HYBRID EVENT: You can participate in person at Paris, France or Virtually from your home or work.

2nd Edition of International Heart Congress

June 20-22,2024 | Hybrid Event

June 20 -22, 2024 | Paris, France
Heart Congress 2024

Dopamine D2 receptor and inverse salt sensitivity

Pedro A Jose, Speaker at Cardiovascular Conference
The George Washington University of School of Medicine & Health Sciences, United States
Title : Dopamine D2 receptor and inverse salt sensitivity


Globally, hypertension is the number one risk factor for death, affecting more than 1 billion people. Hypertension is the result of the interactions among genetics, epigenetics, environment, and lifestyle. The long-term regulation of blood pressure (BP) rests on renal and non-renal mechanisms. The impaired renal sodium handling in hypertension is caused by aberrant counter-regulatory natriuretic/anti-natriuretic pathways. The sympathetic nervous and renin-angiotensin systems are anti-natriuretic pathways. A counter-regulatory natriuretic pathway is the renal dopaminergic system. Aberrant dopaminergic regulation of renal sodium transport in hypertension is caused by a decrease in renal dopamine synthesis and/or dysfunction of any of the 5 dopamine receptors (D1R, D2R, D3R, D4R, & D5R). Normally, an increase in sodium intake increases while a decrease in sodium intake decreases BP, albeit, transiently until sodium balance is achieved. However, ~50 % of hypertensive and ~26% of normotensive subjects have increased BP on high sodium intake, a case of salt sensitivity, while ~20 % have increased BP on a low sodium intake, a case of inverse salt sensitivity (ISS).  Low and high sodium intakes are associated with increased incidence of cardiovascular events/mortality. In humans with ISS, there is a linear relationship between the number of single nucleotide polymorphisms (SNPs) in D2R (rs6276 and 6277) and decreased renal D2R expression. The increase in BP on a low sodium diet may be due to increased activities of the renin-angiotensin and sympathetic nervous system that cannot be counteracted by D2R. Hypertension may be a cause or consequence of inflammation or oxidative stress. Deficient D2R function causes renal inflammation independently of high BP. Subjects carrying D2R SNPs have increased inflammation, mediated by decreased regulation of the miR-217-Wnt5a-Ror2 pathway.  The D2R, via paraoxonase2 and sestrin2, maintains normal redox balance and BP. In summary, the D2R is important in the maintenance of normal BP by regulating renal sodium transport, vascular reactivity, inflammation, and redox balance.

Audience Take Away

  • The audience will recognize the existence of inverse salt-sensitive hypertension, a state in which a low salt diet increases blood pressure
  • The audience may want to make sure that the high blood pressure that is not responsive to a low sodium diet may be caused by inverse salt-sensitive hypertension.
  • Research that leads to an improvement in human health integrates animal and human study data.
  • Integrate pharmacogenetics in the treatment of diseases.


Pedro A. Jose, MD, PhD is Professor of Medicine and Pharmacology and Physiology, The George Washington University of School of Medicine & Health Sciences. Dr. Jose received his MD degree from the University of Santo Tomas, Philippines, in 1965 and his PhD degree in Physiology from Georgetown University, in 1976. The primary goal of Dr. Jose’s research is to determine the genetic and pharmacogenetic bases of human essential hypertension and the metabolic syndrome.  He has 380 publications. Dr. Jose has received several academic and research awards, including the 2015 Excellence Award for Hypertension Research (American Heart Association).