磷酸西他列汀
脂肪性肝炎
脂肪变性
胆碱
蛋氨酸
内科学
内分泌学
医学
脂肪肝
化学
生物
糖尿病
生物化学
2型糖尿病
疾病
氨基酸
作者
Leslye Sámano-Hernández,Reyna Fierro,Aude Marchal,Jean‐Louis Guéant,Humberto González‐Márquez,Rosa-María Guéant-Rodríguez
出处
期刊:Biochimie
[Elsevier]
日期:2020-12-16
卷期号:181: 240-248
被引量:4
标识
DOI:10.1016/j.biochi.2020.12.004
摘要
Non-alcoholic fat liver disease (NAFLD) is the most common chronic liver disease in the world. NAFLD is a spectrum of diseases ranging from simple steatosis to hepatic carcinoma. The complexity of pathomechanisms makes treatment difficult. The oral antidiabetic agents, dipeptidyl peptidase four inhibitors (DPP-4i) have been proposed as possible therapeutic agents. This study was performed using a well-established NAFLD model in rats to elucidate whether sitagliptin could prevent steatohepatitis. Rats were fed a methionine/choline-deficient (MCD) diet with or without sitagliptin treatment for six weeks. Liver tissue was examined to estimate sitagliptin’s effect on the development of NASH. The MCD diet decreased the SAM/SAH ratio, and increased plasma levels of homocysteine , free fatty acids , and long-chain acylcarnitines in the MCD rats. MMP2 and Col1A2 expression also increased under the MCD diet. Sitagliptin treatment did not reverse these effects and increased steatosis and long-chain acylcarnitines. In conclusion, sitagliptin was ineffective to prevent from NAFLD in the MCD rat model. This result challenges previous data reporting beneficial effects and is consistent with the clinical trials’ negative results. • Sagliptin worsens steatosis in the MCD-NASH rat model. • Sitagliptin increased NASH markers in the MCD-NASH model. • Our results are consistent with sitagliptin negative effects in clinical trials. • Our results challenge previous data reporting sitagliptin beneficial effects.
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