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大黄黄连泻心汤通过抑制内质网应激调节脂肪细胞分化和脂质降解改善肥胖。

Dahuang Huanglian Xiexin Decoction ameliorates obesity via modulating adipocyte differentiation and lipid degradation through inhibiting endoplasmic reticulum stress.

机构信息

Department of Pediatrics, Beijing Fangshan District Liangxiang Hospital, Beijing 102400, PR China.

Department of Pediatrics, Guang'anmen Hospital, Chinese Academy of Traditional Chinese Medicine, Beijing 100053, PR China.

出版信息

Prostaglandins Other Lipid Mediat. 2024 Oct;174:106874. doi: 10.1016/j.prostaglandins.2024.106874. Epub 2024 Jul 11.

Abstract

Dahuang Huanglian Xiexin Decoction (DHXD) is the representative clinical formula for treating epigastric oppression. In this study, we aim to explore the effect of DHXD on obesity and attempt to investigate its potential mechanism. 3T3-L1 preadipocytes were differentiated and high-fat diet-induced obese rat model was established. DHXD was used for treatment and tunicamycin, the activator of endoplasmic reticulum (ER) stress, was adopted to investigate the related regulatory mechanism. Cell viability was evaluated using CCK-8 assay. Oil-Red O staining was performed to determine lipid accumulation. Glycerol production and Triglyceride content were measured using their commercial kits. Western blot was conducted to examine the expression of critical proteins. Results indicated that DHXD could greatly reduce intracellular lipid droplets and triglyceride in differentiated 3T3-L1 cells. Moreover, the elevated expression of mature adipocytes markers, PPARγ, aP2, during adipogenesis was decreased by DHXD treatment. In addition, DHXD aggravated the lipolysis in differentiated 3T3-L1 cells, as evidenced by the upregulated ATGL expression and the downregulated HSL expression. Besides, DHXD inhibited endoplasmic reticulum (ER) stress in 3T3-L1 cells. Further experiments indicated that the impacts of DHXD on adipocyte differentiation and lipid degradation were partly abolished by tunicamycin. Finally, DHXD alleviated lipid accumulation and ER stress in obese rats. In conclusion, DHXD ameliorates obesity via modulating adipocyte differentiation and lipid degradation through inhibiting ER stress.

摘要

大黄黄连泻心汤(DHXD)是治疗脘腹痞满的临床代表方剂。本研究旨在探讨 DHXD 对肥胖的影响,并试图探讨其潜在机制。用 3T3-L1 前体脂肪细胞进行分化,并建立高脂肪饮食诱导的肥胖大鼠模型。用 DHXD 进行治疗,并用衣霉素(内质网(ER)应激的激活剂)来研究相关的调节机制。用 CCK-8 法评估细胞活力。用油红 O 染色法测定脂质积累。用其商业试剂盒测定甘油生成和三酰基甘油含量。用 Western blot 检测关键蛋白的表达。结果表明,DHXD 可显著减少分化的 3T3-L1 细胞内的脂质滴和三酰基甘油。此外,DHXD 处理可降低脂肪生成过程中成熟脂肪细胞标志物 PPARγ、aP2 的表达。此外,DHXD 加重了分化的 3T3-L1 细胞中的脂肪分解,表现为 ATGL 表达上调和 HSL 表达下调。此外,DHXD 抑制了 3T3-L1 细胞中的内质网(ER)应激。进一步的实验表明,DHXD 对脂肪细胞分化和脂质降解的影响部分被衣霉素所阻断。最后,DHXD 减轻了肥胖大鼠的脂质积累和 ER 应激。总之,DHXD 通过抑制内质网应激来调节脂肪细胞分化和脂质降解,从而改善肥胖。

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