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CRH-ACTH-POMC-ADRENAL |
Perinatal Research Laboratories, Department of Obstetrics/Gynecology, University of Wisconsin (J.K.P., I.M.B.), Madison, Wisconsin 53715; and Department of Population Health and Reproduction, University of California School of Veterinary Medicine (F.M., A.J.C.), Davis, California 95616
Address all correspondence and requests for reprints to: Dr. Ian M. Bird, 7E Meriter Hospital, 202 South Park Street, Madison, Wisconsin 53715. E-mail: imbird{at}facstaff.wisc.edu
There is mounting evidence that nitric oxide (NO) may inhibit
adrenal steroidogenesis by binding to the heme group of P450 enzymes,
particularly the rate-limiting steps cholesterol side-change cleavage
P450, aldosterone synthase P450, and
17
-hydroxylase/C17/20-lyase P450. Using
immunohistochemistry, nitrotyrosine was detectable throughout the ovine
adrenal cortex, and endothelial NO synthase (eNOS) was further
identified in zona glomerulosa (ZG) and at a higher level throughout
the zona fasciculata, increasing toward the medulla. Caveolin-1, 90-kDa
heat shock protein, ERK-1/2, and Akt, all known and proposed regulators
of eNOS activity, were detected throughout the ovine adrenal cortex.
Western immunoblotting confirmed the identity of these proteins as well
as the absence of neuronal NOS, inducible NOS, caveolin-2, and
caveolin-3. Through dual immunostaining we further identified for the
first time a zona intermedia without strong staining for
17
-hydroxylase/C17/20-lyase P450 or angiotensin II type
1 receptor, but positive for eNOS. Rhesus adrenals also stained
positively for eNOS, but staining was seen only in the ZG and zona
reticularis. We conclude that eNOS may play a role in controlling
zone-specific aldosterone synthase vs. 11ß-hydroxylase
activities of the single CYP11B gene in sheep. In the rhesus monkey, NO
may modulate ZG aldosterone synthase, but it is not needed for control
of the distinct 11ß-hydroxylase in the zona fasciculata. In the zona
reticularis, however, eNOS may control C19 steroid
production at the level of 17
-hydroxylase vs.
17,20-lyase activity otherwise unopposed by 3ß-hydroxysteroid
dehydrogenase.
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