Cargando…

Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination

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. Ho...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Hyeon-Joong, Choi, Sun-Hye, Lee, Na-Eun, Cho, Hee-Jung, Rhim, Hyewhon, Kim, Hyoung-Chun, Hwang, Sung-Hee, Nah, Seung-Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038146/
https://www.ncbi.nlm.nih.gov/pubmed/32013120
http://dx.doi.org/10.3390/ijerph17030838
_version_ 1783500587019534336
author Kim, Hyeon-Joong
Choi, Sun-Hye
Lee, Na-Eun
Cho, Hee-Jung
Rhim, Hyewhon
Kim, Hyoung-Chun
Hwang, Sung-Hee
Nah, Seung-Yeol
author_facet Kim, Hyeon-Joong
Choi, Sun-Hye
Lee, Na-Eun
Cho, Hee-Jung
Rhim, Hyewhon
Kim, Hyoung-Chun
Hwang, Sung-Hee
Nah, Seung-Yeol
author_sort Kim, Hyeon-Joong
collection PubMed
description 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.
format Online
Article
Text
id pubmed-7038146
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-70381462020-03-10 Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination Kim, Hyeon-Joong Choi, Sun-Hye Lee, Na-Eun Cho, Hee-Jung Rhim, Hyewhon Kim, Hyoung-Chun Hwang, Sung-Hee Nah, Seung-Yeol Int J Environ Res Public Health Article 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. MDPI 2020-01-29 2020-02 /pmc/articles/PMC7038146/ /pubmed/32013120 http://dx.doi.org/10.3390/ijerph17030838 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Hyeon-Joong
Choi, Sun-Hye
Lee, Na-Eun
Cho, Hee-Jung
Rhim, Hyewhon
Kim, Hyoung-Chun
Hwang, Sung-Hee
Nah, Seung-Yeol
Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination
title Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination
title_full Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination
title_fullStr Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination
title_full_unstemmed Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination
title_short Effects of Gintonin-Enriched Fraction on Methylmercury-Induced Neurotoxicity and Organ Methylmercury Elimination
title_sort effects of gintonin-enriched fraction on methylmercury-induced neurotoxicity and organ methylmercury elimination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038146/
https://www.ncbi.nlm.nih.gov/pubmed/32013120
http://dx.doi.org/10.3390/ijerph17030838
work_keys_str_mv AT kimhyeonjoong effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination
AT choisunhye effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination
AT leenaeun effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination
AT choheejung effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination
AT rhimhyewhon effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination
AT kimhyoungchun effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination
AT hwangsunghee effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination
AT nahseungyeol effectsofgintoninenrichedfractiononmethylmercuryinducedneurotoxicityandorganmethylmercuryelimination