Key result
In p47(phox-/-) mice, the hypertensive response to angiotensin II infusion was markedly blunted compared to wild-type mice (122+/-4 vs 151+/-6 mm Hg; P<0.05), with no increase in vascular superoxide.
Absolute Event Rate: 122% vs 151%
p-value: p=<0.05
The NAD(P)H oxidase subunit p47phox plays a pivotal role in mediating vascular oxidative stress and the hypertensive response to angiotensin II in vivo.
No takes yet. Share an insight, caveat, or question.
p47phox deletion attenuates Ang II hypertension in mice; extends in vitro data but leaves open human therapeutic targeting.
Landmesser et al. (2002) studied Hypertension caused by angiotensin II. Angiotensin II infusion vs. Wild-type (WT) mice was evaluated on Systolic blood pressure (mm Hg) (p=<0.05). In p47(phox-/-) mice, the hypertensive response to angiotensin II infusion was markedly blunted compared to wild-type mice (122+/-4 vs 151+/-6 mm Hg; P<0.05), with no increase in vascular superoxide.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: