Alpha-2 adrenergic and opioid receptor-mediated gastroprotection

被引:42
|
作者
Gyires, K [1 ]
Müllner, K [1 ]
Fürst, S [1 ]
Rónai, AZ [1 ]
机构
[1] Semmelweis Univ, Fac Med, Dept Pharmacol & Pharmacotherapy, H-1089 Budapest, Hungary
关键词
gastroprotection; clonidine; alpha-2B adrenoceptors; opioid receptors;
D O I
10.1016/S0928-4257(00)00151-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Clonidine inhibited the development of gastric mucosal lesions induced by either acidified ethanol or indomethacin. The ED50 values were: 7.1 and 5.2 mu g.kg(-1) orally, respectively. The gastroprotective effect was antagonised by the pre-synaptic alpha-2 antagonist, yohimbine, the more selective alpha-2 antagonist Ch-38083 and the pre-synaptic alpha-2B antagonist prazosin. Moreover, the non-selective opioid receptor antagonist naloxone, the delta receptor selective naltrindole also reversed the clonidine-induced mucosal protective action. Clonidine was also effective following intracerebroventricular administration with the ED50 of 37 ng/rat against ethanol-induced mucosal damage. Our results suggest that: 1) the gastroprotective effect of clonidine is likely to be mediated by alpha-2B adrenoceptor subtype; 2) there is an interaction between pre-synaptic alpha-2 adrenoceptors and opioid system; and 3) clonidine can induce gastroprotection by central mechanism. (C) 2000 Elsevier Science Ltd. Published by Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:117 / 121
页数:5
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