丙酸盐
炎症
短链脂肪酸
丁酸盐
肾
内科学
内分泌学
纤维化
化学
药理学
医学
生物
生物化学
发酵
作者
Daisuke Mikami,Mamiko Kobayashi,Junsuke Uwada,Takashi Yazawa,Kazuko Kamiyama,Kazuhisa Nishimori,Yudai Nishikawa,Satoru Nishikawa,Seiji Yokoi,Hideki Kimura,Ikuo Kimura,Takanobu Taniguchi,Masayuki Iwano
标识
DOI:10.1016/j.bbalip.2020.158666
摘要
Short-chain fatty acids (SCFAs), including acetate, butyrate, and propionate, are produced when colonic bacteria in the human gastrointestinal tract ferment undigested fibers. Free fatty acid receptor 2 (FFA2) and FFA3 are G-protein-coupled receptors recently identified as SCFA receptors that may modulate inflammation. We previously showed through in vitro experiments that SCFAs activate FFA2 and FFA3, thereby mitigating inflammation in human renal cortical epithelial cells. This study used a murine model of adenine-induced renal failure to investigate whether or not SCFAs can prevent the progression of renal damage. We also examined whether or not these FFA2 and FFA3 proteins have some roles in this protective mechanism in vivo. Immunohistochemical analyses of mouse kidneys showed that FFA2 and FFA3 proteins were expressed mainly in the distal renal tubules and collecting tubules. First, we observed that the administration of propionate mitigated the renal dysfunction and pathological deterioration caused by adenine. Consistent with this, the expression of inflammatory cytokines and fibrosis-related genes was reduced. Furthermore, the mitigation of adenine-induced renal damage by the administration of propionate was significantly attenuated in FFA2−/− and FFA3−/− mice. Therefore, the administration of propionate significantly protects against adenine-induced renal failure, at least in part, via the FFA2 and FFA3 pathways. Our data suggest that FFA2 and FFA3 are potential new therapeutic targets for preventing or delaying the progression of chronic kidney disease.
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