Thomas D A, Williams G M, Iwata K, Kenshalo D R, Dubner R
Neurobiology and Anesthesiology Branch, National Institute of Dental Research, National Institutes of Health, Bethesda, MD 20892.
Brain Res. 1992 Jul 10;585(1-2):315-7. doi: 10.1016/0006-8993(92)91227-6.
Epidural and intrathecal administration of opioids to humans can produce facial pruritus and scratching that is naloxone reversible. It has been proposed that opioids may act at the level of the medulla to produce facial pruritus and associated scratching behavior. We investigated the effects of mu, delta and kappa opioid-receptor agonists microinjected unilaterally into the medullary dorsal horn (MDH) on facial scratching in cynomolgus monkeys. The selective mu opioid-receptor agonist, DAMGO (3.1-25.0 ng) produced large dose-dependent, naloxone-reversible increases in facial scratches. The selective delta opioid-receptor agonist, DPDPE (1.0-5.0 micrograms) and the selective kappa opioid-receptor agonist, U-50,488H (0.1-5.0 micrograms) did not produce significant increases in facial scratching behavior. We conclude that the MDH is a site where DAMGO, a mu opioid-receptor agonist, can act to produce facial scratching in monkeys, and that the MDH is likely the site where centrally administered opioids act to produce facial pruritus in humans.
向人体硬膜外和鞘内注射阿片类药物可引发面部瘙痒和抓挠,且这种反应可被纳洛酮逆转。有人提出,阿片类药物可能作用于延髓水平,从而引发面部瘙痒及相关抓挠行为。我们研究了单侧微量注射到延髓背角(MDH)的μ、δ和κ阿片受体激动剂对食蟹猴面部抓挠的影响。选择性μ阿片受体激动剂DAMGO(3.1 - 25.0纳克)可产生大剂量依赖性、纳洛酮可逆的面部抓挠增加。选择性δ阿片受体激动剂DPDPE(1.0 - 5.0微克)和选择性κ阿片受体激动剂U - 50,488H(0.1 - 5.0微克)未显著增加面部抓挠行为。我们得出结论,MDH是μ阿片受体激动剂DAMGO在猴子中引发面部抓挠的作用部位,并且MDH可能是中枢给予阿片类药物在人体中引发面部瘙痒的作用部位。