Endothelium-independent vasorelaxation of plant-derived estrogen biochanin A and its mechanism in rat aortic rings.
- Author:
Hui-ping WANG
1
;
Fu-yu QIU
;
Cheng CHEN
;
Meng-hui ZHAO
;
Yuan LU
;
Qiang XIA
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Aorta, Thoracic; drug effects; physiology; Genistein; pharmacology; In Vitro Techniques; KATP Channels; metabolism; Male; Muscle, Smooth, Vascular; drug effects; physiology; Rats; Rats, Sprague-Dawley; Vasodilation; drug effects
- From: Chinese Journal of Applied Physiology 2006;22(3):274-277
- CountryChina
- Language:Chinese
-
Abstract:
AIMTo investigate the mechanisms of vasodilatation of plant-derived estrogen biochanin A.
METHODSIsolated aortic ring preparations from Sprague-Dawley rats were suspended in individual organ baths. The tension was measured isometrically.
RESULTSBiochanin A at the range of 10(-9)-10(-4) mol/L provoked concentration-dependent and endothelium-independent relaxation of the rings constricted by phenylephrine (10(-5) mol/L). Biochanin A caused concentration-dependent relaxation of denuded rings precontracted with KCl (6 x 10(-2) mol/L). Glibenclamide (3 x 10(-6) mol/L), a selective inhibitor of ATP-sensitive potassium channels, and tetraethylammonium (5 x 10(-3) mol/L), a Ca2+ -activated K+ channel inhibitor, significantly attenuated the relaxation induced by biochanin A. The vasoconstriction induced by phenylephrine was decreased by biochanin A in Ca2+ -free medium.
CONCLUSIONThe endothelium-independent relaxation of thoracic aorta induced by biochanin A might be mediated by ATP-sensitive K+ channels, Ca2+ -activated K+ channels and intracellular Ca2+ release from sarcoplasmic reticulum.
