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Department of Pharmacology, New York Medical College, Valhalla, New York 10595
We examined whether renal 20-hydroxyeicosatetraenoic acid
(20-HETE) synthesis is altered during gestation. Renal microsomal arachidonic acid
-hydroxylase activity increased by 50 and 48% in
rats on days 12 and 19 of gestation,
respectively. Renal microvessel 20-HETE synthesis increased by 50 and
82% in rats on days 6 and 12 of gestation,
respectively, and returned to control levels at day 19 of
gestation. In contrast, 20-HETE synthesis in isolated medullary thick
ascending limb was unchanged from control levels on days 6 and 12 of gestation, but it increased twofold on day 19 of gestation. This increase on day 19 of gestation
was associated with a twofold increase in urinary 20-HETE excretion,
and it coincided with a 23-mmHg fall in blood pressure. Moreover,
change in the rate of 20-HETE synthesis in microvessels was consistent
with the level of expression of cytochrome P450 (CYP)4A
proteins. Administration of the CYP4A inhibitor
1-aminobenzotriazole (ABT) for 2 days on day 12 of pregnancy
or for 5 days starting on day 15 of pregnancy caused a
transient but significant reduction in systolic blood pressure. ABT
treatment also decreased urinary sodium, urinary 20-HETE, and renal and
microvessel 20-HETE synthesis. This study, to our knowledge, is the
first to demonstrate that 20-HETE synthesis in the kidney is altered in
time- and site-specific manners during pregnancy. The localized pattern
of changes suggests that there are distinct regulatory mechanisms for
20-HETE synthesis in the kidney during pregnancy.
medullary thick ascending limb; renal microvessels; 1-aminobenzotriazole
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