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育亨宾对啮齿动物阿片类激动剂的抗伤害感受和位置条件作用的影响。

Effects of yohimbine on the antinociceptive and place conditioning effects of opioid agonists in rodents.

作者信息

Morales L, Perez-Garcia C, Alguacil L F

机构信息

Lab. Pharmacology, Univ. San Pablo CEU, P.O. Box 67, 28660 Boadilla, Madrid, Spain.

出版信息

Br J Pharmacol. 2001 May;133(1):172-8. doi: 10.1038/sj.bjp.0704057.

Abstract
  1. The pharmacological modulation of opioid actions by drugs acting on heterologous mechanisms could be useful to overcome some of the main problems associated with the use of opiate agonists. Based on previous findings on the interactions between yohimbine and opioid drugs, we have further studied the effects of yohimbine on the antinociceptive and positive-negative reinforcing effects of morphine (mu opioid receptor-preferring agonist), U-50,488 (kappa agonist) and SNC80 (delta agonist). 2. Pretreatment with yohimbine completely blocked the antinociception provided by the three opioid agonists in the mouse tail-immersion test. 3. A similar blockade of SNC80 and U-50,488-induced antinociception was observed with yohimbine in the mouse hot plate test at the same doses. In this paradigm, the effect of the kappa agonist was very slight and the actions of yohimbine rather variable. 4. In place conditioning experiments with SD (Sprague -- Dawley) male rats, yohimbine alone was inactive but it limited the preference induced by morphine and SNC80 and the aversive effect of U-50,488. Impaired novelty preference was also observed with the combination of yohimbine and U-50,488. 5. It is concluded that yohimbine tends to limit opioid antinociception and the addictive potential of mu and delta opioid agonists. More selective drugs could help to understand the mechanisms involved in these actions.
摘要
  1. 通过作用于异源机制的药物对阿片类药物作用进行药理学调节,可能有助于克服与使用阿片激动剂相关的一些主要问题。基于先前关于育亨宾与阿片类药物相互作用的研究结果,我们进一步研究了育亨宾对吗啡(偏爱μ阿片受体激动剂)、U - 50,488(κ激动剂)和SNC80(δ激动剂)的镇痛及正负强化作用的影响。2. 在小鼠尾浸试验中,用育亨宾预处理可完全阻断这三种阿片激动剂产生的镇痛作用。3. 在小鼠热板试验中,相同剂量的育亨宾对SNC80和U - 50,488诱导的镇痛作用也有类似的阻断作用。在这种模式下,κ激动剂的作用非常轻微,育亨宾的作用相当多变。4. 在对Sprague - Dawley雄性大鼠进行的位置条件反射实验中,单独使用育亨宾没有活性,但它限制了吗啡和SNC80诱导的偏好以及U - 50,488的厌恶作用。育亨宾与U - 50,488联合使用时还观察到新奇偏好受损。5. 得出的结论是,育亨宾倾向于限制阿片类药物的镇痛作用以及μ和δ阿片激动剂的成瘾潜力。更具选择性的药物可能有助于了解这些作用所涉及的机制。

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