کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5558376 1561134 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Genipin protects the liver from ischemia/reperfusion injury by modulating mitochondrial quality control
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
Genipin protects the liver from ischemia/reperfusion injury by modulating mitochondrial quality control
چکیده انگلیسی


- Genipin ameliorates IR-induced hepatic injury by reducing oxidative mitochondrial damages.
- Genipin enhances mitochondrial biogenesis during hepatic IR.
- Genipin restores impaired mitophagy during hepatic IR.
- Genipin regulates mitochondrial dynamics during hepatic IR.

Hepatic ischemia and reperfusion (IR) injury is closely linked to oxidative mitochondrial damage. Since mitochondrial quality control (QC) plays a pivotal role in the recovery of impaired mitochondrial function, mitochondrial QC has emerged as a potential therapeutic target. Genipin, an iridoid compound from Gardenia jasminoides, has been showed antioxidant and anti-inflammatory properties. In this study, we investigated the hepatoprotective mechanism of genipin against IR-induced hepatic injury, particularly focusing on mitochondrial QC. Male C57BL/6 mice underwent liver ischemia for 60 min, followed by reperfusion for 6 h. Genipin (100 mg/kg, i.p.) or vehicle (10% Tween 80 in saline) was administrated to mice 1 h before ischemia. Liver and blood samples were collected 6 h after reperfusion. Hepatic IR increased hepatocellular oxidative damage and induced mitochondrial dysfunction. These phenomena were ameliorated by genipin. Hepatic IR also increased the level of mitochondrial fission, such as dynamin-related protein 1 and the level of PINK1 protein expression. In contrast, hepatic IR decreased the levels of mitochondrial biogenesis related proteins (e.g., peroxisome proliferator-activated receptor gamma coactivator 1α, nuclear respiratory factor 1, and mitochondrial transcription factor A), mitophagy related proteins (e.g., Parkin), and fusion related protein (e.g., mitofusin 2). Furthermore, hepatic IR decreased the levels of sirtuin1 protein and phosphorylation of AMP-activated protein kinase. Genipin alleviated these IR-induced changes. These data indicate that genipin protects against IR-induced hepatic injury via regulating mitochondrial QC. (225/250).

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology and Applied Pharmacology - Volume 328, 1 August 2017, Pages 25-33
نویسندگان
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