RELEASE OF ATRIAL-NATRIURETIC-FACTOR INDUCED BY THE A(1)-ADENOSINE RECEPTOR AGONIST 2-CHLORO-N6-CYCLOPENTYL-ADENOSINE IN THE RAT

被引:8
作者
MASSI, M
SAIJA, A
CRISTALLI, G
POLIDORI, C
PERFUMI, M
COSTA, G
机构
[1] UNIV MESSINA,DIPARTIMENTO FARMACOBIOL,I-98100 MESSINA,ITALY
[2] UNIV MESSINA,DIPARTIMENTO SCI CHIM,I-98100 MESSINA,ITALY
关键词
ADENOSINE; ADENOSINE RECEPTOR AGONISTS; ADENOSINE RECEPTOR ANTAGONISTS; ATRIAL NATRIURETIC FACTOR;
D O I
10.1016/1043-6618(92)90676-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of the adenosine receptor agonists, 2-chloro-N6-cyclopentyladenosine (CCPA) and 2-hexynyl-adenosine-5′-N-ethylcar{ballot box}amide (HENECA) on atrial natriuretic factor (ANF) release was investigated. The A1 adenosine receptor agonist CCPA markedly increased plasma ANF levels, following subcutaneous (s.c.), but not intracerebroventricular injection. ANF release evoked by the s.c. injection of CCPA was completely abolished by s.c. pretreatment with the selective A1 adenosine receptor antagonist, 1,3-dipropyl-8-cyclopentylxanthine. The A2 adenosine receptor agonist HENECA did not produce ANF release. The results of the present study suggest that peripheral adenosine mechanisms might be involved in the control of ANF secretion, through the activation of A1 adenosine receptors. Preliminary results show that CCPA produces ANF release also from isolated atria, thus suggesting that its action on ANF release is, at least in part, direct, and not only a consequence of cardiovascular modifications. © 1992 The Italian Pharmacological Society.
引用
收藏
页码:393 / 402
页数:10
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