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[D-精氨酸2]-皮肤吗啡四肽类似物与吗啡之间的抗伤害感受性交叉耐受性。

Antinociceptive cross-tolerance between [D-Arg2]-dermorphin tetrapeptide analogs and morphine.

作者信息

Chaki K, Sakurada S, Sakurada T, Nakata N, Kisara K, Watanabe H, Suzuki K

机构信息

Department of Pharmacology, Tohoku College of Pharmacy, Sendai, Japan.

出版信息

Peptides. 1990 Jan-Feb;11(1):139-44. doi: 10.1016/0196-9781(90)90122-l.

Abstract

Cross-tolerance between [D-Arg2]-dermorphin tetrapeptide analogs and morphine with respect to antinociception was examined in the present set of experiments. Systemic administration of H-Tyr-D-Arg-Phe-Gly-NH2 (TDAPG-NH2), H-Tyr-D-Arg-Phe-beta-Ala-OH (TDAPA) or morphine over a period of 5 days produced the development of tolerance. In the cross-tolerance study, antinociception after subcutaneous (SC), intracerebroventricular (ICV) and intrathecal (IT) administrations of TDAPG-NH2 and TDAPA in morphine-tolerant mice was not significantly different from their respective effects in saline-pretreated control mice. A marked tolerance to SC- and ICV-administered morphine was seen in mice made tolerant to TDAPG-NH2 and TDAPA. However, IT administration of morphine produced no significant decrement in the antinociceptive activity in mice made tolerant to TDAPG-NH2 and TDAPA. These data indicate that [D-Arg2]-dermorphin tetrapeptide analogs can produce significant antinociception in morphine-tolerant mice.

摘要

在本系列实验中,研究了[D-精氨酸2]-皮啡肽四肽类似物与吗啡在抗伤害感受方面的交叉耐受性。连续5天全身给予H-Tyr-D-Arg-Phe-Gly-NH2(TDAPG-NH2)、H-Tyr-D-Arg-Phe-β-Ala-OH(TDAPA)或吗啡会产生耐受性。在交叉耐受性研究中,吗啡耐受小鼠皮下(SC)、脑室内(ICV)和鞘内(IT)给予TDAPG-NH2和TDAPA后的抗伤害感受与生理盐水预处理的对照小鼠中的相应作用无显著差异。在对TDAPG-NH2和TDAPA产生耐受的小鼠中,观察到对皮下和脑室内给予的吗啡有明显耐受性。然而,鞘内给予吗啡对TDAPG-NH2和TDAPA耐受小鼠的抗伤害感受活性没有显著降低。这些数据表明,[D-精氨酸2]-皮啡肽四肽类似物可在吗啡耐受小鼠中产生显著的抗伤害感受。

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