Abstract:
:This study compared the structure-activity relationships of 16 analogues at the A1 and A2 adenosine receptors (A1AR, A2AR) of rat and guinea pig. Radioligand binding studies revealed no marked differences in the affinities of each analogue at the A1AR of brain cortex or the A2AR of brain striatum. Bioassay employing Langendorff heart preparations showed that the guinea pig is more sensitive than the rat to A1AR-mediated slowing of conduction through the atrioventricular node and, in some instances, to A2AR-mediated coronary vasodilation. That difference could reflect factors such as receptor density or efficacy of coupling to effector systems.
journal_name
Life Scijournal_title
Life sciencesauthors
Ueeda M,Thompson RD,Padgett WL,Secunda S,Daly JW,Olsson RAdoi
10.1016/0024-3205(91)90199-lsubject
Has Abstractpub_date
1991-01-01 00:00:00pages
1351-8issue
18eissn
0024-3205issn
1879-0631pii
0024-3205(91)90199-Ljournal_volume
49pub_type
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