| Literature DB >> 24634821 |
Alexandre Picard1, Claude Rouch2, Nadim Kassis2, Valentine S Moullé1, Sophie Croizier3, Raphaël G Denis3, Julien Castel2, Nicolas Coant1, Kathryn Davis4, Deborah J Clegg4, Stephen C Benoit5, Vincent Prévot3, Sébastien Bouret6, Serge Luquet2, Hervé Le Stunff1, Céline Cruciani-Guglielmacci1, Christophe Magnan1.
Abstract
Brain lipid sensing is necessary to regulate energy balance. Lipoprotein lipase (LPL) may play a role in this process. We tested if hippocampal LPL regulated energy homeostasis in rodents by specifically attenuating LPL activity in the hippocampus of rats and mice, either by infusing a pharmacological inhibitor (tyloxapol), or using a genetic approach (adeno-associated virus expressing Cre-GFP injected into Lpl (lox/lox) mice). Decreased LPL activity by either method led to increased body weight gain due to decreased locomotor activity and energy expenditure, concomitant with increased parasympathetic tone (unchanged food intake). Decreased LPL activity in both models was associated with increased de novo ceramide synthesis and neurogenesis in the hippocampus, while intrahippocampal infusion of de novo ceramide synthesis inhibitor myriocin completely prevented body weight gain. We conclude that hippocampal lipid sensing might represent a core mechanism for energy homeostasis regulation through de novo ceramide synthesis.Entities:
Keywords: AAV, adeno-associated virus; ANS, autonomic nervous system; CERS, ceramide synthase; CNS, central nervous system; Ceramides; Energy expenditure; GFP, green fluorescent protein; LPL, lipoprotein lipase; Lipid sensing; Obesity; Parasympathetic nervous system; RQ, respiratory quotient; SMPD1, acid sphingomyelin phosphodiesterase 1; SPHK1, sphingosine kinase 1; SPT, serine palmitoyltransferase; TG, triglycerides
Year: 2013 PMID: 24634821 PMCID: PMC3953702 DOI: 10.1016/j.molmet.2013.11.002
Source DB: PubMed Journal: Mol Metab ISSN: 2212-8778 Impact factor: 7.422