| Literature DB >> 25259918 |
Leandro Z Agudelo1, Teresa Femenía2, Funda Orhan3, Margareta Porsmyr-Palmertz1, Michel Goiny3, Vicente Martinez-Redondo1, Jorge C Correia1, Manizheh Izadi1, Maria Bhat4, Ina Schuppe-Koistinen4, Amanda T Pettersson1, Duarte M S Ferreira1, Anna Krook5, Romain Barres5, Juleen R Zierath6, Sophie Erhardt3, Maria Lindskog7, Jorge L Ruas8.
Abstract
Depression is a debilitating condition with a profound impact on quality of life for millions of people worldwide. Physical exercise is used as a treatment strategy for many patients, but the mechanisms that underlie its beneficial effects remain unknown. Here, we describe a mechanism by which skeletal muscle PGC-1α1 induced by exercise training changes kynurenine metabolism and protects from stress-induced depression. Activation of the PGC-1α1-PPARα/δ pathway increases skeletal muscle expression of kynurenine aminotransferases, thus enhancing the conversion of kynurenine into kynurenic acid, a metabolite unable to cross the blood-brain barrier. Reducing plasma kynurenine protects the brain from stress-induced changes associated with depression and renders skeletal muscle-specific PGC-1α1 transgenic mice resistant to depression induced by chronic mild stress or direct kynurenine administration. This study opens therapeutic avenues for the treatment of depression by targeting the PGC-1α1-PPAR axis in skeletal muscle, without the need to cross the blood-brain barrier.Entities:
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Year: 2014 PMID: 25259918 DOI: 10.1016/j.cell.2014.07.051
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582