Study on the Mechanism of Vascular Relaxation of Ethanol Extract of Persicaria Perfoliata H. Gross

하백초 에탄올 추출물의 혈관이완 기전에 대한 연구

  • Kim, Hye-Yoom (Professional Graduate School of Oriental Medicine, Wonkwang University) ;
  • Choi, Byung-Sun (College of Oriental Medicine, Wonkwang University) ;
  • Choi, Eun-Hee (College of Oriental Medicine, Wonkwang University) ;
  • Cui, Hao-Zhen (Professional Graduate School of Oriental Medicine, Wonkwang University) ;
  • Kang, Dae-Gill (Professional Graduate School of Oriental Medicine, Wonkwang University) ;
  • Lee, Ho-Sub (Professional Graduate School of Oriental Medicine, Wonkwang University)
  • 김혜윰 (원광대학교 한의학전문대학원) ;
  • 최병선 (원광대학교 한의과대학) ;
  • 조은희 (원광대학교 한의과대학) ;
  • 최호진 (원광대학교 한의학전문대학원) ;
  • 강대길 (원광대학교 한의학전문대학원) ;
  • 이호섭 (원광대학교 한의학전문대학원)
  • Published : 2009.04.25

Abstract

The ethanol extract of Persicaria perfoliata (EPP) induced relaxation of the phenylephrine-precontracted aorta in a dose-dependent manner, which was abolished by removal of functional endothelium. Pretreatment of the aortic tissues with NG-nitro-L-arginine methyl ester (L-NAME) or 1H-[1,2,4}-oxadiazole-[4,3-${\alpha}$)-quinixalin-1-one (ODQ) inhibited the relaxation induced by EPP. However, EPP-induced relaxation was not blocked by pretreatment with indomethacine, glibenclamide, tetraethylammonium (TEA), atropine, or propranolol. Incubation of endothelium-intact thoracic aortic ring with EPP increased the production of cGMP, which was also blocked by pretreatment with L-NAME or ODQ. These results suggest that EPP dilates vascular smooth muscle via endothelium-dependent NO/cGMP signaling.

Keywords

References

  1. 통계청 인구 분석과 2001년 사망원인 통계결과. 통계청, 2002
  2. Levi, R. Therapies for perioperative hypertension: Pharmacodynamic consideration. Acta Anaesthesiol., Acand Suppi. 37: 16-19, 1993 https://doi.org/10.1111/j.1399-6576.1993.tb03818.x
  3. Bosnjak, Z.J. Ion channels in vascular smooth muscle. Anesthesiology. 403: 120-127, 1993
  4. Rees, D.D., Palmer, R.M., Schulz, R., Hodson, H.F., Moncada, S. Characterization of three inhibitors endothelial Nitric oxide synthase in vitro and in vivo. Br. J. Pharmacol. 101: 746, 1990 https://doi.org/10.1111/j.1476-5381.1990.tb14151.x
  5. Vane, J.R., Anggard, E.E., Botting, R.M. Regulatory function of the vascular endothelium. New Med. 323: 27, 1990 https://doi.org/10.1056/NEJM199007053230106
  6. Luscher, T.F. The endothelium as a target and mediator of cardiovascular disease. Eur. J. clin. invest. 23: 670, 1993 https://doi.org/10.1111/j.1365-2362.1993.tb01285.x
  7. Moncada, S., Palmer, R.M., Higgs, E.A. Nitric oxide : Physiology. pathophysiology and pharmacology. Phamacol. Rev. 43: 109, 1993
  8. Arnold, W.P., Mittal, C.K., Katsuki, S., Murad, F. Nitric oxide activates guanylate cyclase and increase guanosine 3,5,-cyclic monophosphate level in various tissue preparations. Proc Natl Acad Sci. 74: 3203-3207, 1997 https://doi.org/10.1073/pnas.74.8.3203
  9. Forstermann, U., Closs, E.I., Pollock, J.S., Nakane, M., Schwarz, P., Gath, I. & Kleinert, H. Nitric oxide synthase isozyme-characterization, purification, molecular 4 cloning and function. Hypertension. 23: 1121, 1994. https://doi.org/10.1161/01.HYP.23.6.1121
  10. Moncada, S., Radomski, M.W., Palmer, R.M.J. Endothelium-derived relaxing factor: Identification as nitric oxide and role in the control of vascular tone and platelet function. Biochem Pharmacol. 37: 2495, 1990
  11. Ishii, K., Kerwin, J.F., Huang, Z.Y., Murad, F. NG-Nitro-L-argnine : a potent inhibitor of endotherium- derived relaxing factor formation. Eur. J. Pharmacol. 176: 216, 1990
  12. Furchgott, R.F., Zawadzki, J.V. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. Nature. 288: 373-376, 1980 https://doi.org/10.1038/288373a0
  13. Sakuma, I.D., Stuehr, D.J., Gross, S.S., Nathan, C., Levi, R. Identification of arginine as a precursor of endothelium- derived nitric oxide. Proc. Natl. Acad. Sci. 85: 8864, 1989
  14. Furchgott, R.F., Vanhoutte, P.M. Endothelium-derived relaxing and contracting actors. FASEB J 3(9):2007-2018, 1989 https://doi.org/10.1096/fasebj.3.9.2545495
  15. Kuramochi, T., Chu, J., Suga, T. Gou-Teng (From Uncaria rhynchophylla Miquel)-induced endothelium-dependent and independent relaxations in the isolated rat aorta. Life Sci. 54: 2061-2069, 1994. https://doi.org/10.1016/0024-3205(94)00715-2
  16. Goto, H., Shimada, Y., Tanigawa, K., Sekiya, N., Shitani, T., Terasawa, K. Effect of Uncariae ramulus et Uncus on endothelium in spontaneously hypertensive rats. Am. J. Chin. Med. 27: 339-345, 1999 https://doi.org/10.1142/S0192415X99000380
  17. Kamata, K., Noguchi, M., Nagai, M. Hypotensive effects of lithospermic acid B isolated from the extract of Salviae miltiorrhizae radix in the rat. Gen. Phamacol. 25: 69-73, 1994 https://doi.org/10.1016/0306-3623(94)90011-6
  18. Kim, S.H., Kang, K.W., Kim, K.W., Kim, N.D. Procyanidins in Crataegus extract evoke endothelium-dependent vasorelaxation in rat aorta. Life Sci. 67: 121-131, 2000 https://doi.org/10.1016/S0024-3205(00)00608-1
  19. Kang, D.G., Sohn, E.J., Kwon, E.K., Han, J.H., Oh, H., Lee, H.S. Effects of berberine on angiotensin-converting enzyme and NO/cGMP system in vessels. Vascul. Pharmacol. 39: 281-286, 2002 https://doi.org/10.1016/S1537-1891(03)00005-3
  20. Rodriguez-Cruz, M.E., Perez-Ordaz, L., Serrato-Barajas, B.E., Juarez-Oropeza, M.A., Mascher, D., Paredes-Carbajai, M.C. Endothelium-dependent effects of the ethanolic extract of the mistletoe Psittacanthus calyculatus on the vasomotor responses of rat aortic rings. J. Ethnophamacol. 39: 281-286, 2002
  21. Nishida, S., Satoh, H. Mechanism for the vasodilations induced by Ginkgo biloba extract and its main constituent, bilobalide, in rat aorta. Life Sci. 72: 2659-2667, 2003 https://doi.org/10.1016/S0024-3205(03)00177-2
  22. Lee, T.H., Wang, G.J., Lee, C.K., Kuo, Y.H., Chou, C.H. Inhibitory effects of glycosides from the leaves of Melaleuca quinquenervia on vascular contraction of rats. Planta Med. 68: 891-895, 2002 https://doi.org/10.1055/s-2002-34934
  23. Yuzurihara, M., Ikarashi, Y., Goto, K., Sakakibara, I., Hayakawa, T., Sasaki, H. Geissoschizine methyl ether, an indole alkaloid extracted from Uncariae Ramulus et Uncus, is a poent vasorelaxant of isolated rat aorta. Eur. J. Pharmacol. 444: 183-189, 2002. https://doi.org/10.1016/S0014-2999(02)01623-0
  24. Matsuura, M., Kimura, Y., Nakata, K., Baba, K., Okuba, H. Artery relaxation by chalcones isolated from the roots of Angelica keiskei. Planta. Med. 67: 230-235, 2001 https://doi.org/10.1055/s-2001-12011
  25. Chen, C.X., Kwan, C.Y. Endothelium-independent vasorelaxation by leonurine, a plant alkaloid purified from Chinese motherwort. Life Sci. 68: 953-960, 2001 https://doi.org/10.1016/S0024-3205(00)00987-5
  26. 이우철, 原色 韓國基準植物圖鑑. 아카데미서적, p 78 1996
  27. 임숙자. 한국산 야생식용물의 혈당강하효과 (Hypoglycemic Effects of Korean Wild Vegetables), 한국영양과학회지(KFN) 25(6):511-517, 1992
  28. Rubanyi, G.M. Endothelium-derived relaxing and contracting factors. J. Cell. Biochem. 46: 27-36, 1991 https://doi.org/10.1002/jcb.240460106
  29. MacNaul, K.L., Hutchinson, N.I. Differential of iNOS and cNOS mRNA in human vascular smooth muscle cells and endothelial cells under normal and inflammatory conditions. Biochem. Biophys. Res. Commun. 196: 1330-1334, 1993 https://doi.org/10.1006/bbrc.1993.2398
  30. Meng, W., Ma, J., Ayata, C., Hara, H., Huang, P.L., Fishman, M.C., Moskowitz, M.A. Ach dilates pial arterioles in endothelial and neuronal NOS knockout mice by NO-dependent mechanisms. Am. J. Physiol. 271: H1145-H1150, 1996
  31. Hutcheson, I.R., Griffith, T.M. Central role of intracellular calcium stores in acute flow-and agonist-evoked endothelial nitric oxide release. Br. J. Pharmacol. 122: 117-125, 1997 https://doi.org/10.1038/sj.bjp.0701340
  32. Sharma, N.R., Davis, M.J. Substance P-induced calcium entry in endothelial cells is secondary to depletion of intracellular stores. Am. J. Physiol, 268: H962-H973, 1995
  33. Guerrero, M.F., Puebla, P., Carron, R., Martin, M.L., San Roman, L. Quercetin 3,7-dimethyl ether: a vasorelaxant flavonoid isolated from Croton schiedeanus Schlecht. J. Pharm. Pharmacol. 54: 1373-1378, 2002 https://doi.org/10.1211/002235702760345455
  34. Lemos, V.S., Freitas, M.R., Muller, B., Lino, Y.D., Queiroga, C.E., Cortes, S.F. Dioclein, a new nitric oxide- and endothelium-dependent vasodilator flavonoid. Eur. J. Pharmacol. 386: 41-46, 1999 https://doi.org/10.1016/S0014-2999(99)00747-5
  35. Ko, F.N., Huang, T.F., Teng, C.M. Vasodilatory action mechanisms of apigenin isolated from Apium graveolens in rat thoracic aorta. Biochim. Biophys. Acta. 1115: 69-74, 1991 https://doi.org/10.1016/0304-4165(91)90013-7
  36. Van Breeman, C., Cauvin, C., Johns, A., Leijten, P., Yamamoto, H. $Ca^{2+}$regulation of vascular smooth muscle. Fed. Proc. 45: 2746-2751, 1986
  37. Okabe, K., Kitimura, K., Kuriyama, H. Features of 4-aminopyridine sensitive outward current observed in single smooth muscle cells from the rabbit pulmonary artery. Pflugers Arch. 409: 561-568, 1987 https://doi.org/10.1007/BF00584654
  38. Nevala, R., Paukku, K., Korpela, R., Vapaatalo, H. Calcium-sensitive potassium channel inhibitors antagonize genistein- and daidzein-induced arterial relaxation in vitro. Life Sci. 69: 1407-1417, 2001 https://doi.org/10.1016/S0024-3205(01)01233-4
  39. Furchgott, R.F. Studies on relaxation of rabbit aorta by sodium nitrite: The basis for the proposal that the acid activatable inhibitory factor from bovine retractor penis is inorganic nitrite and the endothelium-derived relaxing factor is nitric oxide, in Vasodilation: Vascular Smooth Muscle, Peptides, Autonomic Nerves, and Endothelium (Vanhoutte PM ed), Raven Press, New York, pp 401-414, 1988