Role of blood pressure in the natriuretic response to acute calcium channel blockade in humans

J Cardiovasc Pharmacol. 1991 May;17(5):724-30. doi: 10.1097/00005344-199105000-00006.

Abstract

Glomerular filtration rate (GFR), effective renal plasma flow (ERPF), and renal excretion of sodium and lithium were measured before and after acute oral administration of 20 mg nifedipine in 19 essential hypertensive patients. In 10 of them, with a diastolic pressure less than 105 mm Hg, nifedipine resulted in a decrease in mean blood pressure toward normal (109 +/- 2 to 97 +/- 2, p less than 0.001), a 27% increase in ERPF (p less than 0.001), no change in GFR, and an increase in fractional sodium excretion (28%, p less than 0.001). In nine subjects with a diastolic pressure greater than or equal to 105 mm Hg, nifedipine produced a decrease in mean blood pressure (133 +/- 6 to 117 +/- 4, p less than 0.001), which however remained higher than in mild hypertensives (p less than 0.001). ERPF rose by 29% (p less than 0.001), GFR remained unchanged, and fractional sodium excretion definitely increased more than in mild hypertensives (126%, p less than 0.001), as did fractional lithium excretion, used as an estimate of proximal tubular sodium handling. Acute nifedipine produces renal vasodilation in hypertensives, but with a greater natriuretic response in those subjects whose blood pressure remains elevated. Thus, acute natriuresis following nifedipine administration is largely dependent on the interaction between changes in arterial pressure and renal hemodynamics.

MeSH terms

  • Blood Pressure / physiology*
  • Calcium Channels / drug effects
  • Female
  • Humans
  • Hypertension / drug therapy
  • Hypertension / physiopathology
  • Kidney / drug effects
  • Kidney / metabolism
  • Kidney Tubules, Distal / drug effects
  • Kidney Tubules, Distal / metabolism
  • Kidney Tubules, Proximal / drug effects
  • Kidney Tubules, Proximal / metabolism
  • Lithium / pharmacokinetics
  • Male
  • Natriuresis / drug effects*
  • Natriuresis / physiology
  • Nifedipine / pharmacology*

Substances

  • Calcium Channels
  • Lithium
  • Nifedipine