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Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study

BACKGROUND: Acrylamide (AA) is a carcinogenic compound that causes severe reproductive impairments and represents a high environmental risk factor. Thymoquinone (TQ) has a unique antioxidant activity and has been widely used as a protective agent against various types of toxicity. OBJECTIVE: To eval...

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Autores principales: AL-ghamdi, Maryam, Huwait, Etimad, Elsawi, Nagwa, Shaker Ali, Soad, Sayed, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982326/
https://www.ncbi.nlm.nih.gov/pubmed/36875499
http://dx.doi.org/10.18502/ijrm.v21i1.12668
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author AL-ghamdi, Maryam
Huwait, Etimad
Elsawi, Nagwa
Shaker Ali, Soad
Sayed, Ahmed
author_facet AL-ghamdi, Maryam
Huwait, Etimad
Elsawi, Nagwa
Shaker Ali, Soad
Sayed, Ahmed
author_sort AL-ghamdi, Maryam
collection PubMed
description BACKGROUND: Acrylamide (AA) is a carcinogenic compound that causes severe reproductive impairments and represents a high environmental risk factor. Thymoquinone (TQ) has a unique antioxidant activity and has been widely used as a protective agent against various types of toxicity. OBJECTIVE: To evaluate the protective effects of TQ against AA-induced reproductive toxicity in female rats. MATERIALS AND METHODS: In this experimental study, 40 female albino rats (120-150 gr, 8-10 wk) were sorted into 4 groups, (n = 10/each), vehicle group (received a daily oral administration of 0.5 ml saline [9%]); AA group (received a daily oral administration with freshly prepared AA, 20 mg/kg body weight) for 21 days which is less than the lethal dose LD [Formula: see text] of AA in rats (20 mg/kg body weight); AA+TQ group (received a daily oral administration of TQ, 10 mg/kg body weight) after AA intoxication for 21 days, and TQ group (received a daily oral administration of TQ only, 10 mg/kg body weight) for 21 consecutive days. Reproductive hormones, carcinogenic biomarkers, and oxidative stress markers were measured. The histological assessment showed the protective effect of TQ against AA-induced ovarian injury. Network pharmacology analysis and molecular docking approach were carried out to determine the binding affinity of TQ with cyclooxygenase 2. RESULTS: TQ administration significantly enhanced the functional capacity of the ovary at hormones, oxidative biomarkers, and tumor markers at a significant level of p [Formula: see text] 0.001. Besides, TQ protects the ovary of AA-treated rats from the severe degeneration effect. CONCLUSION: TQ showed a promising protective effect against AA-induced reproductive toxicity in female rats.
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spelling pubmed-99823262023-03-04 Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study AL-ghamdi, Maryam Huwait, Etimad Elsawi, Nagwa Shaker Ali, Soad Sayed, Ahmed Int J Reprod Biomed Original Article BACKGROUND: Acrylamide (AA) is a carcinogenic compound that causes severe reproductive impairments and represents a high environmental risk factor. Thymoquinone (TQ) has a unique antioxidant activity and has been widely used as a protective agent against various types of toxicity. OBJECTIVE: To evaluate the protective effects of TQ against AA-induced reproductive toxicity in female rats. MATERIALS AND METHODS: In this experimental study, 40 female albino rats (120-150 gr, 8-10 wk) were sorted into 4 groups, (n = 10/each), vehicle group (received a daily oral administration of 0.5 ml saline [9%]); AA group (received a daily oral administration with freshly prepared AA, 20 mg/kg body weight) for 21 days which is less than the lethal dose LD [Formula: see text] of AA in rats (20 mg/kg body weight); AA+TQ group (received a daily oral administration of TQ, 10 mg/kg body weight) after AA intoxication for 21 days, and TQ group (received a daily oral administration of TQ only, 10 mg/kg body weight) for 21 consecutive days. Reproductive hormones, carcinogenic biomarkers, and oxidative stress markers were measured. The histological assessment showed the protective effect of TQ against AA-induced ovarian injury. Network pharmacology analysis and molecular docking approach were carried out to determine the binding affinity of TQ with cyclooxygenase 2. RESULTS: TQ administration significantly enhanced the functional capacity of the ovary at hormones, oxidative biomarkers, and tumor markers at a significant level of p [Formula: see text] 0.001. Besides, TQ protects the ovary of AA-treated rats from the severe degeneration effect. CONCLUSION: TQ showed a promising protective effect against AA-induced reproductive toxicity in female rats. Knowledge E 2023-02-08 /pmc/articles/PMC9982326/ /pubmed/36875499 http://dx.doi.org/10.18502/ijrm.v21i1.12668 Text en Copyright © 2023 AL-ghamdi et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
AL-ghamdi, Maryam
Huwait, Etimad
Elsawi, Nagwa
Shaker Ali, Soad
Sayed, Ahmed
Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study
title Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study
title_full Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study
title_fullStr Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study
title_full_unstemmed Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study
title_short Thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: An experimental study
title_sort thymoquinone ameliorates acrylamide-induced reproductive toxicity in female rats: an experimental study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982326/
https://www.ncbi.nlm.nih.gov/pubmed/36875499
http://dx.doi.org/10.18502/ijrm.v21i1.12668
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