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Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats

OBJECTIVES: Asafetida is traditionally used in folklore medicine for the treatment of various ailments. To validate its use in traditional medicine, it is important to evaluate its toxicity in the animal system. Therefore, this study aimed to evaluate the toxicological effects of asafetida in Wistar...

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Autores principales: Bagheri, Seyyed Majid, Yadegari, Maryam, Mirjalily, Aghdas, Rezvani, Mohammd Ebrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721178/
https://www.ncbi.nlm.nih.gov/pubmed/26862262
http://dx.doi.org/10.4103/0971-6580.172258
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author Bagheri, Seyyed Majid
Yadegari, Maryam
Mirjalily, Aghdas
Rezvani, Mohammd Ebrahim
author_facet Bagheri, Seyyed Majid
Yadegari, Maryam
Mirjalily, Aghdas
Rezvani, Mohammd Ebrahim
author_sort Bagheri, Seyyed Majid
collection PubMed
description OBJECTIVES: Asafetida is traditionally used in folklore medicine for the treatment of various ailments. To validate its use in traditional medicine, it is important to evaluate its toxicity in the animal system. Therefore, this study aimed to evaluate the toxicological effects of asafetida in Wistar albino rats. MATERIALS AND METHODS: Acute toxicity tests were conducted by the oral administration of 250, 500, and 1,000 mg/kg body weight of the animal. In chronic study, animals were administered with various doses of asafetida (25, 50, 100, and 200 mg/kg body weight) for a period of 6 weeks. At end of experiment, the effects of asafetida on hematological, renal, and hepatic markers and histological parameters were analyzed. RESULTS: In acute toxicity study, no mortality was seen up to 72 h of the administration of asafetida. No signs of neurological and behavioral changes were noticed within 24 h. In the chronic study, the asafetida intake has changed the hematological parameters such as red blood cell (RBC), white blood cell (WBC), hematocrit (HCT), and platelets. Aspartate aminotransferase (AST) and lactate dehydrogenase (LDH) were significantly increased in treated animals. The plasma level of urea and creatinine were not altered by the administration of asafetida throughout the study. Histopathology study indicates hepatotoxicity, but no signs of prominent pathological changes in kidney. CONCLUSIONS: Asafetida did not show any acute toxicity, but chronic administration could have undesirable effects on hepatocytes and hematological factors.
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spelling pubmed-47211782016-02-09 Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats Bagheri, Seyyed Majid Yadegari, Maryam Mirjalily, Aghdas Rezvani, Mohammd Ebrahim Toxicol Int Original Article OBJECTIVES: Asafetida is traditionally used in folklore medicine for the treatment of various ailments. To validate its use in traditional medicine, it is important to evaluate its toxicity in the animal system. Therefore, this study aimed to evaluate the toxicological effects of asafetida in Wistar albino rats. MATERIALS AND METHODS: Acute toxicity tests were conducted by the oral administration of 250, 500, and 1,000 mg/kg body weight of the animal. In chronic study, animals were administered with various doses of asafetida (25, 50, 100, and 200 mg/kg body weight) for a period of 6 weeks. At end of experiment, the effects of asafetida on hematological, renal, and hepatic markers and histological parameters were analyzed. RESULTS: In acute toxicity study, no mortality was seen up to 72 h of the administration of asafetida. No signs of neurological and behavioral changes were noticed within 24 h. In the chronic study, the asafetida intake has changed the hematological parameters such as red blood cell (RBC), white blood cell (WBC), hematocrit (HCT), and platelets. Aspartate aminotransferase (AST) and lactate dehydrogenase (LDH) were significantly increased in treated animals. The plasma level of urea and creatinine were not altered by the administration of asafetida throughout the study. Histopathology study indicates hepatotoxicity, but no signs of prominent pathological changes in kidney. CONCLUSIONS: Asafetida did not show any acute toxicity, but chronic administration could have undesirable effects on hepatocytes and hematological factors. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4721178/ /pubmed/26862262 http://dx.doi.org/10.4103/0971-6580.172258 Text en Copyright: © Toxicology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Bagheri, Seyyed Majid
Yadegari, Maryam
Mirjalily, Aghdas
Rezvani, Mohammd Ebrahim
Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats
title Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats
title_full Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats
title_fullStr Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats
title_full_unstemmed Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats
title_short Evaluation of Toxicity Effects of Asafetida on Biochemical, Hematological, and Histological Parameters in Male Wistar Rats
title_sort evaluation of toxicity effects of asafetida on biochemical, hematological, and histological parameters in male wistar rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721178/
https://www.ncbi.nlm.nih.gov/pubmed/26862262
http://dx.doi.org/10.4103/0971-6580.172258
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