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Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide

Currently, living organisms are increasingly exposed to many toxic chemicals in the environment. These substances pose a threat to human life, other living organisms and ecosystem. In fact, there is an increasing requirement to search for safe therapeutic sources today. Medicinal plants and natural...

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Autor principal: Al-Attar, Atef M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716955/
https://www.ncbi.nlm.nih.gov/pubmed/35002463
http://dx.doi.org/10.1016/j.sjbs.2021.10.037
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author Al-Attar, Atef M.
author_facet Al-Attar, Atef M.
author_sort Al-Attar, Atef M.
collection PubMed
description Currently, living organisms are increasingly exposed to many toxic chemicals in the environment. These substances pose a threat to human life, other living organisms and ecosystem. In fact, there is an increasing requirement to search for safe therapeutic sources today. Medicinal plants and natural products have become of great importance globally because of their therapeutic potential and medicinal properties, as well as their availability and the absence of harmful side effects for most of them. The present study was designed to explore the potential protective effect of curcumin (CUR) and thymoquinone (TQ) in male rats exposed to thioacetamide (TAA). The experimental mice were divided into eight groups. Group 1 was served as control. Group 2 was exposed to 50 mg/ kg body weight of TAA. Group 3 was exposed to CUR and TAA. Mice of group 4 were treated with TQ and TAA. Mice of group 5 were exposed to CUR plus TQ and TAA. Group 6 was supplemented with CUR. Group 7 was subjected to TQ. Mice of group 8 were treated with CUR and TQ. Hematological and biochemical alterations were evaluated after one month. Significant increases of white blood corpuscles (WBC), alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total bilirubin (TB), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) values were observed in group 2, while the values of red blood corpuscles (RBC), hemoglobin (Hb(, hematocrit (Hct), glutathione (GSH) and superoxide dismutase (SOD) were statistically decreased. Treatment with CUR, TQ and their combination inhibited the hematological and biochemical alterations induced by TAA toxicity. Moreover, the most protective effect was observed in mice treated with CUR plus TQ. These new results suggested that the protective effect of CUR and TQ attributed to their antioxidant properties.
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spelling pubmed-87169552022-01-06 Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide Al-Attar, Atef M. Saudi J Biol Sci Original Article Currently, living organisms are increasingly exposed to many toxic chemicals in the environment. These substances pose a threat to human life, other living organisms and ecosystem. In fact, there is an increasing requirement to search for safe therapeutic sources today. Medicinal plants and natural products have become of great importance globally because of their therapeutic potential and medicinal properties, as well as their availability and the absence of harmful side effects for most of them. The present study was designed to explore the potential protective effect of curcumin (CUR) and thymoquinone (TQ) in male rats exposed to thioacetamide (TAA). The experimental mice were divided into eight groups. Group 1 was served as control. Group 2 was exposed to 50 mg/ kg body weight of TAA. Group 3 was exposed to CUR and TAA. Mice of group 4 were treated with TQ and TAA. Mice of group 5 were exposed to CUR plus TQ and TAA. Group 6 was supplemented with CUR. Group 7 was subjected to TQ. Mice of group 8 were treated with CUR and TQ. Hematological and biochemical alterations were evaluated after one month. Significant increases of white blood corpuscles (WBC), alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total bilirubin (TB), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) values were observed in group 2, while the values of red blood corpuscles (RBC), hemoglobin (Hb(, hematocrit (Hct), glutathione (GSH) and superoxide dismutase (SOD) were statistically decreased. Treatment with CUR, TQ and their combination inhibited the hematological and biochemical alterations induced by TAA toxicity. Moreover, the most protective effect was observed in mice treated with CUR plus TQ. These new results suggested that the protective effect of CUR and TQ attributed to their antioxidant properties. Elsevier 2022-01 2021-10-22 /pmc/articles/PMC8716955/ /pubmed/35002463 http://dx.doi.org/10.1016/j.sjbs.2021.10.037 Text en © 2021 The Author https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Al-Attar, Atef M.
Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide
title Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide
title_full Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide
title_fullStr Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide
title_full_unstemmed Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide
title_short Hematological and biochemical investigations on the effect of curcumin and Thymoquinone in male mice exposed to Thioacetamide
title_sort hematological and biochemical investigations on the effect of curcumin and thymoquinone in male mice exposed to thioacetamide
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716955/
https://www.ncbi.nlm.nih.gov/pubmed/35002463
http://dx.doi.org/10.1016/j.sjbs.2021.10.037
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