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Skeletal Muscle PGC-1α1 Modulates Kynurenine Metabolism and Mediates Resilience to Stress-Induced Depression
Author(s) -
Leandro Z. Agudelo,
Teresa Femenía,
Funda Orhan,
Margareta PorsmyrPalmertz,
Michel Goiny,
Vicente Martínez-Redondo,
Jorge C. Correia,
Manizheh Izadi,
Maria Bhat,
Ina SchuppeKoistinen,
Amanda Pettersson,
Duarte M. S. Ferreira,
Anna Krook,
Romain Barrès,
Juleen R. Zierath,
Sophie Erhardt,
Maria Lindskog,
Jorge L. Ruas
Publication year - 2014
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2014.07.051
Subject(s) - kynurenine , skeletal muscle , kynurenine pathway , kynurenic acid , biology , depression (economics) , endocrinology , medicine , metabolite , chronic stress , biochemistry , glutamate receptor , tryptophan , receptor , macroeconomics , amino acid , economics
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.

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