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首页> 外文期刊>Behavioural Brain Research: An International Journal >GABAergic mRNA expression is upregulated in the prefrontal cortex of rats sensitized to methamphetamine
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GABAergic mRNA expression is upregulated in the prefrontal cortex of rats sensitized to methamphetamine

机译:甲基苯丙胺致敏的大鼠前额叶皮质中GABA能mRNA的表达上调

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Inhibitory gamma-aminobutyric acid (GABA)-mediated neurotransmission plays an important role in the regulation of the prefrontal cortex (PFC), with increasing evidence suggesting that dysfunctional GABAergic processing of the PFC may underlie certain deficits reported across psychotic disorders. Methamphetamine (METH) is a psychostimulant that induces chronic psychosis in a subset of users, with repeat administration producing a progressively increased vulnerability to psychotic relapse following subsequent drug administration (sensitization). The aim here was to investigate changes to GABAergic mRNA expression in the PFC of rats sensitized to METH using quantitative polymerase chain reaction (qPCR). Male Sprague-Dawley rats (n = 12) underwent repeated methamphetamine (intraperitoneal (i.p.) or saline injections for 7 days. Following 14 days of withdrawal, rats were challenged with acute methamphetamine (1 mg/kg i.p.) and RNA was isolated from the PFC to compare the relative mRNA expression of a range of GABA enzymes, transporters and receptors subunits. METH challenge resulted in a significant sensitized behavioral (locomotor) response in METH pre-treated animals compared with saline pre-treated controls. The mRNAs of transporters (GAT(1) and GAT(3)), ionotropic GABA(A) receptor subunits (alpha 3 and beta 1), together with the metabotropic GABA(B)1 receptor, were upregulated in the PFC of sensitized rats compared with saline controls. These findings indicate that GABAergic mRNA expression is significantly altered at the pre and postsynaptic level following sensitization to METH, with sensitization resulting in the transcriptional upregulation of several inhibitory genes. These changes likely have significant consequences on GABA-mediated neurotransmission in the PFC and may underlie certain symptoms conserved across psychotic disorders, such as executive dysfunction. (C) 2015 Elsevier B.V. All rights reserved.
机译:抑制性γ-氨基丁酸(GABA)介导的神经传递在前额叶皮层(PFC)的调节中起着重要作用,越来越多的证据表明,PFC的功能失调的GABA能处理可能是精神病性疾病报道的某些缺陷的基础。甲基苯丙胺(METH)是一种精神兴奋剂,可在一部分用户中诱发慢性精神病,重复给药在随后的药物给药(致敏)后对精神病复发的抵抗力逐渐增加。本文的目的是使用定量聚合酶链反应(qPCR)研究对METH敏感的大鼠PFC中GABA能mRNA表达的变化。雄性Sprague-Dawley大鼠(n = 12)反复接受甲基苯丙胺(腹膜内(ip)或生理盐水注射)7天。停药14天后,用急性甲基苯丙胺(1 mg / kg ip)攻击大鼠,并从中提取RNA。 PFC比较了一系列GABA酶,转运蛋白和受体亚基的相对mRNA表达。与盐水预处理对照组相比,METH攻击在METH预处理动物中引起了显着的敏化行为(运动)反应。 GAT(1)和GAT(3)),与盐水对照组相比,致敏大鼠的PFC中的离子型GABA(A)受体亚基(α3和β1)以及代谢型GABA(B)1受体被上调。这些发现表明,对METH致敏后,GABA能mRNA的表达在突触前和突触后水平发生了显着改变,致敏导致几种抑制基因的转录上调。 nges可能会对PFC中GABA介导的神经传递产生重大影响,并且可能是精神病性疾病中某些保守的症状(例如执行功能障碍)的基础。 (C)2015 Elsevier B.V.保留所有权利。

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