Activation of AQP2 water channels by protein kinase A: therapeutic strategies for congenital nephrogenic diabetes insipidus

BACKGROUND: Congenital nephrogenic diabetes insipidus (NDI) is primarily caused by loss-of-function mutations in the vasopressin type 2 receptor (V2R). Renal unresponsiveness to the antidiuretic hormone vasopressin impairs aquaporin-2 (AQP2) water channel activity and water reabsorption from urine,...

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Detalles Bibliográficos
Autor principal: Ando, Fumiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Invited Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421276/
https://www.ncbi.nlm.nih.gov/pubmed/34224008
http://dx.doi.org/10.1007/s10157-021-02108-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421276/
https://www.ncbi.nlm.nih.gov/pubmed/34224008
http://dx.doi.org/10.1007/s10157-021-02108-6

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