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DOI: 10.1055/s-2002-32545
© Georg Thieme Verlag Stuttgart · New York
Vascular Effects of a Soy Leaves (Glycine max) Extract and Kaempferol Glycosides in Isolated Rat Carotid Arteries
Publikationsverlauf
August 14, 2001
November 10, 2001
Publikationsdatum:
01. Juli 2002 (online)
Abstract
We have recently purified genistin, and six kaempferol glycosides from a soy leaves (Glycine max L. Merr.) butanol extract. Here we report the vascular effects of the extract and purified genistin and kaempferol glycosides on contractions induced by different constricting agonists in isolated rat carotid arteries. The butanol extract relaxed artery rings preconstricted by 9,11-dideoxy-11α,9α-epoxy-methanoprostaglandin F2 α (U46619) or [5Z,9α,11α,13E,15S]-9,11,15-trihydroxyprosta-5,13-dienoic acid (PGF2 α) in a dose-dependent manner and this effect was independent of the presence of endothelium. The extract also inhibited the concentration-dependent contraction to U46619 with a slight reduction of the maximal response. The extract produced partial relaxation of both phenylephrine-preconstricted endothelium-intact and -denuded rings. In contrast, the extract had no effect on the contractile response to 50 mM extracellular K+. None of the six kaempferol glycosides affected vessel tension induced by U46619. A mixture of kaempferol glycosides prepared according to their relative composition in the extract had no effect either. However, kaempferol relaxed U46619- and high K+-contracted rings to the same extent. Endothelium played no role in kaempferol-induced relaxation. Genistein induced concentration-dependent relaxation and this effect was attenuated in the endothelium-denuded rings. Genistin caused a smaller relaxant effect. The present results indicate that a butanol extract from soy leaves causes endothelium-independent relaxation in rat carotid artery rings. Kaempferol glycosides, accounting for ∼48 % of the extract in weight, are not the ingredients responsible for the extract-induced relaxation. Genistein and genistin also caused relaxation, however, the dose range is beyond that of the extract causing relaxation.
Key words
Soy leaves (Glycine max L. Merr.) - kaempferol - genistin - contraction - relaxation - carotid artery - rat
- 1 Potter S M, Bakhit R M, Essex-Sorlie D L, Weingartner K E, Chapman K M, Nelson R A, Prabhudesai M, Savage W D, Nelson A I, Winter L W, Nelson R, Ham J, avage W, Prabhudesai M, Erdman J W. Depression of plasma cholesterol in men by consumption of baked products containing soy protein. American Journal of Clinical Nutrition. 1993; 58 501-6
- 2 Anderson J W, Johnstone B M, Cook-Newell M E. Meta-analysis of the effects of soy protein intake on serum lipids. New England Journal of Medicine. 1995; 333 276-82
- 3 Kanazawa T, Osanai T, Zhang X S, Uemura T, Yin X Z, Onodera K, Oike Y, Ohkubo K. Protective effects of soy protein on the peroxidizability of lipoproteins in cerebrovascular diseases. Journal of Nutrition. 1995; 125 (Suppl) 639S-46S
- 4 Potter S M. Overview of proposed mechanisms for the hypocholesterolemic effect of soy. Journal of Nutrition. 1995; 125 (Suppl) 606S-11S
- 5 Wilcox J N, Blumenthal B F. Thrombotic mechanisms in atherosclerosis: potential impact of soy proteins. Journal of Nutrition. 1995; 125 631S-38S
- 6 Pan W, Ikeda K, Takebe M, Yamori Y. Genistein, daidzein and glycitein inhibit growth and DNA synthesis of aortic smooth muscle cells from stroke-prone spontaneously hypertensive rats. Journal of Nutrition. 2001; 131 1154-8
- 7 Mishra S K, Abbot S E, Choudhury Z, Cheng M, Khatab N, Maycock N J, Zavery A, Aaronson P I. Endothelium-dependent relaxation of rat aorta and main pulmonary artery by the phytoestrogens genistein and daidzein. Cardiovascular Research. 2000; 46 39-46
- 8 Karamsetty M R, Klinger J R, Hill N S. Phytoestrogens restore nitric oxide-mediated relaxation in isolated pulmonary arteries from chronically hypoxic rats. Journal of Pharmacology and Experimental Therapeutics. 2001; 297 968-74
- 9 Huang Y, Ho I HM. Separate activation of intracellular Ca2+ release, voltage-dependent and receptor-operated Ca2+ channels in the rat aorta. Chinese Journal of Physiology. 1996; 39 1-8
- 10 Shearman M S, Sekiguchi K and Nishizuka Y. Modulation of ion channel activity: a key function of the protein kinase C enzyme family. Pharmacological Review. 1989; 41 211-37
- 11 Huang Y. Inhibitory effect of noradrenaline uptake inhibitors on contractions of rat aortic smooth muscle. British Journal of Pharmacology. 1996; 117 533-9
Yu Huang, Ph. D.
Department of Physiology
Chinese University of Hong Kong
Shatin, NT, Hong Kong
Fax: +852-26035022
eMail: yu-huang@cuhk.edu.hk