Literature DB >> 7212067

Intracellular potentials in rabbit proximal tubules perfused in vitro.

B Biagi, T Kubota, M Sohtell, G Giebisch.   

Abstract

Conventional microelectrodes were used to measure the basolateral membrane potential (VBL) in isolated perfused superficial proximal convoluted (sPCT) and superficial proximal straight (sPST) tubules of the rabbit kidney. Stable recordings for periods up to 2 h can be obtained. The mean +/- SE (n = number of cells) values of VBL were sPCT = -51.0 +/- 1.63 (24) and sPST = -47.0 +/- 0.97 (94) mV. Inhibitors of active transport, ouabain (10(-5) M) and low bath potassium (0.1 mM), caused a significant depolarization of VBL in sPST. In contrast, short-duration bath cooling (10 degrees C) had no significant effect. Removal of luminal glucose caused a larger hyperpolarization in sPCT (-13.9 +/- 1.77 (9) mV) than in sPST (-3.8 +/- 1.02 (5) mV). Removal of luminal glucose and alanine resulted in an even larger hyperpolarization of VBL in sPCT (-19.0 +/- 0.44 (6) mV). Perfusion of the lumen with a solution resembling late proximal tubular fluid in sPST resulted in hyperpolarization of VBL (-4.3 +/- 0.85 (4) mV). Reducing bath pH to 6.7 depolarized VBL (39.9 +/- 1.77 (13) mV). This effect can be associated with a decrease in the relative potassium permeability of the basolateral membrane. These results demonstrate the feasibility of using intracellular electrical measurements to determine both luminal and basolateral membrane characteristics in isolated proximal tubular segments.

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Year:  1981        PMID: 7212067     DOI: 10.1152/ajprenal.1981.240.3.F200

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


  45 in total

1.  Expression of an artificial Cl- channel in microperfused renal proximal tubules.

Authors:  N Matsumoto; S Tsuruoka; T Iwamoto; J M Tomich; K Ito; M Imai; M Suzuki
Journal:  J Membr Biol       Date:  2003-06-01       Impact factor: 1.843

2.  Cell swelling, co-transport activation and potassium conductance in isolated perfused rabbit kidney proximal tubules.

Authors:  J S Beck; D J Potts
Journal:  J Physiol       Date:  1990-06       Impact factor: 5.182

Review 3.  Molecular diversity and regulation of renal potassium channels.

Authors:  Steven C Hebert; Gary Desir; Gerhard Giebisch; Wenhui Wang
Journal:  Physiol Rev       Date:  2005-01       Impact factor: 37.312

4.  Potassium-selective channels in the basolateral membrane of single proximal tubule cells of frog kidney.

Authors:  M Hunter
Journal:  Pflugers Arch       Date:  1991-03       Impact factor: 3.657

5.  Functional heterogeneity in the hamster medullary thick ascending limb of Henle's loop.

Authors:  K Yoshitomi; C Koseki; J Taniguchi; M Imai
Journal:  Pflugers Arch       Date:  1987-05       Impact factor: 3.657

6.  Characterization of a Ca-dependent maxi K channel in the apical membrane of a cultured renal epithelium (JTC-12.P3).

Authors:  H A Kolb; C D Brown; H Murer
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

Review 7.  Molecular aspects of structure, gating, and physiology of pH-sensitive background K2P and Kir K+-transport channels.

Authors:  Francisco V Sepúlveda; L Pablo Cid; Jacques Teulon; María Isabel Niemeyer
Journal:  Physiol Rev       Date:  2015-01       Impact factor: 37.312

Review 8.  Molecular mechanisms and regulation of urinary acidification.

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

9.  Regulation of inwardly rectifying K+ channels by intracellular pH in opossum kidney cells.

Authors:  T Ohno-Shosaku; T Kubota; J Yamaguchi; M Fujimoto
Journal:  Pflugers Arch       Date:  1990-04       Impact factor: 3.657

10.  Effect of bicarbonate, pH, methazolamide and stilbenes on the intracellular potentials of cultured bovine corneal endothelial cells.

Authors:  T J Jentsch; M Koch; H Bleckmann; M Wiederholt
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

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