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Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents

The present study aimed to evaluate the acute and subacute toxicity profiles of Erodium guttatum extracts in mice using the methods described in the guidelines of the OECD. In the acute toxicity study, the LD(50) value was greater than 2000 mg/kg. The subacute toxicity study of E. guttatum extracts...

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Autores principales: Benrahou, Kaoutar, Mrabti, Hanae Naceiri, Assaggaf, Hamza M., Mortada, Salma, Salhi, Najoua, Rouas, Lamiaa, El Bacha, Rim, Dami, Abdellah, Masrar, Azlarab, Alshahrani, Mohammed Merae, Awadh, Ahmed Abdullah Al, Bouyahya, Abdelhakim, Goh, Khang Wen, Ming, Long Chiau, Cherrah, Yahia, Faouzi, My El Abbes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695652/
https://www.ncbi.nlm.nih.gov/pubmed/36355985
http://dx.doi.org/10.3390/toxins14110735
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author Benrahou, Kaoutar
Mrabti, Hanae Naceiri
Assaggaf, Hamza M.
Mortada, Salma
Salhi, Najoua
Rouas, Lamiaa
El Bacha, Rim
Dami, Abdellah
Masrar, Azlarab
Alshahrani, Mohammed Merae
Awadh, Ahmed Abdullah Al
Bouyahya, Abdelhakim
Goh, Khang Wen
Ming, Long Chiau
Cherrah, Yahia
Faouzi, My El Abbes
author_facet Benrahou, Kaoutar
Mrabti, Hanae Naceiri
Assaggaf, Hamza M.
Mortada, Salma
Salhi, Najoua
Rouas, Lamiaa
El Bacha, Rim
Dami, Abdellah
Masrar, Azlarab
Alshahrani, Mohammed Merae
Awadh, Ahmed Abdullah Al
Bouyahya, Abdelhakim
Goh, Khang Wen
Ming, Long Chiau
Cherrah, Yahia
Faouzi, My El Abbes
author_sort Benrahou, Kaoutar
collection PubMed
description The present study aimed to evaluate the acute and subacute toxicity profiles of Erodium guttatum extracts in mice using the methods described in the guidelines of the OECD. In the acute toxicity study, the LD(50) value was greater than 2000 mg/kg. The subacute toxicity study of E. guttatum extracts showed no significant changes in body or organ weights. The administration of E. guttatum extracts to mice at a dose of 200 mg/kg led to an increase in white blood cells, platelets and hemoglobin. Moreover, the aqueous extract of E. guttatum only decreased liver aspartate aminotransferase (ASAT) levels at a dose of 200 mg/kg, and creatinine and urea levels did not show any significant alterations compared to the control group. Our results showed that the extracts of E. guttatum caused a slight increase in alanine aminotransferase (ALAT) and triglycerides. The histological study showed that mice treated with E. guttatum extracts experienced some histopathological changes in the liver, particularly with the methanolic extract, and slight changes in the kidneys and pancreas. Regarding the renal profile, no toxicity was observed. These results provide basic information on the toxicological profile of E. guttatum used in traditional medicine.
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spelling pubmed-96956522022-11-26 Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents Benrahou, Kaoutar Mrabti, Hanae Naceiri Assaggaf, Hamza M. Mortada, Salma Salhi, Najoua Rouas, Lamiaa El Bacha, Rim Dami, Abdellah Masrar, Azlarab Alshahrani, Mohammed Merae Awadh, Ahmed Abdullah Al Bouyahya, Abdelhakim Goh, Khang Wen Ming, Long Chiau Cherrah, Yahia Faouzi, My El Abbes Toxins (Basel) Article The present study aimed to evaluate the acute and subacute toxicity profiles of Erodium guttatum extracts in mice using the methods described in the guidelines of the OECD. In the acute toxicity study, the LD(50) value was greater than 2000 mg/kg. The subacute toxicity study of E. guttatum extracts showed no significant changes in body or organ weights. The administration of E. guttatum extracts to mice at a dose of 200 mg/kg led to an increase in white blood cells, platelets and hemoglobin. Moreover, the aqueous extract of E. guttatum only decreased liver aspartate aminotransferase (ASAT) levels at a dose of 200 mg/kg, and creatinine and urea levels did not show any significant alterations compared to the control group. Our results showed that the extracts of E. guttatum caused a slight increase in alanine aminotransferase (ALAT) and triglycerides. The histological study showed that mice treated with E. guttatum extracts experienced some histopathological changes in the liver, particularly with the methanolic extract, and slight changes in the kidneys and pancreas. Regarding the renal profile, no toxicity was observed. These results provide basic information on the toxicological profile of E. guttatum used in traditional medicine. MDPI 2022-10-27 /pmc/articles/PMC9695652/ /pubmed/36355985 http://dx.doi.org/10.3390/toxins14110735 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Benrahou, Kaoutar
Mrabti, Hanae Naceiri
Assaggaf, Hamza M.
Mortada, Salma
Salhi, Najoua
Rouas, Lamiaa
El Bacha, Rim
Dami, Abdellah
Masrar, Azlarab
Alshahrani, Mohammed Merae
Awadh, Ahmed Abdullah Al
Bouyahya, Abdelhakim
Goh, Khang Wen
Ming, Long Chiau
Cherrah, Yahia
Faouzi, My El Abbes
Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents
title Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents
title_full Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents
title_fullStr Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents
title_full_unstemmed Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents
title_short Acute and Subacute Toxicity Studies of Erodium guttatum Extracts by Oral Administration in Rodents
title_sort acute and subacute toxicity studies of erodium guttatum extracts by oral administration in rodents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695652/
https://www.ncbi.nlm.nih.gov/pubmed/36355985
http://dx.doi.org/10.3390/toxins14110735
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