Pharmacological characterization of A1 adenosine receptors in isolated
rat ventricular myocytes
D. Martens, M. Lohse, B. Rauch, and U. Schwabe. Naunyn Schmiedebergs Arch Pharmacol, 336 (3):
342-8(September 1987)Martens, D Lohse, M J Rauch, B Schwabe, U In Vitro Research Support,
Non-U.S. Gov't Germany, west Naunyn-Schmiedeberg's archives of pharmacology
Naunyn Schmiedebergs Arch Pharmacol. 1987 Sep;336(3):342-8..
Abstract
The aim of the present study was the characterization of adenosine
receptors in isolated rat ventricular myocytes. The cAMP-levels of
rat ventricular myocytes in the presence of 1 mumol/l isoprenaline
were reduced by up to 48% by adenosine analogues; the rank order
of potency was: R-N6-phenylisopropyladenosine (IC50 60 nmol/l), 5'-N-ethylcarboxamidoadenosine
(IC50 360 nmol/l) and S-N6-phenylisopropyladenosine (IC50 16 mumol/l).
The adenosine receptor antagonist XAC ("xanthine amine congener")
antagonized the effect of R-N6-phenylisopropyladenosine in a concentration-dependent
manner with a Ki-value of 20 nmol/l. The A1 receptor-selective radioligand
R-N6-125I-p-hydroxyphenylisopropyladenosine bound to membranes prepared
from rat ventricular myocytes in a saturable manner with a Bmax of
17.7 fmol/mg protein and a KD-value of 1.1 nmol/l. Adenosine analogues
competed for the binding with the same rank order of potency as for
the inhibition of the isoprenaline-induced cAMP-increase. GTP inhibited
radioligand binding with an IC50-value of 73 mumol/l. These results
suggest the presence of A1 adenosine receptors on rat ventricular
myocytes, which mediate an inhibition of adenylate cyclase. The receptors
may be responsible for the effects of adenosine and its analogues
on the heart.
Martens, D Lohse, M J Rauch, B Schwabe, U In Vitro Research Support,
Non-U.S. Gov't Germany, west Naunyn-Schmiedeberg's archives of pharmacology
Naunyn Schmiedebergs Arch Pharmacol. 1987 Sep;336(3):342-8.
%0 Journal Article
%1 Martens1987
%A Martens, D.
%A Lohse, M. J.
%A Rauch, B.
%A Schwabe, U.
%D 1987
%J Naunyn Schmiedebergs Arch Pharmacol
%K & AMP/biosynthesis Adenosine/*analogs Animals Assay Cyclic Heart/*drug Iodine Male Myocardium/metabolism Phenylisopropyladenosine/analogs Purinergic/*drug Radioisotopes/diagnostic Radioligand Rats Strains derivatives/diagnostic derivatives/pharmacology effects effects/metabolism use Receptor Mice
%N 3
%P 342-8
%T Pharmacological characterization of A1 adenosine receptors in isolated
rat ventricular myocytes
%U http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=2825048
%V 336
%X The aim of the present study was the characterization of adenosine
receptors in isolated rat ventricular myocytes. The cAMP-levels of
rat ventricular myocytes in the presence of 1 mumol/l isoprenaline
were reduced by up to 48% by adenosine analogues; the rank order
of potency was: R-N6-phenylisopropyladenosine (IC50 60 nmol/l), 5'-N-ethylcarboxamidoadenosine
(IC50 360 nmol/l) and S-N6-phenylisopropyladenosine (IC50 16 mumol/l).
The adenosine receptor antagonist XAC ("xanthine amine congener")
antagonized the effect of R-N6-phenylisopropyladenosine in a concentration-dependent
manner with a Ki-value of 20 nmol/l. The A1 receptor-selective radioligand
R-N6-125I-p-hydroxyphenylisopropyladenosine bound to membranes prepared
from rat ventricular myocytes in a saturable manner with a Bmax of
17.7 fmol/mg protein and a KD-value of 1.1 nmol/l. Adenosine analogues
competed for the binding with the same rank order of potency as for
the inhibition of the isoprenaline-induced cAMP-increase. GTP inhibited
radioligand binding with an IC50-value of 73 mumol/l. These results
suggest the presence of A1 adenosine receptors on rat ventricular
myocytes, which mediate an inhibition of adenylate cyclase. The receptors
may be responsible for the effects of adenosine and its analogues
on the heart.
@article{Martens1987,
abstract = {The aim of the present study was the characterization of adenosine
receptors in isolated rat ventricular myocytes. The cAMP-levels of
rat ventricular myocytes in the presence of 1 mumol/l isoprenaline
were reduced by up to 48% by adenosine analogues; the rank order
of potency was: R-N6-phenylisopropyladenosine (IC50 60 nmol/l), 5'-N-ethylcarboxamidoadenosine
(IC50 360 nmol/l) and S-N6-phenylisopropyladenosine (IC50 16 mumol/l).
The adenosine receptor antagonist XAC ("xanthine amine congener")
antagonized the effect of R-N6-phenylisopropyladenosine in a concentration-dependent
manner with a Ki-value of 20 nmol/l. The A1 receptor-selective radioligand
R-N6-125I-p-hydroxyphenylisopropyladenosine bound to membranes prepared
from rat ventricular myocytes in a saturable manner with a Bmax of
17.7 fmol/mg protein and a KD-value of 1.1 nmol/l. Adenosine analogues
competed for the binding with the same rank order of potency as for
the inhibition of the isoprenaline-induced cAMP-increase. GTP inhibited
radioligand binding with an IC50-value of 73 mumol/l. These results
suggest the presence of A1 adenosine receptors on rat ventricular
myocytes, which mediate an inhibition of adenylate cyclase. The receptors
may be responsible for the effects of adenosine and its analogues
on the heart.},
added-at = {2010-12-14T18:12:02.000+0100},
author = {Martens, D. and Lohse, M. J. and Rauch, B. and Schwabe, U.},
biburl = {https://www.bibsonomy.org/bibtex/2a6b9fae71a8101794fb5d2ebd8f6cc14/pharmawuerz},
endnotereftype = {Journal Article},
interhash = {2355eec521539b63ec59bff35b0f0dea},
intrahash = {a6b9fae71a8101794fb5d2ebd8f6cc14},
issn = {0028-1298 (Print) 0028-1298 (Linking)},
journal = {Naunyn Schmiedebergs Arch Pharmacol},
keywords = {& AMP/biosynthesis Adenosine/*analogs Animals Assay Cyclic Heart/*drug Iodine Male Myocardium/metabolism Phenylisopropyladenosine/analogs Purinergic/*drug Radioisotopes/diagnostic Radioligand Rats Strains derivatives/diagnostic derivatives/pharmacology effects effects/metabolism use Receptor Mice},
month = Sep,
note = {Martens, D Lohse, M J Rauch, B Schwabe, U In Vitro Research Support,
Non-U.S. Gov't Germany, west Naunyn-Schmiedeberg's archives of pharmacology
Naunyn Schmiedebergs Arch Pharmacol. 1987 Sep;336(3):342-8.},
number = 3,
pages = {342-8},
shorttitle = {Pharmacological characterization of A1 adenosine receptors in isolated
rat ventricular myocytes},
timestamp = {2010-12-14T18:22:56.000+0100},
title = {Pharmacological characterization of A1 adenosine receptors in isolated
rat ventricular myocytes},
url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=2825048},
volume = 336,
year = 1987
}