FACILITATION OF [H-3] ACH RELEASE BY FORSKOLIN DEPENDS ON A(2)-ADENOSINE RECEPTOR ACTIVATION

被引:17
作者
CORREIADESA, P
RIBEIRO, JA
机构
[1] GULBENKIAN INST SCI, PHARMACOL LAB, P-2781 OEIRAS, PORTUGAL
[2] UNIV PORTO, ICBAS, PHARMACOL LAB, OPORTO, PORTUGAL
关键词
PRESYNAPTIC A(2)-ADENOSINE RECEPTOR; FORSKOLIN; H-3]-ACETYLCHOLINE RELEASE; PHRENIC NERVE ENDING;
D O I
10.1016/0304-3940(93)90035-J
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effect of forskolin (FSK) on [H-3]-acetylcholine release ([H-3]-ACh) from the phrenic motor nerve terminals, and its modification by adenosine deaminase (ADA), by the A2-adenosine receptor agonist 2-[p-(2-carboxyethyl)phenethylamino]-5'-N-ethylcarboxamide adenosine (CGS 21680C), by the A1-adenosine receptor agonist R-N6-phenylisopropyl adenosine (R-PIA), by the A2-antagonist N-(2-(dimethylamino)-ethyl)-N-methyl-4-(2,3,6,7-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purine-8-yl)-benzene sulphonamide (PD 115,199), and by the A1-antagonist 1,3-dipropyl-8-cyclopentylxanthine (DPCPX) were studied on the rat phrenic-hemidiaphragm preparation. It is concluded that the excitatory effect of FSK on evoked [H-3]-ACh release depends on tonic A2-adenosine receptor activation.
引用
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页码:21 / 24
页数:4
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