2021
DOI: 10.1016/j.cbi.2020.109314
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Impact of prenatal arsenic exposure on the testes and epididymides of prepubertal rats

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Cited by 16 publications
(18 citation statements)
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“…Chronic As trioxide exposure to parental male at a dose of 1 mg/L showed genotoxic damage in F0-F3, altered methylation patterns, changes in reproductive parameters, morphological damage in the ovaries (F0 and F1) and testicles (F1-F3), and compromised sperm quality (F0-F3, except F2) [138]. Exposure of sodium arsenite at the dose of 10 mg/L in drinking water to pregnant females from GD1-21 affected body weight and initial sexual development in male pups and relative anogenital distance also showed changes in the expression of SOD1, SOD2, CAT, and GSTK1 gene in male pup rat [139]. Administration of sodium arsenite at a concentration of 10 mg/L showed lower sperm production, sperm count, motility, and quality in the epididymis of rats [140].…”
Section: Pre-natal Arsenic Exposure Induced Male Reproductive Toxicit...mentioning
confidence: 99%
“…Chronic As trioxide exposure to parental male at a dose of 1 mg/L showed genotoxic damage in F0-F3, altered methylation patterns, changes in reproductive parameters, morphological damage in the ovaries (F0 and F1) and testicles (F1-F3), and compromised sperm quality (F0-F3, except F2) [138]. Exposure of sodium arsenite at the dose of 10 mg/L in drinking water to pregnant females from GD1-21 affected body weight and initial sexual development in male pups and relative anogenital distance also showed changes in the expression of SOD1, SOD2, CAT, and GSTK1 gene in male pup rat [139]. Administration of sodium arsenite at a concentration of 10 mg/L showed lower sperm production, sperm count, motility, and quality in the epididymis of rats [140].…”
Section: Pre-natal Arsenic Exposure Induced Male Reproductive Toxicit...mentioning
confidence: 99%
“…So, the pathology of metabolically active organs like renal and hepatic tissues is a good experimental tool to study arsenic toxicity. Furthermore, arsenic is also responsible for damaging the male reproductive function in rats and mice and, after that, causing reduced spermatogenesis, sperm counts and motility (Liu et al, 2021;Souza et al, 2021). It also inhibits testosterone release, the function of the testicular enzyme and atrophy of male genital organs.…”
Section: Small Animal Model Using Rodentsmentioning
confidence: 99%
“…It has been reported that sodium arsenite causes declined mRNA expression of epididymal SOD1, SOD2, CAT and GST, which undoubtedly impede epididymal redox status and leads to reproductive disorders (Figure 4). 93 A recent finding has further elucidated that arsenic enhances the NO2/NO3 levels in the epididymis and thereby promotes nitrosative stress. 94 Another study on arsenic exposed epididymis of post-natal rats (52 days age) has reported a significant up-regulation of SOD1, CAT and GSTK1 genes in response to combat with the arsenic-induced oxidative stress.…”
Section: Redox Balancementioning
confidence: 99%
“…87 Increase of MDA level and decrease of enzymatic CAT activity have also been observed also suggesting altered redox state. 87 Recently Souza ACF 93 has reported that arsenic exposure on post-natal rats of 14 and 28 days caused increased activity of CAT to neutralize arsenic induced reactive species but exhaustion occurred finally reducing the activity below normal level. Souza ACF 93 has also stated that arsenic induced reduction of epididymal GST activity in post-natal rats of 28 days validating the malfunction of antioxidant enzyme that act against arsenic mediated oxidative stress.…”
Section: Redox Balancementioning
confidence: 99%