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

Research Authors
Maryam AL-ghamdi, Etimad Huwait1, Nagwa Elsawi, Soad Shaker Ali, Ahmed Sayed
Research Abstract

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 LD50 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 < 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.

Research Department
Research Journal
International Journal of Reproductive BioMedicine
Research Publisher
Knowledge E
Research Vol
21
Research Website
https://doi.org/10.18502/ijrm.v21i1.12668
Research Year
2023
Research Pages
61-70