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β-促胰岛素分泌素/血管生成素样蛋白8与非酒精性脂肪性肝病的关联:动物和人体研究

Association between betatrophin/ANGPTL8 and non-alcoholic fatty liver disease: animal and human studies.

作者信息

Lee Yong-Ho, Lee Sang-Guk, Lee Chan Joo, Kim Soo Hyun, Song Young-Mi, Yoon Mi Ra, Jeon Byung Hun, Lee Jae Hyuk, Lee Byung-Wan, Kang Eun Seok, Lee Hyun Chul, Cha Bong-Soo

机构信息

Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

出版信息

Sci Rep. 2016 Apr 5;6:24013. doi: 10.1038/srep24013.

Abstract

Betatrophin/angiopoietin-like protein 8 (ANGPTL8) is a liver-secreted protein recently identified as a potent stimulator of beta cell proliferation in mice. However, it is unclear how betatrophin is regulated in humans with non-alcoholic fatty liver disease (NAFLD). We investigated the role of betatrophin in mice and in humans with and without NAFLD. Serum betatrophin levels were examined by ELISA in 164 subjects, including 96 patients with NAFLD. Levels were significantly elevated in subjects with NAFLD compared with controls (1.301 ± 0.617 vs. 0.900 ± 0.574 μg/L, P < 0.001), even after stratification by diabetic or obesity status. Circulating betatrophin positively correlated with obesity or glycemic indices, liver enzyme profiles, and NAFLD status, and was confirmed by multivariate regression analyses (β = 0.195, P = 0.040). However, when including insulin resistance index in the model, the significant association between betatrophin level and NAFLD was diminished due to a mediation effect of insulin resistance on this relationship. Palmitate or tunicamycin increased betatrophin expression in HepG2 cells, while a chemical chaperone blocked its induction. Hepatic expression of betatrophin was elevated in mice with NAFLD including db/db or ob/ob mice and mice with a high-fat or methionine-choline deficient diet. In conclusion, circulating betatrophin was increased in mice and humans with NAFLD and its expression was induced by endoplasmic reticulum stress in hepatocytes (Clinical trial no. NCT02285218).

摘要

β-促胰岛素分泌素/血管生成素样蛋白8(ANGPTL8)是一种肝脏分泌的蛋白质,最近被确定为小鼠β细胞增殖的强效刺激因子。然而,目前尚不清楚在非酒精性脂肪性肝病(NAFLD)患者中β-促胰岛素分泌素是如何被调节的。我们研究了β-促胰岛素分泌素在患有和未患有NAFLD的小鼠及人类中的作用。通过酶联免疫吸附测定(ELISA)检测了164名受试者的血清β-促胰岛素分泌素水平,其中包括96名NAFLD患者。与对照组相比,NAFLD患者的β-促胰岛素分泌素水平显著升高(1.301±0.617 vs. 0.900±0.574μg/L,P<0.001),即使按糖尿病或肥胖状态分层后也是如此。循环β-促胰岛素分泌素与肥胖或血糖指标、肝酶谱以及NAFLD状态呈正相关,多变量回归分析证实了这一点(β=0.195,P=0.040)。然而,当在模型中纳入胰岛素抵抗指数时,由于胰岛素抵抗对这种关系的中介作用,β-促胰岛素分泌素水平与NAFLD之间的显著关联减弱。棕榈酸酯或衣霉素可增加HepG2细胞中β-促胰岛素分泌素的表达,而一种化学伴侣可阻断其诱导作用。在患有NAFLD的小鼠中,包括db/db或ob/ob小鼠以及高脂或蛋氨酸-胆碱缺乏饮食的小鼠,肝脏中β-促胰岛素分泌素的表达升高。总之,患有NAFLD的小鼠和人类循环β-促胰岛素分泌素增加,其表达由肝细胞内质网应激诱导(临床试验编号:NCT02285218)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3579/4820743/c47529d8053d/srep24013-f1.jpg

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