Search Results (546)

Background/Objectives: N6-methyladenosine (m⁶A) is a prevalent RNA modification that significantly influences various biological processes. AlkB homologs (ALKBHs) belong to the family of specific demethylases and, by regulating m⁶A methylation, are known to be involved in the modulation of plant stress responses. However, the ALKBH gene family has not been systematically characterized in ginseng. Methods: A genome-wide identification and characterization of the ALKBH gene family in ginseng were performed using a telomere-to-telomere reference genome. Phylogenetic relationships, gene structures, conserved motifs, 3D structures, chromosomal distribution, syntenic relationships, cis-acting regulatory elements, protein-protein interaction (PPI) networks, and expression profiles were analyzed. Transcriptome datasets covering multiple tissues, developmental stages, cultivars, and abiotic stress treatments were examined. Candidate stress-responsive genes were further validated by qRT-PCR. Results: A total of 17 PgALKBH genes were identified and classified into seven subfamilies. Structural analyses revealed conserved motifs, exon–intron organization, and 3D structures among members within the same subfamily. Chromosomal localization and synteny analyses suggested that the PgALKBH family has been evolutionarily conserved between ginseng and Arabidopsis and has primarily undergone purifying selection during its expansion. Promoter analysis identified abundant light-, hormone-, and stress-responsive cis-elements. Expression profiling revealed distinct tissue- and developmental stage-specific patterns. The PPI analysis suggested that PgALKBH proteins, especially PgALKBH10, may play a central role in m⁶A-mediated RNA regulation in ginseng. Transcriptome and qRT-PCR analyses further showed that PgALKBH genes respond differentially to drought, cold, and salt stresses. Notably, PgALKBH10 was induced under all three stress conditions. Conclusions: This study provides a comprehensive characterization of the ALKBH gene family in ginseng and identifies PgALKBH10 as a promising candidate involved in multiple abiotic stress responses. These findings establish a foundation for elucidating the roles of RNA m⁶A demethylation in ginseng and provide valuable genetic resources for developing stress-tolerant ginseng cultivars. Full article

Background: Ginsenoside Rh2 (Rh2), a bioactive metabolite of Panax ginseng, has documented anticancer effects, but its role in cancer–immune crosstalk remains incompletely defined. Thus, we aimed to investigate the role of Rh2 in hepatocellular carcinoma (HCC) cells and immune regulation. Methods: We used a co-culture system of murine Hepa1-6 hepatocellular carcinoma cells or nonmalignant AML12 hepatocytes with primary splenocytes to model cancer–immune interactions during Rh2 exposure. Readouts included cell viability, nuclear morphology, and multiparameter flow cytometry. Results: In a co-culture system of Hepa1-6 cells and splenocytes, Rh2 decreased bulk cell viability and increased apoptosis in Hepa1-6 cells. CD8⁺ T cells exhibited enhanced effector features, with increased CD107a and IFN-γ expression following Rh2 treatment. Rh2 reduced PD-L1 expression on Hepa1-6 cells and splenocytes, and PD-1 expression on CD8⁺ T cells. Rh2 also reduced TGF-β1 and IL-6 levels in both Hepa1-6 cells and splenocytes, and decreased IL-10 levels in splenocytes. This was accompanied by a reduction in CD4⁺CD25⁺FOXP3⁺ regulatory T cells (Tregs). Conclusions: In a physiologically relevant cancer–immune context, Rh2 reprograms suppressive interactions by enhancing CD8⁺ T cell effector function, dampening PD-L1/PD-1 signaling, and reducing key immunosuppressive cytokines and Tregs. These coordinated effects position Rh2 as a candidate multi-target immunomodulatory agent for enhancing anticancer immunity. Full article

Rusty root rot of ginseng (Panax ginseng) caused by Ilyonectria spp. infection is a devastating soil-borne disease restricting the sustainable production of garden-cultivated ginseng (GCG) in Northeast China and causes severe yield and economic losses; GCG is far more susceptible to this pathogen than forest-cultivated ginseng (Lin-Xia-Shan-Shen, LXSS). Ginsenosides, the signature triterpenoid saponin defensive metabolites of ginseng, are characteristic dammarane-type triterpenoid defensive saponins represented by Re, Rg₂, Rb₁, Rd, and Rg₁. These compounds are continuously secreted into the rhizosphere and widely participate in plant–microbe interactions, yet their functional roles in mediating Ilyonectria infection remain poorly clarified. This study aimed to clarify how rhizospheric ginsenosides regulate the infection process of pathogenic Ilyonectria strains. Two pathogenic strains, Ilyonectria sp. SYM-1 and Ilyonectria sp. SYM-2, were found isolated from diseased GCG roots and verified as causal agents via morphological observation, molecular ITS identification and artificial inoculation infection experiments. Interestingly, the concentrations of five ginsenosides, Re, Rg₂, Rb₁, Rd, and Rg₁, in the rhizospheric soil of GCG with rusty root rot were significantly higher than those in the rhizospheric soil of healthy LXSS plants. In addition, the concentrations of ginsenosides in the LXSS rhizospheric soils decreased with increasing age of plants. Non-nutritive suspension co-culture assays showed that high concentrations of the ginsenosides Rg₁ and Rd significantly promoted spore germination of the strains SYM-1 and SYM-2. However, Rb₁ had a certain inhibitory effect on the growth of Ilyonectria sp. SYM-2. Host inoculation experiments further indicated that infection with either fungus significantly reduced the concentrations of ginsenosides produced in ginseng roots. These results demonstrate that the pathogenic fungi SYM-1 and SYM-2 of Ilyonectria can adapt to and utilize ginsenosides. Collectively, these findings prove that the two pathogenic Ilyonectria strains have evolved the capacity to adapt to and exploit rhizospheric ginsenosides to facilitate their infectivity. From an application perspective, reducing rhizospheric ginsenoside release may represent a promising theoretical strategy for ginseng cultivation and germplasm improvement, which warrants further verification by field or greenhouse experiments for validation. Full article

The Cysteine-rich Polycomb-like Protein (CPP) gene family is a class of transcription factors containing conserved CXC domains that are widely involved in the regulation of plant growth and development, cell division, and stress responses. Based on the ginseng genome and transcriptome database, all members of the PgCPP gene family in Panax ginseng were systematically identified, and comprehensive bioinformatics analyses, including phylogenetic, conserved domain, chromosomal localization and collinearity, cis-acting element, and expression pattern analyses, were conducted. In this study, we identified 44 PgCPP gene family members in ginseng, which were unevenly localized on multiple chromosomes. The phylogenetic tree divided them into three subfamilies, with members in the same subfamily being highly conserved. Conserved domain analysis revealed that all PgCPPs contain typical CXC motifs. Cis-acting elements were abundant in light response, hormone responses (abscisic acid, methyl jasmonate, salicylic acid), and stress response elements. Expression heatmaps demonstrated that different members have specific expression patterns across different ages, tissues, and species. After treatment with MeJA, transcriptional suppression of PgCPP03-4 and PgCPP03-13 was observed, and their expression levels demonstrated significant negative correlations with the contents of six protopanaxadiol-type ginsenosides. These findings suggest that PgCPP03-4 and PgCPP03-13 may act as negative regulators of protopanaxadiol-type ginsenoside biosynthesis within the MeJA signaling pathway. This systematic characterization and identification of the CPP gene family members in P. ginseng establishes a foundational framework for future functional validation and molecular breeding initiatives. Full article

Ginseng Alternaria leaf and stem blight (GALSB), caused by Alternaria alternata, poses a severe threat to ginseng cultivation. Although azoxystrobin is a cornerstone fungicide for GALSB management, the emergence of widespread adaptive resistance has severely curtailed its field efficacy. This study integrated molecular, transcriptomic, and genetic approaches to unravel the underlying resistance mechanisms. Targeted gene sequencing and molecular docking revealed that resistant strains harbor a conserved G143A point mutation in the AaCyt b protein. This mutation weakens the azoxystrobin–AaCyt b protein binding affinity by decreasing the binding energy from −8.31 to −7.08 kcal/mol. Additionally, comparative transcriptomics and RT-qPCR demonstrated pronounced upregulation of the alternative oxidase gene (AaAOX) and core energy metabolism pathways in resistant strain TYC8-2, with AaAOX expression increasing 4.45–6.91-fold. Fungicidal inhibition of AOX via salicylhydroxamic acid (SHAM) restored fungal sensitivity, increasing azoxystrobin sensitivity by 11.66-fold. Crucially, genetic knockout of AaAOX enhanced sensitivity by approximately 2.7 × 10⁴-fold. Phenotypic assays further established AaAOX as a multifunctional regulator; the AaAOX mutant exhibited attenuated virulence on ginseng leaves and increased sensitivity to oxidative and osmotic stresses (NaCl, H₂O₂, NaAc). We conclude that the G143A mutation in AaCyt b and the transcriptional overexpression of AaAOX act independently to drive azoxystrobin resistance in A. alternata. These findings provide comprehensive mechanistic insights to guide resistance monitoring, optimize fungicide applications, and develop precision strategies for GALSB management. Full article

The continued rise in atmospheric carbon dioxide (CO₂) concentrations presents a strategic opportunity to harness climate change variables within the framework of precision agriculture. Despite the well-established role of elevated CO₂ (eCO₂) in enhancing biomass accumulation, its largely underexplored potential to drive the biosynthesis of secondary metabolites represents a more significant and promising avenue of investigation. This review appraises the physiological and molecular mechanisms through which eCO₂ enrichment redirects metabolic flux toward secondary metabolite biosynthesis, with far-reaching implications for plant productivity and resilience. Special emphasis is placed on critically evaluating the scientific literature to explore how CO₂-mediated modulation of the carbon–nutrient balance (CNB) can be strategically leveraged to enhance secondary metabolite yields. Moving from observation to application, integrated strategies are proposed to exploit CO₂ enrichment in advanced bioreactor systems and controlled-environment greenhouses as a means of maximizing bioactive compound production in ginseng. Pinpointing the regulatory sweet spots at which carbon saturation elicits maximum ginsenoside expression opens a promising avenue for engineering ginseng cultivation systems with sustainable potency and superior bioactivity. Though the full molecular architecture of these pathways in Panax awaits elucidation, converging evidence from related plant systems furnishes a credible mechanistic scaffold for future research. Full article

Background: Neuroinflammation contributes to the etiopathology and symptom severity of neurodegenerative and neuropsychiatric disorders. Glial cells, especially microglia and astrocytes, play a crucial role in neuroinflammation. It has been reported that ginseng (Panax ginseng) and its bioactive component ginsenoside Rg1 exhibit anti-inflammatory effects and can improve cognitive performance in various models. However, the exact underlying mechanisms remain unclear. Methods: Astrocyte–microglia co-culture models simulating physiological (M5, 5–10% microglia) and pathological/inflammatory (M30, 30–40% microglia) conditions were treated with different concentrations of ginsenoside Rg1 (15, 30, 45 µM) or ginseng extract (derived from Korean red ginseng) at low (12.5, 25, 37.5 µg/mL) or high doses (125, 250, 375 µg/mL) for 24 h. Cell viability was assessed using the MTT assay while microglial reactivity was examined using immunocytochemistry. Astrocytic gap-junctional coupling was investigated using the scrape-loading method, and connexin 43 (Cx43) expression was analyzed using immunocytochemistry and Western blot. Results: Both Rg1 and low-dose ginseng extract reduced microglial activation under inflammatory conditions by promoting a shift in microglia from an activated to homeostatic (resting) phenotype. Rg1 preserved astrocytic gap-junctional function by preventing the inflammation-induced downregulation of Cx43 expression and enhancing Cx43-mediated gap-junctional intercellular communication. Rg1 caused a significant reduction in glial cell viability, but only at high concentrations (30 and 45 µM), under inflammatory conditions. High-dose ginseng extract showed a significant concentration-dependent reduction in glial cell viability under physiological and pathological conditions, without comparable anti-inflammatory benefits. Conclusions: This study demonstrates that low-dose ginseng and its active compound Rg1 exert anti-inflammatory effects by modulating astrocytic coupling and microglial reactivity. These results provide a novel therapeutic perspective for the use of ginseng in the treatment of neurodegenerative and neuropsychiatric diseases related to neuroinflammation. Full article

Ginsenoside Rg1 has a broad spectrum of pharmacological activities, and its concentration is a key indicator of ginseng quality. Because ginsenoside levels are quantitative traits controlled by multiple genes and environmental factors, identifying genes involved in Rg1 biosynthesis is essential to improve its production in ginseng. Transcriptome analysis of 344 4-year-old ginseng roots identified 33 Candidate Genes implicated in Rg1 biosynthesis. These candidates were detected through differential expression analysis, SNP/InDel mutation screening, correlation analysis with Rg1 content variation, and co-expression network analysis. By integrating GO functional annotation, gene expression profiles, and Rg1 content correlations, a putative biosynthetic pathway for Rg1 was inferred and the roles of these genes were preliminarily clarified. Further study of MeJA regulation confirmed that PgRg1-021 is highly associated with ginsenoside Rg1 biosynthesis. Functional verification was performed via overexpression of PgRg1-021 and RNAi in ginseng hairy roots. RT-qPCR analysis showed that PgRg1-021 negatively regulated ginsenoside Rg1 biosynthesis: Rg1 saponin levels decreased after overexpression and increased after RNAi. This study was the first to verify PgRg1-021’s role in Rg1 biosynthesis and provided essential gene resources for pathway analysis. It established a foundation for targeted breeding and serves as a reference for identifying other genes associated with complex traits. Full article

Oxidative stress is a primary driver of sperm deterioration during chilled storage of poultry semen, and identifying effective natural antioxidant supplements for semen extenders is an important practical goal for poultry reproductive management. This study evaluated the protective effects of ginseng extract (Panax ginseng) supplementation on sperm viability, motility, oxidative stress biomarkers, antioxidant defense, and fertility in chilled Leung Hang Kao rooster semen. Pooled semen was diluted in IGGKPh extender supplemented with ginseng extract at 0, 1, 2, 3, or 4 mg/mL and stored at 5 °C for 0, 24, and 48 h. Sperm viability, total motility, progressive motility, malondialdehyde (MDA) concentration, total antioxidant capacity (T-AOC), glutathione peroxidase (GPx) activity, catalase (CAT) activity, and fertility following artificial insemination were evaluated at each time point. All ginseng-supplemented groups showed significantly lower MDA concentrations and higher GPx activity than the unsupplemented control throughout storage. At 48 h, total motility and progressive motility were highest in the 2 and 3 mg/mL groups, while T-AOC was best maintained in the 1 and 2 mg/mL groups. CAT activity did not differ significantly among groups at 48 h (p = 0.2498). Fertility was significantly higher in the 1 and 2 mg/mL groups than in the control after 24 and 48 h of storage, and the alignment between T-AOC and fertility across storage time points indicated that overall antioxidant buffering capacity was a stronger determinant of fertilizing competence than individual enzyme activities or MDA concentration alone. Concentrations of 3–4 mg/mL, despite producing lower MDA at 48 h, did not confer superior fertility outcomes, suggesting a hormetic dose–response relationship. Based on integrated evidence from sperm quality, antioxidant status, and in vivo fertility, ginseng extract supplementation at 1–2 mg/mL is recommended as the most suitable range for preserving chilled Leung Hang Kao rooster semen and may represent a practical natural antioxidant strategy for Thai native poultry breeding programs. Full article

The glucagon-like peptide-1 receptor (GLP-1R) is a class B G protein-coupled receptor (GPCR) central to metabolic regulation, and its potential modulation by dietary phytochemicals is increasingly recognized as physiologically relevant. Understanding how such compounds interact with GLP-1R is important for clarifying mechanisms that may contribute to gut-to-brain signaling. In this study, we examined three structurally related dietary ginsenosides, Rg1, Rg2, and Rg3, as potential modulators of GLP-1R using luciferase reporter assays and computational analyses. Despite sharing similar molecular weights, a common dammarane scaffold, and comparable sugar moieties, the three ginsenosides displayed distinct effects on GLP-1R activity: Rg2 and Rg3 potently reduced receptor activation in a dose-dependent manner when co-administered with Exendin-4, whereas Rg1 had minimal effect. Computational screening of the GLP-1R structure for binding sites identified a putative extracellular pocket on the protein that can accommodate these compounds, while molecular docking and binding free energy calculations provided predicted affinities qualitatively reflecting the phytochemicals’ experimental activities. These findings point to a plausible extracellular mechanism through which dietary ginsenosides may influence GLP-1R responsiveness at the intestinal interface. Our results point to the possibility that non-absorbed phytochemicals can differentially modulate gut-expressed receptors, suggesting a novel pathway for dietary signaling relevant to ethnopharmacology and metabolic health. Full article

Background: Metabolic-associated fatty liver disease (MAFLD) has a high prevalence of 30–40% in China and Asia, with a complex pathogenesis and no specific therapeutic drugs. Phytochemicals have become a research hotspot for MAFLD prevention, and ginsenosides, the core active components of Panax ginseng, show great potential in anti-MAFLD research. This review aims to comprehensively clarify the key mechanisms and targets of ginsenosides in preventing and treating MAFLD, to provide a theoretical basis for their application in metabolic diseases, and to promote the development of natural phytochemical resources. Method: The literature review method was adopted to sort out the regulatory effects and molecular targets of ginsenosides in multiple pathological processes of MAFLD from published studies. Results: Ginsenosides regulated MAFLD through multi-pathway and multi-target effects: antioxidant regulation occurred via Nuclear factor E2-related factor 2 (Nrf2)/Silent information regulator 1/6 (SIRT1/6) pathways, and anti-inflammatory regulation was achieved by inhibiting the Nuclear factor kappa-B (NF-κB)/NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome. Additionally, the measures adopted improved insulin resistance and lipid metabolism disorder, suppressed hepatocyte apoptosis/pyroptosis, repaired autophagy, alleviated hepatocyte senescence, and reshaped gut microbiota to restore gut–liver axis homeostasis. Conclusions: Ginsenosides have good potential for MAFLD prevention and treatment, but there is a prominent lack of human clinical evidence as most existing studies are only based on in vitro cell and in vivo animal models, and the synergistic mechanisms among different ginsenoside components remain unclear. Future research needs multi-omics analysis, formulation optimization, and large-sample clinical trials, and ginsenosides have broad application prospects in MAFLD intervention. Full article

American ginseng (Panax quinquefolius L.) is an important medicinal crop, but its improvement in China is limited by variety degeneration and a shortage of elite cultivars. In this study, phenotypic traits and simple sequence repeat (SSR) markers were integrated to evaluate the genetic diversity of 51 selected accessions from major Chinese production regions. Phenotypic analysis showed that five of the 18 quantitative traits had phenotypic coefficients of variation exceeding 40%, mainly involving root traits such as fresh root weight and lateral root number. Broad-sense heritability for these root traits ranged from 61.70% to 74.80%, indicating substantial genetic contribution under standardized conditions. Principal component analysis identified five candidate elite accessions: CY3 and KD1 for tall stature and high yield, DH1 and LH2 for high ginsenoside content, and AT1 for well-developed lateral roots. A 12-accession representative subset was further proposed for conservation and pre-breeding. SSR-based clustering showed weak geographic differentiation, and Mantel analysis revealed no significant correlation between phenotypic and SSR-based genetic distances. These materials, together with the proposed accession-level conservation strategy, provide useful resources for germplasm preservation, parental selection, QTL mapping, and marker-assisted breeding. Full article

Ginseng (Panax ginseng C. A. Mey.) is a classic traditional Chinese herbal medicine with a history of clinical use that spans millennia. Its utilisation has long been established in the regulation of physical and mental equilibrium, in addition to the amelioration of conditions pertaining to the heart, spleen, and brain. Recent studies have indicated that the core biological activity of the substance under investigation is mediated by key active components such as ginsenosides, polysaccharides, and polyphenols. These components are closely associated with the regulation of the gut-brain axis (GBA). However, extant reviews have predominantly concentrated on individual diseases or specific mechanisms, thereby lacking a thorough investigation into the comprehensive analysis of how ginseng components exert systemic effects via the GBA. This review systematically searched and analyzed published studies in major databases regarding the regulation of the GBA by ginseng bioactive components, summarizing the latest advances in its role as a multifactorial disease intervention regulator targeting the GBA. It has been demonstrated that ginseng components exert a multifaceted GBA regulatory effect through interconnected mechanisms, including modulation of the gut microbiota, protection of the intestinal barrier, anti-inflammatory actions, and regulation of neurotransmitters, showing promising preclinical therapeutic potential in neurodegenerative diseases, mood disorders, metabolic diseases, and gastrointestinal disorders. Contrary to previous reviews, which focused on the description of individual ginseng components or specific diseases, this study provides a comprehensive analysis of how various bioactive components of ginseng modulate the gut-brain axis in relation to multiple disease categories through a systematic review. However, the preponderance of extant evidence derives from preclinical studies and necessitates further validation through clinical trials. This review provides pivotal directions and theoretical underpinnings for the clinical translation of ginseng’s bioactive components and the development of disease intervention strategies targeting the gut-brain axis. Full article

Agriforestry systems are essential for improving the quality of medicinal herbs and ensuring the sustainable management of forests. Forest soil acidification inhibits the growth of medicinal plants. The application of novel dolomite-loaded vermicompost (DOVC) is considered a potential method for promoting plants growth. However, the mechanisms by which it promotes the growth of medicinal plants are poorly understood. This study combined observational analysis and field experimentation, to first elucidate the correlation between under-forest soil pH and root dry weight of American ginseng (Panax quinquefolius L.). Subsequently, the mechanisms by which DOVC promotes the growth of P. quinquefolius were analyzed from the perspectives of plant physiology and soil microbiome. The results indicate: (1) Field survey results demonstrated when the pH was between 5.28 and 5.99, the root dry weight of P. quinquefolius gradually increased with increasing soil pH. (2) Compared with Control, DOVC increased the soil pH by 1.48 units and promoted the growth of P. quinquefolius, with a net photosynthetic rate increase of 60.26%, malondialdehyde content decrease of 71.07%, and root dry weight increase of 50.33%. (3) Compared with Control, DOVC enhanced bacterial community diversity, with Ace and Chao 1 indices increasing significantly by 33.88% and 25.18%, respectively; and increased the relative abundance of Chloroflexi and Basidiomycota. (4) Partial Least Squares Path Modeling revealed that DOVC positively influenced P. quinquefolius growth via the improvement of soil health index and microbial community diversity. The development of this novel soil amendment offers a new approach to improving soil health in agroforestry systems. Full article