Literature DB >> 11512026

The disulfonic stilbene DIDS and the marine poison maitotoxin activate the same two types of endogenous cation conductance in the cell membrane of Xenopus laevis oocytes.

A Diakov1, J P Koch, O Ducoudret, S Müller-Berger, E Frömter.   

Abstract

In the present experiments we exposed the intra- or extracellular surface of excised giant membrane patches of Xenopus laevis oocytes bathed in 140 mmol/l Na-aspartate solution to the anion transport inhibitor 4,4'-diisothiocyanatostilbene-2,2'-disulfonate (DIDS, 250 micromol/l). We observed that DIDS activated at least two cation conductances: (1) a non-selective cation (NSC) conductance that was mediated by channels of approximately 27 pS and resembled the stretch-activated cation conductance that has been observed in the oocyte cell membrane previously, and (2) a Na+-selective conductance, the single-channel events of which could not be resolved and which resembled the depolarization-induced Na+ conductance that has also been observed in the oocyte cell membrane previously. Both conductances were blocked by 1 mmol/l amiloride from the intra- and extracellular surfaces but inhibition of the NSC conductance by extracellular amiloride was less pronounced. Both conductances activated only slowly with a delay of 15-60 s after application of DIDS and remained active even after DIDS was washed off. This suggests that DIDS caused the exocytosis of preformed channels and this interpretation was supported by our additional observation that extracellular application of maitotoxin (MTX) mimicked the effects of DIDS. MTX is a marine toxin that has recently been reported to induce exocytosis in Xenopus laevis oocytes. The fact that DIDS and MTX each carry two sulfonyl groups suggests that they act on the same positively charged binding sites of an exocytosis-inducing protein. Our observations demonstrate that using DIDS to inhibit heterologously expressed anion transporters in the cell membrane of Xenopus laevis oocytes may compromise proper determination of the transporter currents. This effect can be prevented if the DIDS-activated endogenous cation conductances are suppressed by application of amiloride to the cytoplasmic surface of the cell membrane.

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Year:  2001        PMID: 11512026     DOI: 10.1007/s004240100593

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  8 in total

1.  Chloride channel blockers activate an endogenous cationic current in oocytes of Bufo arenarum.

Authors:  M S Cavarra; S M del Mónaco; B A Kotsias
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2004-04-22       Impact factor: 1.836

Review 2.  Marine pharmacology in 2001--2002: marine compounds with anthelmintic, antibacterial, anticoagulant, antidiabetic, antifungal, anti-inflammatory, antimalarial, antiplatelet, antiprotozoal, antituberculosis, and antiviral activities; affecting the cardiovascular, immune and nervous systems and other miscellaneous mechanisms of action.

Authors:  Alejandro M S Mayer; Mark T Hamann
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2005 Mar-Apr       Impact factor: 3.228

3.  Effect of chloride channel inhibitors on cytosolic Ca2+ levels and Ca2+-activated K+ (Gardos) channel activity in human red blood cells.

Authors:  Yuliya V Kucherenko; Lisa Wagner-Britz; Ingolf Bernhardt; Florian Lang
Journal:  J Membr Biol       Date:  2013-02-22       Impact factor: 1.843

4.  HCO(3)(-)-independent conductance with a mutant Na(+)/HCO(3)(-) cotransporter (SLC4A4) in a case of proximal renal tubular acidosis with hypokalaemic paralysis.

Authors:  Mark D Parker; Xue Qin; Rosalind C Williamson; Ashley M Toye; Walter F Boron
Journal:  J Physiol       Date:  2012-02-13       Impact factor: 5.182

5.  Discovery of potent CLC chloride channel inhibitors.

Authors:  Kimberly Matulef; Andrew E Howery; Li Tan; William R Kobertz; J Du Bois; Merritt Maduke
Journal:  ACS Chem Biol       Date:  2008-07-18       Impact factor: 5.100

6.  NHE8 is an intracellular cation/H+ exchanger in renal tubules of the yellow fever mosquito Aedes aegypti.

Authors:  Peter M Piermarini; Dirk Weihrauch; Heiko Meyer; Markus Huss; Klaus W Beyenbach
Journal:  Am J Physiol Renal Physiol       Date:  2009-02-04

7.  Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak.

Authors:  Damien Barneaud-Rocca; Bernard Pellissier; Franck Borgese; Hélène Guizouarn
Journal:  Int J Cell Biol       Date:  2011-08-23

8.  PI3K and PKC contribute to membrane depolarization mediated by alpha2-adrenoceptors in the canine isolated mesenteric vein.

Authors:  Ilia A Yamboliev; Violeta N Mutafova-Yambolieva
Journal:  BMC Physiol       Date:  2005-06-15
  8 in total

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