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

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-11 DOI:10.1016/j.prostaglandins.2024.106874
Long Hao , Mingxi Li , Huan Gu , Ji Li
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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.

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大黄黄连解毒汤通过抑制内质网应激,调节脂肪细胞分化和脂质降解,从而改善肥胖症。
大黄黄连解毒汤(DHXD)是治疗上腹压迫症状的临床代表方剂。本研究旨在探讨大黄黄连解毒汤对肥胖的影响,并尝试研究其潜在机制。研究人员分化了 3T3-L1 前脂肪细胞,并建立了高脂饮食诱导的肥胖大鼠模型。使用 DHXD 进行治疗,并采用内质网(ER)应激激活剂妥尼霉素研究相关调控机制。使用 CCK-8 检测法评估细胞活力。油红 O 染色法测定脂质积累。甘油生成量和甘油三酯含量用商品试剂盒测定。采用 Western 印迹法检测关键蛋白的表达。结果表明,DHXD 能大大减少分化的 3T3-L1 细胞中的细胞内脂滴和甘油三酯。此外,成熟脂肪细胞标志物 PPARγ、aP2 在脂肪生成过程中的升高表达也因 DHXD 的处理而降低。此外,DHXD 还加剧了分化的 3T3-L1 细胞的脂肪分解,这表现在 ATGL 表达的上调和 HSL 表达的下调。此外,DHXD 还能抑制 3T3-L1 细胞的内质网(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在一定程度上被曲安奈德所消除。最后,DHXD 可减轻肥胖大鼠的脂质积累和 ER 压力。总之,DHXD通过抑制ER应激调节脂肪细胞分化和脂质降解,从而改善肥胖。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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