Oxidative Damage and Nrf2 Translocation Induced by Toxicities of Deoxynivalenol on the Placental and Embryo on Gestation Day 12.5 d and 18.5 d.
Oxidative Damage and Nrf2 Translocation Induced by Toxicities of Deoxynivalenol on the Placental and Embryo on Gestation Day 12.5 d and 18.5 d.
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脱氧雪腐镰刀菌烯醇毒性对妊娠12.5天和18.5天胎盘和胚胎的氧化损伤和Nrf2易位
DOI:
10.3390/toxins10090370
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发表时间:
2018-09-13
期刊:
影响因子:
4.2
通讯作者:
Chen JH
中科院分区:
文献类型:
--
作者:
Yu M;Wei ZY;Xu ZH;Pan JQ;Chen JH
Deoxynivalenol (DON) is a kind of natural pollutant belonging to the trichothecenes family. The aim of this study is to use diverse assays to evaluate oxidative damage as well as translocation of nuclear factor erythroid 2-related factor 2 (Nrf2), and to investigate their mechanisms in DON-induced toxicities on a placenta and embryo. Pregnant C57BL/6 mice were randomly assigned to three groups with different doses of DON: 0, 1.0, 2.5 mg/(kg·day). In gestation day (GD) 12.5 d and 18.5 d, DON induced an elevated resorption rate of the embryos as well as structural and functional damage of the placenta. In the placenta, altered levels of the antioxidant enzymes malondialdehyde, superoxide dismutase and glutathione indicated remarkable oxidative stress. Furthermore, an elevated level of heme oxygenase-1 (HO-1) and the translocation of Nrf2 from nucleus to cytoplasm indicated Nrf2/HO-1 pathway activation in DON-L group (1.0 mg/(kg·day)). It is noteworthy that the results in this experiment in GD 12.5 d were similar to those in GD 18.5 d. In conclusion, DON-induced placental oxidative damage and Nrf2 translocation were similar in GD 12.5 d and GD 18.5 d. Oxidative stress is one of the most important molecular mechanisms for embryotoxicity induced by DON, and Nrf2 translocation may play a substantial role against it.
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影响因子:
4.7
作者:
Mitsuishi Y;Motohashi H;Yamamoto M
通讯作者:
Yamamoto M
影响因子:
3.3
作者:
Katika, Madhumohan R.;Hendriksen, Peter J. M.;Peijnenburg, Ad A. C. M.
通讯作者:
Peijnenburg, Ad A. C. M.
影响因子:
4.3
作者:
Duan, Yang;Sun, Fuqiang;Liu, Geli
通讯作者:
Liu, Geli
影响因子:
4.8
作者:
Foresti, R;Clark, JE;Motterlini, R
通讯作者:
Motterlini, R
影响因子:
3.8
作者:
KURMAN, RJ;MAIN, CS;CHEN, HC
通讯作者:
CHEN, HC