Agudelo 2014 Cell: Difference between revisions

From Bioblast
(Created page with "{{Publication |title=Agudelo LZ, FemenΓ­a T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira D...")
Β 
No edit summary
Line 1: Line 1:
{{Publication
{{Publication
|title=Agudelo LZ, FemenΓ­a T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira DM, Krook A, Barres R, Zierath JR, Erhardt S, Lindskog M, Ruas JL (2014) Skeletal muscle PGC-1Ξ±1 modulates kynurenine metabolism and mediates resilience to stress-induced depression. Cell 159:33-45. Β 
|title=Agudelo LZ, FemenΓ­a T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira DM, Krook A, Barres R, Zierath JR, Erhardt S, Lindskog M, Ruas JL (2014) Skeletal muscle PGC-1Ξ±1 modulates kynurenine metabolism and mediates resilience to stress-induced depression. Cell 159:33-45.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/25259918 PMID:25259918]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/25259918 PMID:25259918]
|authors=Agudelo LZ, Femenia T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira DM, Krook A, Barres R, Zierath JR, Erhardt S, Lindskog M, Ruas JL
|authors=Agudelo LZ, Femenia T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira DM, Krook A, Barres R, Zierath JR, Erhardt S, Lindskog M, Ruas JL
|year=2014
|year=2014
|journal=Cell
|journal=Cell
|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-1Ξ±1 induced by exercise training changes kynurenine metabolism and protects from stress-induced depression. Activation of the PGC-1Ξ±1-PPARΞ±/Ξ΄ 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-1Ξ±1 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-1Ξ±1-PPAR axis in skeletal muscle, without the need to cross the blood-brain barrier. Β 
|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-1Ξ±1 induced by exercise training changes kynurenine metabolism and protects from stress-induced depression. Activation of the PGC-1Ξ±1-PPARΞ±/Ξ΄ 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-1Ξ±1 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-1Ξ±1-PPAR axis in skeletal muscle, without the need to cross the blood-brain barrier.
}}
}}
{{Labeling
{{Labeling
Line 13: Line 13:
|model cell lines=Other cell lines
|model cell lines=Other cell lines
|diseases=Other
|diseases=Other
|additional=Labels
}}
}}

Revision as of 09:29, 25 March 2016

Publications in the MiPMap
Agudelo LZ, FemenΓ­a T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira DM, Krook A, Barres R, Zierath JR, Erhardt S, Lindskog M, Ruas JL (2014) Skeletal muscle PGC-1Ξ±1 modulates kynurenine metabolism and mediates resilience to stress-induced depression. Cell 159:33-45.

Β» PMID:25259918

Agudelo LZ, Femenia T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira DM, Krook A, Barres R, Zierath JR, Erhardt S, Lindskog M, Ruas JL (2014) Cell

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-1Ξ±1 induced by exercise training changes kynurenine metabolism and protects from stress-induced depression. Activation of the PGC-1Ξ±1-PPARΞ±/Ξ΄ 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-1Ξ±1 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-1Ξ±1-PPAR axis in skeletal muscle, without the need to cross the blood-brain barrier.


Labels: MiParea: Exercise physiology;nutrition;life style  Pathology: Other 

Organism: Mouse  Tissue;cell: Skeletal muscle 





Cookies help us deliver our services. By using our services, you agree to our use of cookies.