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Am J Physiol Renal Physiol 296: F1194-F1201, 2009. First published February 25, 2009; doi:10.1152/ajprenal.90774.2008
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Potential role of purinergic signaling in lithium-induced nephrogenic diabetes insipidus

Yue Zhang,2,4 Raoul D. Nelson,5 Noel G. Carlson,3,7,8 Craig D. Kamerath,2,4 Donald E. Kohan,1,4,6 and Bellamkonda K. Kishore1,4,6,8

Nephrology 1Service and 2Research and 3Geriatric Research, Education and Clinical Center, Department of Veterans Affairs Salt Lake City Health Care System and Departments of 4Internal Medicine, 5Pediatrics, 6Physiology, and 7Neurobiology and Anatomy and 8Center on Aging, University of Utah Health Sciences Center, Salt Lake City, Utah

Submitted 30 December 2008 ; accepted in final form 20 February 2009

Lithium (Li)-induced nephrogenic diabetes insipidus (NDI) has been attributed to the increased production of renal prostaglandin (PG)E2. Previously we reported that extracellular nucleotides (ATP/UTP), acting through P2y2 receptor in rat medullary collecting duct (mCD), produce and release PGE2. Hence we hypothesized that increased production of PGE2 in Li-induced NDI may be mediated by enhanced purinergic signaling in the mCD. Sprague-Dawley rats were fed either control or Li-added diet for 14 or 21 days. Li feeding resulted in marked polyuria and polydipsia associated with a decrease in aquaporin (AQP)2 protein abundance in inner medulla (~20% of controls) and a twofold increase in urinary PGE2. When acutely challenged ex vivo with adenosine 5'-O-(3-thiotriphosphate) (ATP{gamma}S), UTP, or ADP, mCD of Li-fed rats showed significantly higher increases (50–130% over control diet-fed rats) in PGE2 production, indicating that more than one subtype of P2y receptor is involved. This was associated with a 3.4-fold increase in P2y4, but not P2y2, receptor mRNA expression in the inner medulla of Li-fed rats compared with control diet-fed rats. Confocal laser immunofluorescence microscopy revealed predominant localization of both P2y2 and P2y4 receptors in the mCD of control or Li diet-fed rats. Together, these data indicate that in Li-induced NDI 1) purinergic signaling in the mCD is sensitized with increased production of PGE2 and 2) P2y2 and/or P2y4 receptors may be involved in the enhanced purinergic signaling. Our study also reveals the potential beneficial effects of P2y receptor antagonists in the treatment and/or prevention of Li-induced NDI.

collecting duct; P2 receptors; extracellular nucleotides; prostaglandin E2; cyclooxygenases; bipolar disorder; neurodegeneration; rat



Address for reprint requests and other correspondence: B. K. Kishore, Nephrology Research (151M), VA SCL Health Care System, 500 Foothill Dr., Salt Lake City, UT 84148 (e-mail: bk.kishore{at}hsc.utah.edu)







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