HISTAMINE H1-RECEPTOR IN HEART - UNIQUE ELECTROPHORETIC MOBILITY AND AUTORADIOGRAPHIC LOCALIZATION

被引:27
作者
RUAT, M
BOUTHENET, ML
SCHWARTZ, JC
GANELLIN, CR
机构
[1] UNIV LONDON UNIV COLL, DEPT CHEM, LONDON WC1E 6BT, ENGLAND
[2] FAC PHARM PARIS, PHYSIOL LAB, PARIS, FRANCE
关键词
Autoradiographic localization; Electrophoretic analysis; Photoaffinity labeling; [!sup]125[!/sup]I]Iodoazidophenpyramine; [!sup]125[!/sup]I]Iodobolpyramine;
D O I
10.1111/j.1471-4159.1990.tb04148.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Histamine H1‐receptors, visualized in the guinea pig heart by autoradiography using [125I]iodoboipyramine as a specific probe, are abundant in the nodal tissue and cardiac vessels but also occur heterogeneously in the myocardium. Following photoaffinity labeling with [125I]iodoazidophenpyramine and electrophoresis, the ligand binding domain of the heart H1‐receptor was shown to be present on a major 68‐kDa and a less abundant 54‐ to 58‐kDa protein. The 68‐kDa protein displayed a molecular size higher in heart than in all other tissues (56 kDa). This indicates the existence of at least two isoforms of the H1‐receptor; the cardiac isoform, however, was pharmacologically indistinguishable from the common isoform studied in cerebellar membranes using available ligands. Its distinct electrophoretic properties suggest that the cardiac isoform may have a unique function. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:379 / 385
页数:7
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