首页> 外文期刊>European Journal of Pharmacology: An International Journal >Opioid receptors and the discriminative stimulus effects of ethanol in squirrel monkeys: Mu and delta opioid receptor mechanisms.
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Opioid receptors and the discriminative stimulus effects of ethanol in squirrel monkeys: Mu and delta opioid receptor mechanisms.

机译:阿片受体和乙醇对松鼠猴的歧视性刺激作用:Mu和δ阿片受体机制。

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Mu and delta opioid receptors modulate the reinforcing effects of ethanol, however, their role in the subjective effects of ethanol is not well understood. This study evaluated the contribution of mu and delta opioid receptors to the subjective effects of ethanol using drug discrimination procedures. Monkeys were trained to discriminate ethanol from saline under a schedule of food delivery. In tests, ethanol engendered increases in drug-lever responding, reaching a maximum of >80%. The mu opioid receptor agonists fentanyl and buprenorphine and the delta opioid receptor agonists SNC 80 and SNC 162 did not substitute for the discriminative stimulus effects of ethanol. As pretreatments, the full agonists fentanyl and SNC 80 enhanced the effects of low doses of ethanol and fentanyl attenuated the effects of the ethanol training dose. Although the possibility of pharmacological antagonism of the effects of ethanol cannot be ruled out, a more likely alternative is that the diminished effects of ethanol were due to perceptual masking of the ethanol stimulus. In contrast, the partial agonists buprenorphine and SNC 162 did not alter ethanol's effects. Finally, the discriminative stimulus effects of ethanol were attenuated following administration of presumably mu-selective doses of the antagonist naltrexone, but not after administration of the delta opioid receptor antagonist naltrindole. The ability of naltrexone to block the discriminative stimulus effects of ethanol likely reflects its capacity to attenuate ethanol-induced increases in endogenous opioids, in particular beta-endorphin, because attenuation of the ethanol stimulus was not accompanied by significant suppression of response rate.
机译:Mu和δ阿片样物质受体调节乙醇的增强作用,但是,它们在乙醇的主观作用中的作用尚不清楚。这项研究使用药物区分程序评估了mu和delta类阿片受体对乙醇的主观作用的贡献。训练猴子按照食物分配时间表从盐水中区分乙醇。在测试中,乙醇引起了药物杠杆反应的增加,最高达到> 80%。 mu阿片受体激动剂芬太尼和丁丙诺啡以及δ阿片受体激动剂SNC 80和SNC 162不能替代乙醇的歧视性刺激作用。作为预处理,全激动剂芬太尼和SNC 80增强了低剂量乙醇的作用,芬太尼减弱了乙醇训练剂量的作用。尽管不能排除乙醇作用产生药理拮抗作用的可能性,但更可能的替代方法是乙醇作用减弱,这是由于对乙醇刺激物的感知掩盖了。相反,部分激动剂丁丙诺啡和SNC 162不会改变乙醇的作用。最后,在施用大概μ选择剂量的拮抗剂纳曲酮后,乙醇的歧视性刺激作用减弱,但在施用δ阿片受体拮抗剂纳曲酮后未减弱。纳曲酮阻断乙醇的歧视性刺激作用的能力可能反映了其减弱乙醇诱导的内源性阿片类药物(特别是β-内啡肽)增加的能力,因为乙醇刺激剂的减弱并没有显着抑制响应率。

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