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关于新型具有支气管解痉活性的甲基黄嘌呤衍生物1-丙基-3-甲基-7-(5-羟基己基)黄嘌呤(HWA 153)的生化作用机制

On the biochemical mechanism of action of 1-propyl-3-methyl-7-(5-hydroxy-hexyl)-xanthine (HWA 153), a new bronchospasmolytically active methyl xanthine derivative.

作者信息

Stefanovich V, Porsche E

出版信息

Arzneimittelforschung. 1979;29(6):917-20.

PMID:226104
Abstract

1-Propyl-3-methyl-7-(5-hydroxy-hexyl)-xanthine (HWA 153) is a new bronchospasmolytic agent with a significant influence on the cAMP system of lungs and bronchi. In in vitro experiments HWA 153 inhibits cAMP phosphodiesterase (PDE) isolated from bovine bronchi more than does theophylline. HWA 153 is (in conc. 5 x 10(-4) mol/l) 1.8 and 4.3 times more active as a PDE inhibitor of guinea pig lungs and bronchi, respectively, than theophylline-ethylenediamine. HWA 153 also stabilizes rat erythrocyte membrane against hypoosmotic shock. In isolated guinea pig bronchi HWA 153 (in conc. 5 x 10(-4) mol/l) decreases by 77% bronchial spasm induced by the addition of histamine (5 x 10(-5) mol/l). A significant increase in cAMP level of bronchi was simultaneously observed. In in vivo experiments HWA 153 (25 mg/kg p.o.) inhibits PDE of lungs and bronchi of guinea pigs. Simultaneously, a significant increase in cAMP level in these organs was observed. In in vivo experiments with hypoxic rats, HWA 153 (25 mg/kg p.o.) increases ATP, ATP/ADP ratio and adenylate energy charge (AEC) in hypoxic rats, 1 h after administration. This indicates a positive influence of HWA 153 on the energy metabolism of red blood cells.

摘要

1-丙基-3-甲基-7-(5-羟基己基)黄嘌呤(HWA 153)是一种新型支气管解痉剂,对肺和支气管的环磷酸腺苷(cAMP)系统有显著影响。在体外实验中,HWA 153对从牛支气管分离出的cAMP磷酸二酯酶(PDE)的抑制作用比茶碱更强。HWA 153(浓度为5×10⁻⁴mol/L时)作为豚鼠肺和支气管PDE抑制剂的活性分别比氨茶碱高1.8倍和4.3倍。HWA 153还能稳定大鼠红细胞膜以抵抗低渗休克。在离体豚鼠支气管中,HWA 153(浓度为5×10⁻⁴mol/L)可使因加入组胺(5×10⁻⁵mol/L)引起的支气管痉挛降低77%。同时观察到支气管中cAMP水平显著升高。在体内实验中,HWA 153(25mg/kg口服)可抑制豚鼠肺和支气管的PDE。同时,观察到这些器官中cAMP水平显著升高。在对缺氧大鼠的体内实验中,给药1小时后,HWA 153(25mg/kg口服)可提高缺氧大鼠的三磷酸腺苷(ATP)、ATP/二磷酸腺苷(ADP)比值和腺苷酸能荷(AEC)。这表明HWA 153对红细胞的能量代谢有积极影响。

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