2018
DOI: 10.1016/j.biopha.2018.01.083
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Selenium nanoparticles prevents lead acetate-induced hypothyroidism and oxidative damage of thyroid tissues in male rats through modulation of selenoenzymes and suppression of miR-224

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Cited by 28 publications
(11 citation statements)
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“…In another study, nanoselenium was found to be less toxic than SeMet in inducing liver toxicity in mice [148], although both nanosized Se and SeMet increased the liver and kidney GPx and TrxR activity with similar efficacy [148]. There are reports on the protective effects of nanoselenium against various toxic elements such as lead [149] and chromium (VI) [150] as well as the ameliorative action of nanoselenium against As III already mentioned in earlier chapters [99]. Altogether, nanoselenium appears as a very attractive form of Se for the treatment of As III or Cd intoxication, but more studies on this topic are needed.…”
Section: Discussionmentioning
confidence: 99%
“…In another study, nanoselenium was found to be less toxic than SeMet in inducing liver toxicity in mice [148], although both nanosized Se and SeMet increased the liver and kidney GPx and TrxR activity with similar efficacy [148]. There are reports on the protective effects of nanoselenium against various toxic elements such as lead [149] and chromium (VI) [150] as well as the ameliorative action of nanoselenium against As III already mentioned in earlier chapters [99]. Altogether, nanoselenium appears as a very attractive form of Se for the treatment of As III or Cd intoxication, but more studies on this topic are needed.…”
Section: Discussionmentioning
confidence: 99%
“…For example, co-administration of nano-Se high dose along with di- n -butyl phthalate significantly decreased the level of MDA, and also improved GSH concentration and GPx and SOD activities initially compromised by the toxicant treatment (Rashad et al ., 2018). Similarly, in male rats treated with lead acetate, oxidative stress was observed in thyroid tissues and nano-Se supplementation restored antioxidant defence mechanisms (GPx, catalase (CAT), SOD, and GSH) and expression of iodothyronine deiodinase type 1 which were compromised due to the lead-acetate treatment (Atteia et al ., 2018). Protective effects of nano-Se against oxidative stress and testicular damage induced by free-radical producing chemical bisphenol A (BPA) was also shown (Abdel-Halim et al ., 2016).…”
Section: Discussionmentioning
confidence: 99%
“…In the experiments of proving the effect of Nano-Se on hyperhomocysteinemic rats, SD rats or SHRs or Wistar rats were randomly divided into a Hcy group and a Hcy+Nano-Se group with 6 rats per group, respectively. The protocol of the study, including doses and duration of treatment for Nano-Se, were all designed according to our pilot studies and previous reports, [18][19][20] which have demonstrated its protective effects. Chronic hyperhomocysteinemia was induced as described previously, 21,22 with a minor modification.…”
Section: Animals and Treatmentmentioning
confidence: 99%