4.2 Review

Glycogen synthase kinase-3 regulation of urinary concentrating ability

Journal

CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
Volume 21, Issue 5, Pages 541-546

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MNH.0b013e32835571d4

Keywords

aquaporin 2; cyclooxygenase; glycogen synthase kinase-3; nephrogenic diabetes insipidus; prostaglandin; vasopressin

Funding

  1. National Institutes of Health [R01-DK083525]

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Purpose of review Glycogen synthase kinase-3 (GSK3) is an enzyme that is gaining prominence as a critical signaling molecule in the epithelial cells of renal tubules. This review will focus on recent findings exploring the role of GSK3 in renal collecting ducts, especially its role in urine concentration involving vasopressin signaling. Recent findings Recent studies using inhibition or tissue-specific gene deletion of GSK3 revealed the mechanism by which GSK3 regulates aquaporin 2 water channels via adenylate cyclase or the prostaglandin-E-2 pathway. In other studies, postnatal treatment with lithium, an inhibitor of GSK3, increased cell proliferation and led to microcyst formation in rat kidneys. These studies suggest that loss of GSK3 activity could interfere with renal water transport at two levels. In the short term, it could disrupt vasopressin signaling in collecting duct cells and in the long term it could alter the structure of the collecting ducts, making them less responsive to the hydro-osmotic effects of vasopressin. Summary Ongoing studies reveal the crucial role played by GSK3 in the regulation of vasopressin action in the renal collecting ducts and suggest a possible use of GSK3 inhibitors in disease conditions associated with disrupted vasopressin signaling.

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