吸前皮质强啡肽/κ阿片受体系统调节甲基苯丙胺诱导的认知障碍。

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Addiction Biology Pub Date : 2023-08-23 DOI:10.1111/adb.13323
Ying-jie Cheng, Ying-zhi Deng, Di Deng, Man-qing Wu, Jing-rui Chai, Yu-jun Wang, Jing-gen Liu, Min Zhao
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引用次数: 0

摘要

长期接触甲基苯丙胺会导致严重和持续的认知障碍。本研究旨在探讨强啡肽/κ阿片受体(KOR)系统在METH诱导的认知障碍发展中的作用。我们发现,在连续7天每天注射METH(10 mg/kg)后,小鼠在新型物体识别测试(NOR)中表现出显著的认知障碍。通过预处理选择性KOR拮抗剂norBNI(10mg/kg,i.p.)或KOR缺失,系统性阻断KOR可预防METH诱导的认知障碍。然后,除边缘下皮层外,仅在边缘前皮层(PL)观察到强啡肽和KOR mRNA显著增加。最后,使用NOR和自发交替行为测试,向PL中微量注射norBNI也改善了METH治疗小鼠的认知记忆。我们的研究结果表明,PL中强啡肽/KOR系统的激活可能是METH诱导的认知障碍的一种可能机制,并阐明了KOR拮抗剂作为一种潜在的神经保护剂来对抗药物滥用诱导的认知缺陷。
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Prelimbic cortex dynorphin/κ opioid receptor system modulates methamphetamine-induced cognitive impairment

Chronic exposure to methamphetamine (METH) causes severe and persistent cognitive impairment. The present study aimed to investigate the role of dynorphin/κ opioid receptor (KOR) system in the development of METH-induced cognitive impairment. We found that mice showed significant cognitive impairment in the novel object recognition test (NOR) following daily injections of METH (10 mg/kg) for seven consecutive days. Systemic blockade of KOR prevented METH-induced cognitive impairment by pretreatment of the selective KOR antagonist norBNI (10 mg/kg, i.p.) or KOR deletion. Then, significant increased dynorphin and KOR mRNA were observed exclusively in prelimbic cortex (PL) other than infralimbic cortex. Finally, microinjection with norBNI into PL also improved cognitive memory in METH-treated mice using NOR and spontaneous alternation behaviour test. Our results demonstrated that dynorphin/KOR system activation in PL may be a possible mechanism for METH-induced cognitive impairment and shed light on KOR antagonists as a potential neuroprotective agent against the cognitive deficits induced by drug abuse.

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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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