The long term objectives of this application are to understand the mechanisms by which the Y chromosome from spontaneously hypertensive rats (SHR) produces a significant blood pressure rise. The Y chromosome blood pressure effect has now been documented in two other independent laboratories but the genetic and physiological mechanisms are not known. There appears to be both sympathetic nervous system (SNS) and androgen components to the Y mediated blood pressure effect. This research will benefit our understanding of one of the genetic components of hypertension and parallels what is observed in human populations.
The specific aims will focus on: l) how the SNS may influence testicular development, vascular reactivity and renal metabolism of norepinephrine, 2) if gonadotropin releasing hormone may be released early due to the Y chromosome, 3) if the Y chromosome enhances salt sensitivity, 4) identification and cloning of the heat shock protein sequence on the Y chromosome and 5) determination of the mechanism of the Y chromosome influence on steroid sulfatase in specific tissues.
These aims will be accomplished by using both physiological, genetic and molecular techniques. Blood pressure will be measured by telemetry in several studies throughout' the prepubertal and pubertal stages during which blood pressure rapidly rises. molecular studies measuring components of the renin angiotensin system in testes and kidney will be examined and heat shock protein expression will be determined in relevant target organs, such as, aorta, resistance 'vessels, kidney, heart and adrenal glands. Biochemical measurements of indices of the SNS will evaluate the mechanism of elevated adrenergic responsiveness (increased norepinephrine content, release, turnover) in target' organs influencing blood pressure. in some experiments the genetically testicular feminized male will be studied to determine the interaction of the Y chromosome, androgens, androgen receptor and the SNS upon blood pressure. The results of these studies should enhance our understanding of the mechanism of the Y chromosome effect upon blood pressure.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL048072-07
Application #
2910548
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Project Start
1993-05-01
Project End
2000-04-30
Budget Start
1999-05-01
Budget End
2000-04-30
Support Year
7
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Akron
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
City
Akron
State
OH
Country
United States
Zip Code
44325
Toot, Jonathan; Dunphy, Gail; Turner, Monte et al. (2004) The SHR Y-chromosome increases testosterone and aggression, but decreases serotonin as compared to the WKY Y-chromosome in the rat model. Behav Genet 34:515-24
Caplea, Ann; Seachrist, Darcie; Daneshvar, Hamid et al. (2002) Noradrenergic content and turnover rate in kidney and heart shows gender and strain differences. J Appl Physiol 92:567-71
Caplea, A; Seachrist, D; Dunphy, G et al. (2001) Sodium-induced rise in blood pressure is suppressed by androgen receptor blockade. Am J Physiol Heart Circ Physiol 280:H1793-801
Ely, D; Turner, M; Milsted, A (2000) Review of the Y chromosome and hypertension. Braz J Med Biol Res 33:679-91
Neves, L A; Santos, R A; Khosla, M C et al. (2000) Angiotensin-(1-7) regulates the levels of angiotensin II receptor subtype AT1 mRNA differentially in a strain-specific fashion. Regul Pept 95:99-107
Valigora, S D; Lib, P K; Dunphy, G et al. (2000) Steroid sulfatase inhibitor alters blood pressure and steroid profiles in hypertensive rats. J Steroid Biochem Mol Biol 73:113-22
Seachrist, D; Dunphy, G; Daneshvar, H et al. (2000) Testosterone increases blood pressure and cardiovascular and renal pathology in spontaneously hypertensive rats. Blood Press 9:227-38
Caplea, A; Seachrist, D; Dunphy, G et al. (2000) SHR Y chromosome enhances the nocturnal blood pressure in socially interacting rats. Am J Physiol Heart Circ Physiol 279:H58-66
Dumas, P; Pausova, Z; Kren, V et al. (2000) Contribution of autosomal loci and the Y chromosome to the stress response in rats. Hypertension 35:568-73
Ely, D; Herman, M; Ely, L et al. (2000) Sodium intake is increased by social stress and the Y chromosome and reduced by clonidine. Am J Physiol Regul Integr Comp Physiol 278:R407-12

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