Hypertension, Vol 11, 179-184, Copyright © 1988 by American Heart Association
GM Reid, RG Appel and MJ Dunn
Isolated kidneys of Dahl salt-sensitive rats (DS) excrete sodium less
readily than those of Dahl salt-resistant rats (DR). The collecting tubule
is an important source of papillary prostaglandin E2 and is a site of
significant sodium reabsorption. We cultured renal papillary collecting
tubule cells from 5-week-old, prehypertensive DS and DR on a low salt diet
and also after 14 weeks of high salt feeding, and we measured prostaglandin
E2 synthetic capacity. Unstimulated renal papillary collecting tubule cells
from 5-week-old DS produced 62 +/- 5% less prostaglandin E2 than did
comparable cells from DR (p less than 0.001). The cells from DS also
synthesized less prostaglandin E2 after stimulation with the calcium
ionophore A23187 (67 +/- 6% of control; p less than 0.001) or the addition
of exogenous arachidonate (74 +/- 7% of control; p less than 0.01). Urinary
prostaglandin E2 excretion was also diminished in the 5-week-old DS
compared with their salt-resistant counterparts (18.1 +/- 1.3 vs 23.9 +/-
1.7 ng/24 hr; p less than 0.025). After high salt feeding, the DS became
hypertensive but the DR remained normotensive. Renal papillary collecting
tubule cells cultured from these DS continued to produce less prostaglandin
E2 than those from control rats, both in the basal state (60 +/- 12% of
control; p less than 0.09) and after stimulation with ionophore (62 +/- 2%
of control; p less than 0.002). In these older animals, the DS continued to
underexcrete prostaglandin E2 compared with the DR (29.7 +/- 3.2 vs 42.2
+/- 6.1 ng/24 hr; p less than 0.08). The underproduction of prostaglandin
E2 in the papillary collecting tubule of DS may play a role in their
inadequate renal natriuretic capacity and contribute to the onset and
maintenance of salt-induced hypertension in this strain.
ARTICLES
Papillary collecting tubule synthesis of prostaglandin E2 in Dahl rats
Department of Medicine, Case Western Reserve University, Cleveland, Ohio.
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