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用五种不同的抗精神病药物进行长期治疗会引发对注入伏隔核的阿片类药物的行为超敏反应。

Chronic treatment with five different neuroleptics elicits behavioral supersensitivity to opiate infusion into the nucleus accumbens.

作者信息

Stinus L, Nadaud D, Jauregui J, Kelley A E

出版信息

Biol Psychiatry. 1986 Jan;21(1):34-48. doi: 10.1016/0006-3223(86)90006-5.

Abstract

It has previously been demonstrated that direct opiate infusion into nucleus accumbens elicits psychomotor activation in rats. In the present study, the effects of chronic treatment with five different neuroleptics on this behavioral response were investigated. All neuroleptics tested (haloperidol, sulpiride, flupentixol decanoate, perphenazine enanthate, fluphenazine decanoate, palmitic ester of pipotiazine) induced a marked behavioral supersensitivity to intraaccumbens opiate infusion. A similarly enhanced sensitivity was observed in chronic reserpine-treated rats. The maximum sensitivity to opiates appeared 2-3 weeks after the beginning of neuroleptic treatment and was present up to 1 month after the end of treatment. Naloxone blocked the neuroleptic-induced enhanced response to opiates. It is concluded that chronic blockade of dopaminergic transmission results in considerable functional alterations of the endogenous opiate systems. The results are discussed in terms of possible underlying neuronal mechanisms, and important clinical implications are noted.

摘要

先前已经证明,将阿片类药物直接注入大鼠伏隔核会引发其精神运动激活。在本研究中,研究了五种不同抗精神病药物的长期治疗对这种行为反应的影响。所有测试的抗精神病药物(氟哌啶醇、舒必利、癸酸氟奋乃静、庚酸奋乃静、癸酸氟奋乃静、哌泊噻嗪棕榈酸酯)均诱导出对伏隔核内注入阿片类药物的明显行为超敏反应。在长期接受利血平治疗的大鼠中也观察到了类似增强的敏感性。对抗精神病药物治疗开始后2至3周出现对阿片类药物的最大敏感性,并且在治疗结束后长达1个月仍存在。纳洛酮阻断了抗精神病药物诱导的对阿片类药物的增强反应。得出的结论是,多巴胺能传递的长期阻断导致内源性阿片系统发生相当大的功能改变。从可能的潜在神经元机制方面讨论了结果,并指出了重要的临床意义。

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