Nakata N, Sakurada S, Sakurada T, Kisara K, Sasaki Y, Suzuki K
Pharmacol Biochem Behav. 1986 Jan;24(1):27-31. doi: 10.1016/0091-3057(86)90039-0.
The characteristics of an analog of tetrapeptide dermorphin (H-Tyr-D-Arg-Phe-Sar-OH), [D-Arg2, Sar4]-dermorphin (1-4) were examined in comparison with morphine by the appearance of typical withdrawal signs upon cessation of administration or treatment with naloxone, an opioid antagonist. The dose of [D-Arg2, Sar4]-dermorphin (1-4) or morphine in the physical dependence test can be quantified by determining the ED50 to inhibit the tail-flick response to thermal stimuli. Doses from 8 to 64 times the ED50 doses were employed in the subcutaneous injection schedules. The cessation of [D-Arg2, Sar4]-dermorphin (1-4) or naloxone treatment was largely without effect on body weight, in contrast to a marked loss of weight in morphine-dependent rats. The tetrapeptide failed to substitute for morphine in morphine-dependent rats. The physical dependence of [D-Arg2, Sar4]-dermorphin (1-4) was revealed by the behavioral signs of withdrawal precipitated by naloxone. However, the scores of lacrimation, diarrhea and urination were much lower in chronically tetrapeptide-treated rats than in morphine-treated rats, though the score of teeth chatter was higher. These findings indicate that [D-Arg2, Sar4]-dermorphin (1-4) may differ from morphine in physical dependence.
通过在停止给药或用阿片类拮抗剂纳洛酮治疗时出现典型的戒断症状,将四肽类皮肤吗啡肽类似物(H-Tyr-D-Arg-Phe-Sar-OH),即[D-Arg2,Sar4]-皮肤吗啡肽(1-4)的特性与吗啡进行了比较。在身体依赖性试验中,[D-Arg2,Sar4]-皮肤吗啡肽(1-4)或吗啡的剂量可通过测定抑制对热刺激的甩尾反应的半数有效剂量(ED50)来定量。皮下注射方案采用的剂量为ED50剂量的8至64倍。与吗啡依赖大鼠体重明显减轻相反,停止[D-Arg2,Sar4]-皮肤吗啡肽(1-4)或纳洛酮治疗对体重基本没有影响。该四肽在吗啡依赖大鼠中不能替代吗啡。纳洛酮诱发的戒断行为体征揭示了[D-Arg2,Sar4]-皮肤吗啡肽(1-4)的身体依赖性。然而,尽管牙齿打颤的评分较高,但长期接受四肽治疗的大鼠的流泪、腹泻和排尿评分远低于接受吗啡治疗的大鼠。这些发现表明,[D-Arg2,Sar4]-皮肤吗啡肽(1-4)在身体依赖性方面可能与吗啡不同。