Molecular mechanisms involved in catecholamine regulation of sodium transport

Semin Nephrol. 1993 Jan;13(1):41-9.

Abstract

The catecholamines dopamine and norepinephrine, play a central role in the regulation of sodium homeostasis and blood pressure. Dopamine inhibits tubular Na+, K(+)-ATPase activity and increases sodium excretion. Norepinephrine stimulates Na+, K(+)-ATPase activity and decreases urinary sodium excretion. The signaling pathway by which these two opposite first messengers regulate Na+, K(+)-ATPase activity involves the dopamine-specific protein phosphatase-1 inhibitor, DARPP-32, and the norepinephrine-activated protein phosphatase-2B, calcineurin. Aberrations in the renal dopamine/norepinephrine system may be the cause of alterations in the regulation of sodium excretion during ontogeny and in salt-sensitive hypertension.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Catecholamines / metabolism*
  • Dopamine / biosynthesis
  • Dopamine and cAMP-Regulated Phosphoprotein 32
  • Humans
  • Ion Transport
  • Kidney / metabolism
  • Nerve Tissue Proteins / metabolism
  • Phosphoproteins*
  • Receptors, Adrenergic / metabolism
  • Receptors, Dopamine / metabolism
  • Sodium / metabolism*
  • Sodium-Potassium-Exchanging ATPase / metabolism

Substances

  • Catecholamines
  • Dopamine and cAMP-Regulated Phosphoprotein 32
  • Nerve Tissue Proteins
  • Phosphoproteins
  • Receptors, Adrenergic
  • Receptors, Dopamine
  • Sodium
  • Sodium-Potassium-Exchanging ATPase
  • Dopamine