The purpose of the research outlined in this proposal is to investigate the interrelationship between dietary manipulation and the production and biological activity of a factor(s) isolated from erythrocytes that promotes calcium uptake by vascular tissue and induces a sustained and severe elevation in systolic blood pressure in normotensive rats. Preliminary characterization of the compound that promotes calcium uptake indicates that it is a peptide. Blood levels of this peptide appear to vary in response to situations having a bearing on blood pressure thereby suggesting that it may play a role in blood pressure regulation. The proposed research will assess the effects of certain dietary modifications on blood levels of this peptide or tissue responsiveness to it to determine if changes in these parameters occur which are compatible with the hypothesis that this peptide plays a role in the blood pressure alterations associated with dietary modification. In certain of the proposed studies, food intake will be reduced to 35% of the ad libitum consumption by age-matched controls having free access to food. In other studies, rats will be fed a calcium fortified diet (4% calcium by weight) or a calcium deficient diet (.03% calcium by weight). Spontaneously hypertensive rats and two strains of normotensive rats (Wistar Kyoto and Sprague Dawley) will be maintained on these dietary regimens or standard Purina rodent chow for 8 weeks. At the end of this interval rats will be anesthetized and then bled by cardiac puncture. Blood levels of the peptide will be estimated by a bioassay that measures calcium uptake by aortic rings. Aortae from rats maintained on the different dietary regimens will be incubated with several predetermined concentrations of the purified peptide and the resultant effects on contraction and calcium uptake will be measured in order to determine if dietary modification alters vascular tissue responsiveness to the peptide. Additional studies are proposed to determine the age at which aortic tissue first becomes responsive to the peptide. Subsequently, the effects of reduced food intake or diets with modified calcium content on the onset of tissue responsiveness will be determined. Finally, the effects of the above mentioned dietary manipulations on the capacity of the hypertensive component to elevate systolic blood pressure in normotensive rats will be assessed.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL037661-01
Application #
3353514
Study Section
(SRC)
Project Start
1986-09-30
Project End
1989-09-29
Budget Start
1986-09-30
Budget End
1987-09-29
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Marshall University
Department
Type
Schools of Medicine
DUNS #
036156615
City
Huntington
State
WV
Country
United States
Zip Code
25701
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Simmons, M A; Johnson, E C; Becker, J B et al. (1989) An endogenous 'hypertensive factor' enhances the voltage-dependent calcium current. FEBS Lett 254:137-40
Huang, B S; McCumbee, W D; Wright, G L (1989) Further investigation of a potential calcium channel modulator isolated from rat erythrocytes. Can J Physiol Pharmacol 67:1252-8
Todd, D G; McCumbee, W D; Wright, G L et al. (1989) Hypotensive properties of antibodies directed against an endogenous pressor peptide isolated from rat blood. Can J Physiol Pharmacol 67:1580-5
Huang, B S; McCumbee, W D; Wright, G L (1988) Bay K 8644-like contractile effects of a peptide isolated from spontaneously hypertensive rats. Can J Physiol Pharmacol 66:332-6
McCumbee, W D; Johnson, P; Kasvinsky, P J et al. (1987) An endogenous peptide that stimulates lanthanum-resistant calcium uptake in vascular tissue. Can J Physiol Pharmacol 65:1991-5