Literature DB >> 3942227

Conductive properties of the rabbit outer medullary collecting duct: outer stripe.

B M Koeppen.   

Abstract

Segments of the outer medullary collecting duct were dissected from the outer stripe of the rabbit kidney (OMCDo) and perfused in vitro. The conductive properties of the tubule epithelium and individual cell membranes were determined by means of cable analysis and intracellular voltage-recording microelectrodes. The transepithelial voltage (VT) and resistance (RT) averaged -10.7 +/- 2.5 mV, lumen negative, and 28.5 +/- 2.9 k omega X cm (n = 27), respectively. Two cell types could be defined by their electrophysiological properties. One cell type (n = 7) had a mean basolateral membrane voltage (Vbl) of -30.1 +/- 2.4 mV, a fractional resistance of the apical membrane (fRa = Ra/Ra + Rbl) near unity (0.99 +/- 0.01), and a predominantly Cl(-)-selective basolateral cell membrane. The second cell type (n = 27) had a mean Vbl of -63.7 +/- 2.7 mV, a fRa of 0.81 +/- 0.02, and a predominantly K+-selective basolateral cell membrane. The present study focused on defining the conductive properties of this latter cell type. Amiloride (10(-5) M) and BaCl2 (2 mM) were used as probes of apical cell membrane Na+ and K+ conductive pathways, respectively. Amiloride increased fRa from 0.80 +/- 0.02 to 0.98 +/- 0.01 (n = 12), whereas BaCl2 increased fRa from 0.77 +/- 0.03 to 0.82 +/- 0.03 (n = 9). The conductive properties of the basolateral cell membrane were assessed by ion substitutions of the bath solution. A 10-fold increase in the bath [K+] depolarized Vbl by 34.9 +/- 1.9 mV (n = 16) in less than 1 s, indicating that this membrane was predominantly K+ selective.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3942227     DOI: 10.1152/ajprenal.1986.250.1.F70

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  9 in total

1.  Electrophysiological identification of alpha- and beta-intercalated cells and their distribution along the rabbit distal nephron segments.

Authors:  S Muto; K Yasoshima; K Yoshitomi; M Imai; Y Asano
Journal:  J Clin Invest       Date:  1990-12       Impact factor: 14.808

Review 2.  Molecular mechanisms and regulation of urinary acidification.

Authors:  Ira Kurtz
Journal:  Compr Physiol       Date:  2014-10       Impact factor: 9.090

3.  Electrophysiological identification of principal and intercalated cells in the rabbit outer medullary collecting duct.

Authors:  B M Koeppen
Journal:  Pflugers Arch       Date:  1987-06       Impact factor: 3.657

Review 4.  Renal Tubular Acidosis: H+/Base and Ammonia Transport Abnormalities and Clinical Syndromes.

Authors:  Ira Kurtz
Journal:  Adv Chronic Kidney Dis       Date:  2018-07       Impact factor: 3.620

5.  The swelling-activated chloride channel ClC-2, the chloride channel ClC-3, and ClC-5, a chloride channel mutated in kidney stone disease, are expressed in distinct subpopulations of renal epithelial cells.

Authors:  N Obermüller; N Gretz; W Kriz; R F Reilly; R Witzgall
Journal:  J Clin Invest       Date:  1998-02-01       Impact factor: 14.808

6.  Regulation of rabbit medullary collecting duct cell pH by basolateral Na+/H+ and Cl-/base exchange.

Authors:  M D Breyer; H R Jacobson
Journal:  J Clin Invest       Date:  1989-09       Impact factor: 14.808

7.  Functional characterization of the vertebrate primary ureter: structure and ion transport mechanisms of the pronephric duct in axolotl larvae (Amphibia).

Authors:  Birgitte M Haugan; Kenneth A Halberg; Ase Jespersen; Lea R Prehn; Nadja Møbjerg
Journal:  BMC Dev Biol       Date:  2010-05-27       Impact factor: 1.978

8.  Mechanisms of renal tubular acidification.

Authors:  G Giebisch
Journal:  Klin Wochenschr       Date:  1986-09-15

9.  ROMK inhibitor actions in the nephron probed with diuretics.

Authors:  Sujay V Kharade; Daniel Flores; Craig W Lindsley; Lisa M Satlin; Jerod S Denton
Journal:  Am J Physiol Renal Physiol       Date:  2015-12-09
  9 in total

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