2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a polychlorinated dibenzo-p-dioxin that binds to the

aryl hydrocarbon receptor (AhR), translocates into the nucleus, and up-regulates CYP1A1 and 1B1 expression. The Hepa cells were treated with arachidonic acid with or without TCDD activation. There were two controls, one cells treated Inhibitors,research,lifescience,medical with DMSO alone (the vehicle for the inducer) and one cells treated with TCDD only, where no significant levels of EETs were detected. The total amount of EETs (esterified and free) was determined by the same targeted chiral approach. Enantioselective formation of 8(S),9(R)-EET, 11(S),12(R)-EET, and 14(R),15(S)-EET, was observed (Figure 10). 14(R),15(S)-EET was present in the largest amount, followed by 8(S),9(R)-EET and 11(S),12(R)-EET (Figure 10). The amount of each isomer all targets increased Inhibitors,research,lifescience,medical from 1 h to 4 h treatment, in both stimulated and un-stimulated cells. Figure 10 Analysis of epoxyeicosatrienoic acids by chiral liquid chromatography/electron capture atmospheric pressure chemical ionization mass spectrometry using a [13C]‐analog internal standards. Reprinted with permission from Ref. [138]. After 4 Inhibitors,research,lifescience,medical h of arachidonic acid treatment, all the EET regioisomers increased

by approximately 50 %, and the enantioselectivity of the EETs was preserved. When the cells were pre-treated with TCDD followed by arachidonic acid, the concentration of all the cellular EETs increased. After adding 10 μM arachidonic acid for 1 h to the TCDD pre-treated cells, the most selleck Temsirolimus abundant regioisomer was 14,15-EET (Figure 10) and it showed a preferential formation of the 14(R),15(S)-EET enantiomer. The Inhibitors,research,lifescience,medical second

most abundant regioisomer was 8,9-EET (Figure 10) with the 8(S),9(R)-EET enantiomer being formed preferentially . Surprisingly, 8(S),9(R)-EET was the major arachidonic Inhibitors,research,lifescience,medical acid-derived 8,9-EET in both the non-induced and TCDD-induced Hepa cells. None of the CYPs that were tested produced significant quantities of this enantiomer, which has been shown previously to be a major metabolite of the rat cortex [78]. This suggests that there is another CYP in the mouse Hepa cell line, which is responsible for the formation of 8(S),9(R)-EET. Interestingly, Carfilzomib the 8(S),9(R)-EET enantiomer has potent vasoactive proprieties and undergoes COX-mediated metabolism to a potent mitogen for mesangial cells [147,148]. The low abundance of the 8(R),9(S)-EET in the TCDD-induced cells at 1 h and 4 h, a significant product of both rCYP1A1 and 1B1 suggests that preferential hydrolysis of this EET enantiomer could have occurred as a result of TCDD treatment. 11,12-EET, a minor product of arachidonic acid metabolism of CYP1A1 and 1B1 in the supersomes was also the least abundant product in the Hepa cell incubations. The expected racemic 11,12-EET was observed in the non-induced cells, whereas TCDD induction caused an apparent selective induction of 11(S),12(R)-EET formation.