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Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi 39216
Hepatic angiotensinogen secretion is controlled by a
complex pattern of physiological or pathophysiological mediators.
Because plasma concentrations of angiotensinogen are close to the
Michaelis-Menten constant, it was hypothesized that changes in
circulating angiotensinogen affect the formation rate of ANG I and ANG
II and, therefore, blood pressure. To further test this
hypothesis, we injected purified rat angiotensinogen intravenously
in Sprague-Dawley rats via the femoral vein and measured mean arterial
blood pressure after arterial catheterization. In controls, mean
arterial pressure was 131 ± 2 mmHg before and after the injection
of vehicle (sterile saline). The injection of 0.8, 1.2, and 2.9 mg/kg
angiotensinogen caused a dose-dependent increase in mean arterial blood
pressure of 8 ± 0.4, 19.3 ± 2.1, and 32 ± 2.4 mmHg,
respectively. In contrast, the injection of a purified rabbit anti-rat
angiotensinogen antibody (1.4 mg/kg) resulted in a significant decrease
in mean arterial pressure (
33 ± 3.2 mmHg). Plasma
angiotensinogen increased to 769 ± 32, 953 ± 42, and
1,289 ± 79 pmol/ml, respectively, after substrate and decreased
by 361 ± 28 pmol/ml after antibody administration. Alterations in
plasma angiotensinogen correlated well with changes in plasma renin
activity. In summary, variations in circulating angiotensinogen can
result in changes in blood pressure. In contrast to renin, which is
known as a tonic regulator for the generation of ANG I, angiotensinogen
may be a factor rather important for long-term control of the basal
activity of the renin-angiotensin system.
renin-angiotensin system; Sprague-Dawley rat; hypertension; plasma renin activity; anti-rat angiotensinogen antibody
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