Imidazoline recognition sites and stomach function

被引:10
作者
Molderings, GJ [1 ]
Burian, M [1 ]
Menzel, S [1 ]
Donecker, K [1 ]
Homann, J [1 ]
Nilius, M [1 ]
Göthert, M [1 ]
机构
[1] Univ Bonn, Inst Pharmacol & Toxicol, D-53113 Bonn, Germany
来源
IMIDAZOLINE RECEPTORS AND THEIR ENDOGENOUS LIGANDS: CURRENT CONCEPTS AND THERAPEUTIC POTENTIAL | 1999年 / 881卷
关键词
D O I
10.1111/j.1749-6632.1999.tb09377.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Radioligand binding experiments carried out in cell membranes from rat and human stomach revealed the existence of non-adrenoceptor [H-3]clonidine and [H-3]idazoxan binding sites and of [H-3]DTG (1,2-di-(2-tolyl)guanidine) binding shes. In rat stomach, specific binding was inhibited by imidazolines and guanidines and by non-imidazoline sigma-site ligands, respectively; at different rank orders of affinity, suggesting the existence of non-I-1/non-I-2 [H-3]clonidine binding sites; I-2-imidazoline binding sites as well as sigma(2)-like-sites. These sites are not directly related to a postsynaptic contractile effect on rat gastric smooth muscle or to acid release from isolated gastric glands. Finally, we demonstrated. that the gastric pathogen Helicobacter pylori is able to form and to release the endogenous imidazoline receptor ligand agmatine and that considerable amounts of agmatine are present in human gastric juice. The quantities of; agmatine were higher in gastric juice from H. pylori-positive than H. pylori-negative patients.
引用
收藏
页码:332 / 343
页数:12
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