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   Intracerebroventricular administration of lipopolysaccharide induces indoleamine-2,3-dioxygenase-dependent depression-like behaviors  
   
نویسنده lawson m.a. ,parrott j.m. ,mccusker r.h. ,dantzer r. ,kelley k.w. ,o'connor j.c.
منبع journal of neuroinflammation - 2013 - دوره : 10 - شماره : 0
چکیده    Background: activation of the tryptophan degrading enzyme indoleamine-2,3-dioxygenase 1 (ido1) is associated with the development of behavioral signs of depression. systemic immune challenge induces ido1 in both the periphery and the brain,leading to increased circulating and brain concentrations of kynurenines. however,whether ido1 activity within the brain is necessary for the manifestation of depression-like behavior of mice following a central immune challenge remains to be elucidated.methods: we investigated the role of brain ido1 in mediating depression-like behavior of mice in response to intracerebroventricular injection of saline or lipopolysaccharide (lps,10 ng).results: lps increased the duration of immobility in the tail suspension test and decreased preference for a sucrose solution. these effects were associated with an activation of central but not peripheral ido1,as lps increased brain kynurenine but had no effect on plasma concentrations of kynurenine. interestingly,genetic deletion or pharmacological inhibition of ido1,using 1-methyl-tryptophan,abrogated the reduction in sucrose preference induced by intracerebroventricular lps. 1-methyl-tryptophan also blocked the lps-induced increase in duration of immobility during the tail suspension test.conclusions: these data indicate that activation of brain ido1 is sufficient to induce depression-like behaviors of mice in response to central lps. © 2013 lawson et al.; licensee biomed central ltd.
آدرس neuroscience program,university of illinois at urbana-champaign,urbana,il 61801,united states,integrative immunology and behavior program,department of animal sciences,university of illinois at urbana-champaign,urbana,il 61801, United States, department of pharmacology,university of texas health science center at san antonio,216b medical building mc-7764,7703 floyd curl drive,san antonio,tx 78229-3900,united states,center for biomedical neuroscience,university of texas health science center at san antonio,216b medical building mc-7764,7703 floyd curl drive,san antonio,tx 78229-3900, United States, neuroscience program,university of illinois at urbana-champaign,urbana,il 61801,united states,integrative immunology and behavior program,department of animal sciences,university of illinois at urbana-champaign,urbana,il 61801,united states,department of pathology,university of illinois at urbana-champaign,urbana,il 61801, United States, md anderson cancer center,division of internal medicine,department of symptom research,houston,tx 77030, United States, neuroscience program,university of illinois at urbana-champaign,urbana,il 61801,united states,integrative immunology and behavior program,department of animal sciences,university of illinois at urbana-champaign,urbana,il 61801,united states,department of pathology,university of illinois at urbana-champaign,urbana,il 61801, United States, department of pharmacology,university of texas health science center at san antonio,216b medical building mc-7764,7703 floyd curl drive,san antonio,tx 78229-3900,united states,center for biomedical neuroscience,university of texas health science center at san antonio,216b medical building mc-7764,7703 floyd curl drive,san antonio,tx 78229-3900,united states,mood disorders translational research core,university of texas health science center at san antonio,216b medical building mc-7764,7703 floyd curl drive,san antonio,tx 78229-3900, United States
 
     
   
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