Search Results (3,678)

Pseudorabies (PR) is an acute and highly contagious disease caused by the pseudorabies virus (PRV). This virus has a wide range of susceptible hosts and has caused major economic losses to the global swine industry. While rosmarinic acid possesses broad antioxidant and antiviral properties, its efficacy against PRV has remained unexplored. Therefore, this study aimed to evaluate the anti-PRV activity of rosmarinic acid and to elucidate its underlying mechanism, with a focus on the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway. The results revealed that rosmarinic acid exhibited potent, concentration-dependent antiviral activity in vitro, with a half-maximal inhibitory concentration (IC50) of 0.02654 mg/mL, a half-maximal cytotoxic concentration (CC50) of 0.1043 mg/mL, and a selectivity index (SI) of 3.9. Rosmarinic acid inhibited virus adsorption, entry, and intracellular replication. It also significantly suppressed the expression of the gB protein. In a mouse model, rosmarinic acid treatment (200 mg/kg) significantly enhanced the survival rate to 28.5%. This treatment reduced the viral load in the brain, lungs, kidneys, heart, and spleen. It also alleviated the tissue damage caused by PRV infection. Furthermore, rosmarinic acid counteracted PRV-induced oxidative stress by elevating the activity of the antioxidant factors SOD and CAT and reducing the level of the oxidative factor MDA. Combined network pharmacology and molecular docking analyses predicted the Nrf2 signaling pathway as a key target for rosmarinic acid. Subsequent mechanistic studies confirmed that rosmarinic acid upregulated the expression of the Nrf2, HO-1, GPX, SOD, and CAT genes, as well as Nrf2 and HO-1 proteins, thereby promoting the nuclear translocation of Nrf2. These results identify rosmarinic acid as a promising anti-PRV agent that acts through multi-phase viral inhibition and activation of the Nrf2-mediated antioxidant defense, suggesting its potential as a novel pharmacological strategy against PRV. Full article

Gallic acid (GA) is a natural polyphenol abundantly found in a variety of fruits, including blackberries, apples, pineapples, strawberries, bananas, and grapes. With prominent anti-inflammatory and antioxidant properties, GA effectively mitigates inflammation and oxidative stress. Furthermore, it plays a significant role in modulating various cellular processes and biological activities, ultimately inhibiting the progression of pathogenesis. This review explores the multifaceted health benefits of GA, highlighting its role as antidiabetic, anti-obesity, anti-arthritis, hepatoprotective, cardioprotective, and neuroprotective effects. Additionally, its impact on the respiratory, digestive, and reproductive systems, along with its related pathogenesis, is described. Additionally, its role as an antimicrobial is defined primarily through mechanisms such as disruption of microbial cell membranes, inhibition of efflux pumps, and antibiofilm activity. Moreover, this review provides a novel, integrative analysis of GA by unifying its mechanistic roles across various pathogenesis. It further describes the role of GA in cancer management via the modulation of signaling pathways. In addition, it demonstrates the synergistic effects of GA when used in combination with other drugs/compounds and discusses nanoformulation approaches that improve its therapeutic efficacy. However, despite significant preclinical outcomes, the clinical application of GA is limited by a shortage of human trials, low bioavailability, and an inadequate understanding of its mechanisms of action and optimal dosage. To overcome these limitations, well-designed clinical trials, in vivo studies, and advanced nanoformulation approaches are required to enhance bioavailability, elucidate mechanisms of action, and increase knowledge of safety and long-term toxicity. Addressing these gaps will enable the full exploration of GA’s benefits in disease prevention and management. Full article

Algal carotenoids play a promising role in handling chronic diseases due to their diverse bioactive properties, including anti-inflammatory, antioxidant, and anticancer effects. This study assesses the activity of the antioxidant xanthophyll diatoxanthin (Dt), derived from marine diatoms, against triple-negative breast cancer (TNBC) cells using in vitro models, gene expression evaluation, and explores its role in potentiating the cytotoxic effect of chemotherapy. Dt exhibited selective activity against MDA-MB-231 and BT-549 TNBC cells at concentrations ≥12.5 ng/mL, with maximal effects observed at 25 ng/mL while sparing human umbilical vein endothelial cells (HUVECs) at these doses. When combined with doxorubicin (0.1–0.5 μM), Dt enhanced the anti-tumor efficacy in both TNBC cell lines, further reducing cell viability compared with doxorubicin alone (p < 0.05–0.001). Dt also exerted its activity in inhibiting migration and chemotaxis by approximately 30–50% compared with the controls (p < 0.01) and suppressing 3D-tumor spheroid growth at day 12 (up to >50% reduction, p < 0.001). Notably, secretome analysis revealed Dt-induced changes in inflammatory, oxidative and angiogenic mediators, highlighting its ability to modulate the TNBC microenvironment. Dt also downregulated key pro-survival, pro-angiogenic and pro-tumorigenic genes in both TNBC cell lines, supporting its role in disrupting oncogenic pathways. Angiogenesis-related genes were significantly reduced. Dt also decreased the expression of angiogenic mediators in HUVECs, supporting Dt’s role in inhibiting tumor vascularization. Results on gene expression regulation were also confirmed by RNA-Seq analysis. These findings pose Dt as a promising chemopreventing candidate in the challenging fight against TNBC, a well-known type of cancer that is aggressive and resistant to conventional therapies, targeting critical pathways for tumor survival, such as inflammation, angiogenesis, tumor cell growth, and cell migration. Given its selective activity against TNBC cells, ability to enhance chemotherapy efficacy, and modulation of the tumor microenvironment, Dt holds promise as a complementary drug for cancer prevention and interception. Future studies should focus on validating these effects in vivo and exploring Dt’s potential in combinatorial treatment strategies for cancer. Full article

The transition to a circular bioeconomy enhances the valorization of agricultural by-products. Hawthorn leaves (Crataegus spp.), generated in large quantities from orchard maintenance, represent a promising yet underutilized biomass. This comprehensive narrative review synthesizes recent advances regarding their bioactive compounds, extraction methods, and applications. A systematic literature search was conducted to identify relevant studies. The analysis reveals that hawthorn leaves are rich in polyphenols (e.g., flavonoids, procyanidins), with their content often exceeding that found in fruits. Modern “green” extraction techniques (e.g., ultrasound- and microwave-assisted) demonstrate superior efficiency in recovering these thermolabile compounds compared to conventional methods. The broad spectrum of associated biological activities—including antioxidant, cardioprotective, neuroprotective, antimicrobial, and insecticidal effects—underpins their potential in nutraceuticals, cosmetics, and functional foods. Crucially, this review highlights the significant promise of hawthorn leaf extracts as a source for developing natural, plant-based biopesticides, aligning with sustainable agriculture and integrated pest management principles. To fully realize this “waste-to-wealth” potential, future research should prioritize the scaling of eco-friendly extraction, field trials for crop protection efficacy, and the standardization of extracts. Full article

Background/Objectives: Oleuropein is a bioactive phenolic compound from olive leaves with antimicrobial and antioxidant activity. This study aimed to develop a sprayable oral gel containing an oleuropein-rich aqueous extract and to evaluate its pharmaceutical performance antimicrobial efficacy and in ovo biological response. Methods: Oleuropein content was quantified using a validated chromatographic method. Polymeric systems were screened to select an optimized sprayable formulation. Physicochemical stability, dose uniformity, and antimicrobial activity against major cariogenic bacteria were evaluated. In ovo biological evaluation was conducted using the chick chorioallantoic membrane angiogenesis model together with histopathological examination of embryonic heart and liver tissues. Results: Oleuropein content was determined as 288.6 µg/mL in the olive leaf extract and 255.1 µg/mL in the final formulation. The optimized oral spray showed stable physicochemical properties, with pH maintained at 6.90 ± 0.02 and no relevant changes in viscosity during storage. The mean delivered dose per actuation was 0.128 ± 0.015 g, corresponding to 32.6 µg oleuropein per spray. The formulation exhibited inhibitory activity against all tested cariogenic microorganisms, with MIC values ranging from 13.3 to 170.7 µg/mL and MBC values generally two-fold higher. In the CAM assay, significant concentration- and time-dependent antiangiogenic effects were observed after 24–48 h at moderate and higher concentrations. Histopathological evaluation revealed dose-dependent acute degenerative and congestive changes in heart and liver tissues without evidence of fibrosis or steatosis. Conclusions: The oleuropein-based sprayable oral gel is a promising localized delivery system with adequate stability dose uniformity and antimicrobial efficacy. In ovo findings provide a conservative assessment of systemic exposure and support further development for oral biofilm and caries-related applications. Full article

To investigate the effect of a polysaccharide-based composite film (ASC) composed of Alpinia oxyphylla polysaccharide (its molecular weight was approximately 4.07 kDa, and the monosaccharide composition was predominantly glucose and galacturonic acid), sodium alginate, and calcium chloride on the storage quality of shrimp surimi, this study compared the preservation efficacy of the ASC film with that of treatments using chitosan, potassium sorbate, ascorbic acid, sodium alginate, Alpinia oxyphylla polysaccharide, and distilled water. Samples were stored at 4 °C for 12 days, and evaluations were conducted by measuring film structural characteristics and quality indicators of shrimp surimi. Results showed that the ASC groups (where Alpinia oxyphylla polysaccharide was added at 20%, 30%, and 40% of the sodium alginate mass, designated as ASC 20%, ASC 30%, and ASC 40%) significantly outperformed the control group across all quality indicators. The ASC 30% group demonstrated the best overall preservation performance, effectively delaying oxidative browning, protein degradation, lipid oxidation, and microbial growth in shrimp surimi. The ASC 40% group exhibited particularly strong antibacterial effects, while the ASC 20% group also showed stable preservation performance. The composite film combines the antioxidant and antibacterial activities of Alpinia oxyphylla polysaccharide with the barrier and moisture-retention properties of sodium alginate, forming a stable three-dimensional network structure through calcium chloride cross-linking. It is superior to single/individual chemical preservatives in terms of film-forming ability, functionality, and safety, providing a natural, effective, and environmentally friendly preservation approach for shrimp surimi and other aquatic products. It also offers a theoretical foundation and practical reference for the development of natural preservation technologies in the food industry. Full article

Growing limitations on the use of in-feed antibiotics have accelerated the search for functional feed additives capable of supporting animal health and productivity under antibiotic-free production systems. Postbiotics, defined as non-viable microbial products or metabolic byproducts, and phytogenics, which are plant-derived bioactive compounds, have emerged as promising alternatives due to their stability and biological activity. Recent advances in the application of postbiotics and phytogenics in monogastric and ruminant nutrition are summarized, with emphasis on their mechanisms of action, synergistic effects, and impacts on gut health, immune function, and growth performance. Postbiotics modulate the gut microbiota, enhance epithelial barrier integrity, and regulate immune signaling, whereas phytogenic compounds provide antimicrobial, antioxidant, and digestive-stimulant effects. Available evidence suggests that combined strategies can enhance efficacy, particularly under production-related stress. Key challenges related to formulation, dose–response relationships, stability, and regulatory classification are discussed together with emerging omics-based approaches that support precision formulation. Overall, integration of multi-omics evidence with formulation and regulatory considerations supports the practical use of postbiotics and phytogenics in commercial livestock systems. Full article

Increasing consumer demand for healthier and clean-label meat products, together with health concerns over synthetic antioxidants, has driven interest in natural alternatives. In this context, tannin-rich extracts were evaluated as functional ingredients to improve the quality and shelf life of beef patties. The effect of two different tannin-rich extracts, each tested at three different concentrations (0.005%, 0.02%, and 0.04% w/w), was investigated in beef patties. Obtained results were compared with a commercial rosemary extract (0.2% w/w) and an untreated control. Natural antioxidant supplementation significantly reduced lipid oxidation during refrigerated storage, limiting malondialdehyde (MDA) formation. At the end of the 7-day storage period, the control sample exhibited the highest thiobarbituric acid reactive substance (TBARS) value of 2.99 ± 0.01 mg MDA/kg, whereas treated samples showed markedly reduced oxidation (0.34–0.97 mg MDA/kg), with tannin-rich extracts presenting greater antioxidant efficacy with respect to rosemary extract (p < 0.001). The natural compounds also effectively inhibited hexanal formation and delayed the accumulation of 1-octen-3-ol compared with the control (p < 0.001). Moreover, all extracts enhanced meat redness, as indicated by higher CIELAB a* values, while no significant effects (p > 0.05) were observed on texture, microbial growth, or overall sensory acceptance. These results highlight tannin-rich extracts as promising natural antioxidants for improving oxidative stability and extending the shelf life of beef patties. Full article

Light and antioxidant systems play a crucial role in the life activities of algal cells. This study investigates the algicidal efficacy of hydrogen peroxide (H₂O₂) against the harmful algal bloom (HAB)-forming dinoflagellate Prorocentrum donghaiense Lu, with a focus on the modulating roles of light conditions and iron ion environments. Within 180 min, dark-adapted cells showed 78% greater viability loss than light-exposed ones, and Fe₃O₄ nanoparticles synergistically enhanced H₂O₂ inhibition. Imaging and cytometry confirmed cell damage, including membrane rupture. Mechanistically, H₂O₂ penetrated cells, induced severe oxidative stress, suppressed photosynthesis, and compromised membrane integrity. Darkness likely exacerbated toxicity by depleting antioxidant reserves. This study elucidates an apoptosis-like pathway underlying H₂O₂-induced cell death and highlights the critical influence of ambient light on treatment efficiency. These findings reveal an apoptosis-like death pathway and highlight ambient light’s critical role, suggesting that optimized nighttime H₂O₂ application with nanomaterial synergists could improve HAB control strategies. Full article

Background: Glaucoma is a chronic neurodegenerative disorder characterized by the selective vulnerability of retinal ganglion cells (RGCs), in which mitochondrial dysfunction, redox imbalance, and impaired bioenergetic signaling play central pathogenetic roles. Mitochondrial homeostasis in RGCs critically depends on maintaining intracellular NAD⁺ pools, which support oxidative phosphorylation, sirtuin-mediated deacetylation, and antioxidant gene expression. Nicotinamide riboside (NR), a potent NAD⁺ precursor, and berberine (BBR), an AMPK activator derived from Berberis aristata, have recently emerged as synergistic modulators of mitochondrial metabolism and oxidative stress resistance. Methods: This study retrospectively assessed clinical outcomes associated with combined nutraceutical supplementation of nicotinamide riboside (NR) and berberine (BBR) in patients with primary open-angle glaucoma undergoing stable topical hypotensive therapy. We have included a narrative review in the current literature regarding NAD⁺ biology, AMPK–sirtuin signaling, and oxidative stress responses in retinal ganglion cell (RGC) degeneration. Due to the absence of comparator groups receiving only NR or only berberine in this retrospective cohort, the combined supplementation has been regarded as a biologically complementary strategy, and the potential for synergistic efficacy remains a subject for further investigation. Results: Translationally, a retrospective clinical cohort receiving combined NR and BBR supplementation showed functional stabilization of the visual field and structural preservation of the retinal nerve fiber layer over a six-month follow-up, in line with the proposed mitochondrial protective mechanisms. Conclusions: The clinical trends identified in this retrospective cohort have substantiated the translational significance of NR + BBR supplementation as a potential adjunctive approach in glaucoma management. NAD⁺ repletion and engagement of the AMPK–SIRT–NRF2 pathway may enhance mitochondrial resilience in RGCs. Collectively, these findings offer initial clinical evidence advocating for additional controlled studies on NR + berberine supplementation, while mechanistic interpretations have been derived from the existing literature and are hypothesis-generating. Full article

Colon cancer (CC) remains a leading cause of cancer-related mortality worldwide, with multidrug resistance (MDR) presenting a formidable barrier to successful chemotherapy. Ferroptosis—an iron-dependent, lipid peroxidation-driven form of cell death—offers a novel therapeutic avenue to bypass MDR by exploiting metabolic vulnerabilities distinct from traditional apoptosis pathways. Emerging evidence reveals a dynamic interplay between MDR and ferroptosis: MDR cancer cells suppress ferroptosis through NRF2/GPX4-mediated antioxidant upregulation, iron sequestration by ferritin, and lipid metabolism reprogramming, including SREBP1-driven monounsaturated fatty acid accumulation, while ABC transporters actively efflux ferroptosis inducers. On the other hand, ferroptosis inducers such as erastin and RSL3 have the potential to overcome apoptotic resistance and avoid efflux pathways, which recover therapeutic efficacy. This review first describes the primary mechanisms of chemotherapy resistance in colon cancer and then explains the molecular processes that prevent ferroptosis in resistant cells. We also review recent data on the complex interactions between resistance to chemotherapy and ferroptosis, and outline approaches that may stimulate iron accumulation to reverse MDR. By emphasizing novel methods to induce ferroptosis, this review highlights that this approach is a promising strategy to overcome chemotherapy resistance in colon cancer and will facilitate the development of more precise and efficient treatment. Full article

This study investigated the efficacy of two value-added products derived from silkworm excrement—a concentrated extract (SCE, 20:1) and sodium copper chlorophyllin (SCC)—as functional feed additives for common carp. Diets supplemented with 0.5% SCE, 1.0% SCE, or 0.1% SCC were compared to a basal control. The results revealed a distinct dose-dependent effect for SCE: 0.5% SCE was safe, while 1.0% SCE impaired growth, feed efficiency, and digestive enzyme activity. Both SCE and SCC significantly enhanced lipid metabolism, reducing hepatic lipid deposition and improving serum lipid profiles, albeit through distinct molecular pathways—SCC primarily stimulated catabolism, whereas SCE comprehensively regulated both synthesis and breakdown. Furthermore, SCE demonstrated superior, multi-targeted immunomodulatory capacity by favorably regulating inflammatory cytokine expression, an effect not observed with SCC. Although both additives boosted systemic antioxidant capacity, their specific patterns of enzyme activity and gene expression differed. In conclusion, SCE offers broad-spectrum, synergistic benefits for health modulation, while SCC provides specific, stable bioactivity, highlighting the importance of selecting the appropriate additive form based on desired functional outcomes in aquaculture. Full article

Background: Chronic inflammatory enteropathies (CIEs) in dogs are multifactorial disorders characterized by mucosal immune dysregulation, compromised epithelial barrier function, and increased exposure to microbial components such as lipopolysaccharide (LPS). The resulting oxidative stress and inflammation contribute to local and systemic pathology. Objective: This study aimed to evaluate the immunomodulatory and antioxidant effects of three naturally occurring flavonoids—quercetin, luteolin, and grape seed extract oligomeric proanthocyanidins (GSOPs)—in LPS-stimulated canine duodenal explants. Methods: Duodenal tissue samples were cultured in vitro and challenged with LPS derived from Escherichia coli and Salmonella enterica. Explants were co-incubated with flavonoid compounds, and endpoints included evaluation of histological architecture, inflammatory cytokine production, and reactive oxygen species (ROS) and reactive nitrogen species (RNS) generation. Results: All three flavonoids attenuated LPS-induced mucosal inflammation and ROS production to varying degrees. In addition, GSOPs significantly reduced RNS levels under both basal and LPS-stimulated conditions. Quercetin and luteolin demonstrated pronounced downregulation of TNF-α, while both compounds also reduced IL-6 concentrations under non-stimulated conditions. These effects support the hypothesis that flavonoids can mitigate both inflammatory and oxidative responses under conditions relevant to CIE. Conclusion: Quercetin, luteolin, and GSOPs show promising in vitro efficacy in modulating key mechanisms implicated in canine CIE. Their multimodal actions highlight their potential as adjunctive nutraceuticals for the management of CIE in dogs. However, further in vivo validation is warranted. Full article

Background: Hyperpigmentation disorders lack effective therapies due to efficacy and safety limitations. Spirulina-derived peptides (SPs) show promises as anti-melanogenic agents, but their mechanisms remain unclear. Methods: SPs (<1 kDa, 3–6 amino acids) were isolated and assessed for tyrosinase inhibition, antioxidant, and anti-glycation activities. In vitro effects were tested in B16F10 cells; transcriptomic profiling used RNA sequencing. In vivo efficacy was evaluated in UVB-induced hyperpigmentation mouse models. Results: SPs exhibited mixed-type kinetic inhibition of tyrosinase along with strong antioxidant and anti-glycation activities. In vitro, SP suppressed melanin synthesis by directly inhibiting tyrosinase, downregulating the cAMP/PKA/CREB cascade, and activating the PI3K/Akt/GSK-3β pathway, resulting in reduced MITF and tyrosinase expression. Transcriptomic analysis revealed broad regulation of melanogenesis and inflammatory pathways. In vivo, topical SP treatment significantly reduced UVB-induced hyperpigmentation and skin inflammation, correlating with decreased CREB phosphorylation and tyrosinase expression. Conclusions: SP acts as a dual anti-melanogenic/anti-inflammatory agent through enzyme inhibition and signaling modulation, offering a novel therapeutic strategy for inflammation-associated hyperpigmentation. Full article

The physiological mechanism of melatonin in alleviating combined saline-alkali stress in Fraxinus mandshurica remains unclear. This study aimed to determine the efficacy of exogenous melatonin in enhancing salt tolerance and elucidate the underlying mechanisms through integrated physiological and multi-omics analyses. Seedlings were subjected to 400 mmol L⁻¹ saline-alkali stress and treated with foliar melatonin. We quantified key growth indicators (height, diameter, dry biomass) and measured the activities of antioxidant enzymes (SOD, POD). Melatonin significantly alleviated growth inhibition, increasing biomass and height by 29% and 13%, respectively, while enhancing net photosynthetic rate and antioxidant capacity. To uncover the systemic regulation, conjoint analysis of transcriptome (RNA-seq) and metabolome data was performed. This integrated approach revealed that melatonin specifically activated common KEGG pathways pivotal for stress adaptation, including plant hormone signal transduction, phenylpropanoid biosynthesis, and starch and sucrose metabolism, with coordinated upregulation of associated genes and metabolites. Collectively, our integrated data demonstrate that melatonin enhances Fraxinus tolerance by synergistically improving photosynthesis and antioxidant defense, underpinned by a reconfigured molecular network. This study provides a theoretical basis for using melatonin as an eco-friendly biostimulant to improve woody plant resilience in saline-alkali soils. Full article