Send to:

Choose Destination
See comment in PubMed Commons below
Cardiovasc Res. 2001 Aug 15;51(3):409-15.

The V2 vasopressin receptor mutations and fluid homeostasis.

Author information

  • 1Department of Anesthesiology and Physiology, UCLA School of Medicine, BOX 957115, Los Angeles, CA 90095, USA. marielb@ucla.ed


Although three different G-protein coupled receptors have been identified for arginine vasopressin, a significant physiological role has been recognized only for the V2 subtype that controls water homeostasis. Identification of the gene encoding the V2 vasopressin (or antidiuretic hormone) receptor enabled researchers to test the hypothesis that mutations of this gene were responsible for X-linked recessive nephrogenic diabetes insipidus. The affected patients are unable to concentrate their urine and as a consequence live in constant danger of dehydration that can cause death, particularly in infancy, or lead to severe hypernatremia that can impair their intellectual and physical development. The danger of severe dehydration diminishes in the adult patients, although they remain highly susceptible to this condition for the rest of their lives.

[PubMed - indexed for MEDLINE]
Free full text
PubMed Commons home

PubMed Commons

How to join PubMed Commons

    Supplemental Content

    Icon for HighWire
    Loading ...
    Write to the Help Desk