Dai Li-Li, Cho Sung-Bo, Li Hui-Fang, A Li-Sha, Ji Xiao-Ping, Pan Sirigunqiqige, Bao Ming-Lan, Bai Laxinamujila, Ba Gen-Na, Fu Ming-Hai
NMPA Key Laboratory of Quality Control of Traditional Chinese Medicine (Mongolian Medicine), Inner Mongolia Minzu University, Tongliao 028000, Inner Mongolia Autonomous Region, China.
Key Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Provincial Key Laboratory for Research and Development of Tropical Herbs, Hainan Medical University, Haikou 571199, Hainan Province, China.
World J Diabetes. 2023 Jun 15;14(6):846-861. doi: 10.4239/wjd.v14.i6.846.
(LR) is traditionally used in Mongolian folk medicine as a hypoglycemic agent, but its evidence-based pharmacological effects and me-chanisms of action have not been fully elucidated.
To emphasize the hypoglycemic action mechanism of LR in a type 2 diabetic rat model and examine potential biomarkers to obtain mechanistic understanding regarding serum metabolite modifications.
A high-fat, high-sugar diet and streptozotocin injection-induced type 2 diabetic rat model was established. The chemical composition of the LR was identified by high performance liquid chromatography. LR extract administrated as oral gavage at 0.5 g/kg, 2.5 g/kg, and 5 g/kg for 4 wk. Anti-diabetic effects of LR extract were evaluated based on histopathological examination as well as the measurement of blood glucose, insulin, glucagon-like peptide 1 (GLP-1), and lipid levels. Serum metabolites were analyzed using an untargeted metabolomics approach.
According to a chemical analysis, swertiamarin, sweroside, hesperetin, coumarin, 1.7-dihydroxy-3,8-dimethoxyl xanthone, and 1-hydroxy-2,3,5 trimethoxanone are the principal active ingredients in LR. An anti-diabetic experiment revealed that the LR treatment significantly increased plasma insulin and GLP-1 levels while effectively lowering blood glucose, total cholesterol, triglycerides, low-density lipoprotein cholesterol, and oral glucose tolerance test compared to the model group. Furthermore, untargeted metabolomic analysis of serum samples detected 236 metabolites, among which 86 were differentially expressed between the model and the LR group. It was also found that LR considerably altered the levels of metabolites such as vitamin B6, mevalonate-5P, D-proline, L-lysine, and taurine, which are involved in the regulation of the vitamin B6 metabolic pathway, selenium amino acid metabolic pathway, pyrimidine metabolic pathway, and arginine and proline metabolic pathways.
These findings indicated that LR may have a hypoglycemic impact and that its role may be related to changes in the serum metabolites and to facilitate the release of insulin and GLP-1, which lower blood glucose and lipid profiles.
(LR)在蒙古民间医学中传统上用作降血糖剂,但其循证药理学作用及作用机制尚未完全阐明。
在2型糖尿病大鼠模型中强调LR的降血糖作用机制,并检测潜在生物标志物,以了解血清代谢物修饰的作用机制。
建立高脂高糖饮食联合链脲佐菌素注射诱导的2型糖尿病大鼠模型。采用高效液相色谱法鉴定LR的化学成分。以0.5 g/kg、2.5 g/kg和5 g/kg的剂量对LR提取物进行灌胃给药,持续4周。基于组织病理学检查以及血糖、胰岛素、胰高血糖素样肽1(GLP-1)和血脂水平的测量来评估LR提取物的抗糖尿病作用。使用非靶向代谢组学方法分析血清代谢物。
化学分析表明,獐牙菜苦苷、獐牙菜苷、橙皮素、香豆素、1,7 - 二羟基 - 3,8 - 二甲氧基呫吨酮和1 - 羟基 - 2,3,5 - 三甲氧基呫吨酮是LR的主要活性成分。抗糖尿病实验表明,与模型组相比,LR治疗显著提高了血浆胰岛素和GLP-1水平,同时有效降低了血糖、总胆固醇、甘油三酯、低密度脂蛋白胆固醇,并改善了口服葡萄糖耐量试验。此外,对血清样本的非靶向代谢组学分析检测到236种代谢物,其中86种在模型组和LR组之间差异表达。还发现LR显著改变了维生素B6、甲羟戊酸-5P、D - 脯氨酸、L - 赖氨酸和牛磺酸等高代谢物的水平,这些代谢物参与维生素B6代谢途径、硒氨基酸代谢途径、嘧啶代谢途径以及精氨酸和脯氨酸代谢途径的调节。
这些发现表明LR可能具有降血糖作用,其作用可能与血清代谢物的变化有关,并促进胰岛素和GLP-1的释放,从而降低血糖和血脂水平。