Receptor Gene Produces Renin-dependent Hypertension

نویسندگان

  • Laureano D. Asico
  • Cecilia Ladines
  • Sara Fuchs
  • Domenico Accili
  • Robert M. Carey
  • Claudio Semeraro
  • Felice Pocchiari
  • Robin A. Felder
  • Gilbert M. Eisner
  • Pedro A. Jose
چکیده

Since dopamine receptors are important in the regulation of renal and cardiovascular function, we studied the cardiovascular consequences of the disruption of the D 3 receptor, a member of the family of D 2 -like receptors, expressed in renal proximal tubules and juxtaglomerular cells. Systolic and diastolic blood pressures were higher ( z 20 mmHg) in heterozygous and homozygous than in wild-type mice. An acute saline load increased urine flow rate and sodium excretion to a similar extent in wild-type and heterozygous mice but the increase was attenuated in homozygous mice. Renal renin activity was much greater in homozygous than in wild-type mice; values for heterozygous mice were intermediate. Blockade of angiotensin II subtype-1 receptors decreased systolic blood pressure for a longer duration in mutant than in wild-type mice. Thus, disruption of the D 3 receptor increases renal renin production and produces renal sodium retention and renin-dependent hypertension. ( J . Clin . Invest . 1998. 102:493–498.)

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تاریخ انتشار 1998