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Journal Article

Persistent stimulation of adenylate cyclase and urea transport by an AVP photolabel

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Fahrenholz,  Falk
Department of Physical Chemistry, Max Planck Institute of Biophysics, Max Planck Society;

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Citation

Eggena, P., Ma, C. L., Fahrenholz, F., & Schwartz, I. L. (1985). Persistent stimulation of adenylate cyclase and urea transport by an AVP photolabel. American Journal of Physiology: Cell Physiology, 249(1 Pt 1), C84-C88. doi:10.1152/ajpcell.1985.249.1.C84.


Cite as: https://hdl.handle.net/21.11116/0000-0008-6E5F-4
Abstract
The effects of a photoaffinity label for arginine vasopressin receptors, [Phe2, Phe(p-N3)3]AVP (N3-AVP), on urea permeability and adenylate cyclase activity have been investigated in the toad urinary bladder. This compound, when activated by ultraviolet light, induced a maximal and persistent increase in the urea permeability of the intact bladder and a persistent increase in the adenylate cyclase activity of toad bladder epithelial cell homogenates. Covalent attachment of the analogue to target tissue during photolysis was equivalent at 4 and 20 degrees C. Bladders exposed to N3-AVP in the presence of AVP during photolysis were substantially less permeable to urea than controls that had been exposed to N3-AVP alone. These findings constitute further evidence in support of our previous suggestion that N3-AVP binds covalently to AVP receptors and, in addition, demonstrates that N3-AVP evokes a persistent increase in adenylate cyclase activity which, in turn, triggers a persistent increase in bladder permeability to urea.