Abstract |
De novo lipogenesis (DNL) plays an important role in the pathogenesis of hepatic steatosis and also appears to be implicated in hepatic inflammation and fibrosis. Accordingly, the inhibition of acetyl-CoA carboxylase, which catalyzes the rate-limiting step of DNL, might represent a useful approach in the management of patients with nonalcoholic fatty liver disease ( NAFLD). Animal studies and preliminary data in patients with NAFLD consistently showed an improvement in steatosis with the use of these agents. However, effects on fibrosis were variable and an increase in plasma triglyceride levels was observed. Therefore, more long-term studies are needed to clarify the role of these agents in NAFLD and to determine their risk/benefit profile.
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Authors | Georgios Neokosmidis, Evangelos Cholongitas, Konstantinos Tziomalos |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 27
Issue 39
Pg. 6522-6526
(Oct 21 2021)
ISSN: 2219-2840 [Electronic] United States |
PMID | 34754150
(Publication Type: Editorial)
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Copyright | ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. |
Chemical References |
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Topics |
- Acetyl-CoA Carboxylase
(metabolism)
- Animals
- Humans
- Lipogenesis
- Liver
(metabolism)
- Non-alcoholic Fatty Liver Disease
(drug therapy, metabolism)
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