Interactions of lysyl-bradykinin and antidiuretic hormone in the rabbit cortical collecting tubule

V. L. Schuster, J. P. Kokko, H. R. Jacobson

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Abstract

Although intrarenal infusions of kinens produce diuresis, it is not clear to what extent this response is due to hemodynamically mediated medullary washout and/or to direct epithelial effects of kinins. Recent evidence has shown that bradykinin binds to collecting tubules in vitro. We therefore examined the interactions of lysyl-bradykinin and antidiuretic hormone (ADH) with respect to hydraulic conductivity (L(p)) in the rabbit cortical collecting tubule perfused in vitro. To ensure adequate substrate for prostaglandin synthesis, the bath contained 2.5 μM arachidonic acid. Arachidonic acid produced no change in base-line L(p) and had no effect on the subsequent response to a supramaximal dose of ADH (100 μU/ml). Therefore, all subsequent experiments were done in the presence of arachidonic acid. Lysyl-bradykinin (10-9 M) added to either the lumen or bath had no effect on baseline L(p). Collecting tubules which were exposed for 1 h to bath lysyl-bradykinin (10-9 M) had a significantly diminished subsequent L(p) in response to ADH (P < 0.02). In tubules exposed to bath lysyl-bradykinin plus indomethacin (5 μM), the subsequent ADH response was normal. Lysyl-bradykinin (10-9 M) added to the lumen had no effect on subsequent ADH response. We conclude that lysyl-bradykinin from the basolateral side inhibits the hydroosmotic response of the cortical collecting tubule to ADH, and that this inhibition is probably prostaglandin-mediated. Lysyl-bradykinin does not affect water flow from the luminal surface. These data indicate that the diuresis seen with kinin infusions may result, at least in part, from a direct epithelial effect. They also suggest a role of the renal kallikrein-kinin system in modulating water transport in vivo.

Original languageEnglish (US)
Pages (from-to)1659-1667
Number of pages9
JournalJournal of Clinical Investigation
Volume73
Issue number6
DOIs
StatePublished - Jan 1 1984
Externally publishedYes

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ASJC Scopus subject areas

  • Medicine(all)

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