Browse > Article
http://dx.doi.org/10.5142/jgr.2011.35.3.325

Red Ginseng Saponin Fraction A Isolated from Korean Red Ginseng by Ultrafiltration on the Porcine Coronary Artery  

Jung, Young-Hyun (Department of Physiology, Kyungpook National University College of Veterinary Medicine)
Park, Kwang-Yeol (Department of Physiology, Kyungpook National University College of Veterinary Medicine)
Jeon, Jin-Hong (Department of Physiology, Kyungpook National University College of Veterinary Medicine)
Kwak, Yi-Seong (Korea Ginseng Corporation Central Research Institute)
Song, Yong-Bum (Korea Ginseng Corporation Central Research Institute)
Wee, Jae-Joon (Korea Ginseng Corporation Central Research Institute)
Rhee, Man-Hee (Department of Physiology, Kyungpook National University College of Veterinary Medicine)
Kim, Tae-Wan (Department of Physiology, Kyungpook National University College of Veterinary Medicine)
Publication Information
Journal of Ginseng Research / v.35, no.3, 2011 , pp. 325-330 More about this Journal
Abstract
Red ginseng saponin fraction-A (RGSF-A) contains a high percentage of panaxadiol saponins that were isolated from Korean red ginseng by ultrafiltration. The aim of this study was to elucidate the effects of RGSF-A on the porcine distal left anterior descending (LAD) coronary artery. The relaxant responses to RGSF-A were examined during contractions induced by 100 nM U46619 (9,11-dideoxy-9a,11a-methanoepoxy-prostaglandin F2a), a stable analogue of thromboxane A2. RGSF-A dose-dependently induced biphasic (fast- and slow-) relaxation in the distal LAD coronary artery in the presence of an intact endothelium. The fast-relaxation was quickly achieved in a minute, and then the slow-relaxation was slowly developed and sustained for more than thirty minutes after the administration of RGSF-A. The slow-relaxation had a tendency to be bigger than the fast-relaxation. Fast relaxation induced by RGSF-A was almost blocked by $N_{\omega}$-Nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase synthase inhibitor and 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), a guanylate cyclase inhibitor. However slow relaxation induced by RGSF-A was only partially inhibited by L-NAME and ODQ. In the endothelium-removed ring, RGSF-A evoked only slowrelaxation to a certain extent. These data suggest that RGSF-A induced both endothelium dependent fast- and slow-relaxation and endothelium independent slow-relaxation in the porcine distal LAD coronary artery. The endothelium dependent fast-relaxation is mediated by the nitric oxide (NO)-cGMP pathway, and the endothelium dependent slow-relaxation is at least partially mediated by the NO-cGMP pathway. However, the endothelium-independent slow-relaxation remains to be elucidated.
Keywords
Ginseng; Red ginseng saponin fraction-A; Porcine coronary artery; Endothelium; Nitric oxide;
Citations & Related Records
Times Cited By KSCI : 6  (Citation Analysis)
Times Cited By Web Of Science : 1  (Related Records In Web of Science)
연도 인용수 순위
1 Matsumoto T, Kinoshita M, Toda N. Mechanisms of endothelium-dependent responses to vasoactive agents in isolated porcine coronary arteries. J Cardiovasc Pharmacol 1993;21:228-234.   DOI
2 Kim JH, Lee JH, Jeong SM, Lee BH, Yoon IS, Lee JH, Choi SH, Kim DH, Park TK, Kim BK et al. Stereospecific effects of ginsenoside $Rg_{3}$ epimers on swine coronary artery contractions. Biol Pharm Bull 2006;29:365-370.   DOI   ScienceOn
3 Yang Q, Zhang RZ, Yim AP, He GW. Release of nitric oxide and endothelium-derived hyperpolarizing factor (EDHF) in porcine coronary arteries exposed to hyperkalemia: effect of nicorandil. Ann Thorac Surg 2005;79:2065-2071.   DOI   ScienceOn
4 Kim HB, Kang CW, Kim BS, Kwon JK, Yu IJ, Roh YS, Nah SY, Ejaz S, Kim JH. Beneficial role of ginseng saponin on hemodynamic functions of porcine blood vessel. J Ginseng Res 2010;34:314-320.   과학기술학회마을   DOI   ScienceOn
5 Kim ND, Kang SY, Kim MJ, Park JH, Schini-Kerth VB. The ginsenoside $Rg_{3}$ evokes endothelium-independent relaxation in rat aortic rings: role of $K^{+}$ channels. Eur J Pharmacol 1999;367:51-57.   DOI   ScienceOn
6 Nakaya Y, Mawatari K, Takahashi A, Harada N, Hata A, Yasui S. The phytoestrogen ginsensoside Re activates potassium channels of vascular smooth muscle cells through PI3K/Akt and nitric oxide pathways. J Med Invest 2007;54:381-384.   DOI
7 Kim ND, Kang SY, Schini VB. Ginsenosides evoke endothelium- dependent vascular relaxation in rat aorta. Gen Pharmacol 1994;25:1071-1077.   DOI   ScienceOn
8 Hur MH, Lee MS, Yang HJ, Kim C, Bae IL, Ernst E. Ginseng for reducing the blood pressure in patients with hypertension: a systematic review and meta-analysis. J Ginseng Res 2010;34:342-347.   과학기술학회마을   DOI   ScienceOn
9 Chang SJ, Suh JS, Jeon BH, Nam KY, Park HK. Vasorelaxing effect by protopanaxatriol and protopanaxadiol of Panax ginseng in the pig coronary artery. Korean J Ginseng Sci 1994;18:95-101.   과학기술학회마을
10 Chung I, Kim ND. Ginseng saponins enhance maxi $Ca^{2+}$-activated $K^{+}$ currents of the rabbit coronary artery smooth muscle cells. J Ginseng Res 1999;23:230-234.   과학기술학회마을
11 Kang SY, Kim SH, Schini VB, Kim ND. Dietary ginsenosides improve endothelium-dependent relaxation in the thoracic aorta of hypercholesterolemic rabbit. Gen Pharmacol 1995;26:483-487.   DOI   ScienceOn
12 Kim JY, Kim YC, Lee MG, Kwon JW, Yoo M. Effects of water deprivation on the pharmacokinetics of DA-8159, a new erectogenic, in rats. J Pharm Pharm Sci 2006;9:10- 21.
13 Chung IM, Lim JW, Pyun WB, Kim HY. Korean red ginseng improves vascular stiffness in patients with coronary artery disease. J Ginseng Res 2010;34:212-218.   과학기술학회마을   DOI   ScienceOn
14 Yi XQ, Li T, Wang JR, Wong VK, Luo P, Wong IY, Jiang ZH, Liu L, Zhou H. Total ginsenosides increase coronary perfusion flow in isolated rat hearts through activation of PI3K/Akt-eNOS signaling. Phytomedicine 2010;17:1006- 1015.   DOI   ScienceOn
15 Kim TH, Lee SM. The effects of ginseng total saponin, panaxadiol and panaxatriol on ischemia/reperfusion injury in isolated rat heart. Food Chem Toxicol 2010;48:1516- 1520.   DOI   ScienceOn
16 Cho JG, Lee MK, Lee JW, Park HJ, Lee DY, Lee YH, Yang DC, Baek N. Physicochemical characterization and NMR assignments of ginsenosides $Rb_{1}$, $Rb_{2}$, Rc, and Rd isolated from Panax ginseng. J Ginseng Res 2010;34:113- 121.   과학기술학회마을   DOI   ScienceOn
17 Kaku T, Miyata T, Uruno T, Sako I, Kinoshita A. Chemico- pharmacological studies on saponins of Panax ginseng C. A. Meyer. II. Pharmacological part. Arzneimittelforschung 1975;25:539-547.
18 Chang MS, Lee SG, Rho HM. Transcriptional activation of Cu/Zn superoxide dismutase and catalase genes by panaxadiol ginsenosides extracted from Panax ginseng. Phytother Res 1999;13:641-644.   DOI   ScienceOn
19 Kudo K, Tachikawa E, Kashimoto T, Takahashi E. Properties of ginseng saponin inhibition of catecholamine secretion in bovine adrenal chromaffin cells. Eur J Pharmacol 1998;341:139-144.   DOI   ScienceOn
20 Lee HJ, Kim SR, Kim JC, Kang CM, Lee YS, Jo SK, Kim TH, Jang JS, Nah SY, Kim SH. In Vivo radioprotective effect of Panax ginseng C.A. Meyer and identification of active ginsenosides. Phytother Res 2006;20:392- 395.   DOI   ScienceOn
21 Chen X, Gillis CN, Moalli R. Vascular effects of ginsenosides in vitro. Br J Pharmacol 1984;82:485-491.   DOI   ScienceOn
22 Chen X. Cardiovascular protection by ginsenosides and their nitric oxide releasing action. Clin Exp Pharmacol Physiol 1996;23:728-732.   DOI   ScienceOn
23 Gillis CN. Panax ginseng pharmacology: a nitric oxide link? Biochem Pharmacol 1997;54:1-8.   DOI   ScienceOn
24 Furukawa T, Bai CX, Kaihara A, Ozaki E, Kawano T, Nakaya Y, Awais M, Sato M, Umezawa Y, Kurokawa J. Ginsenoside Re, a main phytosterol of Panax ginseng, activates cardiac potassium channels via a nongenomic pathway of sex hormones. Mol Pharmacol 2006;70:1916- 1924.   DOI   ScienceOn
25 Attele AS, Wu JA, Yuan CS. Ginseng pharmacology: multiple constituents and multiple actions. Biochem Pharmacol 1999;58:1685-1693.   DOI   ScienceOn