Hypertension, Vol 24, 770-778, Copyright © 1994 by American Heart Association
Y Uehara, N Hirawa, Y Kawabata, T Suzuki, N Ohshima, K Oka, T Ikeda, A Goto, T Toyo-oka and K Kizuki
We investigated whether long-term infusion of kallikrein would attenuate
renal injury in salt-induced hypertension in Dahl salt- sensitive rats. A
subdepressor dose of purified rat urinary kallikrein (700 ng/d IV) was
infused by osmotic minipump for 4 weeks in male Dahl salt-sensitive rats
fed a high salt (2% NaCl) diet. This dose did not affect the time-dependent
elevation of blood pressure; however, urinary protein excretion was
significantly decreased, and glomerular filtration rate was increased.
These beneficial effects were reflected morphologically by an attenuation
of glomerulosclerotic lesions and tubular injury seen in the hypertensive
Dahl salt-sensitive rats. Kallikrein infusion increased urinary excretion
of bradykinin and stimulated excretion of cyclic GMP, suggesting that the
kallikrein- kinin-prostaglandin and nitric oxide axes were enhanced by rat
urinary kallikrein infusion. The alterations induced by kallikrein infusion
were potentiated by the concomitant administration of the angiotensin-
converting enzyme inhibitor alacepril. These studies indicated that
long-term replacement with rat tissue kallikrein attenuates renal injury in
hypertensive Dahl salt-sensitive rats.
ARTICLES
Long-term infusion of kallikrein attenuates renal injury in Dahl salt- sensitive rats
Second Department of Medicine, University of Tokyo, Japan.
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