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PMID: 10639100 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Novel action of BAPTA series chelators on intrinsic K+ currents in rat hippocampal neurones.

The Journal of physiology ·Vol. 522 Pt 2 ·2000-01-15 ·Pages 231-46

Lancaster B, Batchelor AM

Abstract

1. Whole-cell recordings were made from rat CA1 neurones in brain slices. When electrodes contained diazo-2 (2 mM) or dibromo BAPTA (1 mM) a large steady-state outward current (hundreds of picoamps) developed within 5 min of breakthrough at a VH of -60 mV. BAPTA itself (1 mM) caused qualitatively similar but smaller effects. 2. The outward current was accompanied by increased conductance with a null potential close to the calculated K+ equilibrium potential (EK) of -110 mV. Development of outward current occurred concurrently with progressive loss of slow AHP tail current (IsAHP) evoked by brief depolarizations. The peak latency of IsAHP increased during the onset of chelator action. 3. The persistent outward current was reversibly inhibited by noradrenaline (10 microM) or isoprenaline (2-5 microM), and completely prevented by 8-bromoadenosine 3',5' cyclic monophosphate (8-Br cAMP; 100 microM) or QX-314 (10 mM) in recording electrodes. After development of outward current, diazo-2 photolysis caused inward current and decreased conductance. Both flash- and noradrenergic-sensitive responses were inwardly rectifying outward currents with null potentials close to EK. 4. The outward current induced by dibromo BAPTA was not blocked by internal EGTA (10 mM). However, experiments incorporating Ca2+ influx or Ca2+ loading of the buffer indicate that Ca2+ facilitated the outward current. 5. The outward currents induced by dibromo BAPTA or diazo-2 were not associated with significant changes in resting [Ca2+]i. Regions of the cell contributing to the outward current were deduced from measurements of fura-2 diffusion. These were compared with regions of [Ca2+]i elevation during IsAHP. 6. These results are consistent with the hypothesis that the BAPTA series Ca2+ buffers can activate those Ca2+-activated K+ channels that underlie the slow AHP, without the predicted elevation of bulk [Ca2+]i. Therefore these results cannot be interpreted solely in terms of Ca2+ concentration changes, although the observations illustrate a novel, investigative role for these compounds in the study of Ca2+-dependent processes.

MeSH Terms
Adrenergic alpha-Agonists/pharmacology Animals Calcium/metabolism Chelating Agents/pharmacology Cyclic AMP/metabolism Diazonium Compounds Egtazic Acid/analogs & derivatives,pharmacology Electric Stimulation Electrophysiology Fluorescent Dyes Fura-2 Hippocampus/cytology,drug effects,metabolism In Vitro Techniques Membrane Potentials/drug effects,physiology,radiation effects Neurons/drug effects,metabolism,ultrastructure Norepinephrine/pharmacology Patch-Clamp Techniques Phenoxyacetates Potassium Channels/drug effects Rats Ultraviolet Rays
Chemicals
Adrenergic alpha-Agonists Chelating Agents Diazonium Compounds Fluorescent Dyes Phenoxyacetates Potassium Channels diazo-2 Egtazic Acid Cyclic AMP 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid Calcium Fura-2 Norepinephrine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lancaster B
Wolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK. [email protected]
Batchelor A M
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Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
2000-01-15
Pages
231-46
Language
English
Region
England
NLM ID
0266262
PMCID
PMC2269749
Subset
IM
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