Cicero T J, Owens D P, Schmoeker P F, Meyer E R
Life Sci. 1984 Sep 17;35(12):1321-8. doi: 10.1016/0024-3205(84)90104-8.
The effects of naloxone pretreatment on opiate agonist-induced depressions in serum luteinizing hormone (LH) levels were examined in male rats. Our results demonstrated a pronounced enhancement of morphine's actions 6 hours after the administration of naloxone (0.5 mg/kg). This effect was characterized by a 10 fold reduction in the ED50 (1.26 mg/kg versus 0.13 mg/kg in saline- and naloxone-pretreated rats, respectively) and much greater depressions in serum LH levels at each dose of morphine. The actions of naloxone were not confined to morphine, since similar increased potencies were found for opioid agonists with selectivity for a variety of opioid receptor subtypes. Because naloxone did not alter the uptake of subsequently administered morphine into brain, our results cannot be explained on the basis of an increased availability of the agonist. Rather, it appears that naloxone pretreatment induces a change in the sensitivity of those receptors involved in the effects of opioid agonists on LH.
在雄性大鼠中研究了纳洛酮预处理对阿片类激动剂诱导的血清促黄体生成素(LH)水平降低的影响。我们的结果表明,在给予纳洛酮(0.5毫克/千克)6小时后,吗啡的作用明显增强。这种效应的特征是ED50降低了10倍(盐水预处理和纳洛酮预处理的大鼠分别为1.26毫克/千克和0.13毫克/千克),并且在每种吗啡剂量下血清LH水平的降低幅度更大。纳洛酮的作用并不局限于吗啡,因为对于对多种阿片受体亚型具有选择性的阿片类激动剂,也发现了类似的效力增加。由于纳洛酮并未改变随后给予的吗啡在脑中的摄取,因此我们的结果无法基于激动剂可用性的增加来解释。相反,似乎纳洛酮预处理会导致参与阿片类激动剂对LH作用的那些受体的敏感性发生变化。