1. Academic Validation
  2. Ginseng Gintonin Contains Ligands for GPR40 and GPR55

Ginseng Gintonin Contains Ligands for GPR40 and GPR55

  • Molecules. 2020 Mar 2;25(5):1102. doi: 10.3390/molecules25051102.
Yeon-Jin Cho 1 Sun-Hye Choi 1 Rami Lee 1 Hongik Hwang 2 Hyewhon Rhim 2 Ik-Hyun Cho 3 Hyoung-Chun Kim 4 Jeong-Ik Lee 5 Sung-Hee Hwang 6 Seung-Yeol Nah 1
Affiliations

Affiliations

  • 1 Ginsentology Research Laboratory and Department of Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Korea.
  • 2 Center for Neuroscience, Korea Institute of Science and Technology, Seoul 02792, Korea.
  • 3 Department of Convergence Medical Science, Department of Science in Korean Medicine and Brain Korea 21 Plus Program, Graduate School, Kyung Hee University, Seoul 02447, Korea.
  • 4 Neuropsychopharmacology and Toxicology program, College of Pharmacy, Kangwon National University, Chunchon 24341, Korea.
  • 5 Department of Veterinary Obstetrics and Theriogenology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Korea.
  • 6 Department of Pharmaceutical Engineering, College of Health Sciences, Sangji University, Wonju 26339, Korea.
Abstract

Gintonin, a novel ginseng-derived glycolipoprotein complex, has an exogenous ligand for lysophosphatidic acid (LPA) receptors. However, recent lipid analysis of gintonin has shown that gintonin also contains other bioactive lipids besides LPAs, including linoleic acid and lysophosphatidylinositol (LPI). Linoleic acid, a free fatty acid, and LPI are known as ligands for the G-protein coupled receptors (GPCR), GPR40, and GPR55, respectively. We, herein, investigated whether gintonin could serve as a ligand for GPR40 and GPR55, using the insulin-secreting beta cell-derived cell line INS-1 and the human prostate Cancer cell line PC-3, respectively. Gintonin dose-dependently enhanced Insulin secretion from INS-1 cells. Gintonin-stimulated Insulin secretion was partially inhibited by a GPR40 receptor antagonist but not an LPA1/3 receptor antagonist and was down-regulated by small interfering RNA (siRNA) against GPR40. Gintonin dose-dependently induced [CA2+]i transients and CA2+-dependent cell migration in PC-3 cells. Gintonin actions in PC-3 cells were attenuated by pretreatment with a GPR55 Antagonist and an LPA1/3 receptor antagonist or by down-regulating GPR55 with siRNA. Taken together, these results demonstrated that gintonin-mediated Insulin secretion by INS-1 cells and PC-3 cell migration were regulated by the respective activation of GPR40 and GPR55 receptors. These findings indicated that gintonin could function as a ligand for both receptors. Finally, we demonstrated that gintonin contained two more GPCR ligands, in addition to that for LPA receptors. Gintonin, with its multiple GPCR ligands, might provide the molecular basis for the multiple pharmacological actions of ginseng.

Keywords

GPR40; GPR55; cell migration; ginseng; gintonin; insulin secretion.

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