Author
Listed:
- Hyeon-Joong Kim
(Ginsentology Research Laboratory and Department of Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Korea
Biomedical Research Imaging Center, University of North Caroline at Chapel Hill, Chapel Hill, NC 27599, USA)
- Sun-Hye Choi
(Ginsentology Research Laboratory and Department of Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Korea)
- Na-Eun Lee
(Ginsentology Research Laboratory and Department of Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Korea)
- Hee-Jung Cho
(Ginsentology Research Laboratory and Department of Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Korea)
- Hyewhon Rhim
(Center for Neuroscience, Korea Institute of Science and Technology, Seoul 02792, Korea)
- Hyoung-Chun Kim
(Neuropsychopharmacology and Toxicology program, College of Pharmacy, Kangwon National University, Chunchon 24341, Korea)
- Sung-Hee Hwang
(Department of Pharmaceutical Engineering, College of Health Sciences, Sangji University, Wonju 26339, Korea)
- Seung-Yeol Nah
(Ginsentology Research Laboratory and Department of Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Korea)
Abstract
Gintonin is a newly discovered ingredient of ginseng and plays an exogenous ligand for G protein-coupled lysophosphatidic acid receptors. We previously showed that gintonin exhibits diverse effects from neurotransmitter release to improvement of Alzheimer’s disease-related cognitive dysfunctions. However, previous studies did not show whether gintonin has protective effects against environmental heavy metal. We investigated the effects of gintonin-enriched fraction (GEF) on methylmercury (MeHg)-induced neurotoxicity and learning and memory dysfunction and on organ MeHg elimination. Using hippocampal neural progenitor cells (hNPCs) and mice we examined the effects of GEF on MeHg-induced hippocampal NPC neurotoxicity, on formation of reactive oxygen species (ROS), and on in vivo learning and memory functions after acute MeHg exposure. Treatment of GEF to hNPCs attenuated MeHg-induced neurotoxicity with concentration- and time-dependent manner. GEF treatment inhibited MeHg- and ROS inducer-induced ROS formations. Long-term treatment of GEF also improved MeHg-induced learning and memory dysfunctions. Oral administration of GEF decreased the concentrations of MeHg in blood, brain, liver, and kidney. This is the first report that GEF attenuated MeHg-induced in vitro and in vivo neurotoxicities through LPA (lysophosphatidic acids) receptor-independent manner and increased organ MeHg elimination. GEF-mediated neuroprotection might achieve via inhibition of ROS formation and facilitation of MeHg elimination from body.
Suggested Citation
Hyeon-Joong Kim & Sun-Hye Choi & Na-Eun Lee & Hee-Jung Cho & Hyewhon Rhim & Hyoung-Chun Kim & Sung-Hee Hwang & Seung-Yeol Nah, 2020.
"Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination,"
IJERPH, MDPI, vol. 17(3), pages 1-14, January.
Handle:
RePEc:gam:jijerp:v:17:y:2020:i:3:p:838-:d:314062
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