丁酸盐
丁酸钠
谷氨酰胺
内分泌学
内科学
谷氨酰胺合成酶
肥胖
卡路里
甘油三酯
化学
代谢综合征
新陈代谢
代谢紊乱
生物
生物化学
医学
氨基酸
胆固醇
基因
发酵
作者
Zeyu Fan,Shaonan Wang,Ying‐Ying Meng,Chenglong Wen,Meixue Xu,Xiao Li
标识
DOI:10.1021/acs.jafc.3c08926
摘要
Obesity has emerged as a worldwide epidemic. Both butyrate and glutamine counteract obesity-related metabolic disorders; however, whether and how they synergistically cooperate with each other remains a mystery. In the study, a high-fat diet (HFD, 60% calories from fat) was used to develop a model of obesity-related metabolic disorder and compared with administrated saline and sodium butyrate (SB, 300 mg/kg body weight) daily by gavage. Compared with HFD counterparts, oral administration of SB in mice exhibited significantly reduced body weight and fat mass and decreased hepatic triglyceride content. The targeted mass spectrum revealed that SB restored serum contents of glutamine, which were significantly decreased by HFD. Furthermore, SB significantly elevated the expression of glutamine synthetase (GS, encoded by GLUL) in the liver, accompanied by more enrichment of H3K27ac modifications within its promoter. In summary, the study verified the contribution of elevated glutamine to the beneficial effects of butyrate on metabolic disorders induced by a high-fat diet, providing a novel pathway for understanding how butyrate benefits metabolic homeostasis.
科研通智能强力驱动
Strongly Powered by AbleSci AI