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Fluoride flux in the rabbit CCD: A pH-dependent event

  • Alexander J. Rouch(corresponding author)
    ,
  • Gary M. Whitford
    ,
  • Harold T. Campbell
*Corresponding author for this work
  • University of Alabama at Birmingham
    ,
  • Unknown
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

We measured fluoride flux (JF; pmol ·; min-1 · mm-1) in the isolated rabbit cortical collecting duct (CCD) to investigate the determining factors of JF. The perfusate contained 100 μM fluoride and the bath was fluoride-free. Osmotically-induced lumen-to-bath water flux did not affect JF. When perfusate pH was reduced from 7.4 to 6.1 and from 6.1 to 5.0, JF increased from 0.008 ± 0.002 to 0.027 ± 0.007 (P < 0.01) and from 0.018 ± 0.003 to 0.040 ± 0.005 (P < 0.01), respectively. Acetazolamide at 10-4 M in the bath reduced JF slightly though not statistically. The anion-transport inhibitor, 4,4′-diisothiocyanato-stilbene-2,2′-disulfonic acid (DIDS), at 10-4 M in the perfusate did not affect JF. Substitution of luminal chloride with gluconate failed to affect JF in tubules from normal rabbits or from rabbits treated with deoxycorticosterone which stimulates chloride-bicarbonate exchange in the CCD. JF showed no correlation with transepithelial voltage which ranged from +4 to -104 mV. We conclude that the luminal pH represents the primary determining factor influencing JF in the rabbit CCD, and fluoride does not use a chloride-mediated or a DIDS-inhibitory transport pathway.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 342-349 (8 pages)

Journal (Volume, Issue Number)

Kidney International (Volume 41, Issue 2)

Publication milestones

  • Published - 02/1992

Publication status

Published - 02/1992

ISSN

0085-2538

Publication IDs

  • Scopus: 0026501152
  • PubMed: 1552707

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Funding Details

Portions of this work have been reported in abstract form: Rouch AJ, Whitford GM, Campbell HT: FASEB J. 2:A1307 1988. This work was supported by USPHS Grant No. DE-06429 from the National Institute of Dental Research, National Institutes of Health, Bethesda, Maryland. We are grateful to Dr. Mark A. Knepper for his keen insight into the planning of this study. We also thank Dr. James A. Schafer for his critical review of this manuscript and for his kindness in allowing some of the experiments to be completed in his laboratory at the Nephrology Research and Training Center, Birmingham, AL. We gratefully ac- knowledge the helpful suggestions from Dr. Jack Ginsburg, Dr. Gary Bond, and Dr. David Pashley.
FundersFunding numbers
NIH
-
NIDCR
R01DE006429
USPHS
DE-06429