Liu Hui-Fen, Zhou Wen-Hua, Zhu Hua-Qiang, Lai Miao-Jun, Chen Wei-Sheng
Ningbo Institute of Microcirculation and Henbane, Ningbo Addiction Research and Treatment Center, Ningbo 315010, China.
Neurosci Bull. 2007 Jan;23(1):1-8. doi: 10.1007/s12264-007-0001-6.
To investigate the effect of M(5) muscarinic receptor subtype on the locomotor sensitization induced by heroin priming, and it's effect on the FosB expression in the nucleus accumbens (NAc) and the hippocampus in the heroin sensitized rats.
Locomotor activity was measured every 10 min for 1 h after subcutaneous injection of heroin. FosB expression was assayed by immunohistochemistry, and the antisense oligonucleotides (AS-ONs) targeting M(5) muscarinic receptor was transferred with the lipofectin.
Microinjection of AS-ONs targeting M(5) muscarinic receptor in the ventral tegmental area (VTA) blocked the expression of behavioral sensitization induced by heroin priming in rats. Meanwhile, the expression of FosB-positive neurons in either the NAc or the dentate gyrus (DG) of the hippocampus increased in heroin-induced locomotor sensitized rats. The enhancement of FosB-positive neurons in the NAc or DG could be inhibited by microinjection of M(5) muscarinic receptor AS-ONs into the VTA before the heroin-induced locomotor sensitization was performed. In contrast, microinjection of M(5) muscarinic receptor sense oligonucleotide (S-ONs) into the VTA did not block the expression of behavioral sensitization or the expression of FosB in the NAc or DG in the heroin sensitized rats.
Blocking M(5) muscarinic receptor in the VTA inhibits the expression of heroin-induced locomotor sensitization, which is associated with the regulation of FosB expression in the NAc and hippocampus neurons. M(5) muscarinic receptor may be a useful pharmacological target for the treatment of heroin addiction.
研究M5毒蕈碱受体亚型对海洛因启动诱导的运动敏化的影响,以及其对海洛因致敏大鼠伏隔核(NAc)和海马中FosB表达的影响。
皮下注射海洛因后,每10分钟测量1小时的运动活动。通过免疫组织化学检测FosB表达,并用脂质体转染靶向M5毒蕈碱受体的反义寡核苷酸(AS-ONs)。
在腹侧被盖区(VTA)微量注射靶向M5毒蕈碱受体的AS-ONs可阻断大鼠海洛因启动诱导的行为敏化表达。同时,海洛因诱导的运动致敏大鼠海马NAc或齿状回(DG)中FosB阳性神经元的表达增加。在进行海洛因诱导的运动致敏之前,向VTA微量注射M5毒蕈碱受体AS-ONs可抑制NAc或DG中FosB阳性神经元的增加。相反,向VTA微量注射M5毒蕈碱受体正义寡核苷酸(S-ONs)不会阻断海洛因致敏大鼠的行为敏化表达或NAc或DG中FosB的表达。
阻断VTA中的M5毒蕈碱受体可抑制海洛因诱导的运动敏化表达,这与NAc和海马神经元中FosB表达的调节有关。M5毒蕈碱受体可能是治疗海洛因成瘾的有用药理学靶点。