Interaction between Opioids and Cannabinoids in the Immune System: Functional Evidence in the Rat

P. Massi, A. Vaccani, D. Parolaro
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Abstract

Cannabinoids and opioids share several pharmacological properties, including antinociception, hypothermia, sedation, hypotension and inhibition of immune function. It has been demonstrated that chronic morphine treatment in rats produced hypersensitivity to Δ9-tetrahydrocannabinol analgesia. As a consequence of those results and the fact that drug abusers often use marijuana and morphine concurrently, we have investigated the possibility of functional interaction between opioid and cannabinoid systems at immune level in the rat. We have evaluated splenocyte proliferative response to a mitogen and natural killer cytolytic activity following chronic administration of the synthetic cannabinoid compound CP-55,940, and morphine. A psychotropic dose of CP-55,940 (0.2 mg kg−1, i.p.) significantly inhibited the splenocyte proliferative response to Concanavalin A and natural killer activity. Similar to the effects of CP-55,940, morphine (5 mg kg−1, s.c.) administration was also accompanied by a significant suppression of both parameters. Animals that received daily injection of either CP-55,940 or morphine developed tolerance to their acute immunosuppressive effects. Once tolerance to the suppressive effects of either cannabinoid or morphine was achieved, animals became cross-resistant to the suppressive effect of either drug. These data suggest the possibility that morphine and CP-55,940 have a common underlying mechanism for the suppression of splenocyte proliferation and natural killer activity.
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阿片类药物和大麻素在大鼠免疫系统中的相互作用:功能证据
大麻素和阿片类药物具有一些共同的药理特性,包括抗痛觉、降低体温、镇静、低血压和抑制免疫功能。已经证明,慢性吗啡治疗大鼠对Δ9-tetrahydrocannabinol镇痛产生超敏反应。由于这些结果以及药物滥用者经常同时使用大麻和吗啡的事实,我们研究了大鼠免疫水平上阿片类药物和大麻素系统之间功能相互作用的可能性。我们评估了慢性给药合成大麻素化合物CP-55,940和吗啡后,脾细胞对有丝分裂原的增殖反应和自然杀伤细胞溶解活性。精神药物剂量CP-55,940 (0.2 mg kg - 1, i.p.)显著抑制脾细胞对刀豆蛋白A的增殖反应和自然杀伤活性。与CP-55,940的作用类似,吗啡(5mg kg - 1, s.c)的施用也伴随着这两个参数的显著抑制。每天注射CP-55,940或吗啡的动物对其急性免疫抑制作用产生了耐受性。一旦对大麻素或吗啡的抑制作用产生耐受性,动物就会对这两种药物的抑制作用产生交叉抗性。这些数据表明吗啡和CP-55,940可能具有抑制脾细胞增殖和自然杀伤活性的共同潜在机制。
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