Please use this identifier to cite or link to this item: https://hdl.handle.net/11000/35429

Skeletal muscle PGC-1α1 modulates kynurenine metabolism and mediates resilience to stress-induced depression

Title:
Skeletal muscle PGC-1α1 modulates kynurenine metabolism and mediates resilience to stress-induced depression
Authors:
Agudelo, Leandro Z.
Femenía Cantó, Teresa
Orhan, Funda
Porsmyr Palmertz, Margareta
Goiny, Michel
Martínez Redondo, Vicente
Correja, Jorge C.
Izadi, Manizheh
Bhat, Maria
Schuppe Koistinen, Ina
Pettersson, Amanda T.
Ferreira, Duarte M.S.
Editor:
Elsevier
Department:
Departamentos de la UMH::Farmacología, Pediatría y Química Orgánica
Issue Date:
2014
URI:
https://hdl.handle.net/11000/35429
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-1a1 induced by exercise training changes kynurenine metabolism and protects from stress-induced depression. Activation of the PGC- 1a1-PPARa/d pathway increases skeletal muscle expression of kynurenine aminotransferases, thus enhancing the conversion of kynurenine into kynurenic acid, a metabolite unable to cross the bloodbrain barrier. Reducing plasma kynurenine protects the brain from stress-induced changes associated with depression and renders skeletal muscle-specific PGC-1a1 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-1a1-PPAR axis in skeletal muscle, without the need to cross the blood-brain barrier.
Knowledge area:
CDU: Ciencias aplicadas: Medicina: Farmacología. Terapéutica. Toxicología. Radiología
Type of document:
info:eu-repo/semantics/article
Access rights:
info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
DOI:
10.1016/j.cell.2014.07.051
Appears in Collections:
Artículos Farmacología, Pediatría y Química Orgánica



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