Effect and mechanism of puerarin on high glucose-induced hypo-responses in vascular contraction.
- Author:
Yi-Miao ZHU
1
;
Chao NI
;
Li ZHU
;
Yue-Liang SHEN
;
Ying-Ying CHEN
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Aorta, Thoracic; drug effects; physiology; Glucose; pharmacology; Heme Oxygenase (Decyclizing); metabolism; In Vitro Techniques; Isoflavones; pharmacology; Male; Rats; Rats, Sprague-Dawley; Vasoconstriction; drug effects; Vasodilator Agents; pharmacology
- From: Chinese Journal of Applied Physiology 2011;27(1):62-65
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo examine the effect of puerarin on high glucose-induced decrease in contraction of isolated rat aortic rings, and to elucidate its underlying mechanism.
METHODSThe thoracic aortic rings with or without endothelium of male Sprague-Dawley rats were mounted on a bath system. Isometric contractions of aortic rings were measured. The activity of heme oxygenase-1 (HO-1) was also measured.
RESULTS(1) After incubation with 44 mmol/L of glucose (high glucose) for 4 h, the vascular contraction responses to phenylephrine (PE) decreased in an endothelium-dependent manner, when compared with the control group (containing 11 mmol/L of glucose). (2) After coincubation with puerarin ( 10(-10) - 10(-8) mol/L) and high glucose, the decrease in contraction responses to PE of arteries was partly inhibited in a dose-dependent manner. (3) After incubation with puerarin for 4 h, the HO-1 activity of thoracic aorta increased; ZnPP, an inhibitor of HO-1, abrogated the protection effect of puerarin.
CONCLUSIONPuerarin could prevent the high glucose-induced decrease in contraction responses to PE in intact aortic rings. The mechanism might be involved in the activation of HO-1.