Wang Rong, Liu Xue-Feng, Yang Kuan, Yu Li-Li, Liu Shao-Jing, Wang Na-Na, Chen Yun-Mei, Hu Ya-Qi, Qin Bei
Xi'an Key Laboratory for Research and Development of Innovative Multi-Target Anti-Hypertensive Drugs, Xi'an Medical University, Xi'an 710021, China.
Xi'an Innovative Anti-Hypertensive Drugs International Science and Technology Cooperation Base, Xi'an Medical University, Xi'an 710021, China.
Curr Issues Mol Biol. 2025 Jul 3;47(7):515. doi: 10.3390/cimb47070515.
: Gypenosides (Gps) are the main active compounds of and show promise in managing diabetes; nevertheless, the mechanism by which Gps exert anti-diabetic effects is still not fully understood. The aim of this study is to clarify the molecular mechanisms of Gps in ameliorating glucose dysregulation. : Qualitative and quantitative analyses on the chemical components of Gps were performed, respectively. Type 2 diabetes mellitus mouse models were established, and the mice were subsequently treated with Gps at doses of 200, 100, or 50 mg/kg for 4 weeks. Biochemical markers were measured. Histopathological assessments of hepatic and colonic tissues were conducted. The compositions of the intestinal microbiota, short-chain fatty acids (SCFAs), and bile acids (BAs) in fecal samples were analyzed. Western blotting was applied to examine the activation of relevant signaling pathways. : Gps have potent regulatory effects on metabolic homeostasis by improving glucose and lipid profiles and alleviating hepatic tissue damage. Treatment with Gps significantly reduced serum levels of lipopolysaccharides and key pro-inflammatory cytokines (interleukin-6 and tumor necrosis factor-α). Moreover, Gps enhanced the integrity of the gut barrier by upregulating the level of tight junction proteins (ZO-1 and occludin). Microbiota profiling revealed that Gps markedly increased microbial diversity and richness, decreased the ratio of /, and elevated abundance from the phylum to the genus level. Targeted metabolomics further demonstrated that Gps modulated gut microbial metabolites by promoting SCFA production and reshaping BA profiles. Specifically, Gps elevated the primary-to-secondary BA ratio while reducing the 12α-hydroxylated to non-12α-hydroxylated BA ratio. Mechanistically, Western blotting demonstrated that Gps triggered the hepatic PI3K/AKT pathway and the intestinal BA/FXR/FGF15 axis, suggesting the coordinated regulation of metabolic and gut-liver axis signaling pathways. : Gps significantly ameliorate hyperglycemia and hyperlipidemia through a multifaceted mechanism involving gut microbiota modulation, the restoration of intestinal barrier function, and the regulation of microbial metabolites such as SCFAs and BAs. These findings offer novel insights into their mechanism of action via the gut-liver axis.
绞股蓝总皂苷(Gps)是绞股蓝的主要活性成分,在糖尿病管理方面显示出前景;然而,Gps发挥抗糖尿病作用的机制仍未完全阐明。本研究的目的是阐明Gps改善葡萄糖调节异常的分子机制。分别对Gps的化学成分进行了定性和定量分析。建立2型糖尿病小鼠模型,随后用200、100或50mg/kg剂量的Gps对小鼠进行4周治疗。检测生化指标。对肝脏和结肠组织进行组织病理学评估。分析粪便样本中肠道微生物群、短链脂肪酸(SCFAs)和胆汁酸(BAs)的组成。应用蛋白质免疫印迹法检测相关信号通路的激活情况。Gps通过改善血糖和血脂水平以及减轻肝组织损伤,对代谢稳态具有强大的调节作用。用Gps治疗可显著降低血清脂多糖和关键促炎细胞因子(白细胞介素-6和肿瘤坏死因子-α)水平。此外,Gps通过上调紧密连接蛋白(ZO-1和闭合蛋白)水平增强肠道屏障的完整性。微生物群分析显示,Gps显著增加微生物多样性和丰富度,降低/的比例,并从门水平到属水平提高丰度。靶向代谢组学进一步证明,Gps通过促进SCFA产生和重塑BA谱来调节肠道微生物代谢产物。具体而言,Gps提高了初级胆汁酸与次级胆汁酸的比例,同时降低了12α-羟基化胆汁酸与非12α-羟基化胆汁酸的比例。从机制上讲,蛋白质免疫印迹法表明,Gps触发了肝脏PI3K/AKT途径和肠道BA/FXR/FGF15轴,提示代谢和肠-肝轴信号通路的协同调节。Gps通过涉及肠道微生物群调节、肠道屏障功能恢复以及对SCFAs和BAs等微生物代谢产物的调节等多方面机制,显著改善高血糖和高血脂。这些发现为其通过肠-肝轴的作用机制提供了新的见解。