Mechanisms of guanylin action via cyclic GMP in the kidney

Annu Rev Physiol. 2000:62:673-95. doi: 10.1146/annurev.physiol.62.1.673.

Abstract

Guanylin, uroguanylin, and lymphoguanylin are small peptides that activate cell-surface guanylate cyclase receptors and influence cellular function via intracellular cGMP. Guanylins activate two receptors, GC-C and OK-GC, which are expressed in intestine and/or kidney. Elevation of cGMP in the intestine elicits an increase in electrolyte and water secretion. Activation of renal receptors by uroguanylin stimulates urine flow and excretion of sodium, chloride, and potassium. Intracellular cGMP pathways for guanylins include activation of PKG-II and/or indirect stimulation of PKA-II. The result is activation of CFTR and/or C1C-2 channel proteins to enhance the electrogenic secretion of chloride and bicarbonate. Similar cellular mechanisms may be involved in the renal responses to guanylin peptides. Uroguanylin serves as an intestinal natriuretic hormone in postprandial states, thus linking the digestive and renal organ systems in a novel endocrine axis. Therefore, uroguanylin participates in the complex physiological processes underlying the saliuresis that is elicited by a salty meal.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cyclic GMP / physiology*
  • Gastrointestinal Hormones*
  • Guanylate Cyclase / metabolism
  • Humans
  • Kidney / physiology*
  • Molecular Sequence Data
  • Natriuretic Peptides
  • Peptides / genetics
  • Peptides / physiology*
  • Signal Transduction / physiology

Substances

  • Gastrointestinal Hormones
  • Natriuretic Peptides
  • Peptides
  • guanylin
  • Guanylate Cyclase
  • Cyclic GMP