Liver specific inactivation of carboxylesterase 3/triacylglycerol hydrolase decreases blood lipids without causing severe steatosis in mice
Hepatology, ISSN: 0270-9139, Vol: 56, Issue: 6, Page: 2154-2162
2012
- 57Citations
- 41Captures
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Metrics Details
- Citations57
- Citation Indexes57
- 57
- CrossRef52
- Captures41
- Readers41
- 41
Article Description
Carboxylesterase 3/triacylglycerol hydrolase (Ces3/TGH) participates in hepatic very low-density lipoprotein (VLDL) assembly and in adipose tissue basal lipolysis. Global ablation of Ces3/Tgh expression decreases serum triacylglycerol (TG) and nonesterified fatty acid levels and improves insulin sensitivity. To understand the tissue-specific role of Ces3/TGH in lipid and glucose homeostasis, we generated mice with a liver-specific deletion of Ces3/Tgh expression (L-TGH knockout [KO]). Elimination of hepatic Ces3/Tgh expression dramatically decreased plasma VLDL TG and VLDL cholesterol concentrations but only moderately increased liver TG levels in mice fed a standard chow diet. Significantly reduced plasma TG and cholesterol without hepatic steatosis were also observed in L-TGH KO mice challenged with a high-fat, high-cholesterol diet. L-TGH KO mice presented with increased plasma ketone bodies and hepatic fatty acid oxidation. Intrahepatic TG in L-TGH KO mice was stored in significantly smaller lipid droplets. Augmented hepatic TG levels in chow-fed L-TGH KO mice did not affect glucose tolerance or glucose production from hepatocytes, but impaired insulin tolerance was observed in female mice. Conclusion: Our data suggest that ablation of hepatic Ces3/Tgh expression decreases plasma lipid levels without causing severe hepatic steatosis. © 2012 American Association for the Study of Liver Diseases.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84867023428&origin=inward; http://dx.doi.org/10.1002/hep.25881; http://www.ncbi.nlm.nih.gov/pubmed/22707181; https://onlinelibrary.wiley.com/doi/10.1002/hep.25881; https://dx.doi.org/10.1002/hep.25881; https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/hep.25881
Ovid Technologies (Wolters Kluwer Health)
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