Life Sciences, Год журнала: 2024, Номер 358, С. 123166 - 123166
Опубликована: Окт. 22, 2024
Язык: Английский
Life Sciences, Год журнала: 2024, Номер 358, С. 123166 - 123166
Опубликована: Окт. 22, 2024
Язык: Английский
Advanced Science, Год журнала: 2024, Номер 11(29)
Опубликована: Июнь 5, 2024
Abstract Glucagon receptor (GCGR) agonism offers potentially greater effects on the mitigation of hepatic steatosis. However, its underlying mechanism is not fully understood. Here, it screened tetraspanin CD9 might medicate GCGR agonist. decreased in fatty livers patients and upregulated upon activation. Deficiency liver exacerbated diet‐induced steatosis via complement factor D (CFD) regulated acid metabolism. Specifically, modulated synthesis oxidation genes through regulating CFD expression ubiquitination‐proteasomal degradation FLI1. In addition, influenced body weight by modulating lipogenesis thermogenesis adipose tissue CFD. Moreover, reinforcement alleviated steatosis, blockage abolished remission induced cotadutide treatment. Thus, medicates beneficial signaling, may server as a promising therapeutic target for
Язык: Английский
Процитировано
3Microbiological Research, Год журнала: 2025, Номер 298, С. 128222 - 128222
Опубликована: Май 14, 2025
Язык: Английский
Процитировано
0Life Sciences, Год журнала: 2024, Номер 358, С. 123166 - 123166
Опубликована: Окт. 22, 2024
Язык: Английский
Процитировано
1