Literature DB >> 8781197

Re-evaluation of the P/Q Ca2+ channel components of Ba2+ currents in bovine chromaffin cells superfused with solutions containing low and high Ba2+ concentrations.

A Albillos1, A G García, B Olivera, L Gandía.   

Abstract

This study was undertaken to reassess the set of voltage-dependent Ca2+ channel subtypes expressed by bovine adrenal chromaffin cells maintained in primary cultures. Previous views on the pharmacology of such channels had to be revised in the light of the novel data which arose from the use in this study of low and high micromolar concentrations of omega-agatoxin IVA, and low (2 mM) and high (10 mM) concentrations of the charge carrier Ba2+. Whole-cell Ba2+ currents (IBa) through Ca2+ channels were elicited in voltage-clamped chromaffin cells, with a holding potential of -80 mV and depolarising pulses to 0 mV. Mean peak IBa was 425 pA in 2 mM Ba2+ (59 cells) and 787 pA in 10 mM Ba2+ (42 cells). In 2 mM Ba2+, omega-conotoxin MVIIC (3 microM) inhibited IBa by 79%; in 10 mM Ba2+, the blockade developed much more slowly and reached only 44%. A low concentration of omega-agatoxin IVA (20 nM) inhibited IBa by 9%; 2 microM inhibited IBa by 60%. This blockade was similar in low and high Ba2+ concentrations. After giving furnidipine (3 microM) and omega-conotoxin GVIA (1 microM), 2 microM omega-agatoxin IVA inhibited the remaining current (about 40-45%); this blockade was independent of the Ba2+ concentration. The current could be fully blocked by the cocktail furnidipine/omega-conotoxin GVIA/high omega-agatoxin IVA, both in low and high Ba2+ concentrations. The large Q-type channel component of IBa is blocked by micromolar concentrations of omega-agatoxin IVA and omega-conotoxin MVIIC. While solutions with a high Ba2+ concentration strongly delayed the development of blockade by omega-conotoxin MVIIC, the blockade by high concentrations of omega-agatoxin IVA was equally effective in solutions with a low or a high Ba2+ concentration. Hence, the use of appropriate Ba2+ and toxin concentrations in this study reveals that P-type Ca2+ channels are poorly expressed in bovine chromaffin cells; in contrast, a robust component of the current depends on Q-type Ca2+ channels. An R-type residual current is not present in these cells.

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Year:  1996        PMID: 8781197     DOI: 10.1007/s004240050231

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


  31 in total

1.  A new Conus peptide ligand for mammalian presynaptic Ca2+ channels.

Authors:  D R Hillyard; V D Monje; I M Mintz; B P Bean; L Nadasdi; J Ramachandran; G Miljanich; A Azimi-Zoonooz; J M McIntosh; L J Cruz
Journal:  Neuron       Date:  1992-07       Impact factor: 17.173

2.  P-type calcium channels blocked by the spider toxin omega-Aga-IVA.

Authors:  I M Mintz; V J Venema; K M Swiderek; T D Lee; B P Bean; M E Adams
Journal:  Nature       Date:  1992-02-27       Impact factor: 49.962

3.  The blocking effects of omega-conotoxin on Ca current in bovine chromaffin cells.

Authors:  M Hans; P Illes; K Takeda
Journal:  Neurosci Lett       Date:  1990-06-22       Impact factor: 3.046

4.  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

5.  Two types of Ca2+ currents are found in bovine chromaffin cells: facilitation is due to the recruitment of one type.

Authors:  C R Artalejo; M K Dahmer; R L Perlman; A P Fox
Journal:  J Physiol       Date:  1991-01       Impact factor: 5.182

6.  Separate binding and functional sites for omega-conotoxin and nitrendipine suggest two types of calcium channels in bovine chromaffin cells.

Authors:  J J Ballesta; M Palmero; M J Hidalgo; L M Gutierrez; J A Reig; S Viniegra; A G Garcia
Journal:  J Neurochem       Date:  1989-10       Impact factor: 5.372

7.  Q- and L-type Ca2+ channels dominate the control of secretion in bovine chromaffin cells.

Authors:  M G López; M Villarroya; B Lara; R Martínez Sierra; A Albillos; A G García; L Gandía
Journal:  FEBS Lett       Date:  1994-08-08       Impact factor: 4.124

8.  Characteristics of [125I]omega-conotoxin MVIIA binding to rat neocortical membranes.

Authors:  S J Stoehr; D J Dooley
Journal:  Neurosci Lett       Date:  1993-10-14       Impact factor: 3.046

9.  Localized L-type calcium channels control exocytosis in cat chromaffin cells.

Authors:  M G López; A Albillos; M T de la Fuente; R Borges; L Gandía; E Carbone; A G García; A R Artalejo
Journal:  Pflugers Arch       Date:  1994-06       Impact factor: 3.657

10.  Calcium channel subtypes in cat chromaffin cells.

Authors:  A Albillos; A R Artalejo; M G López; L Gandía; A G García; E Carbone
Journal:  J Physiol       Date:  1994-06-01       Impact factor: 5.182

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  15 in total

1.  R-Type Ca2+ channels are coupled to the rapid component of secretion in mouse adrenal slice chromaffin cells.

Authors:  A Albillos; E Neher; T Moser
Journal:  J Neurosci       Date:  2000-11-15       Impact factor: 6.167

2.  Inhibition of N and PQ calcium channels by calcium entry through L channels in chromaffin cells.

Authors:  Juliana M Rosa; Luis Gandía; Antonio G García
Journal:  Pflugers Arch       Date:  2009-04-04       Impact factor: 3.657

Review 3.  Regulation by L-type calcium channels of endocytosis: an overview.

Authors:  Juliana M Rosa; Carmen Nanclares; Angela Orozco; Inés Colmena; Ricardo de Pascual; Antonio G García; Luis Gandía
Journal:  J Mol Neurosci       Date:  2012-05-12       Impact factor: 3.444

4.  Methylmercury decreases cellular excitability by a direct blockade of sodium and calcium channels in bovine chromaffin cells: an integrative study.

Authors:  J Fuentes-Antrás; E Osorio-Martínez; M Ramírez-Torres; I Colmena; J C Fernández-Morales; J M Hernández-Guijo
Journal:  Pflugers Arch       Date:  2013-07-03       Impact factor: 3.657

5.  Low-threshold exocytosis induced by cAMP-recruited CaV3.2 (alpha1H) channels in rat chromaffin cells.

Authors:  A Giancippoli; M Novara; A de Luca; P Baldelli; A Marcantoni; E Carbone; V Carabelli
Journal:  Biophys J       Date:  2005-12-16       Impact factor: 4.033

6.  Differential blockade of rat alpha3beta4 and alpha7 neuronal nicotinic receptors by omega-conotoxin MVIIC, omega-conotoxin GVIA and diltiazem.

Authors:  C J Herrero; E García-Palomero; A J Pintado; A G García; C Montiel
Journal:  Br J Pharmacol       Date:  1999-07       Impact factor: 8.739

7.  Calcium-dependent inhibition of L, N, and P/Q Ca2+ channels in chromaffin cells: role of mitochondria.

Authors:  J M Hernandez-Guijo; V E Maneu-Flores; A Ruiz-Nuno; M Villarroya; A G Garcia; L Gandia
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

Review 8.  Chromaffin cells as a model to evaluate mechanisms of cell death and neuroprotective compounds.

Authors:  Cristobal de Los Rios; Maria F Cano-Abad; Mercedes Villarroya; Manuela G López
Journal:  Pflugers Arch       Date:  2017-08-19       Impact factor: 3.657

Review 9.  L-type calcium channels in exocytosis and endocytosis of chromaffin cells.

Authors:  Carmen Nanclares; Andrés M Baraibar; Luis Gandía
Journal:  Pflugers Arch       Date:  2017-09-02       Impact factor: 3.657

10.  Voltage inactivation of Ca2+ entry and secretion associated with N- and P/Q-type but not L-type Ca2+ channels of bovine chromaffin cells.

Authors:  M Villarroya; R Olivares; A Ruíz; M F Cano-Abad; R de Pascual; R B Lomax; M G López; I Mayorgas; L Gandía; A G García
Journal:  J Physiol       Date:  1999-04-15       Impact factor: 5.182

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