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Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice

BACKGROUND/AIMS: It is undetermined if herbal medicines (HM) containing aristolochic acid (AA)-containing have similar nephrotoxicity to AA itself. METHODS: We administered HM containing a high concentration of AA for 5 days (short-term study) or a low concentration of AA for 30 days (long-term stud...

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Autores principales: Quan, Yi, Jin, Long, Luo, Kang, Jin, Jian, Lim, Sun Woo, Shin, Yoo Jin, Ko, Eun Jeong, Chung, Byung Ha, Yang, Chul Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060994/
https://www.ncbi.nlm.nih.gov/pubmed/31739654
http://dx.doi.org/10.3904/kjim.2018.280
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author Quan, Yi
Jin, Long
Luo, Kang
Jin, Jian
Lim, Sun Woo
Shin, Yoo Jin
Ko, Eun Jeong
Chung, Byung Ha
Yang, Chul Woo
author_facet Quan, Yi
Jin, Long
Luo, Kang
Jin, Jian
Lim, Sun Woo
Shin, Yoo Jin
Ko, Eun Jeong
Chung, Byung Ha
Yang, Chul Woo
author_sort Quan, Yi
collection PubMed
description BACKGROUND/AIMS: It is undetermined if herbal medicines (HM) containing aristolochic acid (AA)-containing have similar nephrotoxicity to AA itself. METHODS: We administered HM containing a high concentration of AA for 5 days (short-term study) or a low concentration of AA for 30 days (long-term study) to C57BL/6 mice; for comparison, same dose of AA compound was used as controls. RESULTS: The nephrotoxicity in the HM- and AA-treated mice was compared in terms of renal function, histopathology, oxidative stress, apoptotic cell death, and mitochondrial damage. Short-term HM treatment resulted in acute kidney injury (marked renal dysfunction, acute tubular necrosis, and neutrophil gelatinase-associated lipocalin [NGAL] expression) in which the severity of renal dysfunction and histopathology was comparable with that induced by the administration of AA alone. Long-term HM treatment resulted in features of chronic kidney disease (CKD, mild renal dysfunction and tubular atrophy and dilatation). No significant differences in these parameters were observed between the HM- and AA-treated mice. HM-induced oxidative stress (8-hydroxy-2’-deoxyguanosine and manganese- dependent superoxide dismutase expression) and apoptotic cell death (terminal deoxynucleotidyl transferase dUTP nick end labelling [TUNEL]-positive cells and active caspase-3 expression) were similar in HM- and AA-treated mice in the short-term and long-term studies. Mitochondrial injury, evaluated by electron microscopy, was also similar in HM- and AA-treated mice in the short-term and long-term studies. CONCLUSIONS: The nephrotoxic potential of HM containing AA was similar to that of AA itself.
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spelling pubmed-70609942020-03-16 Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice Quan, Yi Jin, Long Luo, Kang Jin, Jian Lim, Sun Woo Shin, Yoo Jin Ko, Eun Jeong Chung, Byung Ha Yang, Chul Woo Korean J Intern Med Original Article BACKGROUND/AIMS: It is undetermined if herbal medicines (HM) containing aristolochic acid (AA)-containing have similar nephrotoxicity to AA itself. METHODS: We administered HM containing a high concentration of AA for 5 days (short-term study) or a low concentration of AA for 30 days (long-term study) to C57BL/6 mice; for comparison, same dose of AA compound was used as controls. RESULTS: The nephrotoxicity in the HM- and AA-treated mice was compared in terms of renal function, histopathology, oxidative stress, apoptotic cell death, and mitochondrial damage. Short-term HM treatment resulted in acute kidney injury (marked renal dysfunction, acute tubular necrosis, and neutrophil gelatinase-associated lipocalin [NGAL] expression) in which the severity of renal dysfunction and histopathology was comparable with that induced by the administration of AA alone. Long-term HM treatment resulted in features of chronic kidney disease (CKD, mild renal dysfunction and tubular atrophy and dilatation). No significant differences in these parameters were observed between the HM- and AA-treated mice. HM-induced oxidative stress (8-hydroxy-2’-deoxyguanosine and manganese- dependent superoxide dismutase expression) and apoptotic cell death (terminal deoxynucleotidyl transferase dUTP nick end labelling [TUNEL]-positive cells and active caspase-3 expression) were similar in HM- and AA-treated mice in the short-term and long-term studies. Mitochondrial injury, evaluated by electron microscopy, was also similar in HM- and AA-treated mice in the short-term and long-term studies. CONCLUSIONS: The nephrotoxic potential of HM containing AA was similar to that of AA itself. The Korean Association of Internal Medicine 2020-03 2019-11-21 /pmc/articles/PMC7060994/ /pubmed/31739654 http://dx.doi.org/10.3904/kjim.2018.280 Text en Copyright © 2020 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Quan, Yi
Jin, Long
Luo, Kang
Jin, Jian
Lim, Sun Woo
Shin, Yoo Jin
Ko, Eun Jeong
Chung, Byung Ha
Yang, Chul Woo
Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice
title Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice
title_full Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice
title_fullStr Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice
title_full_unstemmed Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice
title_short Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice
title_sort assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060994/
https://www.ncbi.nlm.nih.gov/pubmed/31739654
http://dx.doi.org/10.3904/kjim.2018.280
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