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Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats

Realgar- and cinnabar-containing AnGongNiuHuang Pill (AGNHP) is widely used for treating encephalopathy syndrome. However, it raises great safety concerns due to the adverse effects reported by arsenic or mercury poisoning. Although AGNHP has been generally recognized, little is known about the meta...

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Autores principales: Wu, Xiao, Zhong, Zeling, Lin, Kuangmin, Liu, Xinhe, Wu, Zhichao, Liu, Zitian, Li, Yongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470115/
https://www.ncbi.nlm.nih.gov/pubmed/36110533
http://dx.doi.org/10.3389/fphar.2022.967608
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author Wu, Xiao
Zhong, Zeling
Lin, Kuangmin
Liu, Xinhe
Wu, Zhichao
Liu, Zitian
Li, Yongming
author_facet Wu, Xiao
Zhong, Zeling
Lin, Kuangmin
Liu, Xinhe
Wu, Zhichao
Liu, Zitian
Li, Yongming
author_sort Wu, Xiao
collection PubMed
description Realgar- and cinnabar-containing AnGongNiuHuang Pill (AGNHP) is widely used for treating encephalopathy syndrome. However, it raises great safety concerns due to the adverse effects reported by arsenic or mercury poisoning. Although AGNHP has been generally recognized, little is known about the metabolism of arsenic and mercury and their resulting potential health risk in vivo. Thus, comparative pharmacokinetics and urinary excretion of arsenic and mercury were conducted in rats after oral administration of realgar, cinnabar and AGNHP, respectively. The contents of arsenic and mercury in rat blood and urine were determined by hydride-generation atomic fluorescence spectrometry (HG-AFS) after wet digestion. AGNHP significantly reduced the absorption of arsenic in blood and promoted urinary arsenic excretion. Whereas, it increased the blood mercury absorption and reduced urinary mercury excretion. No significant toxicity was observed in the clinical dose range of AGNHP. However, excessive exposure to arsenic and mercury may still pose risks especially by long-term or excessive medication. The results are helpful for the rational clinical applications of realgar- and cinnabar-containing TCMs.
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spelling pubmed-94701152022-09-14 Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats Wu, Xiao Zhong, Zeling Lin, Kuangmin Liu, Xinhe Wu, Zhichao Liu, Zitian Li, Yongming Front Pharmacol Pharmacology Realgar- and cinnabar-containing AnGongNiuHuang Pill (AGNHP) is widely used for treating encephalopathy syndrome. However, it raises great safety concerns due to the adverse effects reported by arsenic or mercury poisoning. Although AGNHP has been generally recognized, little is known about the metabolism of arsenic and mercury and their resulting potential health risk in vivo. Thus, comparative pharmacokinetics and urinary excretion of arsenic and mercury were conducted in rats after oral administration of realgar, cinnabar and AGNHP, respectively. The contents of arsenic and mercury in rat blood and urine were determined by hydride-generation atomic fluorescence spectrometry (HG-AFS) after wet digestion. AGNHP significantly reduced the absorption of arsenic in blood and promoted urinary arsenic excretion. Whereas, it increased the blood mercury absorption and reduced urinary mercury excretion. No significant toxicity was observed in the clinical dose range of AGNHP. However, excessive exposure to arsenic and mercury may still pose risks especially by long-term or excessive medication. The results are helpful for the rational clinical applications of realgar- and cinnabar-containing TCMs. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9470115/ /pubmed/36110533 http://dx.doi.org/10.3389/fphar.2022.967608 Text en Copyright © 2022 Wu, Zhong, Lin, Liu, Wu, Liu and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Wu, Xiao
Zhong, Zeling
Lin, Kuangmin
Liu, Xinhe
Wu, Zhichao
Liu, Zitian
Li, Yongming
Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats
title Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats
title_full Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats
title_fullStr Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats
title_full_unstemmed Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats
title_short Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats
title_sort comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and angongniuhuang pill to rats
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470115/
https://www.ncbi.nlm.nih.gov/pubmed/36110533
http://dx.doi.org/10.3389/fphar.2022.967608
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