Abbott F V
Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
Pharmacol Biochem Behav. 1990 Dec;37(4):713-6. doi: 10.1016/0091-3057(90)90553-t.
The formalin test assesses the behavioral response of an animal to minor tissue injury-induced pain. Opioid antinociception in this test has been suggested to depend largely on activation of kappa receptors but mu agonists are also potent in reducing pain behavior. The present study used the irreversible mu antagonist, beta-funaltrexamine (beta-FNA), to examine the role of mu receptor activation in this test. beta-FNA given intracranially 4 h before testing fully blocked the effects of morphine and attenuated the effects of ethylketocyclazocine and U50,488H. The results do not support a role for kappa receptors in antinociception in the formalin test. Instead, mu and, possibly, delta receptors are involved.
福尔马林试验评估动物对轻微组织损伤诱导疼痛的行为反应。在该试验中,阿片类药物的镇痛作用很大程度上被认为取决于κ受体的激活,但μ激动剂在减轻疼痛行为方面也很有效。本研究使用不可逆的μ拮抗剂β-氟纳曲胺(β-FNA)来研究μ受体激活在该试验中的作用。在测试前4小时颅内注射β-FNA可完全阻断吗啡的作用,并减弱乙基酮环唑辛和U50,488H的作用。结果不支持κ受体在福尔马林试验镇痛中起作用。相反,μ受体以及可能的δ受体参与其中。