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A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats

Alismatis rhizoma (AR), the dried rhizome of Alisma orientale (Sam.) Juzep, is a well-known, traditional medicine that is used for the various biological activities including as a diuretic, to lower cholesterol and as an anti-inflammatory agent. The present study was carried out to investigate the p...

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Autores principales: Lee, Mu-Jin, Jung, Ho-Kyung, Lee, Ki-Ho, Jang, Ji-Hun, Sim, Mi-Ok, Seong, Tea-Gyeong, Ahn, Byung-Kwan, Shon, Jin-Han, Ham, Seong-Ho, Cho, Hyun-Woo, Kim, Yong-Min, Park, Sung-Jin, Yoon, Ji-Young, Ko, Je-Won, Kim, Jong-Choon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Toxicology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467358/
https://www.ncbi.nlm.nih.gov/pubmed/31015901
http://dx.doi.org/10.5487/TR.2019.35.2.191
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author Lee, Mu-Jin
Jung, Ho-Kyung
Lee, Ki-Ho
Jang, Ji-Hun
Sim, Mi-Ok
Seong, Tea-Gyeong
Ahn, Byung-Kwan
Shon, Jin-Han
Ham, Seong-Ho
Cho, Hyun-Woo
Kim, Yong-Min
Park, Sung-Jin
Yoon, Ji-Young
Ko, Je-Won
Kim, Jong-Choon
author_facet Lee, Mu-Jin
Jung, Ho-Kyung
Lee, Ki-Ho
Jang, Ji-Hun
Sim, Mi-Ok
Seong, Tea-Gyeong
Ahn, Byung-Kwan
Shon, Jin-Han
Ham, Seong-Ho
Cho, Hyun-Woo
Kim, Yong-Min
Park, Sung-Jin
Yoon, Ji-Young
Ko, Je-Won
Kim, Jong-Choon
author_sort Lee, Mu-Jin
collection PubMed
description Alismatis rhizoma (AR), the dried rhizome of Alisma orientale (Sam.) Juzep, is a well-known, traditional medicine that is used for the various biological activities including as a diuretic, to lower cholesterol and as an anti-inflammatory agent. The present study was carried out to investigate the potential toxicity of the Alismatis rhizoma aqueous extract (ARAE) following 90-day repeated oral administration to Sprague-Dawley rats. ARAE was administered orally to male and female rats for 90 days at 0 (control), 500, 1,000 and 2,000 mg/kg/day (n = 10 for male and female rats for each dose). Additional recovery groups from the control group and high dose group were observed for a 28-day recovery period. Chromatograms of ARAE detected main compounds with four peaks. Treatment-related effects including an increase in the red blood cells, hemoglobin, hematocrit, albumin, total protein, and urine volume were observed in males of the 2,000 mg/kg/day group (p < 0.05). However, the diuretic effect of ARAE was considered, a major cause of hematological and serum biochemical changes. The oral no-observed-adverse-effect level (NOAEL) of the ARAE was > 2,000 mg/kg/day in both genders, and no target organs were identified.
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spelling pubmed-64673582019-04-23 A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats Lee, Mu-Jin Jung, Ho-Kyung Lee, Ki-Ho Jang, Ji-Hun Sim, Mi-Ok Seong, Tea-Gyeong Ahn, Byung-Kwan Shon, Jin-Han Ham, Seong-Ho Cho, Hyun-Woo Kim, Yong-Min Park, Sung-Jin Yoon, Ji-Young Ko, Je-Won Kim, Jong-Choon Toxicol Res Original Article Alismatis rhizoma (AR), the dried rhizome of Alisma orientale (Sam.) Juzep, is a well-known, traditional medicine that is used for the various biological activities including as a diuretic, to lower cholesterol and as an anti-inflammatory agent. The present study was carried out to investigate the potential toxicity of the Alismatis rhizoma aqueous extract (ARAE) following 90-day repeated oral administration to Sprague-Dawley rats. ARAE was administered orally to male and female rats for 90 days at 0 (control), 500, 1,000 and 2,000 mg/kg/day (n = 10 for male and female rats for each dose). Additional recovery groups from the control group and high dose group were observed for a 28-day recovery period. Chromatograms of ARAE detected main compounds with four peaks. Treatment-related effects including an increase in the red blood cells, hemoglobin, hematocrit, albumin, total protein, and urine volume were observed in males of the 2,000 mg/kg/day group (p < 0.05). However, the diuretic effect of ARAE was considered, a major cause of hematological and serum biochemical changes. The oral no-observed-adverse-effect level (NOAEL) of the ARAE was > 2,000 mg/kg/day in both genders, and no target organs were identified. Korean Society of Toxicology 2019-04 2019-04-15 /pmc/articles/PMC6467358/ /pubmed/31015901 http://dx.doi.org/10.5487/TR.2019.35.2.191 Text en Copyright © 2019 The Korean Society Of Toxicology http://creativecommons.org/licenses/by-nc/3.0 This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Mu-Jin
Jung, Ho-Kyung
Lee, Ki-Ho
Jang, Ji-Hun
Sim, Mi-Ok
Seong, Tea-Gyeong
Ahn, Byung-Kwan
Shon, Jin-Han
Ham, Seong-Ho
Cho, Hyun-Woo
Kim, Yong-Min
Park, Sung-Jin
Yoon, Ji-Young
Ko, Je-Won
Kim, Jong-Choon
A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats
title A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats
title_full A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats
title_fullStr A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats
title_full_unstemmed A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats
title_short A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats
title_sort 90-day repeated oral dose toxicity study of alismatis rhizoma aqueous extract in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467358/
https://www.ncbi.nlm.nih.gov/pubmed/31015901
http://dx.doi.org/10.5487/TR.2019.35.2.191
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