联合多巴胺受体拮抗剂电刺激杏仁核中央核可减少吗啡诱导的雄性大鼠条件性位置偏好的习得期。

IF 2.1 Q3 CHEMISTRY, MEDICINAL
Zahra Jokar, Saeed Khatamsaz, Hojjatallah Alaei, Mehrdad Shariati
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引用次数: 0

摘要

背景与目的:杏仁核中央核(CeA)是参与奖励系统的核之一。本研究旨在探讨CeA联合多巴胺D1受体拮抗剂对吗啡诱导的雄性大鼠条件位置偏好(CPP)的电刺激作用。实验方法:本研究采用5天CPP程序。吗啡有效剂量为5 mg/kg, SCH23390作为选择性D1受体拮抗剂注入CeA。另外,用150 μA的电流刺激CeA。最后对各实验组进行吗啡依赖性评价。结果:吗啡显著提高CPP。而阻断CeA的D1受体可减少吗啡诱导CPP的获得期。此外,D1受体拮抗剂和e-stim联合使用可抑制吗啡诱导的CPP,即使它引起厌恶。结论与意义:本研究提示多巴胺D1受体拮抗剂联合e-stim在吗啡依赖中发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The electrical stimulation of the central nucleus of the amygdala in combination with dopamine receptor antagonist reduces the acquisition phase of morphine-induced conditioned place preference in male rat.

The electrical stimulation of the central nucleus of the amygdala in combination with dopamine receptor antagonist reduces the acquisition phase of morphine-induced conditioned place preference in male rat.

The electrical stimulation of the central nucleus of the amygdala in combination with dopamine receptor antagonist reduces the acquisition phase of morphine-induced conditioned place preference in male rat.

The electrical stimulation of the central nucleus of the amygdala in combination with dopamine receptor antagonist reduces the acquisition phase of morphine-induced conditioned place preference in male rat.

Background and purpose: The central nucleus of the amygdala (CeA) is one of the nuclei involved in the reward system. The aim of the current study was to investigate the electrical stimulation (e-stim) effect of the CeA in combination with dopamine D1 receptor antagonist on morphine-induced conditioned place preference (CPP) in male rats.

Experimental approach: A 5-day procedure of CPP was used in this study. Morphine was administered at an effective dose of 5 mg/kg, and SCH23390 as a selective D1 receptor antagonist was administrated into the CeA. In addition, the CeA was stimulated with an intensity of the current of 150 μA. Finally, the dependence on morphine was evaluated in all experimental groups.

Findings/results: Morphine significantly increased CPP. While the blockade of the D1 receptor of the CeA reduced the acquisition phase of morphine-induced CPP. Moreover, the combination of D1 receptor antagonist and e-stim suppressed morphine-induced CPP, even it induced an aversion.

Conclusion and implication: The current study suggests that the administration of dopamine D1 receptor antagonist into the CeA in combination with e-stim could play a prominent role in morphine dependence.

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来源期刊
Research in Pharmaceutical Sciences
Research in Pharmaceutical Sciences CHEMISTRY, MEDICINAL-
CiteScore
3.60
自引率
19.00%
发文量
50
审稿时长
34 weeks
期刊介绍: Research in Pharmaceutical Sciences (RPS) is included in Thomson Reuters ESCI Web of Science (searchable at WoS master journal list), indexed with PubMed and PubMed Central and abstracted in the Elsevier Bibliographic Databases. Databases include Scopus, EMBASE, EMCare, EMBiology and Elsevier BIOBASE. It is also indexed in several specialized databases including Scientific Information Database (SID), Google Scholar, Iran Medex, Magiran, Index Copernicus (IC) and Islamic World Science Citation Center (ISC).
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