ADENOSINE-A(3) RECEPTORS MEDIATE HYPOTENSION IN THE ANGIOTENSIN II-SUPPORTED CIRCULATION OF THE PITHED RAT

被引:119
作者
FOZARD, JR
CARRUTHERS, AM
机构
[1] Preclinical Research, Sandoz Pharma Ltd., Basel
关键词
5'-N-ETHYLCARBOXAMIDOADENOSINE (NECA); R-N-6-PHENYLISOPROPYLADENOSINE (R-PIA); S-N-6-PHENYLISOPROPYLADENOSINE (S-PIA); N-6-2-(4-AMINOPHENYL)ETHYL ADENOSINE (APNEA); HYPOTENSION; A3-ADENOSINE RECEPTORS;
D O I
10.1111/j.1476-5381.1993.tb13522.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The cardiovascular effects of N6-2-(4-aminophenyl)ethyladenosine (APNEA), which when radiolabelled with I-125 shows high affinity for the newly described adenosine A3 receptor, have been investigated in the angiotension II-supported circulation of the pithed rat. APNEA induces hypotensive responses which are unaffected by high doses (20-40 mg kg-1) of the broad spectrum, adenosine receptor antagonist, 8-(p-sulphophenyl)theophylline (8-SPT). 8-SPT-resistant falls in blood pressure are also seen, in the absence of bradycardia, with 5'-N-ethylcarboxamidoadenosine (NECA) and the R-and S-enantiomers of N6-phenylisopropyladenosine (PIA). Xanthine insensitivity, high potencies of APNEA, NECA and R-PIA, and an enantiomeric selectivity favouring R- over S-PIA are distinguishing features of the adenosine A3 receptor. We suggest that hypotension in the pithed rat may be a functional correlate of this site.
引用
收藏
页码:3 / 5
页数:3
相关论文
共 9 条