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PMID: 1663157 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Inactivation of calcium currents in granule cells cultured from mouse cerebellum.

The Journal of physiology ·Vol. 435 ·1991-04-00 ·Pages 101-21

Slesinger PA, Lansman JB

Abstract

1. Cells dissociated from mouse cerebellum were grown in vitro. Ca2+ channel currents were recorded from granule cells with the patch-clamp technique under conditions which suppressed currents through Na+ and K+ channels and minimized run-down of current through Ca2+ channels. 2. A strong depolarizing voltage step from a hyperpolarized holding potential produced inward Ca2+ channel current that decayed exponentially to a non-zero level. Inward current decayed to approximately 40% of its peak amplitude (range 20-90%). 3. The inward current increased in amplitude when Ca2+ was replaced with Ba2+ or after raising the concentration of extracellular Ba2+, but the rate of decay of current was unaffected. 4. The current-voltage (I-V) relation showed that peak or sustained current increased with voltage pulses more positive than approximately -30 mV, reached a maximum amplitude near +20 mV and became progressively smaller with larger depolarizations. 5. The tail currents produced after rapidly repolarizing the membrane potential to -70 mV from a positive test pulse decayed along a single exponential time course with a time constant of approximately 0.5 ms. The amplitude of tail current measured at a fixed repolarization potential increased as the pre-pulse was made more positive and reached a maximum with pre-pulses more positive than +40 mV. A plot of normalized amplitude of the tail current as a function of the pre-pulse potential was fitted with a Boltzmann relation with V1/2 = approximately + 8 mV and steepness k = 14 mV. 6. Shifting the holding potential to more positive potentials reduced the amplitude of the Ca2+ channel current elicited by the fixed voltage step and abolished the decay of the inward current. The peak current was normalized to the maximum peak current elicited from a very negative holding potential and plotted as a function of holding potential. The points were fitted with a Boltzmann relation for inactivation with V1/2 = approximately -57 mV and steepness k = 14 mV. 7. The onset of inactivation was studied in two-pulse experiments in which the duration of conditioning pre-pulse was varied. Increasing the duration of a pre-pulse to a fixed potential reduced the peak inward current evoked by the second test pulse. Plotting normalized current as a function of pre-pulse duration showed that inactivation developed along a double exponential time course. Both fast and slow time constants decreased as the pre-pulse potential was made more positive.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Animals Calcium/metabolism Calcium Channels/drug effects,physiology Cells, Cultured Cerebellum/metabolism Dihydropyridines/pharmacology Electrophysiology Ion Channel Gating/physiology Male Membrane Potentials/physiology Mice Mice, Inbred C57BL Time Factors
Chemicals
Calcium Channels Dihydropyridines Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Slesinger P A
Graduate Program in Neuroscience, School of Medicine, University of California, San Francisco 94143-0450.
Lansman J B
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Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1991-04-00
Pages
101-21
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1181452
Subset
IM
Grants
NIGMS NIH HHS · GM07449 · United States
NINDS NIH HHS · NS23720 · United States
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