Lehman T, Peterson G R
Psychopharmacology (Berl). 1978 Dec 8;59(3):305-8. doi: 10.1007/BF00426639.
SKF 525-A, given i.p. to mice at doses from 50 to 100 mg/kg, had analgesic activity approximately 40% the analgesic potency of d-propoxyphene HCl, a chemically similar narcotic. While the analgesia produced by propoxyphene was totally antagonized by naloxone, however, that produced by SKF 525-A was only partly reversed. We suspect that SKF 525-A may exert its antinociceptive actions partly by an interaction with CNS narcotic receptors and partly by a nonspecific sedating action.
以50至100毫克/千克的剂量腹腔注射给小鼠的SKF 525 - A,其镇痛活性约为化学结构相似的麻醉剂盐酸右丙氧芬镇痛效力的40%。然而,虽然右丙氧芬产生的镇痛作用可被纳洛酮完全拮抗,但SKF 525 - A产生的镇痛作用仅部分被逆转。我们怀疑SKF 525 - A可能部分通过与中枢神经系统麻醉受体相互作用,部分通过非特异性镇静作用发挥其抗伤害感受作用。