Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Choi SH
,
Kim HJ
,
Kim BR
,
Shin TJ
,
Hwang SH
,
Lee BH
,
Lee SM
,
Rhim H
,
Nah SY
.
???displayArticle.abstract???
Ginseng, the root of Panax ginseng C.A. Meyer, is used as a general tonic. Recently, we isolated a novel ginsengderived lysophosphatidic acid (LPA) receptor ligand, gintonin. Gintonin activates G protein-coupled LPA receptors with high affinity in cells endogenously expressing LPA receptors, e.g., Xenopus oocytes. P2X receptors are ligandgated ion channels activated by extracellular ATP, and 7 receptor subtypes (P2X1-P2X7) have been identified. Most of the P2X1 receptors are expressed in the smooth muscles of genitourinary organs involved in reproduction. A main characteristic of the P2X1 receptor is rapid desensitization after repeated ATP treatment of cells or tissues expressing P2X1 receptors. In the present study, we examined the effect of gintonin on P2X1 receptor channel activity. P2X1 receptors were heterologously expressed in Xenopus oocytes. ATP treatment of oocytes expressing P2X1 receptors induced large inward currents (I ATP ), but repetitive ATP treatments induced a rapid desensitization of I ATP . Gintonin treatment after P2X1 receptor desensitization potentiated I ATP in a concentration-dependent manner. We further examined the signaling transduction pathways involved in gintonin-mediated potentiation of I ATP . Gintoninmediated I ATP potentiation was blocked by Ki16425, an LPA1/3 receptor antagonist, a PKC inhibitor, a PLC inhibitor, and a PI4-Kinase inhibitor but not by a calcium chelator. In addition, mutations of the phosphoinositide binding site of the P2X1 receptor greatly attenuated the gintonin-mediated I ATP potentiation. These results indicate that G protein-coupled LPA receptor activation by gintonin is coupled to the potentiation of the desensitized P2X1 receptor through a phosphoinositide-dependent pathway.
Ase,
Potentiation of P2X1 ATP-gated currents by 5-hydroxytryptamine 2A receptors involves diacylglycerol-dependent kinases and intracellular calcium.
2005, Pubmed,
Xenbase
Ase,
Potentiation of P2X1 ATP-gated currents by 5-hydroxytryptamine 2A receptors involves diacylglycerol-dependent kinases and intracellular calcium.
2005,
Pubmed
,
Xenbase
Balla,
Phosphatidylinositol 4-kinases.
1998,
Pubmed
Banks,
The purinergic component of human vas deferens contraction.
2006,
Pubmed
Bernier,
Direct modulation of P2X1 receptor-channels by the lipid phosphatidylinositol 4,5-bisphosphate.
2008,
Pubmed
,
Xenbase
Burnstock,
Physiology and pathophysiology of purinergic neurotransmission.
2007,
Pubmed
Burnstock,
The past, present and future of purine nucleotides as signalling molecules.
1997,
Pubmed
Choi,
A novel activation of Ca(2+)-activated Cl(-) channel in Xenopus oocytes by Ginseng saponins: evidence for the involvement of phospholipase C and intracellular Ca(2+) mobilization.
2001,
Pubmed
,
Xenbase
Diao,
Uterine luminal epithelium-specific proline-rich acidic protein 1 (PRAP1) as a marker for successful embryo implantation.
2010,
Pubmed
Dunn,
Fertility: purinergic receptors and the male contraceptive pill.
2000,
Pubmed
Fujiwara,
Regulation of the desensitization and ion selectivity of ATP-gated P2X2 channels by phosphoinositides.
2006,
Pubmed
,
Xenbase
Hwang,
Gintonin, newly identified compounds from ginseng, is novel lysophosphatidic acids-protein complexes and activates G protein-coupled lysophosphatidic acid receptors with high affinity.
2012,
Pubmed
Hwang,
Panax ginseng improves survival and sperm quality in guinea pigs exposed to 2,3,7,8-tetrachlorodibenzo- p-dioxin.
2004,
Pubmed
Jang,
Effects of red ginseng extract on the epididymal sperm motility of mice exposed to ethanol.
2011,
Pubmed
Jarvis,
ATP-gated P2X cation-channels.
2009,
Pubmed
Khakh,
P2X receptors as cell-surface ATP sensors in health and disease.
2006,
Pubmed
Kimura,
Two novel Xenopus homologs of mammalian LP(A1)/EDG-2 function as lysophosphatidic acid receptors in Xenopus oocytes and mammalian cells.
2001,
Pubmed
,
Xenbase
Lopes,
Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies.
2002,
Pubmed
,
Xenbase
Mulryan,
Reduced vas deferens contraction and male infertility in mice lacking P2X1 receptors.
2000,
Pubmed
North,
Molecular physiology of P2X receptors.
2002,
Pubmed
North,
P2X receptors: a third major class of ligand-gated ion channels.
1996,
Pubmed
Park,
The therapeutic effect of tissue cultured root of wild Panax ginseng C.A. Mayer on spermatogenetic disorder.
2006,
Pubmed
Rettinger,
Activation and desensitization of the recombinant P2X1 receptor at nanomolar ATP concentrations.
2003,
Pubmed
,
Xenbase
Sim,
Ectodomain lysines and suramin block of P2X1 receptors.
2008,
Pubmed
Sneddon,
Electrophysiology of autonomic neuromuscular transmission involving ATP.
2000,
Pubmed
Suh,
Regulation of ion channels by phosphatidylinositol 4,5-bisphosphate.
2005,
Pubmed
Surprenant,
P2X receptors bring new structure to ligand-gated ion channels.
1995,
Pubmed
Toullec,
The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C.
1991,
Pubmed
Valera,
A new class of ligand-gated ion channel defined by P2x receptor for extracellular ATP.
1994,
Pubmed
,
Xenbase
Vial,
G-protein-coupled receptor regulation of P2X1 receptors does not involve direct channel phosphorylation.
2004,
Pubmed
,
Xenbase
Werner,
Domains of P2X receptors involved in desensitization.
1996,
Pubmed
,
Xenbase
Zhao,
PIP(2) regulates the ionic current of P2X receptors and P2X(7) receptor-mediated cell death.
2007,
Pubmed
Zhao,
Regulation of ATP-gated P2X receptors by phosphoinositides.
2007,
Pubmed