Social isolation rearing induces mitochondrial, immunological, neurochemical and behavioural deficits in rats, and is reversed by clozapine or N-acetyl cysteine

被引:142
作者
Moeller, Marisa [1 ]
Du Preez, Jan L. [2 ]
Viljoen, Francois P. [1 ]
Berk, Michael [3 ,4 ,5 ]
Emsley, Robin [6 ]
Harvey, Brian H. [1 ,2 ]
机构
[1] North West Univ, Sch Pharm, Div Pharmacol, Potchefstroom, South Africa
[2] North West Univ, Sch Pharm, Ctr Excellence Pharmaceut Sci, Potchefstroom, South Africa
[3] Deakin Univ, Sch Med, Geelong, Vic 3217, Australia
[4] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Orygen Res Ctr, Parkville, Vic 3052, Australia
[5] Univ Melbourne, Dept Psychiat, Parkville, Vic 3052, Australia
[6] Univ Stellenbosch, Dept Psychiat, Cape Town, South Africa
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Schizophrenia; Social isolation rearing; Mitochondrial dysfunction; Tryptophan-kynurenine pathway; Adenosine triphosphate (ATP); Clozapine; N-acetyl cysteine; Dopamine; Immune-inflammatory; Animal model; NECROSIS-FACTOR-ALPHA; OXIDATIVE STRESS; PREPULSE INHIBITION; DOPAMINE RELEASE; QUINOLINIC ACID; OBJECT RECOGNITION; KYNURENINE PATHWAY; STRIATAL DOPAMINE; NUCLEUS-ACCUMBENS; NADPH-OXIDASE;
D O I
10.1016/j.bbi.2012.12.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Apart from altered dopamine (DA) function, schizophrenia displays mitochondrial and immune-inflammatory abnormalities, evidenced by oxidative stress, altered kynurenine metabolism and cytokine release. N-acetyl cysteine (NAC), an antioxidant and glutamate modulator, is effective in the adjunctive treatment of schizophrenia. Social isolation rearing (SIR) in rats is a valid neurodevelopmental animal model of schizophrenia. This study evaluated whether SIR-induced behavioural deficits may be explained by altered plasma pro- and anti-inflammatory cytokines, kynurenine metabolism, and cortico-striatal DA and mitochondrial function (via adenosine triphosphate (ATP) release), and if clozapine or NAC (alone and in combination) reverses these changes. SIR induced pronounced deficits in social interactive behaviours, object recognition memory, and prepulse inhibition (PPI), while simultaneously increasing striatal but reducing frontal cortical accumulation of ATP as well as DA. SIR increased pro- vs. anti-inflammatory cytokine balance and altered kynurenine metabolism with a decrease in neuroprotective ratio. Clozapine (5 mg/kg/day x 14 days) as well as clozapine + NAC (5 mg/kg/day and 150 mg/kg/day x 14 days) reversed these changes, with NAC (150 mg/kg/day) alone significantly but partially effective in some parameters. Clozapine + NAC was more effective than clozapine alone in reversing SIR-induced PPI, mitochondrial, immune and DA changes. In conclusion, SIR induces mitochondrial and immune-inflammatory changes that underlie cortico-striatal DA perturbations and subsequent behavioural deficits, and responds to treatment with clozapine or NAC, with an additive effect following combination treatment. The data provides insight into the mechanisms that might underlie the utility of NAC as an adjunctive treatment in schizophrenia. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:156 / 167
页数:12
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