College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu 610041, China.
Int J Mol Sci. 2024 Aug 18;25(16):8979. doi: 10.3390/ijms25168979.
Chronic low-grade inflammation (CLGI) is associated with obesity and is one of its pathogenetic mechanisms. Lipopolysaccharide (LPS), a component of Gram-negative bacterial cell walls, is the principal cause of CLGI. Studies have found that capsaicin significantly reduces the relative abundance of LPS-producing bacteria. In the present study, -knockout () C57BL/6J mice and the intestinal epithelial cell line Caco-2 () were used as models to determine the effect of capsaicin on CLGI and elucidate the mechanism by which it mediates weight loss in vivo and in vitro. We found that the intragastric administration of capsaicin significantly blunted increases in body weight, food intake, blood lipid, and blood glucose in mice fed a high-fat diet, suggesting an anti-obesity effect of capsaicin. Capsaicin reduced LPS levels in the intestine by reducing the relative abundance of Proteobacteria such as , and . Toll-like receptor 4 (TLR4) levels decreased following decreases in LPS levels. Then, the local inflammation of the intestine was reduced by reducing the expression of tumor necrosis factor (TNF)-α and interleukin (IL)-6 mediated by TLR4. Attenuating local intestinal inflammation led to the increased expression of tight junction proteins zonula occludens 1 (ZO-1) and occludin and the restoration of the intestinal barrier function. Capsaicin increased the expression of ZO-1 and occludin at the transcriptional and translational levels, thereby increasing trans-endothelial electrical resistance and restoring intestinal barrier function. The restoration of intestinal barrier function decreases intestinal permeability, which reduces the concentration of LPS entering the circulation, and reduced endotoxemia leads to decreased serum concentrations of inflammatory cytokines such as TNF-α and IL-6, thereby attenuating CLGI. This study sheds light on the anti-obesity effect of capsaicin and its mechanism by reducing CLGI, increasing our understanding of the anti-obesity effects of capsaicin. It has been confirmed that capsaicin can stimulate the expression of intestinal transmembrane protein ZO-1 and cytoplasmic protein occludin, increase the trans-epithelial electrical resistance value, and repair intestinal barrier function.
慢性低度炎症(CLGI)与肥胖有关,是其发病机制之一。脂多糖(LPS)是革兰氏阴性细菌细胞壁的主要成分,是 CLGI 的主要原因。研究发现,辣椒素可显著降低 LPS 产生菌的相对丰度。本研究以 -敲除()C57BL/6J 小鼠和肠上皮细胞系 Caco-2()为模型,确定辣椒素对 CLGI 的影响,并阐明其在体内和体外介导体重减轻的机制。我们发现,胃内给予辣椒素可显著减轻高脂饮食喂养的小鼠体重增加、食物摄入、血脂和血糖升高,提示辣椒素有抗肥胖作用。辣椒素通过降低变形菌门等 Proteobacteria 的相对丰度来降低肠道 LPS 水平,如 、 。LPS 水平降低后,Toll 样受体 4(TLR4)水平下降。随后,通过降低 TLR4 介导的肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6 的表达,减少了肠道局部炎症。减轻局部肠道炎症导致紧密连接蛋白 ZO-1 和闭合蛋白的表达增加,并恢复肠道屏障功能。辣椒素通过增加 ZO-1 和闭合蛋白的转录和翻译表达,增加跨内皮电阻,恢复肠道屏障功能。肠道屏障功能的恢复降低了肠道通透性,从而减少进入循环的 LPS 浓度,减轻内毒素血症导致 TNF-α和 IL-6 等炎症细胞因子的血清浓度降低,从而减轻 CLGI。本研究揭示了辣椒素通过降低 CLGI 减轻肥胖的作用及其机制,加深了我们对辣椒素抗肥胖作用的认识。已经证实,辣椒素可以刺激肠道跨膜蛋白 ZO-1 和细胞质蛋白闭合蛋白的表达,增加跨上皮电阻值,并修复肠道屏障功能。