Brunello N, Volterra A, Di Giulio A M, Cuomo V, Racagni G
Life Sci. 1984 Apr 23;34(17):1669-78. doi: 10.1016/0024-3205(84)90638-6.
C57 BL/6J (C57) mice display a particular pattern of responses following morphine administration, such as a rapid development of tolerance to the pharmacological action of the opiate and an increase in locomotor activity after a single injection of the drug. We have measured met-enkephalin content and the responsiveness of different opiate receptors after repeated administration of morphine and naloxone. Prolonged morphine administration changes neither met-enkephalin levels, nor the density of the opiate receptors in mice brain. In contrast repeated administration of the opiate antagonist naloxone, produced a marked increase in the number of 3H- DHM and 3H- DADLE binding sites in striatum and brainstem without modifying met-enkephalin concentrations. Behavioral studies have indicated that the morphine-induced increase in locomotor activity is enhanced in naloxone pretreated mice, thus suggesting a possible correlation between the behavioral response to morphine in C57 mice and the higher number of opiate receptors in the striatum.
C57 BL/6J(C57)小鼠在给予吗啡后表现出特定的反应模式,例如对阿片类药物药理作用的耐受性迅速发展,以及单次注射该药物后运动活性增加。我们在重复给予吗啡和纳洛酮后测量了甲硫氨酸脑啡肽含量和不同阿片受体的反应性。长期给予吗啡既不改变小鼠脑中的甲硫氨酸脑啡肽水平,也不改变阿片受体的密度。相反,重复给予阿片拮抗剂纳洛酮会使纹状体和脑干中3H-DHM和3H-DADLE结合位点的数量显著增加,而不改变甲硫氨酸脑啡肽浓度。行为学研究表明,在纳洛酮预处理的小鼠中,吗啡诱导的运动活性增加更为明显,因此提示C57小鼠对吗啡的行为反应与纹状体中较高数量的阿片受体之间可能存在相关性。