Fujibayashi K, Kubota-Watanabe M, Iizuka Y
Biological Research Laboratories, Sankyo Co., Ltd, Tokyo, Japan.
Arch Int Pharmacodyn Ther. 1996 Mar-Apr;331(2):153-62.
The effects of R-84760 [(3R)-3-(1-pyrrolidinylmethyl)-4-[(1S)-5,6-dichloro-l-indancarb onyl] tetrahydro-1,4-thiazine hydrochloride] on nociception, locomotion and respiration were examined in rats. R-84760 induced a potent antinociceptive effect in the formalin test. The potency was 930 and 1500 times higher than that of U-50488 and morphine, respectively, when injected subcutaneously. Intracerebroventricular and intrathecal injection, as well as subcutaneous administration of naloxone antagonized the antinociceptive effect of R-84760, suggesting the sites of action of R-84760 were at the spinal and supraspinal levels. R-84760 disturbed the rotarod performance at doses 16 times higher than those needed for antinociception. R-84760 did not affect the arterial blood Pco2, Po2 and pH at a supramaximal dose for antinociception.
研究了R - 84760 [(3R)-3 - (1 - 吡咯烷基甲基)-4 - [(1S)-5,6 - 二氯 - 1 - 茚满羰基]四氢 - 1,4 - 噻嗪盐酸盐]对大鼠痛觉、运动和呼吸的影响。在福尔马林试验中,R - 84760诱导出强效的镇痛作用。皮下注射时,其效力分别比U - 50488和吗啡高930倍和1500倍。脑室内和鞘内注射以及皮下注射纳洛酮可拮抗R - 84760的镇痛作用,提示R - 84760的作用部位在脊髓和脊髓上水平。R - 84760在比镇痛所需剂量高16倍的剂量下会干扰转棒试验表现。在产生最大镇痛作用的剂量下,R - 84760不影响动脉血二氧化碳分压、氧分压和pH值。