| Literature DB >> 28663239 |
Michael S Kuefner1, Kevin Pham1, Jeanna R Redd2, Erin J Stephenson3, Innocence Harvey4, Xiong Deng1, Dave Bridges2, Eric Boilard5, Marshall B Elam1, Edwards A Park6.
Abstract
Secretory phospholipase A2 group IIA (PLA2G2A) is a member of a family of secretory phospholipases that have been implicated in inflammation, atherogenesis, and antibacterial actions. Here, we evaluated the role of PLA2G2A in the metabolic response to a high fat diet. C57BL/6 (BL/6) mice do not express PLA2g2a due to a frameshift mutation. We fed BL/6 mice expressing the human PLA2G2A gene (IIA+ mice) a fat diet and assessed the physiologic response. After 10 weeks on the high fat diet, the BL/6 mice were obese, but the IIA+ mice did not gain weight or accumulate lipid. The lean mass in chow- and high fat-fed IIA+ mice was constant and similar to the BL/6 mice on a chow diet. Surprisingly, the IIA+ mice had an elevated metabolic rate, which was not due to differences in physical activity. The IIA+ mice were more insulin sensitive and glucose tolerant than the BL/6 mice, even when the IIA+ mice were provided the high fat diet. The IIA+ mice had increased expression of uncoupling protein 1 (UCP1), sirtuin 1 (SIRT1), and PPARγ coactivator 1α (PGC-1α) in brown adipose tissue (BAT), suggesting that PLA2G2A activates mitochondrial uncoupling in BAT. Our data indicate that PLA2G2A has a previously undiscovered impact on insulin sensitivity and metabolism.Entities:
Keywords: hepatic steatosis; high fat diet; insulin resistance; obesity
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Year: 2017 PMID: 28663239 PMCID: PMC5580896 DOI: 10.1194/jlr.M076141
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922