Literature DB >> 7530839

Basolateral K+ efflux is largely independent of maxi-K+ channels in rat submandibular glands during secretion.

T Ishikawa1, M Murakami, Y Seo.   

Abstract

The involvement of large-conductance, voltage- and Ca(2+)-activated K+ channels (maxi-K+ channels) in basolateral Ca(2+)-dependent K(+)-efflux pathways and fluid secretion by the rat submandibular gland was investigated. Basolateral K+ efflux was monitored by measuring the change in K+ concentration in the perfusate collected from the vein of the isolated, perfused rat submandibular gland every 30 s. Under conditions in which the Na+/K(+)-ATPase and Na(+)-K(+)-2Cl- cotransporter were inhibited by ouabain (1 mmol/l) and bumetanide (50 mumol/l) respectively, continuous stimulation with acetylcholine (ACh) (1 mumol/l) caused a transient large net K+ efflux, followed by a smaller K+ efflux, which gradually returned to the basal level within 10 min. These two components of the K+ efflux appear to be dependent on an increase in cytosolic Ca2+ concentration. The initial transient K+ efflux was not affected by charybdotoxin (100 nmol/l) or tetraethylammonium (TEA) (5 mmol/l) but the smaller second component was strongly and reversibly inhibited by charybdotoxin (100 nmol/l) and TEA (0.1 and 5 mmol/l). The initial K+ efflux transient induced by ACh was inhibited by quinine (0.1-3 mmol/l), quinidine (1-3 mmol/l) and Ba2+ (5 mmol/l), but not by verapamil (0.1 mmol/l), lidocaine (1 mmol/l), 4-aminopyridine (1 mmol/l) or apamin (1 mumol/l). Ca(2+)-dependent transient large K+ effluxes induced by substance P (0.01 mumol/l) and A23187 (3 mumol/l) were not inhibited by TEA (5 mmol/l or 10 mmol/l). A23187 (3 mumol/l) evoked a biphasic fluid-secretory response, which was not inhibited by TEA (5 mmol/l). Patch-clamp studies confirmed that the whole-cell outward K+ current attributable to maxi-K+ channels obtained from rat submandibular endpiece cells was strongly inhibited by the addition of TEA (1-10 mmol/l) to the bath. It is concluded that maxi-K+ channels are not responsible for the major part of the Ca(2+)-dependent basolateral K+ efflux and fluid secretion by the rat submandibular gland.

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Year:  1994        PMID: 7530839     DOI: 10.1007/bf00374573

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


  23 in total

1.  Specificity of tetraethylammonium and quinine for three K channels in insulin-secreting cells.

Authors:  S Fatherazi; D L Cook
Journal:  J Membr Biol       Date:  1991-03       Impact factor: 1.843

2.  Decrease in rat submandibular acinar cell volume during ACh stimulation.

Authors:  T Nakahari; M Murakami; H Yoshida; M Miyamoto; Y Sohma; Y Imai
Journal:  Am J Physiol       Date:  1990-06

3.  Purification of charybdotoxin, a specific inhibitor of the high-conductance Ca2+-activated K+ channel.

Authors:  C Smith; M Phillips; C Miller
Journal:  J Biol Chem       Date:  1986-11-05       Impact factor: 5.157

4.  Antimuscarinic effects of chloroquine in rat pancreatic acini.

Authors:  Y Habara; J A Williams; S R Hootman
Journal:  Biochem Biophys Res Commun       Date:  1986-06-13       Impact factor: 3.575

5.  Direct measurement of K movement by 39K NMR in perfused rat mandibular salivary gland stimulated with acetylcholine.

Authors:  M Murakami; E Suzuki; S Miyamoto; Y Seo; H Watari
Journal:  Pflugers Arch       Date:  1989-08       Impact factor: 3.657

6.  Effects of extracellular ATP on ion transport systems and [Ca2+]i in rat parotid acinar cells. Comparison with the muscarinic agonist carbachol.

Authors:  S P Soltoff; M K McMillian; E J Cragoe; L C Cantley; B R Talamo
Journal:  J Gen Physiol       Date:  1990-02       Impact factor: 4.086

7.  Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.

Authors:  O P Hamill; A Marty; E Neher; B Sakmann; F J Sigworth
Journal:  Pflugers Arch       Date:  1981-08       Impact factor: 3.657

8.  Voltage and Ca2+-activated K+ channel in baso-lateral acinar cell membranes of mammalian salivary glands.

Authors:  Y Maruyama; D V Gallacher; O H Petersen
Journal:  Nature       Date:  1983-04-28       Impact factor: 49.962

9.  Tetraethylammonium blocks muscarinically evoked secretion in the sheep parotid gland by a mechanism additional to its blockade of BK channels.

Authors:  D I Cook; E A Wegman; T Ishikawa; P Poronnik; D G Allen; J A Young
Journal:  Pflugers Arch       Date:  1992-02       Impact factor: 3.657

10.  Calcium-dependent K+ efflux from rat submandibular gland. The effects of trifluoperazine and quinidine.

Authors:  R J Kurtzer; M L Roberts
Journal:  Biochim Biophys Acta       Date:  1982-12-22
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  4 in total

1.  Regulation of membrane potential and fluid secretion by Ca2+-activated K+ channels in mouse submandibular glands.

Authors:  Victor G Romanenko; Tetsuji Nakamoto; Alaka Srivastava; Ted Begenisich; James E Melvin
Journal:  J Physiol       Date:  2007-03-22       Impact factor: 5.182

Review 2.  Ca²⁺-dependent K⁺ channels in exocrine salivary glands.

Authors:  Marcelo A Catalán; Gaspar Peña-Munzenmayer; James E Melvin
Journal:  Cell Calcium       Date:  2014-01-31       Impact factor: 6.817

3.  Pharmacological investigation of the role of ion channels in salivary secretion.

Authors:  Tina C Stummann; Jørgen H Poulsen; Anders Hay-Schmidt; Morten Grunnet; Dan A Klaerke; Hanne B Rasmussen; Søren-Peter Olesen; Nanna K Jorgensen
Journal:  Pflugers Arch       Date:  2003-02-15       Impact factor: 3.657

4.  Tetraethylammonium-insensitive, Ca(2+)-activated whole-cell K+ currents in rat submandibular acinar cells.

Authors:  T Ishikawa; M Murakami
Journal:  Pflugers Arch       Date:  1995-03       Impact factor: 3.657

  4 in total

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