Blass E M, Cramer C P, Fanselow M S
Johns Hopkins University, Baltimore, MD 21218.
Pharmacol Biochem Behav. 1993 Mar;44(3):643-9. doi: 10.1016/0091-3057(93)90180-2.
Two parallel experiments in rats 2-21 days of age investigated the onset and characteristics of morphine-induced antinociception. One measure of reactivity to pain, limb retraction from a hotplate, was utilized for three different limbs (forepaw, hindpaw, and tail) to chart the development of opioid sensitivity. Morphine-induced antinociception, even in 2-day-old rats, was obtained for all limbs, in a dose-related fashion, and reached peak sensitivity at 6-7 days of age. Naltrexone did not affect limb retraction latencies in nonmorphine treated rats at any age. These studies demonstrate early antinociception to low doses of an opiate and establish that the pain system, like positive reinforcement systems, is opiate sensitive.
两项针对2至21日龄大鼠的平行实验研究了吗啡诱导的抗伤害感受的起始和特征。采用一种对疼痛的反应性测量方法,即从热板上缩回肢体,对三个不同的肢体(前爪、后爪和尾巴)进行测量,以描绘阿片类药物敏感性的发展情况。即使在2日龄的大鼠中,吗啡诱导的抗伤害感受在所有肢体上均呈剂量相关方式出现,并在6至7日龄时达到峰值敏感性。纳曲酮在任何年龄对未用吗啡治疗的大鼠的肢体缩回潜伏期均无影响。这些研究证明了对低剂量阿片类药物的早期抗伤害感受,并证实疼痛系统与正强化系统一样,对阿片类药物敏感。