Pharmacological Effects of ginseng Saponins on Receptor Stimulation-responses

  • Eiichi Tachikawa (Department of Pharmacology and Department of Orthapedii Surgery, School of Medicine, Iwate Medical University) ;
  • Kenzo Kudo (Department of Pharmacology and Department of Orthapedii Surgery, School of Medicine, Iwate Medical University) ;
  • Kazuho Harada (Department of Pharmacology and Department of Orthapedii Surgery, School of Medicine, Iwate Medical University) ;
  • Takeshi Kashimoto (Department of Pharmacology and Department of Orthapedii Surgery, School of Medicine, Iwate Medical University) ;
  • KatsuroFurumachi (Department of Orthopedic Surgery. School of Medicine, Iwate Medical University) ;
  • Yoshikazu Miyate (Department of Medicine, School of Dentistry, Iwate Medical University) ;
  • Atsushi Kakizaki (Department of Medicine, School of Dentistry, Iwate Medical University) ;
  • Eiji Takahashi (Department of Medicine, School of Dentistry, Iwate Medical University)
  • Published : 1998.06.01

Abstract

We investigated the influence of the root of Panax ginseng C. A. Meyer on the secretion of catecholamines from bovine adrenal chromaffin cells, which are used as a model of nervous systems. In two major parts extracted from the ginseng root, the crude saponin fraction, but not the non-saponin fraction, reduced the secretion from the cells, stimulated by acetylcholine (ACh). Ginseng saponins (ginsenosides) are classified into three groups, the panaxadiol, the panaxatriol and the oleanolic acid groups, on the basis of the chemical structures of their saponins. Both the panaxadiol and the panaxatriol saponins, excluding only one oleanolic acid saponin ginsenoside-Ro, generally reduced the ACh-evoked secretion. The inhibitory effects of the panaxatriol were much stronger than those of the panaxadiol. However, ginsenoside-Rg, and -Rh3 in the panaxadiol saponins were the potent inhibitors comparable to the panaxatriol saponins. Ginsenoside-Rg2 in the panaxatriol was the most effective. It is probable that the ginsenoside inhibition of the catecholamine secretion is due to the suppression of the function of the nicotinic ACh receptor-cation channels. On the other hand, ginsenoside-Rg2 did not affect the angiotensin II-, the bradykinin-, the histamine- and the neurotensin- induced catecholamine secretions from the chromaffin cells and the muscarine- and the histamine- induced contraction of the ileum in guinea-pigs. Ginsenoside-Rbl, a panaxadiol saponin, and ginsenoside-Ro had no or only a slight effect on them. On the contrary, ginsenoside-Rg3 not only competitively inhibited the muscarine-induced ileum contraction but also reduced the angiotensin R -, the bradykinin-, the histamine- and the neurotensin-induced catecholamine secretions. Thus, the ginseng root contains active ingredients, namely some ginsensides, which suppress the responses induced by receptor stimulation. The inhibitory effects of ginseng saponins may be one of the action mechanisms for the pharmacological effects of the Panax ginseng root.

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