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氯胺酮和甲基苯丙胺对大鼠神经递质、谷氨酸受体和条件性位置偏爱影响。

The effects of ketamine and methamphetamine on neurotransmitters, glutamate receptors, and conditioned place preference in rat.

机构信息

School of Forensic Medicine/NHC Key Laboratory of Drug Addiction Medicine, Kunming Medical University, Kunming, China.

School of Forensic Medicine/NHC Key Laboratory of Drug Addiction Medicine, Kunming Medical University, Kunming, China; School of Basic Medicine, Hubei University of Arts and Science, Hubei, China.

出版信息

Leg Med (Tokyo). 2023 Nov;65:102328. doi: 10.1016/j.legalmed.2023.102328. Epub 2023 Sep 25.

Abstract

Combined methamphetamine (MA) and ketamine (KET) abuse is a serious issue. At present, however, few studies have explored the mechanism underlying their combined addiction. We established a rat conditioned place preference (CPP) model. We investigated the role of dopamine (DA), 5-hydroxytryptamine (5-HT), monoamine oxidase (MAO), glutamate receptor 1 (GluR1), and glutamate receptor 2 (GluR2) in combined MA and KET addiction. The expression levels of DA, 5-HT, and MAO were detected by enzyme-linked immunosorbent assay (ELISA), and the expressions levels of GluR1 and GluR2 were detected by western blotting. Our results showed that MA and KET successfully induced CPP in rats respectively, and KET enhanced MA-induced CPP effects, although not significantly, and KET can reduce the MA-induced increase in DA, 5-HT, MAO and promoted the MA-induced increase in GluR1 and GluR2. Therefore, it suggested that DA, 5-HT, MAO, GluR1, and GluR2 expression may be involved in the mechanism underlying MA and KET-induced drug addiction in rats. Moreover, When MA and KET are used in combination, KET appears to play a dual addictive and anti-addictive role in the regulation of MA addiction.

摘要

联合使用甲基苯丙胺(MA)和氯胺酮(KET)是一个严重的问题。然而,目前很少有研究探讨它们联合成瘾的机制。我们建立了大鼠条件性位置偏爱(CPP)模型。我们研究了多巴胺(DA)、5-羟色胺(5-HT)、单胺氧化酶(MAO)、谷氨酸受体 1(GluR1)和谷氨酸受体 2(GluR2)在联合 MA 和 KET 成瘾中的作用。通过酶联免疫吸附测定(ELISA)检测 DA、5-HT 和 MAO 的表达水平,通过 Western blot 检测 GluR1 和 GluR2 的表达水平。我们的结果表明,MA 和 KET 分别成功诱导了大鼠 CPP,KET 增强了 MA 诱导的 CPP 效应,尽管不明显,KET 可以降低 MA 诱导的 DA、5-HT、MAO 增加,并促进 MA 诱导的 GluR1 和 GluR2 增加。因此,这表明 DA、5-HT、MAO、GluR1 和 GluR2 的表达可能参与了大鼠 MA 和 KET 诱导的药物成瘾的机制。此外,当 MA 和 KET 联合使用时,KET 似乎在调节 MA 成瘾方面发挥了双重成瘾和抗成瘾作用。

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