Increasing evidence suggests that vasopressin (VP) may play a role in the development of DOCA/salt hypertension. Of great importance is the finding that VP-deficient Brattleboro rats (DI rats) fail to develop hypertension with DOCA/salt treatment but do so when replaced with VP. Little is known of the mechanism of action of VP in hypertension. The present research plan proposes to identify the mechanism(s) of action of VP in DOCA/salt hypertension. VP may function as a direct vasoconstrictor/pressor agent. We will study the direct vasoconstrictor/pressor effect of VP in light concomitent activity of the sympathetic nervous system and the baroreceptor reflex. Vascular reactivity to VP will be assessed in the unanesthetized DOCA/salt treated rats instrumented with chronic catheters and pulsed-Doppler flow probes at various stages of hypertension before and after blockade of the sympathetic nervous system or sinoaortic deafferentation. VP may act as an antidiuretic agent. This will be tested by assessing changes in body fluid volumes, renal function and water and electrolyte metabolism over the course of development of hypertension. VP may act indirectly to modulate the responsiveness of vascular smooth muscle to other vasoconstrictors particularly catecholamines. This will be tested by assessing vascular reactivity in isolated, perfused vascular beds. Finally, VP may modulate the function of central neural target areas controlling the baroreflex and sympathetic outflow. This will be tested by 1) determining the interaction of VP with the locus coeruleus, nucleus tractus solitarii, and posterior hypothalamus using microinjection, push-pull perfusion and brain punch techniques 2) determining the effects of stimulation of the paraventricular and supraoptic nuclei on the baroreflex function. 3) determining the interaction of VP with central catecholaminergic neurons. The results of these experiments should provide fundamental information on the role of VP in normal cardiovascular regulation as well as in the pathogenesis of hypertension.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL028545-08
Application #
3339919
Study Section
Cardiovascular and Pulmonary Research B Study Section (CVB)
Project Start
1982-04-01
Project End
1990-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
8
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
Overall Medical
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
LeBoeuf, R D; Green, M M; Berecek, K H et al. (1991) Cloning and direct sequencing from lambda cDNA libraries using the polymerase chain reaction: suppressin and the vasopressin receptor as models. Neth J Med 39:295-305
Berecek, K H; Wyss, J M; Swords, B H (1991) Alterations in vasopressin mechanisms in captopril-treated spontaneously hypertensive rats. Clin Exp Hypertens A 13:1019-31
Swords, B H; Wyss, J M; Berecek, K H (1991) Central vasopressin receptors are upregulated by deoxycorticosterone acetate. Brain Res 559:10-6
Berecek, K H; Swords, B H (1990) Central role for vasopressin in cardiovascular regulation and the pathogenesis of hypertension. Hypertension 16:213-24
Swords, B H; Carr, D J; Blalock, J E et al. (1990) An antibody directed against a peptide encoded by RNA complementary to mRNA for vasopressin recognizes putative vasopressin receptors. Neuroendocrinology 51:487-92
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Cheng, S W; Kirk, K A; Robertson, J D et al. (1989) Brain angiotensin II and baroreceptor reflex function in spontaneously hypertensive rats. Hypertension 14:274-81
Cheng, S W; Wilson, K M; Mulchahey, J J et al. (1989) Vasopressin in neuronal cultures from neonatal rat brain. Hypertension 13:902-9
Wilson, K M; Magargal, W; Berecek, K H (1988) Long-term captopril treatment. Angiotensin II receptors and responses. Hypertension 11:I148-52
Berecek, K H; Coshatt, G; Narkates, A J et al. (1988) Captopril and the response to stress in the spontaneously hypertensive rat. Hypertension 11:I144-7

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