Bhargava H N, Cao Y J
Department of Pharmaceutics and Pharmacodynamics, The University of Illinois at Chicago, Health Sciences Center, 60612, USA.
Peptides. 1998;19(3):563-8. doi: 10.1016/s0196-9781(97)00422-1.
The effects of acute and chronic administration of cocaine on the antinociception and tolerance to the antinociceptive actions of mu-(morphine), kappa-(U-50,488H), and delta-([D-Pen2,D-Pen5]enkephalin; DPDPE), opioid receptor agonists were determined in male Swiss-Webster mice. Intraperitoneal injection of 40 mg/kg of cocaine by itself produced weak antinociceptive response as measured by the tail-fick test but the lower doses were ineffective. Administration of morphine (10 mg/kg, SC), U-50,488H (25 mg/kg, IP) or DPDPE (10 microg/mouse, ICV) produced antinociception in mice. Cocaine (20 mg/kg) potentiated the antinociceptive action of morphine and DPDPE but had no effect on U-50,488H-induced antinociception. Administration of morphine (20 mg/kg, SC), U-50,488H (25 mg/kg, IP) or DPDPE (20 microg/mouse, ICV) twice a day for 4 days resulted in the development of tolerance to their antinociceptive actions. Tolerance to the antinociceptive actions of morphine and U-50,488H was inhibited by concurrent treatment with 20 or 40 mg/kg doses of cocaine; however, tolerance to the antinociceptive action of DPDPE was not modified by cocaine. It is concluded that cocaine selectively potentiates the antinociceptive action of mu- and delta- but not of the kappa-opioid receptor agonist. On the other hand, cocaine inhibits the development of tolerance to the antinociceptive actions of mu- and kappa- but not of delta-opioid receptor agonists in mice.
在雄性瑞士韦伯斯特小鼠中,研究了急性和慢性给予可卡因对μ-(吗啡)、κ-(U-50,488H)和δ-([D-青霉胺2,D-青霉胺5]脑啡肽;DPDPE)阿片受体激动剂的抗伤害感受及对其抗伤害感受作用耐受性的影响。腹腔注射40mg/kg可卡因本身通过甩尾试验测量产生较弱的抗伤害感受反应,但较低剂量无效。给予吗啡(10mg/kg,皮下注射)、U-50,488H(25mg/kg,腹腔注射)或DPDPE(10μg/小鼠,脑室内注射)可使小鼠产生抗伤害感受。可卡因(20mg/kg)增强了吗啡和DPDPE的抗伤害感受作用,但对U-50,488H诱导的抗伤害感受无影响。每天两次给予吗啡(20mg/kg,皮下注射)、U-50,488H(25mg/kg,腹腔注射)或DPDPE(20μg/小鼠,脑室内注射),持续4天,导致对其抗伤害感受作用产生耐受性。同时给予20或40mg/kg剂量的可卡因可抑制对吗啡和U-50,488H抗伤害感受作用的耐受性;然而,可卡因并未改变对DPDPE抗伤害感受作用的耐受性。得出的结论是,可卡因选择性地增强μ-和δ-阿片受体激动剂的抗伤害感受作用,但不增强κ-阿片受体激动剂的作用。另一方面,可卡因抑制小鼠对μ-和κ-阿片受体激动剂抗伤害感受作用耐受性的发展,但不抑制对δ-阿片受体激动剂的耐受性发展。