Sokoine University of Agriculture

An investigation of the endocrine disrupting potential of enniatin B using in vitro bioassays

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dc.contributor.author Kalayou, S.
dc.contributor.author Ndossi, D.
dc.contributor.author Frizzell, C.
dc.contributor.author Groseth, P.
dc.contributor.author Connolly, L.
dc.contributor.author Sørlie, M.
dc.contributor.author Verhaegen, S.
dc.contributor.author Ropstad, E.
dc.date.accessioned 2020-04-01T12:10:51Z
dc.date.available 2020-04-01T12:10:51Z
dc.date.issued 2015-01
dc.identifier.issn 0378-4274
dc.identifier.uri http://www.suaire.sua.ac.tz/handle/123456789/2989
dc.description Toxicology Letters 233 (2015) 84–94 en_US
dc.description.abstract Evidence that some of the fungal metabolites present in food and feed may act as potential endocrine disruptors is increasing. Enniatin B (ENN B) is among the emerging Fusarium mycotoxins known to contaminate cereals. In this study, the H295R and neonatal porcine Leydig cell (LC) models, and reporter gene assays (RGAs) have been used to investigate the endocrine disrupting activity of ENN B. Aspects of cell viability, cell cycle distribution, hormone production as well as the expression of key steroidogenic genes were assessed using the H295R cell model. Cell viability and hormone production levels were determined in the LC model, while cell viability and steroid hormone nuclear receptor transcriptional activity were measured using the RGAs. ENN B (0.01–100 m M) was cytotoxic in the H295R and LC models used; following 48 h incubation with 100 m M. Flow cytometry analysis showed that ENN B exposure (0.1– 25 m M) led to an increased proportion of cells in the S phase at higher ENN B doses (>10 m M) while cells at G 0 /G 1 phase were reduced. At the receptor level, ENN B (0.00156–15.6 m M) did not appear to induce any specific (ant) agonistic responses in reporter gene assays (RGAs), however cell viability was affected at 15.6 m M. Measurement of hormone levels in H295R cells revealed that the production of progesterone, testosterone and cortisol in exposed cells were reduced, but the level of estradiol was not significantly affected. There was a general reduction of estradiol and testosterone levels in exposed LC. Only the highest dose (100 m M) used had a significant effect, suggesting the observed inhibitory effect is more likely associated with the cytotoxic effect observed at this dose. Gene transcription analysis in H295R cells showed that twelve of the sixteen genes were significantly modulated (p < 0.05) by ENN B (10 m M) compared to the control. Genes HMGR, StAR, CYP11A, 3 b HSD2 and CYP17 were downregulated, whereas the expression of CYP1A1, NR0B1, MC2R, CYP21, CYP11B1, CYP11B2 and CYP19 were upregulated. The reduction of hormones and modulation of genes at the lower dose (10 m M) in the H295R cells suggests that adrenal endocrine toxicity is an important potential hazard. en_US
dc.language.iso en en_US
dc.publisher ELSEVIER en_US
dc.subject Leydig cell en_US
dc.subject H295R en_US
dc.subject ENN B en_US
dc.subject Emerging mycotoxins en_US
dc.subject Steroidogenesis en_US
dc.subject RGA en_US
dc.subject Endocrine disruption en_US
dc.title An investigation of the endocrine disrupting potential of enniatin B using in vitro bioassays en_US
dc.type Article en_US
dc.url www.elsev ier.com/locate /toxlet en_US


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