2019
DOI: 10.1007/s12011-019-01815-2
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The Footprints of Oxidative Stress and Mitochondrial Impairment in Arsenic Trioxide-Induced Testosterone Release Suppression in Pubertal and Mature F1-Male Balb/c Mice via the Downregulation of 3β-HSD, 17β-HSD, and CYP11a Expression

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Cited by 28 publications
(16 citation statements)
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“…Sperm motility, as a potential index of fertilizing ability, can adversely be affected by environmental (94,95), industrial (96,97), and pharmaceutical agents (98). In line with previous researches (20,21,(26)(27)(28)(29)(30)(31)57), we also observed a significant decrement in sperm viability, forward motility, plasma membrane integrity (HOS test), and sperm count, as well as an increment in sperm abnormality following treatment with CNTs. Severe OS along with mitochondrial dysfunction would impair the spermatogenesis and fertility through decrements in sperm viability, count, motility, and steroidogenesis, and an increment in the percentage of abnormal sperm, as well as alterations in histomorphology of the testes or accessory sex organs (20,(26)(27)(28)30).…”
Section: Discussionsupporting
confidence: 90%
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“…Sperm motility, as a potential index of fertilizing ability, can adversely be affected by environmental (94,95), industrial (96,97), and pharmaceutical agents (98). In line with previous researches (20,21,(26)(27)(28)(29)(30)(31)57), we also observed a significant decrement in sperm viability, forward motility, plasma membrane integrity (HOS test), and sperm count, as well as an increment in sperm abnormality following treatment with CNTs. Severe OS along with mitochondrial dysfunction would impair the spermatogenesis and fertility through decrements in sperm viability, count, motility, and steroidogenesis, and an increment in the percentage of abnormal sperm, as well as alterations in histomorphology of the testes or accessory sex organs (20,(26)(27)(28)30).…”
Section: Discussionsupporting
confidence: 90%
“…Mitochondrial impairment due to OS induction by CNTs in the present experiment could be an essential factor in CNTinduced reproductive toxicity. There are ample data in the literature showing that the abnormal levels of cellular glutathione (oxidized/reduced GSH) are closely interconnected with the induction of OS in reproductive organs (20,21,27,29); therefore, CNT-induced decreases in reduced GSH levels, and increases in oxidized GSH level in male gonads and gametes could trigger severe OS and complications. Spermatozoa are very sensitive to peroxidation due to the high level of polyunsaturated fatty acids (PUFAs) in the plasma membrane (26,32), adversely affecting the fertility potential (26,33,34).…”
Section: Discussionmentioning
confidence: 99%
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