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桑枝生物碱改善2型糖尿病KKAy小鼠的糖代谢,同时调节肠道菌群和回肠炎症损伤

Ramulus Mori (Sangzhi) Alkaloids (SZ-A) Ameliorate Glucose Metabolism Accompanied by the Modulation of Gut Microbiota and Ileal Inflammatory Damage in Type 2 Diabetic KKAy Mice.

作者信息

Liu Quan, Liu Shuainan, Cao Hui, Ji Wenming, Li Caina, Huan Yi, Lei Lei, Fu Yaxin, Gao Xuefeng, Liu Yuling, Shen Zhufang

机构信息

Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

State Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Key Laboratory of Polymorphic Drugs of Beijing, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Front Pharmacol. 2021 Apr 15;12:642400. doi: 10.3389/fphar.2021.642400. eCollection 2021.

Abstract

The novel Traditional Chinese Medicine Ramulus Mori (Sangzhi) alkaloid tablets (SZ-A) are approved by The China National Medical Products Administration for the treatment of type 2 diabetes mellitus (T2DM). However, the extensive pharmacological characteristics and the underlying mechanism are unknown. This study investigated the mechanisms by which SZ-A ameliorates glucose metabolism in KKAy mice, an animal model of T2DM. Diabetic KKAy mice were treated intragastrically with SZ-A once daily for 8 weeks, after which glucose levels, lipid metabolism, gut microbiome, systemic inflammatory factors, luminal concentrations of short-chain fatty acids (fecal samples), and ileal proteomic changes were evaluated. The ileum tissues were collected, and the effects of SZ-A on pathological inflammatory damage were evaluated by hematoxylin and eosin staining, immunofluorescence, and immunohistochemistry. The mRNA and protein expression levels of various inflammatory markers, including monocyte chemoattractant protein-1 and phosphorylated nuclear factor kappa B p65, were detected in the ileum tissues. SZ-A improved glucose metabolism with enhanced insulin response and elevated glucagon-like peptide 1 (GLP-1) nearly 2.7-fold during the glucose tolerance test in diabetic KKAy mice. Gut microbiota analysis demonstrated that SZ-A administration elevated the abundance of and , reduced the levels of and and increased the concentrations of fecal acetic and propionic acids compared to the diabetic model group. Additionally, SZ-A markedly improved ileal inflammatory injury and pro-inflammatory macrophage infiltration and improved intestinal mucosal barrier function in diabetic KKAy mice. SZ-A also attenuated the levels of circulating endotoxin, pro-inflammatory cytokines, and chemokines in the mice sera. Collectively, SZ-A ameliorated the overall metabolic profile including glucose and lipid metabolism in KKAy mice, which may be associated with an improvement in GLP-1 and insulin secretion, at least in part by modulating the gut microbiome and relieving the degree of ileal and systemic inflammation.

摘要

新型中药桑枝生物碱片(SZ-A)已获国家药品监督管理局批准用于治疗2型糖尿病(T2DM)。然而,其广泛的药理特性和潜在机制尚不清楚。本研究探讨了SZ-A改善T2DM动物模型KKAy小鼠葡萄糖代谢的机制。将糖尿病KKAy小鼠每日一次灌胃给予SZ-A,持续8周,之后评估血糖水平、脂质代谢、肠道微生物群、全身炎症因子、短链脂肪酸的肠腔浓度(粪便样本)以及回肠蛋白质组变化。收集回肠组织,通过苏木精-伊红染色、免疫荧光和免疫组织化学评估SZ-A对病理性炎症损伤的影响。检测回肠组织中各种炎症标志物的mRNA和蛋白表达水平,包括单核细胞趋化蛋白-1和磷酸化核因子κB p65。在糖尿病KKAy小鼠的葡萄糖耐量试验中,SZ-A改善了葡萄糖代谢,增强了胰岛素反应,并使胰高血糖素样肽1(GLP-1)升高了近2.7倍。肠道微生物群分析表明,与糖尿病模型组相比,给予SZ-A提高了[具体菌种1]和[具体菌种2]的丰度,降低了[具体菌种3]和[具体菌种4]的水平,并增加了粪便中乙酸和丙酸的浓度。此外,SZ-A显著改善了糖尿病KKAy小鼠的回肠炎症损伤和促炎性巨噬细胞浸润,并改善了肠道黏膜屏障功能。SZ-A还降低了小鼠血清中循环内毒素、促炎细胞因子和趋化因子的水平。总体而言,SZ-A改善了KKAy小鼠的整体代谢状况,包括葡萄糖和脂质代谢,这可能与GLP-1和胰岛素分泌的改善有关,至少部分是通过调节肠道微生物群和减轻回肠及全身炎症程度实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f1/8082153/31610b4e0460/fphar-12-642400-g001.jpg

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