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(Received for publication, June 12, 1996, and in revised form, August 9, 1996)
From the Department of Biochemistry and Molecular Biology, Medical
University of South Carolina, Charleston,
South Carolina 29425
The kallikrein-kinin system participates in blood
pressure regulation. One of the kallikrein-kinin system components,
kallikrein-binding protein, binds to tissue kallikrein and inhibits its
activity in vitro. To investigate potential roles of rat
kallikrein-binding protein (RKBP) in vivo, we have
developed transgenic mice that express an RKBP gene under the control
of the mouse metallothionein metal-responsive promoter. Expression of
the transgene, RKBP, was detected in the liver, kidney, lung, heart,
pancreas, salivary glands, spleen, brain, testis, and adrenal gland at
the mRNA and protein levels. Systolic blood pressures of homozygous
transgenic mice were 88.5 ± 0.8 mm Hg (mean ± S.E.,
n = 19, P < 0.001) for one line and
88.8 ± 1.6 mm Hg (mean ± S.E., n = 19, P < 0.001) for another, as compared with 100.5 ± 0.8 mm Hg (mean ± S.E., n = 18) for control
mice. Direct blood pressure measurements of these transgenic mice
through an arterial cannula showed similar reductions of blood
pressure. Intravenous injection of purified RKBP into mice via a
catheter produced a dose-dependent reduction of the mean
arterial blood pressure. Our findings suggest that RKBP may function as
a vasodilator in vivo, independent of regulating the
activity of tissue kallikrein.
Volume 271, Number 44,
Issue of November 1, 1996
pp. 27590-27594
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
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