2011
DOI: 10.1016/j.toxlet.2011.08.005
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Congener-specific action of PBDEs on steroid secretion, CYP17, 17β-HSD and CYP19 activity and protein expression in porcine ovarian follicles

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Cited by 30 publications
(19 citation statements)
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“…Difference in the changes of NaR and GST responding to different PBDEs may be as the result of congener-specific action of PBDEs on NaR and GST activities. Similar phenomena were observed in the effects of PBDEs on GST, deiodinase, and CYP17 activities in porcine ovarian follicles (Karpeta et al, 2011) and fishes (Roberts et al, 2011). The degradation reaction of PBDEs stopped gradually with the NaR and GST became inactive.…”
Section: Responses Of Root Enzymes To the Exposure Of Pbdessupporting
confidence: 74%
“…Difference in the changes of NaR and GST responding to different PBDEs may be as the result of congener-specific action of PBDEs on NaR and GST activities. Similar phenomena were observed in the effects of PBDEs on GST, deiodinase, and CYP17 activities in porcine ovarian follicles (Karpeta et al, 2011) and fishes (Roberts et al, 2011). The degradation reaction of PBDEs stopped gradually with the NaR and GST became inactive.…”
Section: Responses Of Root Enzymes To the Exposure Of Pbdessupporting
confidence: 74%
“…Certain PBDEs have been shown to decrease P 4 synthesis in mouse Leydig tumor cells (Han et al 2012) while other PBDEs have been shown to increase P 4 synthesis in the ovarian follicles of pigs (Karpeta & Gregoraszczuk 2010). Proposed mechanisms of action in the latter study include modulation of key steroidogenic genes, many of which are highly conserved among vertebrates (Karpeta et al 2011).…”
Section: Discussionmentioning
confidence: 84%
“…TOXLET 8730 1-7 BDE-47 increased androgen secretion by directly enhancing the expression and activity of 17␤-hydroxysteroid dehydrogenase (17␤-HSD) (Karpeta et al, 2011), whereas 5-hydroxy-2,2 ,4, 4-tetrabromodiphenyl ether (5-OH-BDE-47) and 6-hydroxy-2,2 ,4,4 -tetrabromodiphenyl ether (6-OH-BDE-47) stimulated estradiol secretion by stimulating aromatase expression and activity (Karpeta et al, 2013).…”
Section: G Modelmentioning
confidence: 99%
“…The medium was then changed to M199 with 5% FBS and the cells were cultured for an additional 3, 6, 24 and 48 h with 50 ng/ml of BDE-47, 5-OH-or 6-OH-BDE-47. The dose of reagents was chosen based on our previously published studies (Karpeta et al, 2011(Karpeta et al, , 2012(Karpeta et al, , 2013. In these dose dependent studies we showed that BDE-47 in a dose of 50 ng/ml was the most potent for stimulation of testosterone secretion and CYP2B1 activity (Karpeta et al, 2011(Karpeta et al, , 2012 and metabolites were the most potent for stimulation of estradiol secretion (Karpeta et al, 2013).…”
Section: Cell Culturementioning
confidence: 99%