AKAP150 from nucleus accumbens dopamine D1 and D2 receptor-expressing medium spiny neurons regulates morphine withdrawal

被引:5
作者
Bai, Xiaohui [1 ,2 ]
Zhang, Kun [1 ]
Ou, Chaopeng [1 ]
Mu, Yanyu [1 ]
Chi, Dongmei [1 ]
Zhang, Jianxing [1 ]
Huang, Jingxiu [1 ]
Li, Xile [1 ]
Zhang, Yingjun [1 ]
Huang, Wan [1 ]
Ouyang, Handong [1 ]
机构
[1] Sun Yat Sen Univ, Guangdong Prov Clin Res Ctr Canc, Dept Anesthesiol, State Key Lab Oncol South China,Canc Ctr, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Anesthesiol, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
OPIATE WITHDRAWAL; STRIATAL NEURONS; KINASE; PHOSPHORYLATION; MODULATION; PLASTICITY; ADDICTION; AVERSION; PATHWAY; REWARD;
D O I
10.1016/j.isci.2023.108227
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dopamine D1 receptor-expressing medium spiny neurons (D1R-MSNs) and dopamine D2 receptor -expressing MSNs (D2R-MSNs) in nucleus accumbens (NAc) have been demonstrated to show different effects on reward and memory of abstinence. A-kinase anchoring protein 150 (AKAP150) expression in NAc is significantly upregulated and contributes to the morphine withdrawal behavior. However, the underlying mechanism of AKAP150 under opioid withdrawal remains unclear. In this study, AKAP150 expression in NAc is upregulated in naloxone-precipitated morphine withdrawal model, and knockdown of AKAP150 alleviates morphine withdrawal somatic signs and improves the performance of conditioned place aversion (CPA) test. AKAP150 in NAc D1R-MSNs is related to modulation of the performance of morphine withdrawal CPA test, while AKAP150 in NAc D2R-MSNs is relevant to the severity of somatic responses. Our results suggest that AKAP150 from D1R-MSNs or D2R-MSNs in NAc contributes to the developmental process of morphine withdrawal but plays different roles in aspects of behavior or psychology.
引用
收藏
页数:19
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