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Characterization of the AT1 angiotensin II receptor expressed in guinea pig liver

Characterization of the AT1 angiotensin II receptor expressed in guinea pig liver AbstractIn guinea pig hepatocytes angiotensin II induced phosphorylase a activation. This effect was mimicked by other angiotensins with the potency order: angiotensin II (EC50 ≈1 nm)>angiotensin III (EC50 ≈30 nm)>angiotensin I (EC50 ≈300 nm). The effect of 10 nm angiotensin II was blocked by the angiotensin II receptor AT1-selective antagonists irbesartan and losartan (Ki values of ≈1 nm and ≈10 nm for irbesartan and losartan respectively) but not by the AT2-selective antagonist PD123177.Similar data were obtained when the production of [3H]IP3 from [3H]myo-inositol-labeled cells was studied. Angiotensin II induced a dose-dependent increase in [3H]IP3 production; the maximal effect (≈3-fold) was observed at a concentration of 10 μm. This effect of angiotensin II was completely blocked by the AT1-selective antagonists irbesartan and losartan, but only in a very limited fashion by PD123177. [125I][Sar1-Ile8]angiotensin II bound with high affinity (≈3·8 nm) to a moderately abundant number of sites (≈660 fmol/mg protein) in guinea pig liver membranes. Binding competition experiments indicate the following orders of potency for agonists: angiotensin II (≈1·5 nm)>angiotensin III (≈7 nm)>angiotensin I (≈176 nm), and for antagonists: irbesartan (≈0·5 nm)>losartan (≈36 nm)>> PD123177 (>> 10 000 nm).The functional and binding data strongly indicate that the effects of angiotensin II were mediated through AT1 receptors. Expression of the mRNA for these receptors was confirmed by RT-PCR and hybridization of the reaction product with a radiolabeled rat AT1 receptor cDNA probe.Journal of Endocrinology (1997) 154, 133–138 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Endocrinology Bioscientifica

Characterization of the AT1 angiotensin II receptor expressed in guinea pig liver

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Publisher
Bioscientifica
Copyright
Copyright © 1997 The Authors. All Rights Reserved.
ISSN
0022-0795
eISSN
1479-6805
DOI
10.1677/joe.0.1540133
Publisher site
See Article on Publisher Site

Abstract

AbstractIn guinea pig hepatocytes angiotensin II induced phosphorylase a activation. This effect was mimicked by other angiotensins with the potency order: angiotensin II (EC50 ≈1 nm)>angiotensin III (EC50 ≈30 nm)>angiotensin I (EC50 ≈300 nm). The effect of 10 nm angiotensin II was blocked by the angiotensin II receptor AT1-selective antagonists irbesartan and losartan (Ki values of ≈1 nm and ≈10 nm for irbesartan and losartan respectively) but not by the AT2-selective antagonist PD123177.Similar data were obtained when the production of [3H]IP3 from [3H]myo-inositol-labeled cells was studied. Angiotensin II induced a dose-dependent increase in [3H]IP3 production; the maximal effect (≈3-fold) was observed at a concentration of 10 μm. This effect of angiotensin II was completely blocked by the AT1-selective antagonists irbesartan and losartan, but only in a very limited fashion by PD123177. [125I][Sar1-Ile8]angiotensin II bound with high affinity (≈3·8 nm) to a moderately abundant number of sites (≈660 fmol/mg protein) in guinea pig liver membranes. Binding competition experiments indicate the following orders of potency for agonists: angiotensin II (≈1·5 nm)>angiotensin III (≈7 nm)>angiotensin I (≈176 nm), and for antagonists: irbesartan (≈0·5 nm)>losartan (≈36 nm)>> PD123177 (>> 10 000 nm).The functional and binding data strongly indicate that the effects of angiotensin II were mediated through AT1 receptors. Expression of the mRNA for these receptors was confirmed by RT-PCR and hybridization of the reaction product with a radiolabeled rat AT1 receptor cDNA probe.Journal of Endocrinology (1997) 154, 133–138

Journal

Journal of Endocrinology – Bioscientifica

Published: Jul 1, 1997

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