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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9695652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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