The genetic causes of Na+ sensitivity of blood pressure (BP) are not well known. The kidney is critical to the long-term regulation of fluid and electrolyte balance and BP. Thus, the pathogenesis of salt sensitivity must involve a perturbation of renal Na+ handling. Salt-sensitive hypertension is associated with intronic variants of the electrogenic NaHCO3 cotransporter gene (SLC4A5). Although Na+ load without Cl- may not elicit a pressor effect, NaHCO3 can cause hypertension in some individuals but its pressor effect is less than NaCl. Hence, in most cases of Na+-sensitive hypertension, there must be Na+ and Cl- retention. Essential hypertension is associated with low serum HCO3-, implying an imbalance between renal Cl- and HCO3- transport. The renal Na+/H+ exchanger type 3 (NHE3), Cl-/HCO3- exchanger, and NaHCO3 cotransporter are negatively regulated by renal dopamine and positively regulated by angiotensin II. A disruption of these two systems may result in hypertension with an imbalance of renal Cl- and HCO3- transport.Aberrant renal dopamine regulation of Na+ transport in hypertension can be caused by decreased expression or function of any of the five dopamine receptors. The impaired function of dopamine receptors may be secondary to their constitutive desensitization by G protein-coupled receptor kinase type 4 (GRK4), in the case of D1R and D3R. GRK4 variants (65L, 142V, and 486V) are associated with hypertension and/or salt sensitivity. GRK4-65L, in particular, is also associated with salt sensitivity in the cohort that we reported to have salt-sensitive hypertension associated with SLC4A5 variants. Human GRK4?65L (hGRK4?65L) transgenic mice are salt-sensitive and hGRK4-65L, alone or in association with SLC4A5 intronic variants, increases the expression of SLC4A5, that may involve acetylation (e.g., histone deacetylase 1, HDAC1), an instance of genetics regulating epigenetics which, in turn, then regulates gene transcription (hGRK4, HDAC1, hepatocyte nuclear factor ? [HNF4A]38a-c, and SLC4A5). Project 3 will test the hypothesis that in some cases of salt-sensitive hypertension, hGRK4?65L and intronic variants of SLC4A5 increase SLC4A5 expression in response to aberrant genetic regulation of epigenetic pathways that also increase renal NHE3, NBCe2, and Cl-/HCO3- exchanger activities, The inter-regulation of genetics and epigenetics plays a crucial role in the development of salt-sensitive BP.

Public Health Relevance

This study will help us understand the role of renal and membrane transporters in salt sensitivity, and ultimately, blood pressure. This is of vital importance, since salt sensitivity is an underdiagnosed condition of hypertension in the United States, and costs US tax payers billions in medical bills and treatments.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL074940-15
Application #
9949772
Study Section
Special Emphasis Panel (ZHL1)
Program Officer
OH, Youngsuk
Project Start
Project End
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
15
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Virginia
Department
Type
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
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