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GLP-1 Receptor Agonist and Non-Alcoholic Fatty Liver Disease

Journal

DIABETES & METABOLISM JOURNAL
Volume 36, Issue 4, Pages 262-267

Publisher

KOREAN DIABETES ASSOC
DOI: 10.4093/dmj.2012.36.4.262

Keywords

Fatty acid oxidation; Glucagon-like peptide 1; Non-alcoholic fatty liver disease

Funding

  1. Young Investigator Award from the Korean Diabetes Association and the Korea Science and Engineering Foundation
  2. Ministry of Education, Science and Technology [S-2010-1115-000]

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Non-alcoholic fatty liver disease (NAFLD), one of the most common liver diseases, is caused by the disruption of hepatic lipid homeostasis. It is associated with insulin resistance as seen in type 2 diabetes mellitus. Glucagon- like peptide-1 (GLP-1) is an incretin that increases insulin sensitivity and aids glucose metabolism. In recent in vivo and in vitro studies, GLP-1 presents a novel therapeutic approach against NAFLD by increasing fatty acid oxidation, decreasing lipogenesis, and improving hepatic glucose metabolism. In this report, we provide an overview of the role and mechanism of GLP-1 in relieving NAFLD.

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