2017
DOI: 10.1021/acs.jafc.6b05308
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Selenomethionine Alleviates AFB1-Induced Damage in Primary Chicken Hepatocytes by Inhibiting CYP450 1A5 Expression via Upregulated SelW Expression

Abstract: This study aims to evaluate the protective effects of selenomethionine (SeMet) on aflatoxin B1 (AFB1)-induced hepatotoxicity in primary chicken hepatocytes. Cell viability and lactic dehydrogenase activity assays revealed the dose dependence of AFB1 toxicity to chicken hepatocytes. AFB1 concentrations of >0.05 μg/mL significantly reduced glutathione and total superoxide dismutase levels and increased the malondialdehyde concentration and cytochrome P450 enzyme 1A5 (CYP450 1A5) mRNA levels (P < 0.05). AFB1, how… Show more

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Cited by 33 publications
(11 citation statements)
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References 55 publications
(106 reference statements)
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“…Surely, it would be interesting to use realistic AFB1 concentrations; however, treating cells with an amount of AFB1 slightly higher may help to highlight the molecular mechanisms involved in the toxicity. Notably, the increasing AFB1 concentrations chosen in the present study were in accordance to those selected in previous cytotoxic experiments conducted in human and chicken hepatocytes, as well as in similar transcriptomic studies aimed at unveiling AFB1 mechanism of toxicity in chicken hepatocellular carcinoma (LMH) and HepG2 cell lines [29][30][31][32][33]. Overall, these data confirm AFB1 is cytotoxic to bovine hepatocytes, as previously reported [24].…”
Section: Afb1 Cytotoxicity and Mechanism Of Cell Deathsupporting
confidence: 89%
“…Surely, it would be interesting to use realistic AFB1 concentrations; however, treating cells with an amount of AFB1 slightly higher may help to highlight the molecular mechanisms involved in the toxicity. Notably, the increasing AFB1 concentrations chosen in the present study were in accordance to those selected in previous cytotoxic experiments conducted in human and chicken hepatocytes, as well as in similar transcriptomic studies aimed at unveiling AFB1 mechanism of toxicity in chicken hepatocellular carcinoma (LMH) and HepG2 cell lines [29][30][31][32][33]. Overall, these data confirm AFB1 is cytotoxic to bovine hepatocytes, as previously reported [24].…”
Section: Afb1 Cytotoxicity and Mechanism Of Cell Deathsupporting
confidence: 89%
“…SelW is a selenoprotein with an essential role in maintaining normal liver function. According to this recent report, SeMet suppressed the expression of CYP450 1A5 enzyme which activates AFB1 to transform to toxic AFBO form; while SelW knockdown with SelW-specific siRNA significantly increased mRNA and protein levels of CYP450 1A5, thus indicating the protective role of SeMet [ 102 ].…”
Section: Selenium-mediated Afb1 Toxicity Control and Protective Mementioning
confidence: 99%
“…Deoxynivalenol, zearalenone, nivalenol, ochratoxin A (OTA), aflatoxin B1 (AFB1), and fumonisin B1 (FB1) are some of the most predominant mycotoxins [75]. Among them, AFB1 is listed as group I carcinogens by the International Agency for Research on Cancer [76] and is claimed as the most toxic mycotoxin due to its capacity to bind with the DNA of cells increasing the risk of liver cancer in human beings [77]. The US Food and Drug Administration (FDA) has set the limited level of AFB1 in corn and peanut feeds for finishing beef cattle at 300 ng•mL −1 [78].…”
Section: Toxinsmentioning
confidence: 99%