2022
DOI: 10.1016/j.toxrep.2022.07.015
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Evaluating effect of acrylamide and ascorbic acid on oxidative stress and apoptosis in ovarian tissue of wistar rat

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Cited by 13 publications
(12 citation statements)
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“…This gene is a protective factor against oxidative stress damage, so its up-regulation in the FA group indicates the external induction of oxidative stress. Similarly, several studies have reported that KL can attenuate oxidative damage and apoptosis [ 24 , 25 ].…”
Section: Resultsmentioning
confidence: 96%
“…This gene is a protective factor against oxidative stress damage, so its up-regulation in the FA group indicates the external induction of oxidative stress. Similarly, several studies have reported that KL can attenuate oxidative damage and apoptosis [ 24 , 25 ].…”
Section: Resultsmentioning
confidence: 96%
“…Oxidative stress response was activated by all chemicals in the ARE- bla and the AREc32 assay (Table and Figures S2 and S4), which is in line with previous studies which identified acrylamide as an activator of oxidative stress response in vitro , and in vivo . NMBA showed the strongest effect in both assays.…”
Section: Resultsmentioning
confidence: 99%
“…AA can damage the reproductive system by damaging normal Sertoli cells in male rats and the function of Leydig cells, as well as induce the abnormal secretion of testosterone and luteinizing hormone, resulting in abnormal sperm-related gene expression, decreasing the number of sperm to reduce the activity of sperm, and increasing the sperm deformity rate [49,50]. Further, AA can induce ovarian dysfunction in female Wistar rats by upregulating apoptosis-related genes [51]. d. Other toxicities: AA can damage the liver, kidneys, lungs, bladder, and digestive tract and may even cause testicular mesothelioma, adrenal cortical adenoma, astrocytoma, and oral tumors [52].…”
Section: Potential Hazards Of Aamentioning
confidence: 99%