化学
糖尿病肾病
甘油三酯
肾功能
脂质代谢
脂肪甘油三酯脂肪酶
分解代谢
肌酐
肾
肾病
内分泌学
内科学
药理学
新陈代谢
糖尿病
生物化学
胆固醇
医学
作者
Jing Zhang,Si-lan Li,Lin Wen,Ronghua Pan,Yue Dai,Yufeng Xia
标识
DOI:10.1016/j.jpba.2022.115028
摘要
Tripterygium glycoside tablet (TGT) has been used clinically to alleviate diabetic nephropathy (DN) for decades. However, the mechanism of its anti-DN has not been fully clarified. The aim of this study was to elucidate molecular mechanism of TGT in repairing renal function injury. The results of biochemical parameters and renal histopathology implied that TGT intervention could attenuate creatinine, albumin excretion rate and histological injury of kidney in DN mouse model. Moreover, UHPLC-QTOF-MS/MS-based untargeted metabolomic analysis indicated that 11 metabolites in kidney of mice with DN were restored after TGT treatment, and the most prominent metabolic alteration was triglyceride (TG) metabolism. Mechanistically, TGT effectively improved the function of impaired kidney by promoting TG catabolism via modulation of adipose triglyceride lipase in DN mice. Our findings identified the link between circulating metabolites and DN, suggesting that it might be a possibility to intervene in DN by targeting metabolism.
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