Hypertension, Vol 7, 554-561, Copyright © 1985 by American Heart Association
S Katayama and JB Lee
To investigate mechanisms involved in the high incidence of hypertension in
diabetes mellitus, the relationship between renin- angiotensin production
and renal prostaglandin E2 synthesis was studied in rats 1 week after
diabetes mellitus had been induced by streptozotocin injection. The
diabetic rats became hypertensive, although plasma renin activity did not
increase despite the plasma volume contraction resulting from polyuria and
natriuresis. Subcutaneous insulin injection resulted in a marked increase
in plasma renin activity, while more rigid control of diabetes mellitus
achieved by constant insulin infusion decreased blood pressure. Cortical
renin content and renin release as well as papillary prostaglandin E2
synthesis in vitro were significantly lower in diabetic rats than in
nondiabetic controls. Isoproterenol and prostaglandin E2 stimulated renin
release in controls, while diabetic rats responded only to isoproterenol.
Insulin infusion by pump reversed these abnormalities. An additive effect
of a maximum dose of isoproterenol (10(-5) M) and prostaglandin E2 (10(-4)
M) on renin release was observed in nondiabetic controls and in diabetic
rats treated with insulin pump, but not in untreated diabetic rats. The
results suggest that 1) renal renin release and prostaglandin E2 synthesis
in diabetes mellitus are insulin dependent, 2) inappropriately lower plasma
renin activity in diabetes mellitus may be attributed to a diminished renal
renin pool and a lack of renin release in response to renal prostaglandin
E2, the synthesis of which is also impaired in diabetes, prostaglandin E2-
induced renin release may operate independently from isoproterenol- induced
renin release, and impaired renal prostaglandin E2 synthesis may contribute
to the development of hypertension in the face of an unchanged
prohypertensive renin-angiotensin II system.
ARTICLES
Hypertension in experimental diabetes mellitus. Renin-prostaglandin interaction
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