Search Results (24,019)

Lilac (Syringa oblata Lindl.) is an important eco-economic aromatic shrub in northern China; however, the key volatile organic compounds (VOCs) responsible for its floral aroma and their origin remain largely unexplored. In this study, we conducted an integrated analysis of volatile metabolomics and transcriptomics to elucidate the composition, dynamic changes, and potential regulatory network of VOCs across different floral organs and petal developmental stages. A total of 1440 VOCs were identified in the stamens, pistils, and petals, with petals being the primary contributors to the overall floral aroma. Analysis of different petal developmental stages revealed that the full-bloom stage (S3) is critical for VOCs emission. The floral aroma of S. oblata is primarily composed of terpenoids, alcohols, and aldehydes. By relative odor activity value (rOAV) with multivariate statistical screening, seven key VOCs with high contributions to the floral aroma were identified. Transcriptome analysis identified 69,935 differentially expressed genes (DEGs) across petal developmental stages, which were predominantly enriched in metabolic pathways and the biosynthesis of secondary metabolites. The expression patterns of these DEGs were highly consistent with the accumulation trends of VOCs, increasing at stages S2 and S3 and subsequently declining at stage S4. Integrative analysis of VOCs and gene expression further identified candidate genes significantly correlated with the key aroma volatiles. Specifically, the carotenoid pathway-related genes CYP97A3 and LYC may influence the formation of carotenoid-derived volatiles and floral aroma. Additionally, genes associated with the fatty acid-lipoxygenase pathway, transport-related genes, and transcription factors are potentially involved in the formation and regulation of aldehyde and alcohol volatiles. These findings advance our understanding of the floral aroma formation in S. oblata and provide metabolic basis, candidate gene resources and a theoretical foundation for the genetic improvement of aroma traits and the breeding of new cultivars. Full article

Reducing reliance on supplemental fish oil is central to sustainable aquaculture, but the molecular consequences of replacing it with vegetable oils remain poorly characterized in the juvenile Chinese soft-shelled turtle (Pelodiscus sinensis). We evaluated whether full substitution of the supplemental dietary fish oil (FO) with linseed oil (LO) or soybean oil (SO) compromises hepatic lipid metabolism in Pelodiscus sinensis. Three isonitrogenous and isolipidic diets, sharing identical fish meal and other ingredient bases and differing only in the supplemental lipid (4% FO, LO or SO), were fed to triplicate groups of juvenile turtles (initial body weight 55.0 ± 0.05 g) for 8 weeks. Growth performance, survival, feed conversion ratio, and serum biochemistry were unaffected. However, both vegetable oil diets altered tissue fatty acid composition, raising n-6 PUFA and lowering n-3 LC-PUFA and the n-3/n-6 ratio in liver and muscle (muscle EPA and DHA each decreased by approximately 40%); the SO group additionally exhibited elevated hepatic malondialdehyde, whereas hepatic lipid droplet area and lipid content did not differ significantly among groups. Liver transcriptomic profiling identified 262 (LO vs. FO) and 214 (SO vs. FO) differentially expressed genes, converging on lipid storage and bile acid metabolism. RT-qPCR confirmed the up-regulation of PLIN3, G0S2 and APOF and the down-regulation of CYP7A1. Over 8 weeks, replacement of supplemental FO maintained growth without overt impairment while altering tissue fatty acid profiles and the hepatic expression of key lipid metabolism genes. Full article

Finger millet (Eleusine coracana L.) is rich in bioactive compounds, including flavonoids. Following exogenous substance regulation, its sprouts can achieve efficient flavonoid enrichment. This study investigates the regulatory effects of exogenous salicylic acid (SA) and γ-aminobutyric acid (GABA) on the physiological metabolism, oxidative stress response, and flavonoid biosynthesis of finger millet sprouts subjected to 5 mM zinc sulfate (ZnSO₄) stress. Compared to treatment solely with ZnSO₄, the application of both 50 μM salicylic acid (SA) and 1 mM gamma-aminobutyric acid (GABA) markedly enhanced flavonoid biosynthesis, with respective yields of 8.53 μg/sprout and 8.85 μg/sprout observed by 6 days post-germination. Concurrently, SA and GABA attenuated ZnSO₄-induced oxidative damage. During days 4 and 6 post-germination, malondialdehyde and hydrogen peroxide levels in sprouts were significantly reduced, with levels at 6 days showing a particularly notable decrease. Moreover, the catalytic activities of catalase, peroxidase, superoxide dismutase, and ascorbate peroxidase were significantly upregulated. Further analysis revealed that both treatments significantly activated the phenylpropanoid biosynthesis pathway. The activities of key rate-limiting enzymes, phenylalanine ammonia-lyase, cinnamate-4-hydroxylase, and 4-coumarate-CoA ligase, along with the expression levels of their corresponding genes, were markedly upregulated. Concurrently, the expression of genes and transcription factors, specifically myeloblastosis and NAC transcription factors, involved in regulating reactive oxygen species homeostasis also increased. These findings suggest that exogenous SA, GABA, and ZnSO₄ cotreatment can effectively enhance the accumulation of flavonoids and the nutritional quality of finger millet sprouts by bolstering antioxidant capacity and modulating the flavonoid biosynthesis pathway. This investigation establishes a theoretical framework for the production of superior, bioactive finger millet sprout ingredients. Full article

Background: Epilepsy is a complex neurological disorder in which growing evidence supports a significant role for the microbiota–gut–brain axis (MGBA) in modulating neuroinflammation, neuronal excitability, and treatment responsiveness. Beyond their traditional role in inducing ketosis, dietary therapies may influence epilepsy by modulating gut microbial ecology, intestinal barrier integrity, immune signaling, and microbiota-derived metabolites. Methods: This narrative review critically examines current clinical and experimental evidence regarding the relationship between epilepsy, gut microbiota, and dietary interventions. Particular attention was given to ketogenic dietary therapies, the Modified Atkins Diet (MAD), low-glycemic-index treatment (LGIT), Mediterranean dietary patterns, restrictive diets, and microbiota-targeted supplementation, including probiotics, prebiotics, and postbiotics. Results: Available evidence suggests that patients with epilepsy exhibit alterations in gut microbial composition associated with impaired short-chain fatty acid production, intestinal inflammation, and altered neuroimmune regulation. Ketogenic and microbiota-supportive dietary approaches may modulate these pathways beyond ketosis alone, potentially contributing to seizure reduction through integrated metabolic, inflammatory, and microbial mechanisms. Emerging evidence also supports a role for probiotics, prebiotics, and postbiotics in modulating gut–brain communication and neuroinflammatory signaling, although current clinical data remain limited. Conclusions: Dietary therapies in epilepsy should no longer be viewed exclusively as metabolic interventions aimed at inducing ketosis, but rather as potential modulators of the microbiota–gut–brain axis and neuroimmune homeostasis. While further mechanistic and clinical studies are needed, microbiota-targeted nutritional approaches may represent valuable complementary strategies to be integrated alongside conventional antiseizure therapies within more personalized models of epilepsy management. Full article

Prostate cancer remains one of the most biologically heterogeneous malignancies in men and continues to present major therapeutic challenges despite advances in androgen receptor-targeted therapy and molecular stratification. Increasing evidence suggests that prostate cancer progression is influenced not only by tumor-intrinsic genetic alterations but also by complex interactions involving androgen receptor signaling, inflammatory pathways, metabolic reprogramming, oxidative stress, epigenetic remodeling, immune dysregulation, and gut microbiome-associated signaling. Within this evolving systems-level framework, natural products have attracted increasing attention because of their ability to modulate multiple interconnected molecular pathways. This review examines the molecular basis of prostate cancer progression with particular emphasis on crosstalk among androgen receptor signaling, microbiome-associated regulation, epigenetic adaptation, inflammatory signaling, and tumor microenvironment remodeling. The emerging role of the gut microbiome in androgen metabolism, microbial metabolite production, immune regulation, and endocrine resistance is critically discussed, together with current evidence describing the biological effects of selected phytochemicals including curcumin, epigallocatechin-3-gallate, resveratrol, sulforaphane, quercetin, and genistein. These compounds may influence prostate cancer-associated pathways through modulation of inflammatory signaling, oxidative stress, metabolic adaptation, chromatin remodeling, and microbiome dynamics. Major translational limitations including poor bioavailability, pharmacokinetic variability, microbiome heterogeneity, inconsistent clinical evidence, and incomplete mechanistic understanding are additionally discussed. Rather than considering natural products as isolated anticancer agents, this review adopts a systems-level perspective in which dietary bioactive compounds may function as modulators of interconnected regulatory networks relevant to prostate cancer biology and therapeutic responsiveness. Full article

Background: Physical exercise is strongly recommended for breast cancer survivors due to its beneficial effects on physical function, metabolic health, and quality of life. Lactate, traditionally considered a metabolic byproduct of glycolysis, is increasingly recognized as a signaling molecule involved in metabolic regulation and exercise adaptation. However, exercise-induced circulating lactate responses in breast cancer survivors remain poorly characterized. The aim of this systematic review and exploratory meta-analysis was to synthesize and critically appraise current evidence on exercise-induced circulating lactate responses in breast cancer survivors Methods: A systematic review and exploratory meta-analysis were conducted according to PRISMA guidelines and prospectively registered in PROSPERO (CRD42024504288). PubMed, Scopus, and Web of Science were searched to identify controlled trials investigating exercise-induced changes in circulating lactate concentrations in breast cancer survivors. Random-effects meta-analysis was performed using pooled mean differences. Results: Among 173 screened records, four studies met eligibility criteria for qualitative synthesis and three contributed to quantitative analysis. Pooled results demonstrated no statistically significant effect of exercise on circulating lactate concentrations (weighted mean difference: 0.03 mmol/L; 95% CI: −0.24 to 0.31; p = 0.81), with low heterogeneity (I² = 31.1%). Considerable variation was observed across exercise protocols, intervention duration, and lactate assessment timing. Conclusions: Exercise-induced circulating lactate responses in breast cancer survivors appear modest and inconsistently reported across available studies. Current evidence remains limited by small sample sizes and methodological heterogeneity. These findings provide a physiological overview of lactate responses to exercise in breast cancer survivorship and highlight the need for standardized exercise interventions and metabolic outcome assessment in future research. Full article

Codonopsis lanceolata has long been used in traditional medicine across East Asia; however, recent scientific investigations have increasingly highlighted its broad therapeutic potential. This review provides an updated and comprehensive overview of the pharmacological properties of C. lanceolata and its bioactive constituents, focusing on their roles in disease prevention and therapy. Evidence from in vitro, in vivo, and limited clinical studies suggests that C. lanceolata possesses antidiabetic, anti-obesity, and anti-cancer properties while showing protective effects in experimental models of cardiovascular dysfunction, liver injury, neurodegenerative disorders, skeletal muscle atrophy, and pulmonary damage. Additionally, its immunomodulatory effects contribute to improved host defense and regulation of inflammatory responses. These diverse actions are mediated by mechanisms involving antioxidant activity, inhibition of inflammatory signaling, regulation of metabolic pathways, modulation of apoptosis, and maintenance of tissue integrity. Despite promising findings, challenges remain regarding extract standardization, identification of key active compounds, and the translation of preclinical results into clinical efficacy. Future research integrating molecular, pharmacokinetic, and clinical approaches is essential to clarify the therapeutic value and establish its potential as a nutraceutical or therapeutic agent. This review highlights the promising pharmacological potential and identifies key directions for future research to support its potential application in modern medicine. Full article

Trehalose-6-phosphate (T6P) is involved in the regulation of plant growth and stress-related responses; however, its potential role in post-drought recovery remains unclear in legume crops. This study evaluated whether foliar application of native T6P could improve growth, yield formation, and physiological recovery in adzuki bean after pre-flowering drought stress. We aimed to propose a model for the production and drought tolerance regulation in adzuki bean. A three-year field experiment was conducted by applying T6P at both the budding stage and the initial pod stage. The plant architecture, yield, photosynthetic characteristics, defensive enzyme activity, sugar metabolism and hormone changes were evaluated. The results indicated that T6P significantly increased root, stem and leaf parameters in adzuki bean it also increased all yield traits except for the main stem branches and sections during post-drought recovery. Indeed, the yield per block of 5μM and 10μM of T6P application during post-drought recovery increased by 20.66% and 31.60% on average compared to the control under well-watered conditions and by 47.68% and 60.20% under drought stress during the three experimental years. Foliar T6P treatment was associated with higher antioxidant enzyme activities and related gene expression, lower ROS accumulation and proline content, and changes in sugar- and hormone-related traits during post-drought recovery. Therefore, foliar application of T6P at the budding and initial pod stages improved growth, yield formation, and post-drought recovery in adzuki bean. The result provide a novel strategy for T6P application for coordinating the high production potential and crop resilience. Full article

Neurodegenerative diseases, such as Alzheimer’s, Parkinson’s, and Amyotrophic lateral sclerosis, are distinguished by progressive neuronal dysfunction caused primarily by oxidative stress, mitochondrial impairment, neuroinflammation, and redox imbalance. Growing evidence suggests that indole-derived compounds have significant neuroprotective potential due to their antioxidant, anti-inflammatory, and redox-modulating properties. This review summarizes the structural and biological significance of indole scaffolds, focusing on the mechanisms by which natural, endogenous, microbiota-derived, and synthetic indole compounds protect neuronal networks. Indole-3-carbinol, 3,3′-diindolylmethane, indole-3-propionic acid, and melatonin are major indole derivatives that control important neuroprotective pathways like Nrf2/ARE signaling, mitochondrial bioenergetics, neurotrophic factor expression, apoptotic regulation, and suppression of proinflammatory mediators. These compounds also maintain synaptic plasticity, reduce reactive oxygen species production, and improve neuronal survival in neurodegenerative disease models. Additionally, updated information from translational and clinical research indicates that indole-based compounds may have promising therapeutic applications; however, obstacles like low bioavailability, metabolic instability, and blood–brain barrier penetration continue to be major obstacles to clinical application. Development in nanoparticle delivery systems, microbiome-targeted interventions, and rational structural optimization may improve therapeutic efficacy and translational potential. Overall, indole-derived compounds are a versatile class of redox modulators with potential applications in the prevention and treatment of neurodegenerative diseases via integrated antioxidant and neuroprotective mechanisms. Full article

Differential fecundity in goats is a complex trait governed by coordinated molecular regulation across reproductive and endocrine tissues. In this study, we performed integrated metabolomic profiling of follicular fluid, serum, thyroid tissue, and uterine luminal fluid together with transcriptomic sequencing of follicular, thyroid, and uterine horn tissues from high-fecundity (HF) and low-fecundity (LF) Yangtze River Delta White goats. In addition, weighted gene co-expression network analysis (WGCNA) was conducted to elucidate the molecular mechanisms underlying differential litter size. High-fecundity goats exhibited enhanced follicular steroidogenesis, superior corpus luteum function, and more stable hypothalamic–pituitary–thyroid (HPT) axis activity, accompanied by increased uterine gland density and greater myometrial thickness. Metabolomic profiling identified 6640 metabolites displaying tissue-specific differential abundance patterns. Pathway enrichment analysis highlighted steroid hormone biosynthesis and energy metabolism in follicular fluid, PPAR signaling and tyrosine metabolism in thyroid tissue, and glycerophospholipid and one-carbon metabolism in uterine luminal fluid as major pathways associated with fecundity. Transcriptomic analysis identified 1596 differentially expressed genes (DEGs), including 20 genes shared across all examined tissues, constituting a systemic molecular signature associated with fecundity. WGCNA further revealed three functional tissue axes associated with follicular development (ELOVL4, INHA, NR5A2), thyroid endocrine regulation (GRHL2, NAPRT), and uterine receptivity (RSPO1, AGTR2, PTGER3). Low-fecundity-associated modules were predominantly concentrated in follicular and thyroid tissues, whereas the high-fecundity-specific module was mainly enriched in uterine horn. These findings provide a multi-tissue molecular framework underlying differential fecundity in goats and identify candidate hub genes and metabolites that may serve as candidate biomarkers for fecundity assessment and selective breeding programs. Full article

Follistatin (FST) binds to and neutralizes members of the transforming growth factor-beta (TGF-β) superfamily, thereby regulating diverse physiological processes, including regulation of skeletal muscle, adipose, and bone homeostasis. FST also promotes adipose browning and enhances energy metabolism, leading to improved plasma lipid profiles and metabolic health in mice. Given the emerging association between brown adipose tissue (BAT) activation and reduced atherosclerosis, we investigated the anti-atherogenic potential of FST. Transcriptomic and metabolomic analyses of the Hybrid Mouse Diversity Panel (HMDP) revealed that Fst expression was negatively correlated with aortic lesion area and positively correlated with the expression of multiple adipose browning-associated genes. Adeno-associated viral delivery of Fst (AAV1-FST344) in Ldlr^−/− mice significantly reduced aortic lesion area, improved plasma lipid profiles, and decreased expression of adhesion (VCAM1) and inflammatory (iNOS, TNF-α) markers in white adipose tissue (WAT), liver, and heart. Fst gene delivery also markedly increased uncoupling protein 1 (UCP1) expression in WAT, consistent with WAT browning. Integrated correlation analyses of Fst expression with tissue metabolites, together with plasma metabolite–lesion associations identified in the HMDP, implicated the arginase 1 (Arg1)-mediated metabolic pathway as a key regulator of atherogenesis. Consistent with these findings, Arg1 expression was significantly elevated in WAT, liver, and heart of AAV1-FST344-treated mice and in wild-type versus Fst-knockout mouse embryonic fibroblasts (MEFs). Immunostaining localized Arg1 predominantly to CD68⁺ macrophages in heart and liver. Given recent evidence identifying Arg1 as a novel mediator of efferocytosis, these findings suggest that Arg1 may promote macrophage metabolic reprogramming and resolution of inflammation by enhancing the clearance of apoptotic cells. Furthermore, Fst gene delivery increased the expression of fibroblast growth factor 21 (Fgf21) and adiponectin (AdipoQ) in WAT. Collectively, these findings identify Fst as a novel anti-atherogenic regulator that protects against vascular disease by promoting adipose browning, improving lipid metabolism, and activating Arg1-mediated metabolic pathways. Full article

The increase in the prevalence of non-communicable diseases globally has been attributed in part to poor lifestyle choices, including unhealthy dietary habits. Dietary polysaccharides, including resistant starch and non-starch polysaccharides, have gained increasing attention due to their potential role in the regulation of glucose and lipid metabolism. Therefore, the aim of this review was to evaluate the role of dietary polysaccharides in the regulation of blood glucose and lipid parameters. Method: A narrative review approach was adopted for this review. Searches were conducted through EBSCOHost and involved the following databases: Medline, APA PsycInfo, CINAHL Plus with Full Text, Psychology and Behavioural Sciences collection, Academic Search Premier and APA PsycArticles. Searches were conducted on 14 April 2026 and covered all records available from database inception to the search date. Search terms were combined using Boolean operators (AND/OR). The reference list of articles was also searched for more articles. Results: Twenty-one studies from thirteen different countries were included in this review. Based on narrative synthesis, five themes were identified: the effects of dietary polysaccharides on glycaemia, insulin, lipids, energy intake and satiety/appetite. The findings demonstrated considerable heterogeneity across studies. While several studies reported improvements in fasting glucose, postprandial glucose, glycated haemoglobin and insulin responses following resistant starch and non-starch polysaccharide interventions, other studies found no significant effects on glycaemic control or insulin levels. Lipid outcomes were similarly inconsistent, although some studies reported reductions in total cholesterol and low density lipoprotein cholesterol. Effects on energy intake and satiety varied according to the type and physicochemical characteristics of the polysaccharide investigated. Conclusion: The findings of this review suggest that dietary polysaccharides may contribute to improvements in glucose control and lipid metabolism, although the magnitude and consistency of these effects vary across populations, intervention types and study designs. The most frequently reported beneficial findings related to blood glucose parameters, although substantial heterogeneity remained across studies. Further, well-designed studies, including randomised controlled trials with longer durations, are needed to fully establish the role of dietary polysaccharides in the control of blood glucose and lipid parameters. Full article

Neuroinflammation, driven by microglial activation and oxidative stress, is a key pathological feature of various neurodegenerative diseases. Dendropanax morbifera Léveille (DM) is a medicinal plant known for its diverse pharmacological activities; however, the influence of leaf developmental stage on its neuroprotective potential remains poorly understood. In this study, we compared the phytochemical profiles of young DM (YDM) and mature DM leaves and evaluated their effects on neuronal metabolism and microglia-mediated neuroinflammation. HPLC analysis revealed that YDM contained approximately 2.4-fold higher levels of chlorogenic acid than DM, while DM exhibited higher quercetin content. In differentiated N2A neuronal cells, YDM treatment significantly upregulated the expression of key metabolic and mitochondrial regulators, including PGC-1α, PPARγ, and CPT2, suggesting enhanced mitochondrial and metabolic regulatory signaling related to biogenesis and fatty acid β-oxidation. Under inflammatory conditions, YDM more potently suppressed the secretion of pro-inflammatory cytokines (IL-6 and TNF-α) in LPS-stimulated BV2 microglia compared to DM. Furthermore, in N2A cells treated with BV2-conditioned medium, both extracts effectively mitigated reactive oxygen species production and restored brain-derived neurotrophic factor expression. These findings demonstrate that leaf age is a critical determinant of the phytochemical composition and biological activity of DM. Our results suggest that chlorogenic acid-rich YDM preparations may offer superior therapeutic advantages in targeting neuroinflammatory and metabolic dysregulation in the central nervous system. Full article

Climate change is expected to increase temperatures in agricultural producing regions, potentially affecting fruit development and quality. To date, the molecular responses of raspberry fruits to moderate warming under field conditions have not been explored. In this paper, raspberry plants (Rubus idaeus L. cv. Heritage) growing in two contrasting agroclimatic regions of Chile were exposed to a moderate increase in temperature during fruit development. Fruit phenotyping, histological analyses, and RNA sequencing were used to evaluate physiological and transcriptomic responses to warming. Elevated temperature increased fruit weight and fruit dimensions in both orchards and was associated with larger drupelet and cell areas, which was accompanied by reduced cell density. Moreover, transcriptomic analyses revealed marked differences in gene expression responses between raspberries fruits from different locations with only a small number of heat-responsive genes shared across locations. Nevertheless, the common enrichment of oxylipin-related processes was observed, suggesting a conserved response. In addition, a combined treatment model identified the enrichment of processes like ribosome biogenesis, RNA metabolism, cell cycle regulation, cytokinesis, and structural cellular remodeling. These transcriptional changes were consistent with the cellular phenotypes observed in heat-treated fruits. Overall, our results show that moderate warming promotes larger raspberry fruits through changes in cellular organization, while the underlying molecular responses are strongly influenced by agroclimatic context. Full article

Background/Objectives: Gamma-aminobutyric acid (GABA) is increasingly recognized as an important modulator of pancreatic beta-cell function, but the mechanisms by which it regulates intracellular Ca²⁺ oscillations and coordinated beta-cell activity remain insufficiently understood. The aim of this study was to investigate how GABA influences the amplitude, frequency, phase adjustment, entrainment, and synchronization of beta-cell Ca²⁺ oscillations. Methods: We developed a reduced ATP–Ca²⁺ oscillation model, based on established beta-cell oscillatory frameworks, and coupled it to the GABA-shunt subsystem derived from our previously established Dual Anaplerotic Model. The model incorporates explicit dynamics of cytosolic Ca²⁺, endoplasmic reticulum Ca²⁺, ATP, and a regulatory variable controlling Ca²⁺ influx, while the interstitial GABA signal is represented as a delayed feedback signal acting on cellular excitability. Single-cell and two-cell simulations were performed to analyze GABA-dependent oscillatory regulation and intercellular coupling. Results: The model reproduced key experimental observations under both control and GABA-deficient conditions, including reduced Ca²⁺-oscillation amplitude and a prolonged oscillation period when GABA production was suppressed. Mechanistically, GABA affected single-cell oscillations through two complementary pathways: metabolically, by modulating ATP production through PEP-related and TCA-related contributions linked to the GABA shunt, and as an interstitial/paracrine signal, by adjusting the phase of Ca²⁺ influx through fast and delayed inhibitory feedback. In the reduced two-cell model, delayed interstitial GABA signaling could phase-lock non-identical oscillators over finite ranges of parameter mismatch. When included as an additional weak effective term, electrical coupling broadened these ranges, consistent with a complementary interaction between GABA-mediated phase adjustment and established electrical coupling. Conclusions: GABA acts as a dual regulator of beta-cell dynamics, linking intracellular metabolism to Ca²⁺-oscillation patterning and promoting coordinated activity through intercellular phase adjustment. The model provides a mechanistic framework connecting GABA metabolism, ATP dynamics, Ca²⁺ signaling, and beta-cell synchronization in pancreatic islets. Full article