Y. Kitagawa et al., DETERMINATION OF BETA-ADRENOCEPTOR SUBTYPE ON RAT ISOLATED VENTRICULAR MYOCYTES BY USE OF HIGHLY SELECTIVE BETA-ANTAGONISTS, British Journal of Pharmacology, 116(1), 1995, pp. 1635-1643
1 The relative proportions of beta(1)- and beta(2)-adrenoceptors were
determined by radioligand binding studies in three different rat myoca
rdial preparations: membranes prepared from rat ventricle (ventricular
membranes), membranes prepared from rat isolated ventricular myocytes
(myocyte membranes), and myocytes isolated from rat ventricle (myocyt
es). 2 Competition experiments using CCP 20712A or ICI 118,551 with [I
-125]-iodocyanopindolol ([I-125]-ICYP) revealed high- and low-affinity
binding sites in ventricular membranes. The concentration at which ea
ch beta-antagonist occupied 100% of its high-affinity binding sites wa
s 300 nM for CGP 20712A (beta(1)-adrenoceptor) and 50 nM for ICI 118,5
51 (beta(2)-adrenoceptor). 3 The density of high-affinity (beta(1)-adr
enoceptor) and low-affinity (beta(2)-adrenoceptor) binding sites for C
GP 20712A was measured by a saturation experiment using [I-125]-ICYP i
n the presence and absence of 300 nM CGP 20712A. In ventricular membra
nes, the proportions of high-affinity and low-affinity binding sites f
or CGP 20712A were 73% and 27%, respectively, whereas in myocyte membr
anes, the corresponding figures were 90% and 10%, respectively. The de
nsity of low-affinity binding sites for CGP 20712A in ventricular memb
ranes, defined as [I-125]-ICYP-specific binding in the presence of 300
nM CGP 20712A, was decreased by addition of 50 nM ICI 118,551, wherea
s that in myocyte membranes was not affected. 4 In myocytes, specific
binding of [I-125]-ICYP and [H-3]-CGP 12177 was not detected by satura
tion experiments performed in the presence of 300 nM CGP 20712A. 5 In
myocytes, the activation of adenylate cyclase caused by beta(2)-adrena
ceptors was not detected in the presence of 10 nM, 100 nM or 1000 nM C
GP 20712A, which selectively antagonized beta(1)-adrenoceptors. Furthe
rmore, the concentration-response curve for isoprenaline-stimulated cy
clic AMP accumulation was not shifted by 10 nM or 100 nM ICI 118,551,
which selectively antagonized beta(2)-adrenoceptors, but was shifted t
o the right by 1000 nM ICI 118,551. 6 These results indicate that beta
(2)-adrenoceptors are not present on rat ventricular myocytes and that
beta(2)-adrenoceptor stimulation does not cause any detectable produc
tion of cyclic AMP. We conclude that only beta(1)-adrenoceptors exist
on rat ventricular myocytes.