郭慧慧, 申浩然, 张红娟, 王璐璐, 韩燕星, 蒋建东. 灯盏生脉通过调节肠道微环境抑制非酒精性脂肪肝进程J. 药学学报, 2022, 57(12): 3524-3534. DOI: 10.16438/j.0513-4870.2022-0908
引用本文: 郭慧慧, 申浩然, 张红娟, 王璐璐, 韩燕星, 蒋建东. 灯盏生脉通过调节肠道微环境抑制非酒精性脂肪肝进程J. 药学学报, 2022, 57(12): 3524-3534. DOI: 10.16438/j.0513-4870.2022-0908
GUO Hui-hui, SHEN Hao-ran, ZHANG Hong-juan, WANG Lu-lu, HAN Yan-xing, JIANG Jian-dong. Dengzhan Shengmai inhibits nonalcoholic fatty liver disease via regulating intestinal microenvironmentJ. Acta Pharmaceutica Sinica, 2022, 57(12): 3524-3534. DOI: 10.16438/j.0513-4870.2022-0908
Citation: GUO Hui-hui, SHEN Hao-ran, ZHANG Hong-juan, WANG Lu-lu, HAN Yan-xing, JIANG Jian-dong. Dengzhan Shengmai inhibits nonalcoholic fatty liver disease via regulating intestinal microenvironmentJ. Acta Pharmaceutica Sinica, 2022, 57(12): 3524-3534. DOI: 10.16438/j.0513-4870.2022-0908

灯盏生脉通过调节肠道微环境抑制非酒精性脂肪肝进程

Dengzhan Shengmai inhibits nonalcoholic fatty liver disease via regulating intestinal microenvironment

  • 摘要: 本研究旨在探讨灯盏生脉(Dengzhan Shengmai, DZSM) 对高脂饮食引起的非酒精性脂肪肝病(non-alcoholic fatty liver diseases, NAFLD) 的改善作用及机制。动物实验方案由中国医学科学院药物研究所伦理委员会审核并批准。高脂饮食建立叙利亚金黄地鼠的NAFLD模型, DZSM治疗6周后测定各组动物的血脂、肝脂、肝功能、炎症反应等指标; 采用16S rRNA基因测序技术和气相-质谱联用技术检测给药后对肠道菌群及短链脂肪酸(short-chain fatty acids, SCFAs) 的调节作用; 采用ELISA (enzyme linked immunosorbent assay)、RT-qPCR (reverse transcription-quantitative polymerase chain reaction)、Western blot及组织病理学方法检测肠屏障功能; 并在体外HepG2细胞中进行验证和机制研究。结果发现, DZSM改善NAFLD的作用在抗生素处理杀灭肠道菌群后明显减弱。进一步的机制研究表明, DZSM可明显调节肠道菌群结构和组成, 促进肠道内SCFAs产生和吸收进入肝脏, 从而减轻肝细胞内的脂质堆积; 而且DZSM通过改善肠屏障功能减少肠内毒素脂多糖(lipopolysaccharide, LPS) 进入机体, 抑制LPS激活的Toll样受体4 (Toll like receptor 4, TLR4)-核因子KB (nuclear factor kappa B, NFKB) 信号通路, 减轻肝脏炎症反应。以上结果表明, DZSM可通过调节肠道微环境改善NAFLD进程。

     

    Abstract: The aim of this study was to investigate the efficacy and mechanism of Dengzhan Shengmai (DZSM) against nonalcoholic fatty liver diseases (NAFLD). The animal experiment program was reviewed and approved by the Ethics Committee of Institute of Materia Medica, Chinese Academy of Medical Sciences. The NAFLD model of Syrian golden hamsters was established by high fat diets. After 6 weeks of DZSM treatment, the serum lipid, hepatic lipid accumulation, liver function and inflammatory response were determined. The regulations of gut microbiota and short-chain fatty acids were detected by 16S rRNA gene sequencing and gas chromatography-mass spectrometry method, respectively. The gut barrier function was evaluated by enzyme linked immunosorbent assay (ELISA), reverse transcription-quantitative polymerase chain reaction (RT-qPCR), Western blot and histopathological methods and further verified in HepG2 cells. The results showed that the efficacy of DZSM against NAFLD was remarkably reduced after removal of the gut microbiota. The study of mechanism showed that DZSM significantly regulated the composition of gut microbiota, promoted the production and absorption of intestinal short-chain fatty acids, then leading to the reduction of hepatic lipid accumulation. Moreover, after DZSM treatment, the decreased lipopolysaccharide (LPS) level by improving the intestinal barrier function significantly inhibited the hepatic inflammation through down-regulating Toll like receptor 4 (TLR4)-nuclear factor kappa B (NFKB) signaling pathway. These results indicate that DZSM inhibits NAFLD via regulating intestinal microenvironment.

     

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