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Research Article Free access | 10.1172/JCI113732

Epidermal growth factor inhibits the hydroosmotic effect of vasopressin in the isolated perfused rabbit cortical collecting tubule.

M D Breyer, H R Jacobson, and J A Breyer

Department of Internal Medicine, Veterans Administration Medical Center, Nashville, TN 37232.

Find articles by Breyer, M. in: PubMed | Google Scholar

Department of Internal Medicine, Veterans Administration Medical Center, Nashville, TN 37232.

Find articles by Jacobson, H. in: PubMed | Google Scholar

Department of Internal Medicine, Veterans Administration Medical Center, Nashville, TN 37232.

Find articles by Breyer, J. in: PubMed | Google Scholar

Published October 1, 1988 - More info

Published in Volume 82, Issue 4 on October 1, 1988
J Clin Invest. 1988;82(4):1313–1320. https://doi.org/10.1172/JCI113732.
© 1988 The American Society for Clinical Investigation
Published October 1, 1988 - Version history
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Abstract

Epidermal growth factor (EGF) is a 53-amino acid polypeptide which is a potent mitogen for cultured cells. The kidney has recently been shown to be a major site of synthesis for the EGF precursor. EGF infusions in sheep result in a diuresis and natriuresis despite a fall in GFR, suggesting a direct tubular effect. Using in vitro microperfusion of rabbit cortical collecting tubules (CCTs) at 37 degrees C, we examined the effect of EGF on the transepithelial voltage (Vt) and arginine vasopressin (AVP)-stimulated hydraulic conductivity (Lp). Pretreatment with peritubular EGF at concentrations from 10(-8) to 10(-12) M resulted in a 50% inhibition of both AVP- and 8-chlorophenythio-cyclic AMP-stimulated peak Lp. This effect was reversed by the protein kinase C inhibitor, staurosporine, but unaffected by indomethacin. CCTs with an initially negative Vt, depolarized after exposure to bath EGF. 10(-8) M EGF applied from the lumen had no effect on either Lp or Vt. Specific binding of 20 nM 125I-EGF to microdissected CCTs was also demonstrated. These results suggest that EGF can modulate both salt and water transport in the CCT via a receptor linked to protein kinase C activation.

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