犬尿氨酸
骨骼肌
巴比妥酸
生物
萧条(经济学)
犬尿氨酸途径
内分泌学
内科学
代谢物
慢性应激
医学
生物化学
谷氨酸受体
色氨酸
受体
氨基酸
经济
宏观经济学
作者
Leandro Z. Agudelo,Teresa Femenía,Funda Orhan,Margareta Porsmyr‐Palmertz,Michel Goiny,Vicente Martínez-Redondo,Jorge C. Correia,Manizheh Izadi,Maria Bhat,Ina Schuppe‐Koistinen,Amanda Pettersson,Duarte M. S. Ferreira,Anna Krook,Romain Barrés,Juleen R. Zierath,Sophie Erhardt,Maria Lindskog,Jorge L. Ruas
出处
期刊:Cell
[Cell Press]
日期:2014-09-01
卷期号:159 (1): 33-45
被引量:606
标识
DOI:10.1016/j.cell.2014.07.051
摘要
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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