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. Author manuscript; available in PMC: 2008 Aug 1.
Published in final edited form as: Am J Physiol Renal Physiol. 2007 May 30;293(2):F586–F593. doi: 10.1152/ajprenal.00489.2006

Table 2.

SBP, drinking and renal excretory responses to ANG II infusion alone or concurrent administration of ANG II and the AT1 receptor antagonist losartan during the 1st week in wild-type, Agtr1a+/−, and Agtr1a−/− mice

Wild-type
Agtr1a+/−
Agtr1a−/−
Responses C ANG II ANG II+L C ANG II ANG II+L C ANG II ANG II+L
SBP, mmHg 113±4 153±7b 132±4b,d 104±3 145±4b 135±2b,c 89±5f 99±4f 95±3f
Drinking, ml/24 h 2.6±0.3 4.3±0.6a 2.9±0.2 5.2±0.2 5.5±0.4 4.4±0.4 9.3±0.7f 8.0±0.8f 7.6±0.5f
UNaV, μmol/24 h 158±6.8 150±5.9 184±7.8 235±4.6 229±9.5 263±4.1 236±9.4f 252±14f 186±9.9
UKV, μmol/24 h 397±18.1 263±10.5a 435±14.8a 539±5.6 354±24.7b 553±11.3d 527±19.3e 479±25f 426±16.7

Results are expressed as means ± SE. C, control or basal; L, losartan. The differences in the same response between different groups for the same strain of mice were analyzed by one-way ANOVA:

a

P < 0.05 or

b

P < 0.01 vs. control;

c

P < 0.05 or

d

P < 0.01 vs. ANG II. The differences in the same response between wild-type or Agtr1a+/− and Agtr1a−/− mice were analyzed by unpaired t-test:

e

P < 0.05 or

f

P < 0.01 versus wild-type or Agtr1a+/− mice.