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Am J Physiol Renal Physiol 279: F144-F152, 2000;
0363-6127/00 $5.00
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Vol. 279, Issue 1, F144-F152, July 2000

Downregulation of aquaporin-2 and -3 in aging kidney is independent of V2 vasopressin receptor

L. Preisser1, L. Teillet1,2, S. Aliotti1, R. Gobin1, V. Berthonaud1, J. Chevalier3, B. Corman1, and J.-M. Verbavatz1

1 Service de Biologie Cellulaire, Commissariat à l'Énergie Atomique/Saclay, Gif-sur-Yvette; 2 Assistance-Publique-Hôpital de Paris, Hôpital Ste. Périne, Paris 16; and 3 Institut National de la Santé et de la Recherche Médicale U-430, Hôpital Broussais, Paris 14, France

The mechanisms underlying age-related polyuria were investigated in 10- and 30-mo-old female WAG/Rij rats. Urinary volume and osmolality were 3.9 ± 0.3 ml/24 h and 2,511 ± 54 mosmol/kgH2O in adult rats and 12.8 ± 0.8 ml/24 h and 1,042 ± 44 mosmol/kgH2O in senescent animals. Vasopressin V2 receptor mRNA did not significantly differ between 10 and 30 mo, and [3H]vasopressin binding sites in membrane papilla were reduced by 30%. The cAMP content of the papilla was unchanged with age, whereas papillary osmolality was significantly lowered in senescent animals. The expression of aquaporin-1 (AQP1) and -4 was mostly unaltered from 10 to 30 mo. In contrast, aquaporin-2 (AQP2) and -3 (AQP3) expression was downregulated by 80 and 50%, respectively, and AQP2 was markedly redistributed into the intracellular compartment, in inner medulla of senescent animals, but not in renal cortex. These results indicate that age-related polyuria is associated with a downregulation of AQP2 and AQP3 expression in the medullary collecting duct, which is independent of vasopressin-mediated cAMP accumulation.

aquaporins


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