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. 2011 Mar 11;300(6):H1990–H1996. doi: 10.1152/ajpheart.01267.2010

Table 1.

Plasma concentrations of individual cis- and trans-EETs in WKY and SHR treated with vehicle or AUCB for 1 wk

WKY
SHR
Vehicle AUCB Vehicle AUCB
14,15-
    cis-EET 5.8 ± 0.6 5.2 ± 0.7 4.5 ± 0.6 4.4 ± 0.7
    trans-EET 1.6 ± 0.2 3.4 ± 0.6* 1.1 ± 0.1 2.3 ± 0.7*
11,12-
    cis-EET 2.1 ± 0.3 2.7 ± 0.3 1.4 ± 0.3 1.6 ± 0.2
    trans-EET 2.0 ± 0.2 3.6 ± 0.8* 0.9 ± 0.1 2.0 ± 0.5*
8,9-
    cis-EET 4.9 ± 0.4 3.3 ± 0.4 3.2 ± 0.4 3.0 ± 0.3
    trans-EET 1.8 ± 0.3 2.7 ± 0.7* 0.9 ± 0.1 1.9 ± 0.3*
5,6-
    cis-EET 5.5 ± 0.4 4.8 ± 0.3 3.2 ± 0.4 3.1 ± 0.2
    trans-EET 2.4 ± 0.1 2.8 ± 0.5 1.2 ± 0.1 1.7 ± 0.3
Total
    cis-EET 18.3 ± 1.4 16.0 ± 1.5 12.3 ± 1.6 12.1 ± 1.3
    trans-EET 7.8 ± 0.5 12.5 ± 1.9* 4.1 ± 0.2 7.9 ± 1.5*
Overall
    EETs 26.1 ± 1.8 28.5 ± 3.2 16.4 ± 1.6 20.0 ± 2.4*

Values were determined by LC/MS/MS and expressed as means ± SE (ng/ml); n = 6–8 rats in each group. EET, epoxyeicosatrienoic acid; AUCB, cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid. Eleven-week-old Wistar-Kyoto (WKY) and spontaneously hypertensive (SHR) rats were treated with vehicle or AUCB (2 mg · kg−1 · day−1 in the drinking water) for 7 days.

*

P < 0.05 compared with plasma concentrations of vehicle rats of the same strain.