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PMID: 1625192 Published · ppublish English Comparative Study Journal Article

In vitro pharmacology of L-158,809, a new highly potent and selective angiotensin II receptor antagonist.

The Journal of pharmacology and experimental therapeutics ·Vol. 262 ·No. 1 ·1992-07-00 ·Pages 133-8

Chang RS, Siegl PK, Clineschmidt BV, Mantlo NB, Chakravarty PK, Greenlee WJ, Patchett AA, Lotti VJ

Abstract

L-158,809 interacted in a competitive manner with rabbit aortic angiotensin II (AII) receptors as determined by Scatchard analysis of the specific binding of [125I]Sar1Ile8-AII. The affinity of L-158,809 (IC50 = 0.3 nM) for AII receptors in this tissue was appreciably greater than that of other reported nonpeptide AII antagonists such as DuP-753 (IC50 = 54 nM) and EXP3174 (IC50 = 6 nM) and similar to the natural ligand, AII. L-158,809 also exhibited a high potency at AII receptors in several other tissues from different animal species (IC50 = 0.2-0.8 nM). In vitro functional assays utilizing AII-induced aldosterone release in rat adrenal cortical cells demonstrated further that L-158,809 acts as a competitive, high affinity antagonist of AII (pA2 = 10.5) and lacks agonist activity. L-158,809 also potently inhibited AII-induced inositol phosphate accumulation in vascular smooth muscle cells and contractile responses to AII in isolated blood vessels. The specificity of L-158,809 for AII receptors was demonstrated by its lack of activity (IC50 greater than 1 microM) in several other receptor binding assays and its inability to affect in vitro functional responses produced by other agonists. L-158,809 demonstrated a very high selectivity for the AT1 compared to the AT2 receptor subtype (AT2 IC50 greater than or equal to 10 microM). The high affinity and selectivity makes L-158,809 a valuable new tool for investigating the physiological and pharmacological actions of AII.

MeSH Terms
Aldosterone/metabolism Angiotensin II/antagonists & inhibitors,metabolism Angiotensin Receptor Antagonists Animals Antihypertensive Agents/pharmacology Binding, Competitive Biphenyl Compounds/metabolism Brain/drug effects,metabolism Cell Membrane/drug effects,metabolism Culture Techniques Humans Imidazoles/metabolism,pharmacology Losartan Macaca mulatta Muscle, Smooth, Vascular/drug effects,metabolism Rabbits Rats Species Specificity Tetrazoles/metabolism,pharmacology
Chemicals
Angiotensin Receptor Antagonists Antihypertensive Agents Biphenyl Compounds Imidazoles Tetrazoles Angiotensin II Aldosterone L 158809 losartan carboxylic acid Losartan
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Chang R S
Merck Research Laboratories, West Point, Pennsylvania.
Siegl P K
Clineschmidt B V
Mantlo N B
Chakravarty P K
Greenlee W J
Patchett A A
Lotti V J
Article Info
Journal
The Journal of pharmacology and experimental therapeutics
Abbr.
J Pharmacol Exp Ther
ISSN
0022-3565
Published
1992-07-00
Pages
133-8
Language
English
Region
United States
NLM ID
0376362
Subset
IM
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