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基于网络药理学的策略探索枳术颗粒改善代谢综合征大鼠糖脂代谢的作用及机制

Network Pharmacology-Based Strategy to Explore the Effect and Mechanism of Zhizhu Granule Improving Glucose-Lipid Metabolism in Rats with Metabolic Syndrome.

作者信息

Wang Jiali, Liu Yiqing, Xiu Chengkui, Wang Xue, Liu Yinan, Hu Yanhong, Yang Jing, Lei Yan

机构信息

Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing, People's Republic of China.

Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2024 Oct 18;17:3833-3846. doi: 10.2147/DMSO.S477410. eCollection 2024.

Abstract

OBJECTIVE

To explore the mechanism of the traditional Chinese medicine (TCM), Zhizhu granule (ZZG), in treating metabolic syndrome (MS) based on network pharmacology and pharmacodynamic experiment.

MATERIALS AND METHODS

Network pharmacology combined with a pharmacodynamic experiment was used to elucidate the therapeutic mechanism of ZZG in MS. Serum samples were collected from rats with MS, induced by a high-sugar-fat-salt diet (HSFSD) combined with streptozotocin (STZ), to measure the levels of biochemical markers. The glucose (GLU), total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), systolic blood pressure (SBP), and diastolic blood pressure (DBP) were detected. The liver tissue of rats was used for histological examination and Western blot analysis.

RESULTS

Network pharmacology analysis generated 69 drug-disease common targets and 10 hub genes closely related to ZZG against MS. KEGG pathway analysis revealed that the PI3K/AKT signaling pathway was the most potential pathway, which took part in the therapeutic mechanisms. In the animal experiments section, the therapeutic effect of ZZG on MS and the therapeutic pathway of ZZG on MS were verified. ZZG could significantly decrease the body weight, TC, TG, LDL-C and GLU levels in MS rats (all <0.01), alleviate hepatocyte steatosis and decrease liver lipid droplet deposition. Western blot analysis indicated that compared with the model group, the expression levels of PI3K, AKT, and IRS-1 protein were significantly increased (all <0.05), and the FOXO-1 was significantly decreased (all <0.05) in the ZZG group.

CONCLUSION

ZZG can improve glucose-lipid metabolism disorder in rats with metabolic syndrome. The reported results provide experimental evidence for ZZG in the treatment of MS.

摘要

目的

基于网络药理学和药效学实验探索中药枳术颗粒(ZZG)治疗代谢综合征(MS)的机制。

材料与方法

采用网络药理学结合药效学实验阐明ZZG治疗MS的机制。从高糖高脂高盐饮食(HSFSD)联合链脲佐菌素(STZ)诱导的MS大鼠中采集血清样本,检测生化标志物水平。检测血糖(GLU)、总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、收缩压(SBP)和舒张压(DBP)。取大鼠肝脏组织进行组织学检查和蛋白质免疫印迹分析。

结果

网络药理学分析得到69个药物-疾病共同靶点和10个与ZZG抗MS密切相关的枢纽基因。KEGG通路分析显示PI3K/AKT信号通路是最具潜力的参与治疗机制的通路。在动物实验部分,验证了ZZG对MS的治疗作用及治疗途径。ZZG可显著降低MS大鼠的体重、TC、TG、LDL-C和GLU水平(均P<0.01),减轻肝细胞脂肪变性,减少肝脏脂质滴沉积。蛋白质免疫印迹分析表明,与模型组相比,ZZG组PI3K、AKT和IRS-1蛋白表达水平显著升高(均P<0.05),FOXO-1显著降低(均P<0.05)。

结论

ZZG可改善代谢综合征大鼠的糖脂代谢紊乱。本研究结果为ZZG治疗MS提供了实验依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09da/11495215/8f3f71ec2ed5/DMSO-17-3833-g0001.jpg

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