李灵源, 叶菜英, 张佩文, 田民, 金荫昌. 纳洛肼及14-羟基双氢吗啡肼与阿片受点结合的可逆性J. 药学学报, 1984, 19(4): 251-255.
引用本文: 李灵源, 叶菜英, 张佩文, 田民, 金荫昌. 纳洛肼及14-羟基双氢吗啡肼与阿片受点结合的可逆性J. 药学学报, 1984, 19(4): 251-255.
LI Ling-yuan, YE Cai-ying, ZHANG Pei-wen, TIAN Min , JIN Yin-chang, . REVERSIBLE BINDING OF NALOXAZINE AND 14-HYDROXYDIHYDROMORPHAZINE WITH OPIATE RECEPTORSJ. Acta Pharmaceutica Sinica, 1984, 19(4): 251-255.
Citation: LI Ling-yuan, YE Cai-ying, ZHANG Pei-wen, TIAN Min , JIN Yin-chang, . REVERSIBLE BINDING OF NALOXAZINE AND 14-HYDROXYDIHYDROMORPHAZINE WITH OPIATE RECEPTORSJ. Acta Pharmaceutica Sinica, 1984, 19(4): 251-255.

纳洛肼及14-羟基双氢吗啡肼与阿片受点结合的可逆性

REVERSIBLE BINDING OF NALOXAZINE AND 14-HYDROXYDIHYDROMORPHAZINE WITH OPIATE RECEPTORS

  • 摘要: 用纳洛肼(NZI,1×10-5M)或14-羟基双氢吗啡肼(HZI,1×10-6)与大鼠脑匀浆P2膜制备保温后,以Tris缓冲液反复洗涤,阿片受点可完全恢复与3H双氢吗啡(3HDHM)的结合能力。在离体豚鼠回肠纵肌(GPI)试验中,HZI对电刺激收缩的抑制及NZI对吗啡(Mor)抑制作用的对抗亦皆可被洗掉,此外HZI对收缩的抑制还可被纳洛酮(Nal)所逆转,说明它们与阿片受点的结合都是可逆的。HZI镇痛作用ED50为1.3 mg/kg(小鼠热板法SC),略强于Mor(3 mg/kg),持续时间与Mor相似。NZI对Mor镇痛的对抗可持续十余小时。

     

    Abstract: Snyder et al reported that naloxazine (NZI) was an irreversible ligand of opiate receptors. But, in the experiment reported here, it was found that after incubation (30℃, 15 min) of NZI (1×10-5) with rat brain P2 membrane preparation, repeated washing could restore completely the reactivity of opiate receptors. The antagonizing effect of NZI on the inhibition of electrically induced contraction of the longitudinal muscle of guinea-pig ileum (GPI) by morphine could also be eliminated by repeated washings. An N-methyl analog of naloxazine, 14-hydroxydihydromorphazine (HZI), is an agonist of opiate receptors. Both receptor binding and GPI experiments revealed that neither the latter compound nor NZI reacted with opiate receptors as irreversible ligand. The duration of analgesic action of HZI in mice was no longer than that of morphine, although, it's ED50, 1.3 mg/kg (Hot-plate, i.p.), was smaller than that of morphine (3 mg/kg).

     

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