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吗啡诱导的免疫状态改变的巴甫洛夫条件反射:阿片受体参与的证据。

Pavlovian conditioning of morphine-induced alterations of immune status: evidence for opioid receptor involvement.

作者信息

Coussons-Read M E, Dykstra L A, Lysle D T

机构信息

Department of Psychology, University of North Carolina at Chapel Hill 27599-3270.

出版信息

J Neuroimmunol. 1994 Dec;55(2):135-42. doi: 10.1016/0165-5728(94)90003-5.

DOI:10.1016/0165-5728(94)90003-5
PMID:7829663
Abstract

Prior work in our laboratory has shown that morphine's immunomodulatory effects can become conditioned to environmental stimuli that predict drug administration. These immune alterations include conditioned changes in natural killer cell activity, interleukin-2 production, and mitogen-induced lymphocyte proliferation. The present study examined the involvement of opioid receptor activity in the establishment and expression of conditioned morphine-induced alterations of immune status. During the training phase of the experiment, Lewis rats received two conditioning sessions during which a subcutaneous injection of 15 mg/kg morphine sulfate was paired with exposure to a distinctive environment. On the test day, animals were re-exposed to the distinctive environment alone prior to sacrifice. Saline or naltrexone (0.3, 1.0, 3.0 or 10.0 mg/kg) was administered during either the training or the test session. Administration of naltrexone prior to training antagonized the development of all of the conditioned alterations of immune status including changes in the mitogenic responsiveness of splenocytes, suppression of natural killer cell activity, and interleukin-2 production by splenocytes. Naltrexone administration prior to testing also was effective in antagonizing the expression of a subset of morphine-induced conditioned alterations in immune status. Taken together, these studies indicate that opioid receptor activity is involved in the establishment of conditioned morphine-induced immune alterations, as well as in the expression of a subset of these conditioned alterations of immune status.

摘要

我们实验室之前的研究表明,吗啡的免疫调节作用能够与预测药物给药的环境刺激形成条件反射。这些免疫改变包括自然杀伤细胞活性、白细胞介素 - 2产生以及丝裂原诱导的淋巴细胞增殖的条件性变化。本研究考察了阿片受体活性在条件性吗啡诱导的免疫状态改变的建立和表达过程中的作用。在实验的训练阶段,Lewis大鼠接受了两个条件反射训练环节,期间皮下注射15mg/kg硫酸吗啡并同时暴露于一个独特的环境中。在测试日,动物在处死前单独再次暴露于该独特环境。在训练或测试环节给予生理盐水或纳曲酮(0.3、1.0、3.0或10.0mg/kg)。训练前给予纳曲酮可拮抗所有条件性免疫状态改变的发展,包括脾细胞促有丝分裂反应性的变化、自然杀伤细胞活性的抑制以及脾细胞白细胞介素 - 2的产生。测试前给予纳曲酮也有效地拮抗了吗啡诱导的部分条件性免疫状态改变的表达。综上所述,这些研究表明阿片受体活性参与了条件性吗啡诱导的免疫改变的建立,以及这些条件性免疫状态改变的部分表达。

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