Next Article in Journal
Modulating One-Carbon Metabolism with B-Vitamins to Protect the Retinal Barrier and Prevent Retinal Degeneration
Next Article in Special Issue
Dietary (−)-Epigallocatechin Gallate (EGCG): State-of-the-Art Advances in Bioactivities, Bioavailability Enhancement Strategies, and Applications in Nutrition and Health
Previous Article in Journal
Best Practices for the Nutritional Management of Infantile-Onset Lysosomal Acid Lipase Deficiency: A Case-Based Discussion
Previous Article in Special Issue
Aloysia citrodora Polyphenolic Extract: From Anti-Glycative Activity to In Vitro Bioaccessibility and In Silico Studies
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

From Traditional Medicinal Plant to Modern Pharmacotherapy: A Comprehensive Review of the Bioactive Compounds and Health Applications of Eucommia ulmoides

1
School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China
2
Hunan Provincial Key Laboratory for Synthetic Biology of Traditional Chinese Medicine, School of Medical Laboratory Science, Hunan University of Medicine, Huaihua 418000, China
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Nutrients 2026, 18(2), 234; https://doi.org/10.3390/nu18020234
Submission received: 9 December 2025 / Revised: 8 January 2026 / Accepted: 9 January 2026 / Published: 12 January 2026
(This article belongs to the Special Issue Bioactive Ingredients in Plants Related to Human Health—2nd Edition)

Abstract

Eucommia ulmoides Oliv. (E. ulmoides), an endemic tree species in China, holds significant value in traditional Chinese medicine industry and health food. The plant is rich in diverse bioactive compounds, including lignans, iridoids, flavonoids, polysaccharides, E. ulmoides gum, amino acids, and minerals. These components contribute to a range of pharmacological activities such as anti-inflammatory, antioxidant, antihypertensive, immunomodulatory, and bone-protective effects, which support its long-standing traditional use and emerging clinical and adjunctive applications. While current research has predominantly focused on the bark and leaves, other parts, such as flowers, seeds, stems and roots, remain underexplored despite their substantial potential for medicinal and edible applications. Based on the recent literature, this paper systematically summarized the chemical composition, health benefits, and comprehensive utilization of different parts of E. ulmoides (bark, leaves, flowers, and seeds), aiming to provide a theoretical foundation for the high-value utilization of the entire plant resources of E. ulmoides. As a health-promoting plant resource, E. ulmoides has extensive development potential in applications such as health foods, natural medicines, and agricultural inputs. Future research should prioritize elucidating the synergistic mechanisms among different active compounds, advancing technologies for multi-part utilization, and establishing standardized quality evaluation systems to facilitate broader applications in functional foods, pharmaceuticals, and related interdisciplinary fields.

Graphical Abstract

1. Introduction

E. ulmoides, a perennial deciduous tree belonging to the Eucommiaceae family, is a unique species native to China. E. ulmoides is primarily distributed in the central, southwestern, and northwestern regions of China, typically growing in sparse forests at altitudes ranging from 300 to 500 m. With a long history of use in traditional Chinese medicine (TCM), E. ulmoides was first documented over 2000 years ago in Shen Nong Ben Cao Jing (Divine Farmer’s Materia Medica), where it was classified as a superior herb with health benefits such as “tonifying essence, strengthening tendons and bones, enhancing mental fortitude, and promoting longevity with prolonged consumption” [1]. In TCM, the dried bark of E. ulmoides is used as medicine. It is believed to tonify the liver and kidneys, strengthen bones and muscles, and prevent miscarriage. It is primarily indicated for conditions such as liver and kidney deficiency, lower back and knee pain, weakness of tendons and bones, dizziness, blurred vision, gestational bleeding, and restless fetus [2]. In addition to the bark, its flowers, seeds, and leaves are also widely used in medicinal diets and health supplements. Modern pharmacological studies have revealed that E. ulmoides exhibits anticancer and antitumor activities, protects the liver and kidneys, regulates immune and endocrine functions, and promotes bone health [3]. Its major bioactive compounds include lignans, iridoids, flavonoids, and polysaccharides [4].
As an important medicinal plant resource, the traditional utilization of E. ulmoides has long relied on “felling trees or stripping bark,” which often resulted in slow bark regeneration or even tree death after partial harvesting. The rapidly growing market demand led to over exploitation and severe destruction of E. ulmoides resources. In contrast, other parts of the plant, such as leaves, flowers, fruits, and stems, possess strong regenerative capacity and are abundant in supply. Therefore, comprehensive development of E. ulmoides resources is of great significance for the sustainable and healthy growth of the E. ulmoides industry. Studies have shown that non-traditional medicinal parts, including leaves, male flowers, and fruits, are rich in bioactive constituents also found in the bark, such as lignans, iridoids, flavonoids, polysaccharides, and E. ulmoides gum (EUG) [5]. These components demonstrate various functions, including antihypertensive, lipid-lowering, antioxidant, anti-inflammatory, immunomodulatory, and bone maturation-promoting effects [6]. In China, E. ulmoides leaves have been included in the catalog of substances that are both food and medicinal herbs, E. ulmoides male flowers and E. ulmoides seeds oil have been approved as Novel Food Ingredients. These developments signify the expansion of E. ulmoides applications from traditional medicine to broader health-related fields. Based on the recent scientific literature, this review systematically summarizes the advances in the chemistry, pharmacological mechanisms, and innovative food applications of E. ulmoides. This paper aims to provide a theoretical basis for the high-value, comprehensive utilization of E. ulmoides resources within the modern health and food industries (Figure 1). In addition to summarizing the chemical composition and biological activities of different botanical parts, this review attempts to assess the quality and level of available evidence, with particular attention to the translational relevance of preclinical findings to clinical and functional food applications, and highlights potential research gaps that may currently limit clinical validation and industrial utilization.

2. Material and Methods

This review was conducted as a narrative literature review based on a structured search strategy. Relevant studies related to E. ulmoides were retrieved from PubMed, Web of Science, CNKI, Google Scholar, and the Pharmacopoeia of the People’s Republic of China. The literature search covered publications from January 1995 to June 2025 using the keywords “Eucommia ulmoides”, “botany”, “traditional uses”, “chemical constituents”, “bioactive compounds”, “pharmacological activities”, “health functions”, and “comprehensive utilization”, alone or in combination. Original research articles and authoritative reviews published in peer-reviewed journals in English or Chinese that reported on the chemical composition, pharmacological effects, or health-related applications of E. ulmoides and its different botanical parts were included, whereas duplicate publications, studies lacking clear experimental design or outcome description, and non-scientific materials such as conference abstracts or editorials were excluded. Retrieved records were screened based on titles and abstracts, followed by full-text evaluation, and the eligible literature was qualitatively analyzed and synthesized to provide an integrated overview of the chemical basis, pharmacological mechanisms, and utilization potential of E. ulmoides.

3. Compositional Basis of E. ulmoides Resources

E.ulmoides contained diverse phytochemicals including lignans, iridoids, phenylpropanoids, flavonoids, terpenoids, steroids, polysaccharides, amino acids, vitamins, minerals, and substantial EUG, with compositional distribution across botanical parts illustrated in Figure 2 [4]. Traditional analytical efforts predominantly focused on the medicinal bark. However, subsequent investigations have identified rich phytochemical profiles in leaves, flowers, seeds and stems. Iridoids, phenolics, and flavonoids constitute major constituents in leaves, while male flowers are primarily characterized by flavonoid components. The highest lignan and iridoid concentrations were detected in the bark, whereas leaves exhibit peak levels of flavonoids and chlorogenic acid. EUG content is maximal in seeds. Iridoid, lignan, and phenylpropanoid concentrations correlate with plant parts, while flavonoid content associates with tree age [7]. At the molecular level, we systematically summarize how these compounds exert their pharmacological activities, offering a scientific basis for future drug development and clinical applications.

3.1. Lignans

Lignans, natural products derived from oxidative polymerization of phenylpropanoids, exhibit pharmacological properties including anti-osteoporotic [8], blood metabolism-regulating [9], and antihypertensive effects [10,11]. Fifty-two lignan compounds have been identified in E. ulmoides, primarily categorized as bisepoxylignans, monoepoxylignans, neolignans, and cyclolignans [12]. In the quality control of Eucommia ulmoides bark, pinoresinol diglucoside, which is the active constituent responsible for antihypertensive effects, is specified in the Chinese Pharmacopoeia (2020 edition) as a quality control marker with a required minimum content of 0.10%. The highest lignan concentration was detected in the bark, with lower levels present in fruits and leaves. As the most extensively studied phytochemicals in E. ulmoides with well-characterized structures, lignans underlie its antioxidant, hypotensive, and immunomodulatory activities (Table 1 and Figure 3) [13,14]. However, most of these activities have been demonstrated primarily in cellular or animal models, and direct clinical evidence supporting lignans as independent therapeutic agents remains limited. Therefore, while lignans represent important bioactive markers for quality control, their contribution to clinical efficacy likely depends on multi-component interactions rather than single-compound effects.

3.2. Iridoids

Iridoids are acetal derivatives of iridodial, classified as monoterpenoids characterized by an iridoid alcohol backbone typically stabilized through glycosylation to form iridoid glycosides, featuring hemiactal and cyclopentane ring structures [4,20]. The antitumor, antidiabetic (including complication-alleviating), antiarrhythmic, antispasmodic, immunostimulatory, hepatoprotective, and anti-inflammatory properties of E. ulmoides are closely associated with its iridoid constituents. The bark and leaves contain abundant iridoids (~5.07 mg/g) [21], primarily genipin, geniposide, geniposidic acid, and aucubin (Table 2 and Figure 4).

3.3. Phenylpropanoids

Phenylpropanoids in E. ulmoides-precursors to lignan biosynthesis-included caffeic acid, coniferyl alcohol, guaiacylglycerol, coniferin, syringin, chlorogenic acid, methyl chlorogenate, vanillic acid, and coumaroyl glycosides, distributed in the bark, leaves, and rhizomes. Chlorogenic acid is a critical quality control marker for E. ulmoides leaves, with content specified to exceed 0.08% in the Chinese Pharmacopoeia [2]. These compounds exhibited antihypertensive, hypolipidemic, immunostimulatory, antibacterial, and anticancer activities. Chlorogenic acid has been observed to reduce blood pressure in spontaneously hypertensive rats (Table 3 and Figure 5) [24]. Nevertheless, these findings are derived from animal models, and their relevance to human blood pressure regulation requires further clinical validation.

3.4. Flavonoids

Flavonoids are compounds formed by two phenolic hydroxyl-bearing benzene rings linked via a central three-carbon chain, predominantly constituting derivatives of chromone. As one of the primary active constituents in E. ulmoides, flavonoids were primarily distributed in male flowers and leaves. Key flavonoid components included quercetin, rutin, kaempferol, astragalin, and hyperoside [28,29], which exhibited antioxidant, cardiovascular-regulatory, immunoenhancing, antibacterial, expectorant, and antitussive properties (Table 4 and Figure 6) [30,31].

3.5. EUG

EUG constitutes a renewable natural rubber resource, primarily composed of a high polymer of trans-isoprene. Its molecular structure represents an isomer of natural rubber (Figure 7). As China’s most promising alternative and supplemental natural rubber resource, the development of the EUG industry not only addresses domestic the development of the EUG industry, but also establishes a new global rubber industry paradigm centered on China’s innovative EUG products. Owing to its combination of low yield strength, rigidity, and toughness, EUG is suitable for manufacturing orthopedic fixation splints [33]. Concurrently, shape-memory materials based on EUG represent a research focus in this field [34].
Studies indicated that EUG serves both as a natural rubber supplement and as a synergist for enhancing composite properties. For instance, EUG/natural rubber composites with optimized ratios could modulate stress–strain curve behavior, improved application characteristics, and exhibited dual rubber–plastic properties, yielding superior functional materials with broader utility [35]. Elasticity improvement was achieved by Yan Ruifang through pervulcanization, creating novel polymeric materials with rubber–plastic duality [36]. High-performance EMI shielding biocomposites can be fabricated using crystalline EUG as the matrix and CNT/GNP hybrids as conductive fillers, demonstrating attractive mechanical properties and high thermal stability [37]. Recent research reveals that composite films prepared from lignin and EUG exhibit exceptional UV-shielding capacity, enhanced thermal stability, improved mechanical properties, and superior aging resistance, indicating potential applications in sustainable packaging and agricultural coatings [38]. Although EUG itself does not function as a pharmacologically active compound, its unique physicochemical properties expand the application scope of E. ulmoides beyond bioactivity-driven uses toward biomedical materials and health-related technologies.

3.6. Steroids and Other Terpenoids

Steroids exhibit diverse structures and extensive applications in pharmaceuticals. Common biologically active steroids include cholesterol, bile acids, sex hormones, vitamin D, and certain antibiotics. They possess anti-inflammatory, antitoxic, antiallergic, and antishock properties, serving as critical adjunct therapies for collagen diseases, anaphylactic shock, Addison’s disease, breast cancer, and prostate cancer (Table 5 and Figure 8) [39].
The terpenoid composition in E. ulmoides is complex, encompassing not only the primary active iridoids but also significant quantities of other terpenoids such as triterpenes. Triterpenes constitute a class of terpenoids polymerized from six isoprene units, featuring a fundamental skeleton of 30 carbon atoms. They existed in plants either in free form or as glycosides/esters, demonstrating diverse biochemical activities.

3.7. Others

Additional components in E. ulmoides include polysaccharides, amino acids, vitamins, and minerals. Anticarcinogenic effects of E. ulmoides polysaccharides have been demonstrated through scavenging nitrite (NO2), a precursor of N-nitrosamine synthesis [41]. Exercise-induced fatigue in mice could be alleviated by these polysaccharides via regulation of glucose metabolism and protein-sparing effects [42]. An antifungal protein isolated from the bark has been shown to effectively inhibit fungal growth, exhibiting significant application potential in pharmaceuticals, food safety, and environmental protection.
In conclusion, the chemical constituents of E. ulmoides are diverse, mainly consisting of lignans, iridoids, flavonoids, and other compounds. These constituents show a broad range of pharmacological activities, including antioxidant, anti-inflammatory, Liver and kidney protection, cardiovascular protective, neuroprotective, and anti-fatigue effects. Overall, these findings support the medicinal value of E. ulmoides.

4. Research on Chemical Composition and Pharmacological Functions of E. ulmoides Botanical Parts

Traditional utilization of E. ulmoides primarily focused on the medicinal use of its bark, which remains the predominant resource in TCM clinical practice. With advancing research and industrial technology, the value of other botanical parts—including leaves, male flowers, fruits, and stems—has gained increasing attention. Consequently, the whole-plant resources of E. ulmoides have entered practical applications (Figure 9).

4.1. E. ulmoides Bark

4.1.1. Chemical Composition of E. ulmoides Bark

Studies revealed similar chemical profiles across E. ulmoides plant parts, though with quantitative variations [4]. Key bioactive constituents in the bark encompass lignans, iridoids, phenylpropanoids, flavonoids, and polysaccharides [5], supplemented by EUG, amino acids, antifungal proteins, and trace minerals (e.g., Ca, Fe). The bark contains all characteristic compound classes of E. ulmoides, with lignans and EUG being predominant. As the principal component of E. ulmoides resources, the bark represents the most extensively utilized segment in current resource development.

4.1.2. Pharmacology and Health Functions of E. ulmoides Bark

E. ulmoides is a prized traditional Chinese medicinal herb with a documented history dating back to the Shen Nong Ben Cao Jing from the Eastern Han Dynasty. As stipulated by the pharmacopoeia of the People’s Republic of China [2], the official medicinal part is the bark. Pharmacological actions of E. ulmoides bark primarily include antihypertensive [43], hepatoprotective [44], anti-inflammatory, anti-osteoporotic, neuroprotective, and antioxidant effects [4]. The antifungal protein isolated from the bark by Liu et al. [45] effectively inhibited fungal growth, indicating significant application potential in pharmaceuticals, food safety, and environmental protection. Recent animal studies have revealed potential efficacy against postpartum depression through suppression of hypothalamic–pituitary–adrenal axis hyperactivation, downregulation of corticotropin-releasing factor receptor 2, inhibition of voltage-dependent anion channel 1, and reduced neuronal apoptosis [46]. Neuroprotective effects observed in experimental models against optic neuropathy are exerted via AMPK signaling activation that mitigates oxidative stress [47]. In KGN cell lines used pregnenolone as substrate, iridoids were investigated for progesterone, testosterone, and estradiol modulation by Zuo et al. [48]. Elevated genipin concentrations significantly upregulated the expression of 3β-hydroxysteroid dehydrogenase, CYP17A1, and 17β-hydroxysteroid dehydrogenase, thereby stimulating testosterone and estradiol synthesis. Renal oxidative stress in diabetic nephropathy mice was alleviated by E. ulmoides flavonoids through mediation of the Nrf2/HO-1 pathway, thereby reducing fasting blood glucose and improving renal function [49]. Monomers such as quercetin, rutin, and hyperoside have been shown to promote osteogenic differentiation [50]. Astragalin and baicalein significantly stimulate MC3T3-E1 Subclone 14 osteoblast proliferation and maturation, counteracting osteoporosis-induced bone loss [51]. Additionally, quercetin exerts antithrombotic and antihypertensive effects through inhibition of platelet lipoxygenase and cyclooxygenase enzymes [52]. Anti-inflammatory effects were demonstrated by Tang et al. [53] through inhibition of NO release in lipopolysaccharide-induced RAW264.7 cells, thereby alleviating joint inflammation and bone destruction in collagen-induced arthritis rats. Osteoclastogenesis inhibition and bone protection were achieved through activation of the β-catenin signaling pathway, effectively ameliorating postmenopausal osteoporosis [54] (Figure 10). Their natural origin and low toxicity provide a valuable direction for developing new drugs to regulate bone metabolism, especially in an aging society, which has significant clinical relevance. Overall, pharmacological evidence for E. ulmoides bark is relatively robust at the preclinical level, whereas clinical validation relies largely on traditional usage and compound formulations rather than standardized monotherapies.
Widely utilized in health foods as extract ingredients, According to the National Medical Products Administration (NMPA) (excluding leaf-based products), as of June 2025, a total of 250 registered health food products using E. ulmoides bark as the raw material have been documented. The claimed health benefits of these products include alleviation of physical fatigue, enhancement of immune function, assistance in lowering blood pressure and blood lipid levels, increase in bone mineral density, improvement of sleep quality, and protection against chemical liver injury. Specific data are presented in Figure 11.

4.1.3. Comprehensive Utilization of the Bark

E. ulmoides bark served as an additive in animal feeds to enhance product quality or prevent specific diseases. Incorporation into fish feed could improve growth performance, elevate muscle collagen content, and enhance fish quality [55,56]. Supplementation with 5% bark powder in poultry diets boosts laying performance, augments antioxidant capacity, and modulates gut microbiota in hens. Research demonstrated that incorporating E. ulmoides into feed inhibits aspergillus flavus growth, spore germination, and toxin synthesis by compromising cell wall integrity, reducing energy metabolism, and modulating toxin synthesis gene expression, thereby effectively mitigating aflatoxin contamination in feed [57].
Advancement in clean energy technologies have expanded industrial applications. Yang [58] utilized post-extraction bark residues to synthesize biomass-derived porous carbon via carbonization and activation processes. This material demonstrated superior electrochemical performance as a lithium–sulfur battery cathode. Within high-value utilization strategies, EUG constitutes a critical component. Lei compared extraction techniques [59], establishing that subcritical ultrasound-assisted extraction outperforms conventional methods, enabling scalable EUG production while advancing green and sustainable resource utilization. Novel wound dressings fabricated from E. ulmoides oligomeric gum and carboxymethyl chitosan significantly reduced infection incidence by establishing optimal sterile environments, thereby mitigating risks of wound deterioration and infection-related complications [60]. Despite these developments, non-pharmaceutical applications remain limited. Current use as a plant-based feed additive fails to achieve high-value utilization. Future research should intensify exploration of multifunctional applications to maximize economic potential.

4.2. E. ulmoides Leaves

4.2.1. Chemical Composition of the Leaves

The chemical composition of E. ulmoides leaves resembles that of the bark, though each possesses unique constituents with quantitative and qualitative variations in shared compounds. Geniposidic acid, geniposide, and pinoresinol diglucoside are more abundant in the bark, whereas chlorogenic acid predominates in leaves. Studies indicated chlorogenic acid exerts antibacterial effects and modulates blood lipid/glucose levels, suggesting leaves substitution for bark in disease management due to its higher yield and accessibility [61]. Additionally, leaves serve as the primary reservoir for micronutrients including polysaccharides, amino acids, proteins, peptides, vitamins, and minerals.

4.2.2. Pharmacological and Health Functions of the Leaves

According to the Chinese Pharmacopoeia [2], E. ulmoides leaves are mildly pungent and warm, acting on the liver and kidney meridians to tonify these organs and strengthen bones/tendons. The leaves have been shown to possess similar compositions and pharmacological activities to the bark [62], primarily including antihypertensive, hypoglycemic, hypolipidemic, anti-fatigue, antioxidant, and antitumor effects. Endothelial dysfunction is prevented both in vivo and in vitro through modulation of the Nrf2/HO-1 signaling pathway [63]. Significant neuroprotection is also achieved by enhanced expression of HO-1, NAD(P)H quinone oxidoreductase 1, and catalase proteins, along with elevated superoxide dismutase and glutathione peroxidase activities through regulation of the PI3K/AKT/GSK-3β/Nrf2 axis [64]. Thirteen anti-neuroinflammatory compounds were isolated from E. ulmoides by Han et al. [65], with ursane-type C29 triterpenoid significantly suppressed proinflammatory mediators while down regulated inducible nitric oxide synthase and cyclooxygenase-2 expression, indicating therapeutic potential for neurodegenerative diseases. β-sitosterol extracted from leaves by Zeng et al. [66] stimulated OPG mRNA expression while suppressing ODF expression, directly promoting osteogenesis.
As a medicinal-food homologous resource, E. ulmoides leaves are widely used in health foods. The NMPA database documents 43 registered health products containing E. ulmoides leaves, collectively demonstrating seven health functions, with 33 products exhibiting a single function and 8 products demonstrating dual functions. (Figure 12) Beyond overlapping benefits with bark-derived products, leaf formulations uniquely provide auxiliary protection against chemical hepatotoxicity Guo et al. [67] revealed potential hepatoprotective mechanisms involving modulation of vitamin A-related pathways (retinoic acid) and antioxidant activity. Zhang [68] established that suppression of TLR-4/NF-κB signaling through reducing HMGB1 secretion and expression mitigates sterile inflammation in hepatic ischemia–reperfusion injury. Aucubin in leaves may confer liver protection by inhibiting mitochondrial damage-mediated apoptotic pathways [69,70], while chlorogenic acid exhibits comparable hepatoprotective efficacy. Total flavonoids and polysaccharides demonstrated protective effects against CCl4-induced acute liver injury and hepatic fibrosis in experimental models [71,72].
Overall, E. ulmoides leaves exhibit notable therapeutic and nutritional value, as evidenced by both traditional medicinal use and modern experimental studies. As a material with dual use as food and medicine, E. ulmoides leaves have been widely incorporated into health products and functional foods, reflecting their practical applicability and favorable safety profile. Collectively, current findings highlight the versatility of E. ulmoides leaves and emphasize their relevance for further exploration in disease prevention, health promotion, and functional food development.

4.2.3. Comprehensive Utilization of the Leaves

Currently, E. ulmoides leaves have been developed into health food products including E. ulmoides tea [73], vinegar [74], wine, and jelly, along with daily necessities like toothpaste. Renn et al. [75] innovatively incorporated leaves as functional additives into glutinous rice (Semen Oryzae Glutinosae) fermentation, developing sweet rice wine with potential health benefits including blood glucose reduction, blood pressure regulation, and lipid metabolism modulation. E. ulmoides leaves-derived vinegar has been proved to enhance overall antioxidant capacity [76]. Leaf extracts are widely utilized as phytogenic feed additives in aquatic, poultry, and livestock diets (studies indicated that dietary supplementation with E. ulmoides leaves or extracts increases unsaturated fatty acid content in muscle tissues, and optimizes egg quality in laying poultry by elevating egg white protein and yolk α-linolenic acid while reducing cholesterol and crude fat content) [77]. When added to fish feed, E. ulmoides leaves reduce lipid deposition, elevate muscle collagen content, and improve sensory quality [55,78]. while enhancing meat quality through promoted protein synthesis [79]. Additionally, supplementation reduced livestock disease susceptibility, potentially via immunomodulatory mechanisms. The flavonoid components improved growth performance and intestinal morphology in weaned piglets, reduced coliform colonization and diarrhea incidence, suggesting potential as antibiotic growth promoter alternatives [80]. Jelly developed by Li Zhiying [81] protected against acute alcohol-induced organ damage in mice, while toothpaste formulations showed antibacterial, anti-inflammatory, and analgesic effects against oral diseases [82]. Despite these advances, food and cosmetic applications remain underexplored. Future efforts should expand innovative utilization in these sectors to maximize resource value and economic returns.

4.3. Male Flowers

4.3.1. Chemical Composition

E. ulmoides is a dioecious plant, with male flowers containing diverse nutritional and functional components including lignans, phenylpropanoids, iridoids, flavonoids, amino acids, polysaccharides, EUG, vitamins, and minerals [83]. Comparative analysis with bark and leaves reveals significant compositional differences in chlorogenic acid, cryptochlorogenic acid, geniposidic acid, quercetin, aucubin, rutin, geniposide, and pinoresinol diglucoside, indicating distinct phytochemical profiles across plant parts [84].

4.3.2. Pharmacological and Health Functions of Male Flowers

E. ulmoides male flowers represent a precious medicinal resource with longstanding therapeutic value. Current pharmacological evidence for male flowers is primarily derived from animal models and in vitro studies. Flavonoids and polysaccharides have been demonstrated by Sun Lanping et al. to confer antioxidant properties [30], while pharmacological functions encompassed sedation, hypnotic effects, anti-aging, anti-inflammatory, analgesic, antibacterial, and immunomodulatory activities. Chen Xiaojun [85] found that high-dose aqueous extracts of male flowers show superior efficacy in anti-inflammatory, analgesic, antibacterial, and immunomodulatory activities compared to bark or leaf extracts. Guo Yangjing [86] reported significant reduction in malondialdehyde levels alongside enhanced superoxide dismutase activity and total antioxidant capacity in murine skin tissues, indicating anti-aging effects. Iridoids further increased collagen fiber content and synthesis, synergizing with flavonoids to exert potent anti-photoaging activity. Wang Jianying [87] identified mechanisms involving suppression of Th2 cytokines, restoration of Th1/Th2 balance, downregulation of Th17 cells, inhibition of inflammatory chemotaxis and matrix metalloproteinase activity, and reduced IgE production—collectively alleviating airway inflammation and improving pulmonary pathology. Additionally, components such as rutin and geniposidic acid modulated the CYP11A1 and 17β-HSD signaling pathways to regulate testosterone secretion, conferring anti-fatigue effects. Additionally, four compounds were found to markedly inhibit proliferation of rat fibroblast-like synoviocytes, demonstrating anti-arthritic activity [88].
In summary, E. ulmoides male flowers exhibit a broad spectrum of bioactivities, and their multifaceted pharmacological effects suggest considerable potential as a valuable medicinal resource. Nevertheless, the paucity of well-designed clinical studies precludes definitive conclusions regarding their efficacy and safety in humans, highlighting the need for further translational research and rigorous clinical investigations to support their rational development and practical application.

4.3.3. Comprehensive Utilization of Male Flowers

According to Announcement No. 6 (2014) of the National Health Commission of China, E. ulmoides male flowers were approved as a novel food ingredient. Their richness in flavonoids, essential amino acids, vitamin C, and trace mineral elements enables broad applications in meal replacements, tea beverages, and medicinal pollens. Zhong Xueting et al. demonstrated that meal replacement powders supplemented with male flowers exhibit lower glycemic index, enhancing suitability for obese individuals and those with glucose metabolism disorders. As of July 2025, 27 invention patents for E. ulmoides male flowers tea have been granted. Han Weijuan [89] and Du Hongyan [90] developed formulations containing abundant flavonoids with potent Fe2+/Cu2+ chelating capacity and significant antioxidant activity. Additionally, these teas demonstrate efficacy in preventing hyperlipidemia [91], counteracting hypertension [92], and conferring hepatoprotection [93]. Noodles incorporating male flowers pollen retained antioxidant, antibacterial, and anti-inflammatory properties while exhibiting a pleasing color and fragrance [94].

4.4. Seeds

4.4.1. Chemical Composition

E. ulmoides seeds, termed “winged fruits” due to their insect-wing-like appearance, consist of kernels and pericarps. Kernels are rich in unsaturated fatty acids, proteins, amino acids, polysaccharides, vitamins, and bioactive aucubin [95]. Pericarps primarily contain cellulose, lignin, and EUG, with rubber content significantly higher than in bark or leaves. Designated as a novel food ingredient per Announcement No. 12 (2009) of China’s Ministry of Health, E. ulmoides seed oil was standardized for properties, production methods, and fatty acid composition. Its fatty acid profile is dominated by ALA (≥45%), followed by OA (≥13%), LA (≥10%), PA (≥6%), and SA (≥2%) (Table 6).

4.4.2. Pharmacological and Health Functions of the Seeds

Li Sen [96] demonstrated that the seeds glycosides directly target osteoblasts, stimulating proliferation and enhancing activity through elevated alkaline phosphatase levels while promoting collagen synthesis to augment bone strength, thereby exerting anti-osteoporotic effects. Additionally, these glycosides might act directly on the reproductive system, significantly increasing indices of the prostate, seminal vesicles, adrenal glands, and testes to enhance reproductive function. Song Linqi [97] found that E. ulmoides seed glycosides markedly reduce xylene-induced ear edema in mice and carrageenan-induced paw swelling in rats, significantly prolong thermal pain threshold time, decrease acetic acid-induced writhing responses, and extend photo-electric tail-flick latency, indicating substantial anti-inflammatory and analgesic effects. Miao Jingjing [98] established that seed meal extracts enhance activity of peritoneal macrophages and splenic lymphocytes in postmenopausal osteoporosis rats with immune dysfunction, modulating immune surveillance to restore systemic balance.
Rich in unsaturated fatty acids with α-linolenic acid exceeding 60%, E. ulmoides seed oil exhibited lipid-lowering, antiplatelet aggregation, antitumor, immunostimulatory, neurodevelopmental, and cardioprotective properties [99]. Intervention studies indicated amelioration of high-fat diet-induced metabolic dysregulation in mice, improving insulin resistance and reducing hepatic lipid droplets. Potential mechanisms involved modulation of gut microbiota (elevated Bacteroides and Lactobacillus abundance) and bile salt hydrolase-mediated regulation of glycine/taurine-conjugated bile acids to normalize lipid metabolism [100].
In summary, E. ulmoides seeds and their derived products demonstrate diverse and complementary biological activities. Collectively, existing evidence highlights the multifunctional potential of E. ulmoides seeds, supporting their further exploration in the prevention and management of metabolic, skeletal, and immune-related disorders.

4.4.3. Comprehensive Utilization of the Seeds

E. ulmoides seeds are rich in oil, which is approved as a novel food ingredient. Free from poorly digestible substances like erucic acid and behenic acid, the seed oil represents a promising functional resource for food, pharmaceutical, and cosmetic applications [101]. Its utilization in food products continues to expand. The fruit is exceptionally rich in ALA acid (≥60%), a precursor to EPA and DHA [102,103] with demonstrated hypolipidemic, cholesterol-lowering, cardioprotective, developmental, anti-inflammatory, and antioxidant properties [104]. Humans lack ω-3/Δ-15 FAD, making dietary α-linolenic acid essential. Thus, E. ulmoides fruit serves as an oil source supplying EPA/DHA precursors or as raw material for EPA/DHA synthesis (Figure 13), enhancing economic value. Wang Xiaoyuan et al. [105] developed ALA-fortified soft candies with seed oil centers, while Niuhan [106] created functional beverages. Seed oil encapsulated in chitosan nanoparticles demonstrates enhanced antibacterial and antioxidant capacities, revealing deeper medicinal potential [107]. Additionally, it is utilized in health foods and pharmaceuticals targeting hyperlipidemia, aging delay, and hyperglycemia [108,109]. The interest in plant-derived interventions for metabolic disorders, including diabetes, has been extensively discussed in recent reviews, which summarize a wide range of botanicals, bioactive compounds, and underlying mechanisms [110]. Within this context, studies on E. ulmoides seed oil provide preliminary evidence supporting its metabolic regulatory potential.
E. ulmoides seeds contain the highest EUG content among all botanical parts. As a premium renewable rubber resource, its exploitation holds significant importance for national rubber industry development. Xu Zhenchuan [111] utilized crushed seed shells to investigate H2O2 pretreatment effects on extraction yield, demonstrating that H2O2 pretreatment significantly enhanced EUG extraction without altering molecular chain structures or chemical composition. Zhang Yue [112] designed and optimized a focused microwave-assisted extraction process, where cellulose removal via microwave treatment prior to petroleum ether extraction substantially improved efficiency. Current application research on seed-derived EUG remains insufficient. Considering abundant oil co-presence, targeted studies on rubber extraction from post-oil-pressing residues could enhance economic value-added benefits.

4.5. Other Botanical Parts

Current bark harvesting practices for E. ulmoides primarily involve tree felling, generating substantial stem residues that are largely discarded as fuel or timber. However, their use as fuel yields minimal economic return, and their structural instability and processing difficulties limit their applications as timber. The imperative for sustainable utilization of these residues has become an urgent environmental and resource challenge. Recent studies leveraged the high cellulose and lignin content of stems for edible fungus cultivation substrates; for instance, post-bark-harvested trunks can be used to effectively cultivate Auricularia fungi enriched with chlorogenic acid [113]. Discarded branches further served as raw material for nanocellulose production, isolating nanocellulose from E. ulmoides cellulose to establish novel pathways for high-value utilization [114]. Future research should prioritize comprehensive investigations into the cellulose and lignan-rich characteristics of stem resources to maximize their valorization potential (Table 7).

5. Clinical Research on E. ulmoides

In clinical applications, the bark of E. ulmoides is mainly used, followed by the leaves. It has been applied in the treatment of orthopedic diseases such as osteoporosis, osteoarthritis, and lumbar disc herniation, as well as hypertension, neurological disorders, and gynecological conditions including threatened abortion and polycystic ovary syndrome. The clinical efficacy of E. ulmoides is closely related to its traditional functions of tonifying the liver and kidneys and strengthening tendons and bones.

5.1. Orthopedic Diseases

In TCM, bone and joint diseases are generally classified as “Bi syndrome,” which primarily affects the joints and is closely associated with the functions of the liver, spleen, and kidneys. As a representative herb for tonifying the liver and kidneys, E. ulmoides exhibits significant therapeutic effects in the prevention and treatment of bone fractures [115], osteoporosis [116], and lumbar disc herniation [117].
The Quan-Du-Zhong capsule, composed of E. ulmoides as a single herb, improves joint function and prevents femoral head necrosis by increasing bone mineral density and trabecular number [118]. The classic prescription Qing-E Pill, which uses E. ulmoides as the principal ingredient together with Psoralea corylifolia, Juglans regia, and Allium sativum, regulates bone metabolism through its effects of warming and tonifying the liver and kidneys and strengthening muscles and bones. It promotes osteoblast proliferation and exerts estrogen-like activity, thereby improving clinical symptoms and enhancing patients’ quality of life [119]. In addition, E. ulmoides often serves as a key herb for tonifying the liver and kidneys in compound formulations, working synergistically with Taxillus sutchuenensis, Achyranthes bidentata, Dipsacus asper, and Epimedium brevicornu. It is widely used in clinically approved traditional Chinese patent medicines such as Fufang Duzhong Jian’gu Granules, Duzhong Yaotong Pills, Duhuo Jisheng Decoction [120], and Danlu Tongdu Tablets. However, most clinical evidence in this area is derived from observational studies or small-scale interventions, and high-quality randomized controlled trials are still limited.

5.2. Cardiovascular Diseases

In TCM, hypertension is categorized under the patterns of “vertigo” and “headache,” involving primarily the liver, spleen, and kidneys. Clinically, E. ulmoides is often combined with Western medicines to treat hypertension, including mild essential hypertension [121], renal hypertension [122], and pregnancy-induced hypertension [123]. In addition to the Quan-Du-Zhong capsule, E. ulmoides granules, prepared from both the bark and leaves, can improve endothelial function in patients with hypertensive nephropathy, thereby alleviating vascular constriction and protecting renal function [122].
Professor Tong formulated a prescription composed of Achyranthes bidentata, fried E. ulmoides, and Taxillus sutchuenensis for the “kidney-deficiency” type of hypertension, achieving significant antihypertensive efficacy and improvement of symptoms such as insomnia, headache, and irritability [124]. The Duzhong Jiangya tablet, which consists of E. ulmoides, Leonurus japonicus, Prunella vulgaris, Scutellaria baicalensis, and Uncaria rhynchophylla, exerts antihypertensive effects through the regulation of nitric oxide and endothelin balance, enhancement of antioxidant capacity, and promotion of reactive oxygen species clearance [125]. While these studies suggest potential antihypertensive benefits, variability in formulations and outcome measures limits the strength of clinical conclusions.

5.3. Neurological Disorders

In TCM, the treatment of neurological disorders emphasizes nourishing the liver and kidneys, clearing the heart, calming the liver, resolving phlegm, and promoting blood circulation. Tian-Zhi granules, which consist of ingredients such as Gastrodia elata, E. ulmoides, Uncaria rhynchophylla, Taxillus sutchuenensis, Haliotis diversicolor, Leonurus japonicus, Polygonum multiflorum, Sophora japonica flower, and Gardenia jasminoides, are effective in alleviating neuropsychiatric symptoms or liver-yang hyperactivity syndrome in patients with Parkinson’s disease. Additionally, this formula enhances cognitive function and mental well-being, showing synergistic effects when used in combination with donepezil [126]. Current evidence mainly supports adjunctive use, and further controlled trials are needed to confirm efficacy.

5.4. Tocolytic Effects

E. ulmoides exerts tocolytic effects by improving vascular endothelial function, enhancing maternal–fetal immune capacity, supplementing trace elements, strengthening adrenocortical function, and providing antioxidant protection [127]. In clinical practice, it is often combined with spleen-strengthening and stomach-regulating herbs such as Astragalus mongholicus, Dioscorea opposita, and Atractylodes macrocephala. This combination reinforces spleen qi and kidney essence, stabilizes the Chong and Ren meridians, and nourishes the fetus. Current clinical evidence supports the broad therapeutic potential of E. ulmoides in orthopedic. However, definitive conclusions are currently limited by a reliance on observational studies and a scarcity of high-quality randomized controlled trials. Future rigorous research is therefore essential to validate these therapeutic claims and support the translational development of E. ulmoides in modern medicine and functional foods.

6. Prospects for Whole-Plant Resource Utilization

E. ulmoides, as a relict plant and traditional medicinal resource unique to China, contains abundant bioactive compounds in its various tissues with broad pharmacological effects. Extensive studies have confirmed that E. ulmoides extracts and their monomeric compounds exhibit significant efficacy in lowering blood pressure, regulating glucose and lipid metabolism, anti-inflammatory and antioxidant activities, immune modulation, and promoting bone formation, indicating great potential for the prevention and auxiliary intervention of chronic diseases such as hypertension, diabetes, hyperlipidemia, osteoporosis, and inflammation-related disorders. The material basis for these pharmacological activities primarily includes lignans, iridoids, flavonoids, phenylpropanoids, and polysaccharides. Notably, in addition to the aforementioned small-molecule active compounds, various tissues of E. ulmoides are also rich in EUG—a natural polymer that is an isomer of natural rubber, possessing unique dual characteristics of rubber and plastic, shape memory effect, and good biocompatibility. These properties make EUG particularly suitable for applications in biomedical materials, tissue engineering scaffolds, smart responsive materials, and environmentally friendly composites, especially in the context of medical rehabilitation and health-related materials.
Although E. ulmoides bark has historically been the most extensively utilized medicinal resource, its traditional harvesting practice—removal of bark following tree felling—raises concerns regarding resource depletion, limited renewability, and ecological sustainability. Continued reliance on bark therefore poses long-term challenges for both environmental conservation and industrial development. By contrast, renewable plant tissues such as leaves, male flowers, and fruits provide a more sustainable and safer utilization pathway. E. ulmoides leaves can be harvested on an annual basis without compromising plant vitality and are officially recognized as a medicinal–food homologous resource, supporting their safety for long-term dietary consumption. Similarly, the periodic collection of male flowers and fruits does not interfere with normal growth or reproductive processes, further underscoring their suitability for sustainable exploitation and functional food development. It is particularly important to note that E. ulmoides seeds not only contain extremely high levels of EUG in their shells but are also rich in E. ulmoides seed oil—a functional oil characterized by α-linolenic acid as its main fatty acid, which possesses various physiological functions such as regulating lipid metabolism and improving insulin resistance, suggesting promising applications in the dietary intervention of cardiovascular and metabolic diseases, including atherosclerosis and type 2 diabetes. This provides an important direction for the comprehensive development of E. ulmoides resources. Chemical composition studies have shown that E. ulmoides leaves, flowers, fruits, and bark share high similarity in their active component profiles, all containing lignans, iridoid glycosides, flavonoids, chlorogenic acid, and phenolic acids. Consequently, they exhibit common pharmacological activities in areas such as antihypertensive, hypoglycemic, antioxidant, anti-inflammatory, and bone-protective effects, supporting their potential functional application in chronic disease prevention, bone health maintenance, and metabolic health management. Based on the similarity in composition and function, E. ulmoides leaves, male flowers, and seed oil have been approved as new food ingredients or medicinal and edible substances in China, providing a regulatory basis for their application in health products. Various products, such as E. ulmoides tea, fermented E. ulmoides wine, and E. ulmoides seed oil soft capsules, have been developed, demonstrating promising prospects and market potential.
Despite significant advancements in characterizing the chemical profile and pharmacological properties of E. ulmoides, critical knowledge gaps continue to impede its clinical translation and industrial scalability. While extensive in vitro and in vivo studies underscore its multi-target therapeutic potential, robust clinical evidence remains scarce. Furthermore, standardized toxicological evaluations—particularly regarding long-term, high-dose administration and the safety of bark-derived functional foods—are currently insufficient. These limitations underscore the urgent need for rigorous, systematic research to establish a foundation for evidence-based applications.
Future research should prioritize the clinical validation of standardized extracts and primary bioactive compounds, alongside comprehensive safety assessments to define precise dosage regimens. Concurrently, a comparative functional analysis of renewable tissues (leaves, male flowers, and seeds) is essential to evaluate their potential as sustainable substitutes for bark. Elucidating the synergistic multi-component interactions and structure–function relationships will also be pivotal in providing a scientific rationale for their health-promoting effects.
From a sustainability perspective, prioritizing renewable resources is imperative for future development. E. ulmoides leaves, recognized as a “medicinal-food dual-use” resource, offer a safe and sustainable matrix for long-term dietary intervention, while the α-linolenic acid-rich seed oil holds significant promise for cardiovascular and metabolic health. Additionally, advancing green extraction and modification technologies for EUG could catalyze its application in biomedical and eco-friendly materials. Integrating chemical characterization, functional evaluation, and safety assessments will facilitate the transition of E. ulmoides into high-value products, contributing to both public health and the global bio-based economy.
In summary, the high-value development and utilization of the entire E. ulmoides resource should adhere to the principle of sustainable development, prioritizing the in-depth development and industrial application of renewable parts such as leaves, flowers, and fruits, and constructing a diversified industrial chain covering pharmaceuticals, functional foods, cosmetics, feed, and bio-based materials. By closely linking functional efficacy with disease prevention and health promotion needs, the utilization of E. ulmoides bark in the health product sector must be cautiously advanced based on scientific safety evaluations, while resource-saving and environmentally friendly harvesting and processing models should be explored. Through the synergistic advancement of compositional research, technological innovation, and industrial chain integration, E. ulmoides resources are expected to become an important component of the regional bioeconomy, achieving harmony among ecological, economic, and social benefits.

Author Contributions

W.X. and Y.X.: writing—original draft preparation, visualization, investigation. P.X., H.Z., X.Z., Y.W., J.J., F.J. and J.Y.: writing—reviewing and editing. Y.Y. and T.Z.: Supervision, Project administration, Methodology, Funding acquisition, Conceptualization. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by Hunan Agriculture Research System (No. HARS-11).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Cui, L. Shen Nong Ben Cao Jing; Tianjin Ancient Books Publishing House: Tianjin, China, 2009. [Google Scholar]
  2. Committee, T.P. Pharmacopoeia of the People’s Republic of China; China Medical Science Press: Beijing, China, 2025. [Google Scholar]
  3. He, X.; Wang, J.; Li, M.; Hao, D.; Yang, Y.; Zhang, C.; He, R.; Tao, R. Eucommia ulmoides Oliv.: Ethnopharmacology, phytochemistry and pharmacology of an important traditional Chinese medicine. J. Ethnopharmacol. 2014, 151, 78–92. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  4. Liu, C.; Guo, F.; Wei, J.; Tang, L.; Yang, H. Research advances in chemical constituents and pharmacological activities of different parts of Eucommia ulmoides. China J. Chin. Mater. 2020, 45, 497–512. [Google Scholar]
  5. Huang, W.; Yao, T.; Ding, L.; Li, W. Chemical constituents from barks of Eucommia ulmoides. Chin. Tradit. Herb. Drugs 2019, 50, 3279–3283. [Google Scholar]
  6. Zhang, R.; Li, Q.; Pei, J.; Dang, R.; Yang, Y.; Wang, C. Overview of the Chemical Components and Pharmacological Effects of Eucommia ulmoides. J. Shaanxi Univ. Chin. Med. 2024, 47, 87–91. [Google Scholar]
  7. Wang, Q.; Zhou, H.; Zhou, X.; Zhang, Q.; Jia, D.; Lu, X.; Xiao, S.; Zhou, J.; Chen, M.; Zhan, Z. Herbal Textual Research on Eucommiae Cortex in Famous Classical Formulas. Chin. J. Exp. Tradit. Med. Formulae 2023, 29, 88–96. [Google Scholar]
  8. Zhang, R.; Pan, Y.; Hu, S.; Kong, X.; Juan, W.; Mei, Q. Effects of total lignans from Eucommia ulmoides barks prevent bone loss in vivo and in vitro. J. Ethnopharmacol. 2014, 155, 104–112. [Google Scholar] [CrossRef] [Scilit]
  9. Luo, L.; Wu, W.; Zhou, Y.; Yan, J.; Yang, G.; Ouyang, D. Antihypertensive effect of Eucommia ulmoides Oliv. extracts in spontaneously hypertensive rats. J. Ethnopharmacol. 2010, 129, 238–243. [Google Scholar] [CrossRef] [Scilit]
  10. Xu, J.; Song, Y.; Ji, H. Vasodilation effect of EUL on rat thoracic artery. China J. Chin. Mater. Med. 2006, 31, 1976–1978. [Google Scholar]
  11. Li, Z.; Gu, J.; Yan, J.; Wang, J.; Huang, W.; Tan, Z.; Zhou, G.; Chen, Y.; Zhou, H.; Ouyang, D. Hypertensive cardiac remodeling effects of lignan extracts from Eucommia ulmoides Oliv. Bark—A famous traditional Chinese medicine. Am. J. Chin. Med. 2013, 41, 801–815. [Google Scholar] [CrossRef] [Scilit]
  12. Gao, H.; Li, Y.; Li, S. Study Advances in Chemical Constituents and Pharmacological Effects of Eucommia ulmoides Oliv. Inf. Tradit. Chin. Med. 2021, 38, 73–81. [Google Scholar]
  13. Chen, J.J. Influence of Eucommia on Growth Performance, Immune Function and Antioxidant Capability in Weaning Piglet. Master’s Thesis, Fujian Agriculture and Forestry University, Fuzhou, China, 2017. [Google Scholar]
  14. Ding, Y.; Guo, Y.; Ren, Y.; Dou, D.; Li, Q. Isolation of flavonoids from male flowers of Eucommia ulmoides and their anti-oxidantive activities. Chin. Tradit. Herb. Drugs 2014, 45, 323–327. [Google Scholar]
  15. Zeng, M.; Long, Y.; Zeng, J.; Yang, M.; Zhou, X.; Zhou, R.; Liu, X. Comparison of chemical constituents in different parts of Eucommiae Cortex. Chin. Tradit. Pat. Med. 2023, 45, 1184–1194. [Google Scholar]
  16. Bao, L.; Sun, Y.; Wang, J.; Li, W.; Liu, J.; Li, T.; Liu, Z. A review of “plant gold” Eucommia ulmoides Oliv.: A medicinal and food homologous plant with economic value and prospect. Heliyon 2024, 10, e24851. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  17. Wang, X.; Wang, J.; Zhu, H.; Ping, Y.; Wang, F.; Wang, Y.; Wang, H. Main chemical components and health care function and application of Eucommia ulmoides. J. Food Saf. Qual. 2021, 12, 2292–2303. [Google Scholar]
  18. Huang, Q.; Tan, J.B.; Zeng, X.C.; Wang, Y.Q.; Zou, Z.X.; Ouyang, D.S. Lignans and phenolic constituents from Eucommia ulmoides Oliver. Nat. Prod. Res. 2021, 35, 3376–3383. [Google Scholar] [CrossRef] [Scilit]
  19. Fan, Y.B.; Zhou, Y.; Liu, D.P.; Zhang, Y.S.; Zhou, C.X. Classified Summary of Main Components in Eucommia ulmoides. Front. Pharm. Sci. 2014, 17, 1756–1760. [Google Scholar]
  20. Zuo, Y.; Zhang, Z.; Wang, Y.; Chen, L.; Liu, R.; Li, Y. Study on Chemical Constituents of Iridoids from Eucommiae Folium. J. Chin. Med. Mater. 2014, 37, 252–254. [Google Scholar]
  21. Zhang, Q.; Gao, Y.; Li, Q.; Lou, F.; Zhao, M. Study on the Extraction of Iridoids from Eucommia ulmoids Leaves. J. Anhui Agric. Sci. 2010, 38, 4051–4052. [Google Scholar]
  22. Takamura, C.; Hirata, T.; Ueda, T.; Ono, M.; Miyashita, H.; Ikeda, T.; Nohara, T. Iridoids from the green leaves of Eucommia ulmoides. J. Nat. Prod. 2007, 70, 1312–1316. [Google Scholar] [CrossRef] [Scilit]
  23. Liu, X. Comparison of Chemical Composition and Contents in Different Parts of Eucommia ulmoides and Its Application in Chinese Patent Medicines. Master’s Thesis, Nanjing University of Chinese Medicine, Nanjing, China, 2022. [Google Scholar]
  24. Li, X.; Liu, T.; Chen, S.; Li, M.; Huang, Y. Optimization of extraction process for chlorogenic acid from Eucommia ulmoides leaves and its hypotensive effect on spontaneously hypertensive rats. Food Sci. 2013, 34, 30–34. [Google Scholar]
  25. Peng, M.; Liu, B.; Yan, P.; Li, C.; Zhang, X.; Zheng, Y.; Song, Y.; Liu, T.; Yang, L.; Miao, M. Review of chemical constituents, pharmacological effects, and quality control status of Eucommiae Cortex and prediction of its Q-markers. China J. Chin. Mater. Med. 2025, 50, 946–958. [Google Scholar]
  26. Feng, H.; Zhou, H.H.; Ouyang, D.S. Chemical constituents and pharmacology of Eucommia ulmoides Oliv. Chin. J. Clin. Pharmacol. Ther. 2015, 20, 713–720. [Google Scholar]
  27. Sun, Y.R.; Dong, J.X.; Wu, S.G. Studies on Chemical Constituents from Eucommia ulmoides Oliv. J. Chin. Med. Mater. 2004, 27, 341–343. [Google Scholar]
  28. Chen, J.; Zhao, Y.Y.; Cui, Y.X.; Cheng, T.M. Studies on Flavonoids from Leave of Eucommia ulmoides Oliv. China J. Chin. Mater. Med. 2000, 25, 28–30. [Google Scholar]
  29. Zhang, K.; Dong, J.; Ma, B.; Gao, J.; Han, X. Studies on the distribution differences of the secondary metabolites in Eucommia ulmoides. Sci. Silvae Sin. 2002, 38, 12–16. [Google Scholar]
  30. Sun, L.; Ma, L.; Zhang, B.; Xu, H. Research progress of flavonoids in Eucommia ulmoides. Sci. Technol. Food Ind. 2009, 30, 359–363. [Google Scholar]
  31. Mu, W.; Chen, Q.; Duan, C.; Zhang, J. Advances in Research on Active Ingredients and Pharmacokinetics of Eucommia ulmoides Oliv. Chin. J. Mod. Appl. Pharm. 2019, 36, 2598–2604. [Google Scholar]
  32. Chai, X.; Wang, Y.; Su, Y.; Bah, A.J.; Hu, L.; Gao, Y.; Gao, X. A rapid ultra performance liquid chromatography-tandem mass spectrometric method for the qualitative and quantitative analysis of ten compounds in Eucommia ulmodies Oliv. J. Pharm. Biomed. Anal. 2012, 57, 52–61. [Google Scholar] [CrossRef] [Scilit]
  33. Zhang, W.; Huang, Z.; Zhao, R.; Liang, H.; Ma, Y.; Shen, Y.; Zhong, H.; Chen, Z.; Zhang, J.; Chen, W. Efficacy of gutta-percha splint on a rabbit fracture model. Chin. J. Tissue Eng. Res. 2023, 27, 1055–1061. [Google Scholar]
  34. Han, Z.Y. Extraction, Modification, and Functional Properties of Eucommia ulmoides Gum. Ph.D. Thesis, East China Normal University, Shanghai, China, 2024. [Google Scholar]
  35. Zhu, H. Research Progress of Eucommia ulmoides Gum. Rubber Sci. Technol. 2020, 18, 605–610. [Google Scholar]
  36. Yan, R. Prospects and Research Progress on Eucommia ulmoides gum. Prog. Chem. 1995, 7, 65–71. [Google Scholar]
  37. Kang, H.; Luo, S.; Du, H.; Han, L.; Li, D.; Li, L.; Fang, Q. Bio-Based Eucommia ulmoides Gum Composites with High Electromagnetic Interference Shielding Performance. Polymers 2022, 14, 970. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  38. Zhao, J.; Tang, M.; Zhang, Q.; Feng, W.; Xu, Q.; Chen, H.; Lu, M.; Chen, C.; Min, D. Enhancing mechanical and anti-aging properties of Eucommia ulmoides rubber UV shielding film through lignin incorporation. Int. J. Biol. Macromol. 2025, 312, 144237. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  39. Wang, H.; Zhou, F.; Wu, Q.; Chen, S. Recent advances in steroid biotransformation. J. Zhejiang Univ. Technol. 2015, 43, 556–561. [Google Scholar]
  40. Huang, T.; Dong, F.; Wu, G.H.; Chen, Y.; Gu, W.; Zhang, J.X. Study on ~1H-NMR fingerprint of the Leaves of Eucommia ulmoides in Guizhou. J. Mt. Agric. Biol. 2015, 34, 92–94. [Google Scholar]
  41. Liu, X.; Wang, Z.; Liang, H.; Zhu, L. Study on the Scavenging Effect of Eucommia to Nitrite. Acta Neuropathol. 2009, 26, 11–12. [Google Scholar]
  42. Wang, Y.; Guo, F.; Xiong, B.; Chi, A. Study of Eucommia ulmoides polysaccharide on improvement in exercise fatigue. Chin. J. Appl. Physiol. 2016, 32, 151–153. [Google Scholar]
  43. Jiang, C.; Xu, J.; Bian, X.; Shen, J.; Kan, J.; Xu, Y. Combination of hypotensive components of Eucommia ulmoides and vasodilator effect. Chin. J. Exp. Tradit. Med. Formulae 2010, 16, 218–220. [Google Scholar]
  44. Fan, G.; Feng, Z.; Peng, C.; Zhang, S.; Duan, Y.; Li, K. Preventive and therapeutic effects of water extract and alcohol extract of Eucommia ulmoides bark on rats with hepatic ischemia-reperfusion injury. Shandong Med. J. 2021, 61, 21–25. [Google Scholar]
  45. Li, B.; Liu, X.; Hu, Z.; Li, Y.; Yang, J. Isolation and characterization of an antifungal protein from the bark of Eucommia ulmoides. Plant Divers. 1994, 16, 385–391. [Google Scholar]
  46. Li, Y.; Chen, W.; Zhang, L.; Wu, Y.; Xu, Y.; Wang, X.; Hou, J.; Yang, L. Regulatory effect mechanism of Eucommia ulmoides on postpartum depression in rats. China Pharm. 2024, 35, 1303–1308. [Google Scholar]
  47. Li, C.; Qiu, G.; Liu, B.; Chen, J.; Fu, H. Neuroprotective effect of lignans extracted from Eucommia ulmoides Oliv. on glaucoma-related neurodegeneration. Neurol. Sci. 2016, 37, 755–762. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  48. Zuo, T.; Song, H. Regulation effects of eucommia iridoids on sex hormone transformation. Chem. Ind. Eng. Prog. 2016, 35, 319–323. [Google Scholar]
  49. Xu, B.; Dai, Y.; Fu, Q.; Liang, T. Effects of Eucommia Flavonoids on Nrf2/HO-1 Oxidative Stress Signaling Pathway in Diabetic Nephropathy Mice. J. Jilin Chin. Med. 2020, 40, 788–791. [Google Scholar]
  50. Du, C. Experiment Research of Eucommia ulmoides Flavonoids Monomersquercetin, Rutin and Hyperin Which Stimulate the SD Ratmesenchymal Stem Cells Osteogenetic Differentiation. Master’s Thesis, Nanchang University, Nanchang, China, 2014. [Google Scholar]
  51. Lan, B.; Liu, T.; Xie, Y.; Wang, A.; Li, Y. Effects of Two Kinds of Eucommia ulmoides Flavonoids on Osteoblast OPG/RANKL and Osteogenic Transcription Factor. Chin. J. Exp. Tradit. Med. Formulae 2014, 20, 180–184. [Google Scholar]
  52. Oh, T.; Do, H.; Jeon, J.; Kim, K. Quercitrin inhibits platelet activation in arterial thrombosis. Phytomedicine 2021, 80, 153363. [Google Scholar] [CrossRef] [Scilit]
  53. Tang, L.; Wang, J.; Tan, D.; Zhang, L.; Yuan, Y. Effects of triterpenoid and iridoid of Eucommia Cortex on collagen-induced arthritis in rats. China J. Chin. Mater. Med. 2022, 47, 5591–5598. [Google Scholar]
  54. Jiang, Y.; Wang, Z.; Wang, R.; Xiang, S.; Jin, Z.; Tong, P.; Lv, S. Study on the Intervention Effect of β-sitosterol in the Postmenopausal Osteoporosis. J. Zhejiang Univ. Chin. Med. 2024, 48, 131–137, 146. [Google Scholar]
  55. Yang, H.; Xu, Z.; Tan, S.; Li, X.Q.; Cheng, Z.; Leng, X. Influences of Dietary Eucommia Bark and Leaf on Growth, Muscle Quality and Collagen Related Genes Expression in Grass Carp (Ctenopharyngodon idellus). Chin. J. Anim. Nutr. 2020, 32, 5827–5838. [Google Scholar]
  56. Luo, X.; Zhang, A.; Yuan, G.; Jiang, H.; Wen, M. Effect of water extract of Eucommia ulmoides Oliver on the expression of MRFs gene in muscle of rainbow trout. Feed Ind. 2019, 40, 10–16. [Google Scholar]
  57. Li, Q.; He, J.; Li, Y.; Tian, X.; Gong, W.; Lan, D. Inhibition of Aspergillus flavus by Eucommia ulmoides Oliv. and Its Beneficial Effects in Animal Husbandry. Feed Ind. 2024, 45, 133–136. [Google Scholar]
  58. Yang, Y.; Yan, Y.; Zhao, Y.; Zhou, Y.; Feng, Z.; Yang, R. Preparation and electrical property of eucommia bark residue-based porous C/S composite. New Chem. Mater. 2022, 50, 141–146. [Google Scholar]
  59. Lei, Y.; Zhang, X.; Gan, Q.; Chen, D.; Li, D.; Chen, S. Comparative Study on Different Extraction and Separation Processes of Gutta-percha. J. Shanxi Agric. Univ. 2022, 68, 49–51. [Google Scholar]
  60. Yang, Y.; Ou, Z.; Wang, Z.; Yang, T.; Zhu, J.; Liu, X. Preparation and characterization of a novel oligomeric gum from Eucommia ulmoides crosslinked with carboxymethyl chitosan antibacterial wound dressing for quick hemostasis. Int. J. Biol. Macromol. 2025, 308, 142652. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  61. Guo, S.; Liu, J.; Li, N.; Ma, F.; Gao, J.; Xue, P.; Dong, Q. Evaluation of the Possibility of Eucommia ulmoides Leaves Replacing its Barks by Fingerprint Combined with Multi-components Quantitive by One Marker Method. J. Chin. Med. 2020, 43, 896–902. [Google Scholar]
  62. Qi, W.; Wang, M.Z. Comparison of chemical composition for Eucommia ulmoides and Eucommia folium. Clin. Res. Pract. 2017, 2, 121–122. [Google Scholar]
  63. Liu, B.; Li, C.; Wang, W.; Song, S.; Liu, X. Lignans Extracted from Eucommia ulmoides Oliv. Protects Against AGEs-Induced Retinal Endothelial Cell Injury. Cell Physiol. Biochem. 2016, 39, 2044–2054. [Google Scholar] [CrossRef] [Scilit]
  64. Han, R.; Yu, Y.; Zhao, K.; Wei, J.; Hui, Y.; Gao, J. Lignans from Eucommia ulmoides Oliver leaves exhibit neuroprotective effects via activation of the PI3K/Akt/GSK-3β/Nrf2 signaling pathways in H2O2-treated PC-12 cells. Phytomedicine 2022, 101, 154124. [Google Scholar] [CrossRef] [Scilit]
  65. Han, R.; Yuan, T.; Yang, Z.; Zhang, Q.; Wang, W.; Lin, L.; Zhu, M.; Gao, J. Ulmoidol, an unusual nortriterpenoid from Eucommia ulmoides Oliv. Leaves prevents neuroinflammation by targeting the PU.1 transcriptional signaling pathway. Bioorg. Chem. 2021, 116, 105345. [Google Scholar] [CrossRef] [Scilit]
  66. Zeng, L.; Xu, X.; Rao, H.; Wang, M.; Cai, X.; Rao, Y. Regulation of β–sitosterol in Duzhongye on Homeostasis of Bone Metabolism. Lishizhen Med. Mater. Medica Res. 2012, 23, 1051–1053. [Google Scholar]
  67. Guo, F.; Tang, X.; Tang, L.; Wei, J.; Xiao, J.; Yang, H. Possible pharmaceutical effect and active components in different parts of Eucommia ulmoides based on network pharmacology. J. Chin. Mater. Med. 2020, 45, 1800–1807. [Google Scholar]
  68. Zhang, S.L. Protective Effect and Mechanism of Aucubin from Eucommia ulmoideson Hepatic Ischemia-Reperfusion Injury in Rats. Master’s Thesis, Zunyi Medical University, Zunyi, China, 2021. [Google Scholar]
  69. Shi, X.; Gao, Y. Protective Effects of Chlorogenic Acid on Liver Injury in Mice. Chin. J. Exp. Tradit. Med. Formulae 2011, 17, 199–202. [Google Scholar]
  70. Xiong, K. The Protective Effect and Potential Mechanism of Chlorogenic Acid from Eucommia ulmoides Oliver on Hepatic Ischemia Reperfusion Injury in Rats. Master’s Thesis, Zunyi Medical University, Zunyi, China, 2018. [Google Scholar]
  71. Jiang, Z.; Yuan, D.; Hu, Q.; Liu, W. Study on the Protective Effect of Total Flavonoids of Eucommia Elmoides on Acute Liver Injury in Mice. Guangzhou Chem. Ind. 2016, 44, 69–70. [Google Scholar]
  72. Zhou, C.; Ai, L.; Wang, M.; Wang, X. Protection of Eucommia ulmoides polysaccharide on liver fibrosis. Chin. Tradit. Herb. Drugs 2011, 42, 324–329. [Google Scholar]
  73. Yang, Q.; Tang, L.; Meng, Y.; Xiao, L.; Xiao, B. Processing Technology of a Compound Fucha Tea. Acta Agric. Boreali-Occident. Sin. 2020, 29, 630–640. [Google Scholar]
  74. Fu, H.; Liu, X.; Jia, J.; Yang, W. Study on the Technological Formula of Eucommia ulmoides Leaf, Red Date, and Goji Berry Composite Beverage. Agric. Prod. Process. 2024, 14, 53–57. [Google Scholar]
  75. Ren, N.; Gong, W.; Zhao, Y.; Zhao, D.G.; Xu, Y. Innovation in sweet rice wine with high antioxidant activity: Eucommia ulmoides leaf sweet rice wine. Front. Nutr. 2022, 9, 1108843. [Google Scholar] [CrossRef] [Scilit]
  76. Jia, C.; Yu, W.; Zhang, B. Manufacture and antibacterial characteristics of Eucommia ulmoides leaves vinegar. Food Sci. Biotechnol. 2020, 29, 657–665. [Google Scholar] [CrossRef] [Scilit]
  77. Lü, G.; He, F.; Qing, J.; Meng, Y.; Du, H.; Zhong, J.; Wang, L. Effect of Eucommia ulmoides leaves powder on production performance and egg quality in Hubei tribute chickens. Feed Res. 2021, 44, 50–54. [Google Scholar]
  78. Tang, Y.; Chen, Y.; Li, P.Q. Current status of Eucommia ulmoides leaves active components and their application in chicken rearing. Anim. Agric. 2015, 1, 33–36. [Google Scholar]
  79. Li, Y.; Jiang, B.; Wen, H.; Wang, J. Active constituents of Eucommia ulmoides leaves and their application in aquaculture. Feed China 2017, 42–44. [Google Scholar] [CrossRef]
  80. Yuan, D.; Wang, J.; Xiao, D.; Li, J.; Liu, Y.; Tan, B.; Yin, Y. Eucommia ulmoides Flavones as Potential Alternatives to Antibiotic Growth Promoters in a Low-Protein Diet Improve Growth Performance and Intestinal Health in Weaning Piglets. Animals 2020, 10, 1998. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  81. Li, Y.Z. Protective Effect of Polysaccharides from Eucommia ulmoides Oliv. Leaves on Mice with Acute Alcoholism and Anti-Alcoholism Jellyproduct Development. Master’s Thesis, NanChang University, Nanchang, China, 2024. [Google Scholar]
  82. Zhang, J.J. Development of Eucommia ulmoides Leaves HealthToothpaste. Master’s Thesis, Henan University, Kaifeng, China, 2020. [Google Scholar]
  83. Du, Q.X. Study on the Diversity of Main Morphological Traits and Active Ingredients Content in Male Flower of Eucommia ulmoides. Master’s Thesis, Chinese Academy of Forestry, Beijing, China, 2017. [Google Scholar]
  84. Yan, Y. Studies on Quality Evaluation of Eucommiae Cortex. Master’s Thesis, Nanjing University of Chinese Medicine, Nanjing, China, 2018. [Google Scholar]
  85. Chen, X.; Wang, F.; Yuan, Y.; Zhang, L.; Li, X.; Jin, S.; He, S.; Wang, J. Comparative study of bark, leaf and male flower of Eucommia on pharmacodynamics. J. Gansu Univ. Chin. Med. 2016, 33, 5–8. [Google Scholar]
  86. Guo, Y.J. Study of Active Ingredients of Eucommia ulmoides Male Flowers Against Skin Photoaging. Master’s Thesis, Henan University, Kaifeng, China, 2014. [Google Scholar]
  87. Wang, J.; Chen, X.; Zhang, L.; Wang, K.; Hou, J.; Fu, S.; Pan, Y.; Yuan, Y. Effects of Alcohol Extracts of Bark and Male Flower of Eucommia ulmoides Oliv. on Airway Allergic Inflammation of Model Mice. Chin. J. Inf. Tradit. Chin. Med. 2018, 25, 42–47. [Google Scholar]
  88. Li, X.; Deng, S.; Li, J.; Gong, S.; Song, T.; Ge, J.; Zhao, Y.; Zhang, J.; Ma, L.; Zheng, Y.; et al. UPLC-MS analysis and network pharmacology-based investigation into the active ingredients and molecular mechanisms of anti-fatigue of male flowers with Eucommia ulmoides Oliv. Fundam. Clin. Pharmacol. 2022, 36, 1083–1098. [Google Scholar] [CrossRef] [Scilit]
  89. Han, W.; Zhang, J.; Du, G.; Sun, P.; Diao, S.; Fu, J.M. Comparative Studies on the Antioxidant Activity of Persimmon Leaf Tea, Eucommia ulmoides Male Flower Tea, Green Tea and Black Tea in vitro. J. Northwest For. Univ. 2017, 32, 144–148. [Google Scholar]
  90. Du, H.; Lou, L.; Fu, J.; Du, L.; Chen, B.; Li, Q. The effect of Eucommia ulmoides male flower tea on the activities of SOD, GSH-Px, and the levels of MDA in D-galactose-induced aging mice model. Chin. Tradit. Pat. Med. 2011, 33, 331–333. [Google Scholar]
  91. Lou, L.; Chen, B.; Du, H.; Fu, J.; Du, L.; Li, Q. Regulation effects of Eucommia ulmoides male flower tea on lipid parameters of mice fed with high fat emul. J. Henan Univ. Med. Sci. 2009, 28, 273–275. [Google Scholar]
  92. Chen, B.; Lou, L.; Du, H.; Fu, J.; Du, L.; Li, Q. Hypnosis effects of Eucommia ulmoides male flower tea on mice. J. Henan Univ. Med. Sci. 2011, 30, 22–23. [Google Scholar]
  93. Lou, L.; Chen, B.; Du, H.; Fu, J.; Du, L.; Li, Q. Protection effects of Eucommia ulmoides male flower tea on carbon tetrachloride induced liver injury in mice. J. Henan Univ. Med. Sci. 2011, 30, 24–26. [Google Scholar]
  94. Hong, R. Study on the Effect of Eucommia ulmoides Maleflower Powder on Dough Characteristics and Dough Product Quality. Master’s Thesis, Chengdu University, Chengdu, China, 2023. [Google Scholar]
  95. Zhang, Y.; Zhou, Q.; Chen, G.; Shen, X.; Hu, J.Y. Research Status and Progress on Comprehensive Development and Utilization of Samara of Eucommia ulmoides Oliver. Chin. Wild Plant Resour. 2015, 34, 53–59. [Google Scholar]
  96. Li, S.; Xie, R.; Sun, W. Experimental study of total glucosides from Eucommia ulmoides seeds against glucocorticoid-induced osteoporosis in mice. Chin. Tradit. Pat. Med. 2010, 32, 205–208. [Google Scholar]
  97. Song, L.; Du, X.; Lin, F.; Xie, R.; Sun, W. Anti-inflammatory and analgesic activity of Eucommiae ulmoides seed total glycoside. Acad. J. Nav. Med. Univ. 2009, 30, 413–415. [Google Scholar] [CrossRef] [Scilit]
  98. Miao, J.J. Immunity Regulation Effect of Eucommia ulmoides Seed-Draff Extract on the Osteoporotic Rats. Master’s Thesis, Northwest University, Xi’an, China, 2015. [Google Scholar]
  99. Wu, Q.; Du, B.; Cai, Y.; Liang, Z.; Lin, Z.; Qiu, G.; Dong, L.; Bao, L. Research developmentof alpha–linolenic acid. Sci. Technol. Food Ind. 2016, 37, 386–390. [Google Scholar]
  100. Wu, Y.; Gao, M.; Li, P.; Xue, K.; Li, Q. Effects of Eucommia ulmoides seed oil on glycolipid metabolism and gut microbiota in KKAy mice with type 2 diabetes mellitus. J. Food Saf. Qual. 2022, 13, 728–736. [Google Scholar]
  101. Han, L.; Hou, Z.; Wen, J.; Wu, Y.; Qian, Y.; Gong, S. Recent Progress on Functional Oils Rich in Alpha-Linoleic Acid and Its Microencapsulation. Food Res. Dev. 2015, 36, 185–189. [Google Scholar]
  102. Kim, K.B.; Nam, Y.A.; Kim, H.S.; Hayes, A.W.; Lee, B.M. alpha-Linolenic acid: Nutraceutical, pharmacological and toxicological evaluation. Food Chem. Toxicol. 2014, 70, 163–178. [Google Scholar] [CrossRef] [Scilit]
  103. Xiao, M.; Ou, Z. Research Progress of the Physiological Function and Mechanism of Two Kinds of Fatty Acid (EPA and DHA) in the Fish Oil of Deep Sea. Food Sci. 2005, 26, 522–526. [Google Scholar]
  104. Chen, Y.; Tang, J.; Gong, X.; Huang, K.; Shan, Q.; Bao, J. Research progress on extraction of fish oil, enrichment of polyunsaturated fatty acids and application progress of EPA and DHA. Food Mach. 2021, 37, 205–210. [Google Scholar]
  105. Wang, X.; Ma, B.; Zong, W. Optimization of process and texture analysis of Eucommia ulmoides seed oil soft sweet. J. Cereals Oilseeds 2021, 34, 131–134. [Google Scholar]
  106. Niu, H. Study on Preparation and Storage Quality of Eucommia ulmoides Seed Oil–Apple Juice Beverage. Master’s Thesis, Zhengzhou University of Light Industry, Zhengzhou, China, 2022. [Google Scholar]
  107. Jiang, X.; Yu, Y.; Ma, S.; Li, L.; Yu, M.; Han, M.; Yuan, Z.; Zhang, J. Chitosan nanoparticles loaded with Eucommia ulmoides seed essential oil: Preparation, characterization, antioxidant and antibacterial properties. Int. J. Biol. Macromol. 2024, 257, 128820. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  108. Wang, H.; Wei, C.; Su, P.; Yang, J.; Qiao, B. Effect of Eucommia ulmoides Oliver Oil Soft Capsules on Regulating the Level of Blood Lipid in Model Rats. China Pharm. 2019, 28, 20–22. [Google Scholar]
  109. Yuan, D.; Yuan, Z.; Li, Z. Anti-aging Effect of Eucommia Fruit Mea on D-Galactose-induced Mouse Aging Model. Lishizhen Med. Mater. Med. Res. 2012, 23, 2968–2970. [Google Scholar]
  110. Chahrour, J.A.; Abdel Baki, Z.; El Badan, D.; Nasser, G.; Maresca, M.; Hijazi, A. Herbal Medicines in the Management of Diabetes Mellitus: Plants, Bioactive Compounds, and Mechanisms of Action. Biomolecules 2025, 15, 1674. [Google Scholar] [CrossRef] [Scilit]
  111. Xu, Z.C. Effect of Chemical Pretreatment of Eucommia ulmoides Seed Shell on Extraction Efficiency and Properties of Eucommia ulmoides Gum. Master’s Thesis, Shenyang University of Chemical Technology, Shengyang, China, 2020. [Google Scholar]
  112. Zhang, Y.; Wang, S.; Li, H.; Xiang, C. Focused Microwave-Assisted Removal of Cellulose Coupled with Solvent Extraction of Gutta-percha from Eucommia ulmodies Seeds Shell. Nat. Prod. Res. Dev. 2016, 28, 904–909. [Google Scholar]
  113. Du, H. “Functional E. ulmoides fungus” won the national invention patent. Forest Sci. Tech. 2013, 19. [Google Scholar] [CrossRef]
  114. Zhao, W.; Geng, L.; Zhao, F.; Hou, M.L.; Su, T.Y.; Guo, W.T.; Zhang, Q. Preparation and characterization of nanocellulose from Eucommia ulmoides twigs. Appl. Chem. Ind. 2024, 53, 2057–2060. [Google Scholar]
  115. Wang, P.; Sun, Q.M. Clinical Observation of Quanduzhong Capsule for 60 Cases with Postoperative Osteoporotic Lower Limb Fracture. Liaoning J. Tradit. Chin. Med. 2022, 49, 135–137. [Google Scholar]
  116. Sun, C.F.; Wang, B.; Ju, X.F. Clinical Effect of Compound Duzhong Jiangu Granules in the Treatment of Type II Primary Osteoporosis. Chin. Foreign Med. Res. 2022, 20, 132–134. [Google Scholar]
  117. Wang, G.H.; Zhao, J.R.; Zhao, N. Clinical Observation of Quan Duzhong Capsule Combined with Acupuncture and Moxibustion in the Treatment of Knee Osteoarthritis. J. Tradit. Chin. Med. 2019, 28, 522–524. [Google Scholar]
  118. Du, G.Q.; Liu, L.Y. Clinical study on the combined treatment of Whole Eucommia Capsules and cannulated screw fixation for Garden III–IV femoral neck fractures. Guangdong Med. J. 2024, 45, 1028–1032. [Google Scholar]
  119. Wang, X.Y.; Chang, S.X.; Li, G.W.; Zhou, Z.M.; Yuan, J.; Wang, L.; Song, Y.Y.; Miu, Y. Experimental study on the effect of Qing E Formula on postmenopausal osteoporosis in rats induced by ovariectomy. Chin. J. Osteoporosis 2017, 23, 197–202. [Google Scholar]
  120. Lai, J.Y.; Fu, Y.F.; Tan, H.S.; Feng, H.L.; Lan, Z.M.; Li, G.; Jiang, Y.; He, S.H. Clinical Efficacy of Modified Duhuo Jisheng Decoction in Treating Lumbar Disc Herniation Complicated with Sarcopenia Based on Infrared Thermography. Chin. J. Tradit. Med. Traumatol. Orthop. 2025, 33, 62–67. [Google Scholar]
  121. Zhang, G.X.; Song, X.; Guo, L.L.; Zhao, J.W. Clinical effect of Quan Duzhong capsule in the treatment of newly onset mild hypertension. Chin. J. Ration. Drug Use 2022, 15, 54–56. [Google Scholar]
  122. Chen, Y.W.; Chen, M.L.; Wang, X.Q.; Zhang, M.X. Effects of Duzhong Granules on vascular endothelial function, blood pressure and microalbuminuria level in patients with hypertensive nephropathy. Guangxi Med. J. 2021, 43, 1932–1934. [Google Scholar]
  123. Yang, H.L.; Yang, J.J.; Zhai, G.R.; Song, Y.L. Clinical observation of Duzhong Granules combined with labetalol in treatment of hypertensive disorder complicating pregnancy. Drugs Clin. 2021, 36, 279–282. [Google Scholar]
  124. Zhang, C.Q.; Yao, C.K. Achyranthes, Eucommia and Mulberry Parasitic in the Treatment of IKidney Deficiency Hypertension—Three Prescription by Professor TONG Xiaolin. Jilin J. Chin. Med. 2019, 39, 1576–1578. [Google Scholar]
  125. Zhao, X.M.; Zhong, X.T.; Sun, X.M.; Zhang, Z.W. Pharmacodynamic Study of Different Extracts of Eucommia ulmoides. Chin. J. Exp. Tradit. Med. Formulae 2009, 15, 75–77. [Google Scholar]
  126. Chai, S.W.; Ma, J.; Zhuang, P.W.; Zhang, Y.J.; Guo, H. Research progress on pharmacological effects of effective components of Eucommia ulmoides on Parkinson’s disease. Drug Eval. Res. 2019, 42, 1003–1009. [Google Scholar]
  127. Xiao, L.M.; Wang, C.R.; Feng, X.; Yao, W.H.; Yu, D.R.; Tang, H.B. Research progress of miscarriage prevention of Eucommia ulmoides Oliv. Glob. Tradit. Chin. Med. 2020, 13, 2189–2192. [Google Scholar]
Figure 1. The bark (a), the seeds (b), the leaves (c), the flowers (d) and the morphology of plants (e) of E. ulmoides.
Figure 1. The bark (a), the seeds (b), the leaves (c), the flowers (d) and the morphology of plants (e) of E. ulmoides.
Nutrients 18 00234 g001
Figure 2. Distribution of components and compounds of resources from different parts of E. ulmoides.
Figure 2. Distribution of components and compounds of resources from different parts of E. ulmoides.
Nutrients 18 00234 g002
Figure 3. Chemical structures of lignans compounds in E. ulmoides.
Figure 3. Chemical structures of lignans compounds in E. ulmoides.
Nutrients 18 00234 g003
Figure 4. Chemical structures of Iridoids compounds in E. ulmoides.
Figure 4. Chemical structures of Iridoids compounds in E. ulmoides.
Nutrients 18 00234 g004
Figure 5. Chemical structures of Phenylpropanoids compounds in E. ulmoides.
Figure 5. Chemical structures of Phenylpropanoids compounds in E. ulmoides.
Nutrients 18 00234 g005
Figure 6. Chemical structures of Flavonoids compounds in E. ulmoides.
Figure 6. Chemical structures of Flavonoids compounds in E. ulmoides.
Nutrients 18 00234 g006
Figure 7. Structure of Gutta-percha and natural rubber.
Figure 7. Structure of Gutta-percha and natural rubber.
Nutrients 18 00234 g007
Figure 8. Chemical structures of Terpenoids compounds in E. ulmoide.
Figure 8. Chemical structures of Terpenoids compounds in E. ulmoide.
Nutrients 18 00234 g008
Figure 9. E. ulmoides pharmacological mechanism of action.
Figure 9. E. ulmoides pharmacological mechanism of action.
Nutrients 18 00234 g009
Figure 10. Antiosteoporosis mechanisms of E. ulmoides.
Figure 10. Antiosteoporosis mechanisms of E. ulmoides.
Nutrients 18 00234 g010
Figure 11. Functional distribution of health food related to E. ulmoides bark.
Figure 11. Functional distribution of health food related to E. ulmoides bark.
Nutrients 18 00234 g011
Figure 12. Functional distribution of health food related to E. ulmoides leaves.
Figure 12. Functional distribution of health food related to E. ulmoides leaves.
Nutrients 18 00234 g012
Figure 13. Synthesis of EPA and DHA from ALA metabolism.
Figure 13. Synthesis of EPA and DHA from ALA metabolism.
Nutrients 18 00234 g013
Table 1. Lignans in E. ulmoides.
Table 1. Lignans in E. ulmoides.
NO.CompoundFormulaPartReference
1pinoresinol diglucosideC32H42O16leaf/bark/seeds[15]
2(+)-syringaresinolC22H26O8leaf/bark/seeds[15]
3guaiacylglycerol-8-O-4′- (sinapyl aldehyde) etherC20H24O7bark[15]
4pruninC20H24O7bark[15]
5syringaresinol-di-O-glucosideC34H46O18bark[15]
6(+)-CycloolivilC20H24O7bark[15]
7lariciresinolC22H28O6bark[16]
8(+)-epicycloolivilC20H24O7bark[16]
9noreucol AC19H20O6bark[16]
10citrusin BC27H36O13bark[16]
11dihydrodehydrodiconiferyl alcoholC20H24O6leaf[16]
12forsythialanside EC26H32O12leaf[16]
13balanophoninC34H42O20bark[17]
14(+)-pinoresinolC10H18Obark[17]
15(+)-epinoresinolC20H22O6bark[17]
16aectiinC27H34O11bark[17]
17(-)-olivilC20H24O7bark[17]
18medioresinolC21H24O7bark[4]
19vladinolD C20H22O7bark[18]
20liriodendrinC34H46O18bark[18]
21erythro-dihydroxydehydro-di-coniferyl alcoholC20H24O8Bark/leaf[19]
22threo-dihydroxydehydro-di-coniferyl alcoholC20H24O8bark[19]
Table 2. Iridoids in E. ulmoides.
Table 2. Iridoids in E. ulmoides.
NO.CompoundFormulaPartReference
23aucubinC15H22O9leaf/bark/flowers/seeds[15]
24geniposidic acidC16H22O10leaf/bark/flowers/seeds[15]
25catalpolC15H22O10leaf/bark/flowers/seeds[15]
26ulmoidoside AC48H62O28seed[15]
27ulmoidoside BC50H64O29seeds[15]
28ulmoidoside CC64H82O37seeds[15]
29ulmoidoside DC66H84O38seeds[15]
30deacetylasperulosidic acidC16H22O11leaf[15]
31eucomosides AC18H22O11leaf[22]
32eucomosides BC25H31NO11leaf[22]
33eucomosides CC27H32N2O11leaf[22]
34loganinC17H26O10leaf[16]
35deacetyl asperulosidic acid methyl esterC17H24O11leaf[16]
364-dihydro-3-methoxypaederosideC19H26O12Sflowers[16]
37linarideC15H22O8seeds[16]
38deoxyeucommiolC9H16O3bark[16]
39asperulosidic acidC18H24O12leaf/flowers[23]
40asperulosideC18H22O11flowers/leaf[23]
41geniposideC15H18O9leaf/flowers[23]
42gardendiolC10H14O4bark[17]
43artselaeninC15H22O5flowers[17]
44ajugosideC17H26O10leave[4]
45daphyllosideC20H28O11flowers[4]
46borreriageninC10H14O5leaf[20]
Table 3. Phenylpropanoids in E. ulmoides.
Table 3. Phenylpropanoids in E. ulmoides.
NO.CompoundFormulaPartReference
48caffeic acidC9H8O4leaf/bark/flowers/seeds[15]
49ferulic acidC10H10O4leaf/bark/flowers/seeds[15]
50protocatechuic acidC7H6O4leaf/bark/flowers/seeds[15]
51chlorogenic acidC16H18O9leaf/bark/flowers/seeds[15]
52isochlorogenic acid isomerC22H28O14leaf/flowers[16]
533-p-coumaroylquinic acid or isomerC16H18O8leaf/flowers/seeds[16]
54methyl chlorogenateC17H20O9leaf/flowers[16]
55forsythinC27H34O11leaf[25]
56p-Coumaric acidC9H8O3leaf[25]
57coniferinC16H22O8bark[26]
58coniferolC10H12O3stems[26]
59catechinC15H14O6Bark/leaf[26]
60L-EpicatechinC15H14O6bark[27]
Table 4. Flavonoids in E. ulmoides.
Table 4. Flavonoids in E. ulmoides.
NO.CompoundFormulaPartReference
61hyperinC21H20O12leaf/bark[15]
62baicaleinC15H10O5leaf/flowers/seeds[15]
63astragalinC21H18O11leaf[15]
64kaempferolC15H10O6leaf/flowers/seeds[15]
65rutinC27H30O16leaf/bark/flowers/seeds[15]
66isoquercitrinC21H20O12leaf/flowers/seeds[15]
67luteolinC15H10O6leaf/bark/flowers/seeds[15]
68quercetinC15H10O7leaf/flowers/seeds[15]
69naringeninC15H12O5flowers[16]
70pruninC21H22O10flowers[16]
71procyanidin B2C30H26O12bark[16]
72wogoninC16H12O5bark[17]
73wogonosideC22H20O11bark[17]
74liquiritigeninC15H12O4bark[25]
75formononetineC16H12O4bark[5]
76paratocarpin EC20H18O5bark[5]
77loureirin CC16H16O4bark[5]
78oroxylinC16H12O5bark[32]
79nicotiflorinC27H30O15bark[26]
80hyperosideC21H20O12bark[26]
Table 5. Terpenoids in E. ulmoides.
Table 5. Terpenoids in E. ulmoides.
NO.CompoundFormulaPartReference
81swerosideC16H22O9leaf/bark/flowers/seeds[15]
82genipin 1-gentiobiosideC23H34O15leaf/bark/flowers[15]
83atractyloside AC21H36O10leaf/bark/seeds[15]
84artemisinic acidC15H22O2leaf/bark/flowers/seeds[15]
85oleanolic acidC30H48O3leaf/bark/flowers/seeds[15]
86ginsenoside Rh1C36H62O9bark/seeds[15]
87catecholC6H6O2leaf[16]
88glucosyringic acidC15H20O10bark[16]
89α-amyrinC30H50Oflowers[16]
90betulinC30H50O2bark/seeds[16]
91ursolic acidC30H48O3bark/seeds[16]
923-O-acetyl oleanolic acidC30H48O3flowers[16]
93β-sitosterolC29H50Obark/leaf[4]
94daucosterolC35H60O6bark/seeds[26]
95cycloeucalenolC30H50Obark[40]
Table 6. Indicators and specifications of E. ulmoides seed oil as a new food ingredient.
Table 6. Indicators and specifications of E. ulmoides seed oil as a new food ingredient.
Indicators for New Food IngredientsRelevant Indicator Specifications
NatureYellowish brown transparent oily liquid
Production processSeed removal, separation of shells and kernels, followed by pressing and filtration
Fatty acid composition (% of total fatty acid content)ALA(C18:3)≥45%
OA (C18:1)≥13%
LA (C18:2)≥10%
PA (C16:0)≥6%
SA (C18:0)≥2%
Table 7. Pharmacological activities and related mechanisms of E. ulmoides.
Table 7. Pharmacological activities and related mechanisms of E. ulmoides.
Pharmacological EffectsMaterialsSubjects ContentAdministration DosageEffect/MechanismReferences
Lower blood pressureLignansSpontaneously hypertensive rats150 and 300 mg/kg Twice daily, for 14 daysIncreasing NO↑ modulating renin–angiotensin system↑ relaxing vessel↑[9]
Chlorogenic acidSpontaneously hypertensive rats5 and 20 mg/kg for 8 weeksAntihypertensive effect↑[24]
Bone protectionAstragalin and baiacaleinOsteoprotegerin7.5, 40, 80 mg/L for 24 hProliferation of MC3T3-E1 subclone 14 osteoblasts↑ expression of OPG and Osterix↑ protein expression of RANKL↓[51]
LignansSprague-Dawley rats20, 40, or 80 mg/kg for 12 weeksOsteoprotegrin↑ NF-κB ligand expression↓[8]
FlavonoidsBone marrow mesenchymal stem cells0.08, 0.4, 2, 10, 50 μg/mL for 24 dOsteogenic differentiation of BMSCs↑[50]
IridoidsOvarian granulosa cells10, 22, 50 μM for 24 hThe expression levels of 3β-HSD, CYP17A1, and 17β-HSD↑[48]
Seeds glycosidesOsteoporotic mice55, 110, 220 mg/kg for 12 weeksDirect action on the reproductive system synthesize collagen↑ bone strength↑[96]
β-sitosterolOsteoblasts and ovarian granulosa cells0.25 μM for 3 dOPGmRNA expression↑ secretion of ODF↓[66]
β-sitosterolC57BL/6J mice5 mg/kg for 8 weeksOsteoblast differentiation↑ β-catenin signaling pathway↑[54]
Seeds extractsOsteoporosis rats180 mg/kg/dThe activity of macrophages and lymphocytes in the spleen and abdomen↑ levels of TNF-α, IGF-1 and IL-6↓[98]
Liver and kidney protectionAucubinHepatic ischemia–reperfusion injury rats1, 5, 10 mg/kg/dExpression of HMGB1↓ TLR-4/NF-kB signaling pathway↓ the sterile inflammatory response of HIRI↓[68]
Chlorogenic acidHepatic ischemia–reperfusion injury rats25, 50, 100 mg/kg/dAnti-inflammatory and antioxidant effects expression of HMGB1↑[70]
FlavonoidsAcute liver injury rats50, 200 mg/kg for 7 dThe content of SOD and GSH↑ the levels of ALT, AST, and MDA↓[71]
PolysaccharideHepatic fibrosis rats35, 70, 140 mg/kg for 8 weeksThe content of ALT, AST, HA, LN, IV-C, GLOB, MDA and Hyp↓ the content of TP, ALB, A/G, SOD, GSH-Px↑ expression of TGF-β1↓[72]
Water extracts; alcohol extractsHepatic ischemia–reperfusion injury rats20, 40, 80 mg/kg for 10 dDegree of liver injury↓ inflammatory response and oxidative stress in liver tissue↓[44]
Anti-inflammationSeeds glycosidesPaw edema and ear swelling mice55, 110, 220 mg/kg for 7dExhibits anti-inflammatory and analgesic effects[97]
Triterpenoid and iridoidCollagen-induced arthritis mice60 mg/kg for 2 weeks and 4 weeksExpression of TNF-α, IL-17, and IL-23↓ proliferation of HFLS-RA↓ RAW264.7 cells release NO↓[53]
Alcohol extract of bark and male flowerAsthmatic mice4 g/kg/dThe production of OVA-Ig E↓ secretion of Th2 cytokines ↓ expression of pro-inflammatory cytokines↓[87]
Anti-depressionBark extractsPostpartum depressive rats1.34, 2.68 g/kg for 3 weeksActivation of the HPA axis↓ expression of CRFR2↓ expression of VDAC1↓[46]
Effect on Improving Insulin ResistanceSeed oilKK-Ay mice0.9 mg/gThe content of fasting blood glucose, fasting insulin, total cholesterol, total triglyceride and low-density lipoprotein↓ microbial diversity↑[100]
AntioxidantFlavonoidsDiabetic nephropathy mice80, 160 mg/(kg·d)The content of SOD↑ the content of MDA↓ the expression of Nrf2 and HO-1 protein↑[49]
Male flowers extractsSkin photoaging miceTopical applicationVitality and capacity in mouse skin tissue↑ accumulation of peroxidation products↓[86]
NeuroprotectionUlmoidolBV-2 cells1, 3, 10 μMThe expression of iNOS and COX-2↓ TLR4/MAPK/NF-κB signaling pathways↓[65]
LignansDiabetic mice RF/6A cells10 μg/mL for 2 months, 25, 50, 75 and 100 μMRegulate oxidative stress response in retinal endothelial cell line, retina, and liver regulation of Nrf2/HO-1 signal transduction pathway[63]
Anti-fatiguePolysaccharideLong-term exercise-induced fatigue mice100, 200 mg/kgThe activity of serum CK and the level of BUN↓ regulates glucose metabolism and conserves protein[42]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Xie, W.; Xiao, Y.; Xu, P.; Zheng, H.; Zeng, X.; Wu, Y.; Jiang, J.; Jia, F.; Yan, J.; Zheng, T.; et al. From Traditional Medicinal Plant to Modern Pharmacotherapy: A Comprehensive Review of the Bioactive Compounds and Health Applications of Eucommia ulmoides. Nutrients 2026, 18, 234. https://doi.org/10.3390/nu18020234

AMA Style

Xie W, Xiao Y, Xu P, Zheng H, Zeng X, Wu Y, Jiang J, Jia F, Yan J, Zheng T, et al. From Traditional Medicinal Plant to Modern Pharmacotherapy: A Comprehensive Review of the Bioactive Compounds and Health Applications of Eucommia ulmoides. Nutrients. 2026; 18(2):234. https://doi.org/10.3390/nu18020234

Chicago/Turabian Style

Xie, Wanting, Yubo Xiao, Pan Xu, Hui Zheng, Xianping Zeng, Yuhang Wu, Jiani Jiang, Fan Jia, Jianye Yan, Tao Zheng, and et al. 2026. "From Traditional Medicinal Plant to Modern Pharmacotherapy: A Comprehensive Review of the Bioactive Compounds and Health Applications of Eucommia ulmoides" Nutrients 18, no. 2: 234. https://doi.org/10.3390/nu18020234

APA Style

Xie, W., Xiao, Y., Xu, P., Zheng, H., Zeng, X., Wu, Y., Jiang, J., Jia, F., Yan, J., Zheng, T., & Yang, Y. (2026). From Traditional Medicinal Plant to Modern Pharmacotherapy: A Comprehensive Review of the Bioactive Compounds and Health Applications of Eucommia ulmoides. Nutrients, 18(2), 234. https://doi.org/10.3390/nu18020234

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop