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Comparison of green tea extract and epigallocatechin gallate on blood pressure and contractile responses of vascular smooth muscle of Rats

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Abstract

The present study was conducted to investigate the effects of green tea extract (GTE) on arte-rial blood pressure and contractile responses of isolated aortic strips of the normotensive rats and to establish the mechanism of action. The phenylephrine (10~p6~10~p5M)-induced contrac-tile responses were greatly inhibited in the presence of GTE (0.3–1.2 mg/mL) in a dose-depen-dent fashion. Also, high potassium (3.5x10-p2~5.6x1CTp2 M)-induced contractile responses were depressed in the presence of 0.6–1.2 mg/mL of GTE, but not affected in low concentration of GTE (0.3 mg/mL). However, epigallocatechin gallate (EGCG, 4–12 ug/mL) did not affect the contractile responses evoked by phenylephrine and high Kp+. GTE (5–20 mg/kg) given into a femoral vein of the normotensive rat produced a dose-dependent depressor response, which is transient. Interestingly, the infusion of a moderate dose of GTE (10 mg/kg/30 min) made a significant reduction in pressor responses induced by intravenous norepinephrine. However, EGCG (1 mg/kg/30 min) did not affect them. Collectively, these results obtained from the present study demonstrate that intravenous GTE causes a dose-dependent depressor action in the anesthetized rat at least partly through the blockade of adrenergic α1-receptors. GTE also causes the relaxation in the isolated aortic strips of the rat via the blockade of adrenergic α1-receptors, in addition to the unknown direct mechanism. It seems that there is a big differ-ence in the vascular effect between GTE and EGCG.

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Correspondence to Dong -Yoon Lim.

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This paper was presented at the 24th Annual Meeting of The Japanese Society of Hypertension held in Osaka, Japan, October 25–27, 2001

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Lim, D.Y., Lee, E.S., Park, H.G. et al. Comparison of green tea extract and epigallocatechin gallate on blood pressure and contractile responses of vascular smooth muscle of Rats. Arch Pharm Res 26, 214–223 (2003). https://doi.org/10.1007/BF02976833

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