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- W4205087403 endingPage "57" @default.
- W4205087403 startingPage "57" @default.
- W4205087403 abstract "The liver is extremely active in oxidizing triglycerides (TG) for energy production. An imbalance between TG synthesis and hydrolysis leads to metabolic disorders in the liver, including excessive lipid accumulation, oxidative stress, and ultimately liver damage. Adipose triglyceride lipase (ATGL) is the rate-limiting enzyme that catalyzes the first step of TG breakdown to glycerol and fatty acids. Although its role in controlling lipid homeostasis has been relatively well-studied in the adipose tissue, heart, and skeletal muscle, it remains largely unknown how and to what extent ATGL is regulated in the liver, responds to stimuli and regulators, and mediates disease progression. Therefore, in this review, we describe the current understanding of the structure–function relationship of ATGL, the molecular mechanisms of ATGL regulation at translational and post-translational levels, and—most importantly—its role in lipid and glucose homeostasis in health and disease with a focus on the liver. Advances in understanding the molecular mechanisms underlying hepatic lipid accumulation are crucial to the development of targeted therapies for treating hepatic metabolic disorders." @default.
- W4205087403 created "2022-01-25" @default.
- W4205087403 creator A5041026222 @default.
- W4205087403 creator A5065858901 @default.
- W4205087403 creator A5067110746 @default.
- W4205087403 date "2021-12-31" @default.
- W4205087403 modified "2023-10-01" @default.
- W4205087403 title "Adipose Triglyceride Lipase in Hepatic Physiology and Pathophysiology" @default.
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