Molecular Mechanisms of Large-Conductance Ca2+-Activated Potassium Channel Activation by Ginseng Gintonin

Authors
Choi, S. H.Lee, B. H.Hwang, S. H.Kim, H. J.Lee, S. M.Kim, H. C.Rhim, H. W.Nah, S. Y.
Issue Date
2013-04
Publisher
HINDAWI LTD
Citation
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, v.2013
Abstract
Gintonin is a unique lysophosphatidic acid (LPA) receptor ligand found in Panax ginseng. Gintonin induces transient [Ca2+](i) through G protein-coupled LPA receptors. Large-conductance Ca2+-activated K+ (BKCa) channels are expressed in blood vessels and neurons and play important roles in blood vessel relaxation and attenuation of neuronal excitability. BKCa channels are activated by transient [Ca2+](i) and are regulated by various Ca2+-dependent kinases. We investigated the molecular mechanisms of BKCa channel activation by gintonin. BKCa channels are heterologously expressed in Xenopus oocytes. Gintonin treatment induced BKCa channel activation in oocytes expressing the BKCa channel alpha subunit in a concentration-dependent manner (EC50 = 0.71 +/- 0.08 mu g/mL). Gintonin-mediated BKCa channel activation was blocked by a PKC inhibitor, calphostin, and by the calmodulin inhibitor, calmidazolium. Site-directed mutations in BKCa channels targeting CaM kinase II or PKC phosphorylation sites but not PKA phosphorylation sites attenuated gintonin action. Mutations in the Ca2+ bowl and the regulator of K+ conductance (RCK) site also blocked gintonin action. These results indicate that gintonin-mediated BKCa channel activations are achieved through LPA1 receptor-phospholipase C-IP3-Ca2+-PKC-calmodulin-CaM kinase II pathways and calcium binding to the Ca2+ bowl and RCK domain. Gintonin could be a novel contributor against blood vessel constriction and over-excitation of neurons.
Keywords
PROTEIN-KINASE-C; ENDOTHELIUM-DEPENDENT RELAXATION; LYSOPHOSPHATIDIC ACID RECEPTORS; MAXI-K-CA; XENOPUS-OOCYTES; NEUROTRANSMITTER RELEASE; SMOOTH-MUSCLE; BK CHANNEL; CALCIUM; GINSENOSIDES; PROTEIN-KINASE-C; ENDOTHELIUM-DEPENDENT RELAXATION; LYSOPHOSPHATIDIC ACID RECEPTORS; MAXI-K-CA; XENOPUS-OOCYTES; NEUROTRANSMITTER RELEASE; SMOOTH-MUSCLE; BK CHANNEL; CALCIUM; GINSENOSIDES
ISSN
1741-427X
URI
https://pubs.kist.re.kr/handle/201004/128221
DOI
10.1155/2013/323709
Appears in Collections:
KIST Article > 2013
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