Inhibitory Effects of Ginsenoside Metabolites, Compound K and Protopanaxatriol, on GABAC Receptor-Mediated Ion Currents.
10.4196/kjpp.2013.17.2.127
- Author:
Byung Hwan LEE
1
;
Sung Hee HWANG
;
Sun Hye CHOI
;
Hyeon Joong KIM
;
Joon Hee LEE
;
Sang Mok LEE
;
Yun Gyong AHN
;
Seung Yeol NAH
Author Information
1. Ginsentology Research Laboratory and Department of Physiology, College of Veterinary Medicine and Bio/Molecular Informatics Center, Konkuk University, Seoul 143-701, Korea. synah@konkuk.ac.kr
- Publication Type:Original Article
- Keywords:
GABAC receptor;
Ginsenoside metabolites;
Panax ginseng;
Xenopus oocytes
- MeSH:
Brain;
Eye;
gamma-Aminobutyric Acid;
Ginsenosides;
Humans;
Oocytes;
Panax;
Retinal Bipolar Cells;
RNA, Complementary;
Sapogenins;
Xenopus
- From:The Korean Journal of Physiology and Pharmacology
2013;17(2):127-132
- CountryRepublic of Korea
- Language:English
-
Abstract:
Ginsenosides, one of the active ingredients of Panax ginseng, show various pharmacological and physiological effects, and they are converted into compound K (CK) or protopanaxatriol (M4) by intestinal microorganisms. CK is a metabolite derived from protopanaxadiol (PD) ginsenosides, whereas M4 is a metabolite derived from protopanaxatriol (PT) ginsenosides. The gamma-aminobutyric acid receptorC (GABAC) is primarily expressed in retinal bipolar cells and several regions of the brain. However, little is known of the effects of ginsenoside metabolites on GABAC receptor channel activity. In the present study, we examined the effects of CK and M4 on the activity of human recombinant GABAC receptor (rho1) channels expressed in Xenopus oocytes by using a 2-electrode voltage clamp technique. In oocytes expressing GABAC receptor cRNA, we found that CK or M4 alone had no effect in oocytes. However, co-application of either CK or M4 with GABA inhibited the GABA-induced inward peak current (IGABA). Interestingly, pre-application of M4 inhibited IGABA more potently than CK in a dose-dependent and reversible manner. The half-inhibitory concentration (IC50) values of CK and M4 were 52.1+/-2.3 and 45.7+/-3.9 microM, respectively. Inhibition of IGABA by CK and M4 was voltage-independent and non-competitive. This study implies that ginsenoside metabolites may regulate GABAC receptor channel activity in the brain, including in the eyes.
