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HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway

This study aims to reveal the potential relationship between 5-HT and oxidative stress in the organism. Our in vitro experiments in RIN-14B cells showed that anoxia leads the cells to the state of oxidative stress. Administration of exogenous 5-HT exacerbated this effect, whereas the inhibition of T...

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Autores principales: He, Qiangqiang, Ma, Ji, Kalavagunta, Praveen Kumar, Zhou, Liangliang, Zhu, Junyi, Dong, Jing, Ahmad, Owais, Du, Yuzhi, Wei, Lixin, Shang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471647/
https://www.ncbi.nlm.nih.gov/pubmed/30889910
http://dx.doi.org/10.3390/ijms20061364
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author He, Qiangqiang
Ma, Ji
Kalavagunta, Praveen Kumar
Zhou, Liangliang
Zhu, Junyi
Dong, Jing
Ahmad, Owais
Du, Yuzhi
Wei, Lixin
Shang, Jing
author_facet He, Qiangqiang
Ma, Ji
Kalavagunta, Praveen Kumar
Zhou, Liangliang
Zhu, Junyi
Dong, Jing
Ahmad, Owais
Du, Yuzhi
Wei, Lixin
Shang, Jing
author_sort He, Qiangqiang
collection PubMed
description This study aims to reveal the potential relationship between 5-HT and oxidative stress in the organism. Our in vitro experiments in RIN-14B cells showed that anoxia leads the cells to the state of oxidative stress. Administration of exogenous 5-HT exacerbated this effect, whereas the inhibition of Tph1, LP533401 alleviated the oxidative stress. Several research articles reported that Cinnabar (consists of more than 96% mercury sulfide, HgS), which is widely used in both Chinese and Indian traditional medicine prescriptions, has been involved in the regulation of 5-HT. The present research revealed that HgS relieved the level of oxidative stress of RIN-14B cells. This pharmacological activity was also observed in the prescription drug Zuotai, in which HgS accounts for 54.5%, and these effects were found to be similar to LP533401, an experimental drug to treat pulmonary hypertension. Further, our in vivo experiments revealed that the administration of cinnabar or prescription drug Zuotai in zebrafish reduced the reactive oxygen species (ROS) induced by hypoxia and cured behavioral abnormalities. Taken together, in organisms with hypoxia induced oxidative stress 5-HT levels were found to be abnormally elevated, indicating that 5-HT could regulate oxidative stress, and the decrease in the 5-HT levels, behavioral abnormalities after treatment with cinnabar and Zuotai, we may conclude that the therapeutic and pharmacologic effect of cinnabar and Zuotai may be based on the regulation of 5-HT metabolism and relief of oxidative stress. Even though they aren’t toxic at the present dosage in both cell lines and zebrafish, their dose dependent toxicities are yet to be evaluated.
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spelling pubmed-64716472019-04-26 HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway He, Qiangqiang Ma, Ji Kalavagunta, Praveen Kumar Zhou, Liangliang Zhu, Junyi Dong, Jing Ahmad, Owais Du, Yuzhi Wei, Lixin Shang, Jing Int J Mol Sci Article This study aims to reveal the potential relationship between 5-HT and oxidative stress in the organism. Our in vitro experiments in RIN-14B cells showed that anoxia leads the cells to the state of oxidative stress. Administration of exogenous 5-HT exacerbated this effect, whereas the inhibition of Tph1, LP533401 alleviated the oxidative stress. Several research articles reported that Cinnabar (consists of more than 96% mercury sulfide, HgS), which is widely used in both Chinese and Indian traditional medicine prescriptions, has been involved in the regulation of 5-HT. The present research revealed that HgS relieved the level of oxidative stress of RIN-14B cells. This pharmacological activity was also observed in the prescription drug Zuotai, in which HgS accounts for 54.5%, and these effects were found to be similar to LP533401, an experimental drug to treat pulmonary hypertension. Further, our in vivo experiments revealed that the administration of cinnabar or prescription drug Zuotai in zebrafish reduced the reactive oxygen species (ROS) induced by hypoxia and cured behavioral abnormalities. Taken together, in organisms with hypoxia induced oxidative stress 5-HT levels were found to be abnormally elevated, indicating that 5-HT could regulate oxidative stress, and the decrease in the 5-HT levels, behavioral abnormalities after treatment with cinnabar and Zuotai, we may conclude that the therapeutic and pharmacologic effect of cinnabar and Zuotai may be based on the regulation of 5-HT metabolism and relief of oxidative stress. Even though they aren’t toxic at the present dosage in both cell lines and zebrafish, their dose dependent toxicities are yet to be evaluated. MDPI 2019-03-18 /pmc/articles/PMC6471647/ /pubmed/30889910 http://dx.doi.org/10.3390/ijms20061364 Text en © 2019 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
He, Qiangqiang
Ma, Ji
Kalavagunta, Praveen Kumar
Zhou, Liangliang
Zhu, Junyi
Dong, Jing
Ahmad, Owais
Du, Yuzhi
Wei, Lixin
Shang, Jing
HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway
title HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway
title_full HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway
title_fullStr HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway
title_full_unstemmed HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway
title_short HgS Inhibits Oxidative Stress Caused by Hypoxia through Regulation of 5-HT Metabolism Pathway
title_sort hgs inhibits oxidative stress caused by hypoxia through regulation of 5-ht metabolism pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471647/
https://www.ncbi.nlm.nih.gov/pubmed/30889910
http://dx.doi.org/10.3390/ijms20061364
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