Zambotti F, Zonta N, Tammiso R, Conci F, Hafner B, Ferrario P, Zecca L, Mantegazza P
Department of Pharmacology, School of Medicine, University of Milano, Italy.
Naunyn Schmiedebergs Arch Pharmacol. 1987 Nov;336(5):526-9. doi: 10.1007/BF00169309.
The antinociceptive effect of morphine, as determined by the tail-flick test, was dose-dependently increased by the intraperitoneal injection of zopiclone. The benzodiazepine antagonists Ro 15-1788 (flumazepil) and Ro 15-3505, when intraperitoneally injected, significantly antagonized the effect of intraperitoneal injection of zopiclone on morphine antinociception. Intrathecal injection of zopiclone potentiated morphine antinociception, while the intracerebroventricular injection of zopiclone failed to enhance morphine antinociception and the intracerebroventricular injection of flumazepil to antagonize the intraperitoneal-zopiclone-induced increase in morphine antinociception. These results suggest that benzodiazepine sites are specifically involved in the potentiating effect of zopiclone on morphine antinociception. The anatomical locations of the receptors involved seem to be at the spinal level.
通过甩尾试验测定,腹腔注射佐匹克隆可使吗啡的镇痛作用呈剂量依赖性增强。苯二氮䓬拮抗剂Ro 15 - 1788(氟马西尼)和Ro 15 - 3505腹腔注射时,可显著拮抗腹腔注射佐匹克隆对吗啡镇痛作用的影响。鞘内注射佐匹克隆可增强吗啡的镇痛作用,而脑室内注射佐匹克隆未能增强吗啡的镇痛作用,脑室内注射氟马西尼也未能拮抗腹腔注射佐匹克隆所致的吗啡镇痛作用增强。这些结果表明,苯二氮䓬位点特异性参与了佐匹克隆对吗啡镇痛作用的增强效应。所涉及受体的解剖位置似乎在脊髓水平。