INTERACTIONS OF GINSENOSIDES WITH LIGAND-BINDINGS OF GABA(A) AND GABA(B) RECEPTORS

被引:77
作者
KIMURA, T
SAUNDERS, PA
KIM, HS
RHEU, HM
OH, KW
HO, IK
机构
[1] UNIV MISSISSIPPI,MED CTR,DEPT PHARMACOL & TOXICOL,JACKSON,MS 39216
[2] CHUNGBUK NATL UNIV,COLL PHARM,DEPT PHARMACOL,CHONGJU 360763,SOUTH KOREA
来源
GENERAL PHARMACOLOGY | 1994年 / 25卷 / 01期
关键词
D O I
10.1016/0306-3623(94)90032-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Total saponin fraction decreased the affinity of specific [H-3]muscimol binding without changes in B-max. Ginsenoside Rb-1 Rb-2, Rc, Re, Rf and Rg, inhibited the specific [H-3]muscimol binding to the high-affinity site. 2. Total saponin fraction increased the affinity of specific [H-3]flunitrazepam binding. Ginsenoside Re and Rf enhanced specific [H-3]flunitrazepam binding. 3. Total saponin fraction decreased the affinity of specific [S-35]TBPS binding without changes in B-max. Ginsenosides did not affect specific or non-specific [S-35]TBPS binding. 4. Total saponin fraction decreased the affinity of specific [H-3]baclofen binding without changes in B-max. Ginsenoside Rc inhibited specific [H-3]baclofen binding.
引用
收藏
页码:193 / 199
页数:7
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