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Planta Med 2002; 68(10): 891-895
DOI: 10.1055/s-2002-34934
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Mechanisms of Relaxant Action of a Pyranocoumarin from Peucedanum japonicum in Isolated Rat Thoracic Aorta

Jong Wha Lee1 , Tae Cheol Roh2 , Mun-Chual Rho2 , Young Kook Kim2 , Hyun Sun Lee2
  • 1Department of Environmental Health Science, Soonchunhyang University, Asan, Korea
  • 2Cardiovascular Research Laboratory, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Taejon, Korea
Further Information

Publication History

Received: January 25, 2002

Accepted: May 5, 2002

Publication Date:
21 October 2002 (online)

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Abstract

The CHCl3-soluble fraction obtained from the MeOH extract of Peucedanum japonicum Thunb. inhibited phenylephrine-induced vasoconstriction in isolated rat thoracic aorta. We isolated a vasorelaxing compound, as one of the bioactive components, which was identified as (+)-cis-4′-O-acetyl-3′-O-angeloylkhellactone (1), a pyranocoumarin, and examined the mechanisms of vasorelaxant effect caused by 1. This compound (1) (10-6 - 10-4 M) concentration-dependently relaxed the isolated rat thoracic aorta pre-contracted with phenylephrine (PE). This vasorelaxant potency was diminished by endothelial removal (by 20 %), L-N G-nitro-arginine or methylene blue (MB), but not indomethacin treatment. These findings indicate that the vasorelaxant effect of 1 was partially endothelium dependent and mediated by nitric oxide and cyclic GMP pathway. To determine if the effect of 1 was mediated through the activation of some of the receptors known to lead to vascular relaxation, the effects of atropine, triprolidine and propranolol were determined. 1-induced vasorelaxation was not affected by atropine, triprolidine and propranolol. Compound 1 inhibited high potassium (80 mM)-induced, calcium-dependent contractions in a concentration-dependent manner. But it slightly relaxed the rat aorta precontracted with PE in the presence of nifedipine, a blocker of voltage-operated calcium channels. Tetraethylammonium (TEA, a non-specific K+ channel blocker) did not affect the vasodilatory effect of 1 against PE-induced contraction. Mechanisms of the vasorelaxant effect of 1 were multiple, including endothelium dependence and Ca2+ channel blockade.

Key words

Peucedanum japonicum Thunb. - Umbelliferae - (+)-cis-4′-O- acetyl-3′-O-angeloylkhellactone - vasorelaxation (rat aorta)

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Dr. Hyun Sun Lee

Cardiovascular Research Laboratory

Korea Research Institute of Bioscience and Biotechnology

P.O. Box 115, Yusong, Taejon 305-333

Korea

Email: leehs@mail.kribb.re.kr

Fax: +82-42-861-2675

Phone: +82-42-860-4314

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