Volume 15, Issue 3 p. 235-239
Research Article

Andrographis paniculata (Ness) induces relaxation of uterus by blocking voltage operated calcium channels and inhibits Ca+2 influx

Rafael A. Burgos

Corresponding Author

Rafael A. Burgos

Institute of Pharmacology, Faculty of Veterinary Science, Universidad Austral de Chile, P.O. Box 567, Valdivia, Chile

Institute of Pharmacology, Faculty of Veterinary Science, Universidad Austral de Chile, PO Box 567, Valdivia, ChileSearch for more papers by this author
Marcela J. Aguila

Marcela J. Aguila

Institute of Pharmacology, Faculty of Veterinary Science, Universidad Austral de Chile, P.O. Box 567, Valdivia, Chile

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Elson. T. Santiesteban

Elson. T. Santiesteban

Institute of Pharmacology, Faculty of Veterinary Science, Universidad Austral de Chile, P.O. Box 567, Valdivia, Chile

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Nury S. Sánchez

Nury S. Sánchez

Institute of Pharmacology, Faculty of Veterinary Science, Universidad Austral de Chile, P.O. Box 567, Valdivia, Chile

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Juan L. Hancke

Juan L. Hancke

Laboratorios Garden House Av. Jorge Alessandri 12310, Santiago, Chile

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First published: 08 May 2001
Citations: 6

Abstract

The possible relaxation of uterine smooth muscle by Andrographis paniculata dried extract via a blockade of voltage operated calcium channels was investigated in rats. Uterine horns pretreated with oestradiol were incubated in Ca+2-free Jalon's solution and stimulated with KCl (20–60 mM) in order to produce depolarization of the membrane. The isometric contractile response to 1 mM or cumulative concentrations of CaCl2 were blockaded by 0.2, 0.4 and 0.8 mg/mL of A. paniculata. The maximum contractile response induced by acetylcholine was moderately antagonized by A. paniculata. The possible blockade of Ca+2 entry by A. paniculata was evaluated with 45Ca+2 uptake in uterine rings incubated with free-Ca+2-Ringer's solution high in K+ (KCl 40 mM). The influx was completely blockaded with 0.4 mg/mL of A. paniculata. These results strongly suggest that A. paniculata blockades voltage operated calcium channels inhibiting the entry of Ca+2 from the external medium. Copyright © 2001 John Wiley & Sons, Ltd.

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