Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke

被引:18
|
作者
Bennion, Douglas M. [1 ]
Rosado, Christian A. [2 ]
Haltigan, Emily A. [1 ]
Regenhardt, Robert W. [1 ]
Sumners, Colin [1 ]
Waters, Michael F. [2 ]
机构
[1] Univ Florida, Dept Physiol & Funct Genom, POB 100274, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Neurol, Neurovasc Div, Gainesville, FL USA
关键词
Angiotensin converting enzyme 2 (ACE2); angiotensin converting enzyme (ACE); renin-angiotensin system; ischemic stroke; angiotensin-(1-7); SYSTEM; TYPE-2; AXIS;
D O I
10.1177/1470320316661060
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Levels of angiotensin converting enzyme 2 (ACE2), a cardio and neuro-protective carboxypeptidase, are dynamically altered after stroke in preclinical models. We sought to characterize the previously unexplored changes in serum ACE2 activity of stroke patients and the mechanism of these changes. Serum samples were obtained from patients during acute ischemic stroke (n=39), conditions mimicking stroke (stroke-alert, n=23), or from control participants (n=20). Enzyme activity levels were analyzed by fluorometric assay and correlated with clinical variables by regression analyses. Serum ACE2 activity was significantly lower in acute ischemic stroke as compared to both control and stroke-alert patients, followed by an increase to control levels at three days. Serum ACE2 activity significantly correlated with the presence of ischemic stroke after controlling for other factors (P=0.01). Additional associations with ACE2 activity included a positive correlation with systolic blood pressure at presentation in stroke-alert (R-2=0.24, P=0.03), while stroke levels showed no correlation (R-2=0.01, P=0.50). ACE2 sheddase activity was unchanged between groups. These dynamic changes in serum ACE2 activity in stroke, which concur with preclinical studies, are not likely to be driven primarily by acute changes in blood pressure or sheddase activity. These findings provide new insight for developing therapies targeting this protective system in ischemic stroke.
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页数:7
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