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. 2009 Jun 30;157(8):1368–1379. doi: 10.1111/j.1476-5381.2009.00210.x

Table 3C.

Effects of urocortin and CRF1/2 receptor antagonists on rat blood rheology

Erythrocyte sedimentation rate (mm·h1) Haematocrit (%) Blood viscosity
Plasma viscosity (mPa s)
200 S1(mPa s) 5 S−1 (mPa s)
Normal 1.08 ± 0.23 40.88 ± 1.34 5.68 ± 0.03 11.34 ± 1.39 1.39 ± 0.03
Sham operated 1.15 ± 0.09 40.03 ± 0.31 5.77 ± 0.28 12.01 ± 2.80 1.34 ± 0.05
TAO model 1.11 ± 0.05 39.60 ± 0.18 5.81 ± 0.41 11.73 ± 0.47 1.36 ± 0.02
Ucn 1.09 ± 0.17 39.21 ± 0.99 5.69 ± 0.18 11.58 ± 1.19 1.39 ± 0.04
Ucn + NBI-27914 1.13 ± 0.20 39.67 ± 2.12 5.71 ± 0.33 11.21 ± 1.30 1.34 ± 0.04
Ucn + antisauvagine-30 1.16 ± 0.09 40.30 ± 2.08 5.61 ± 0.01 11.94 ± 1.71 1.31 ± 0.01
Ucn + astressin 1.01 ± 0.17 39.63 ± 1.62 5.73 ± 0.17 11.84 ± 1.55 1.33 ± 0.02

CRF1/2, corticotrophin-releasing factor type 1 and 2 receptors; TAO, thromboangiitis obliterans; TAO model, single injection of sodium laurate only; Ucn, TAO model + daily urocortin for 12 days; Ucn + NBI 27914 or + antisauvagine-3 or + astressin, Ucn + daily injections of each antagonist for 12 days Values are presented as means ± SEM (n= 8).