Regulation of the Intracellular Free Calcium Concentration in Acutely Dissociated Neurones from Rat Nucleus Basalis
Overview
Authors
Affiliations
1. Neurones were acutely dissociated from the rat nucleus basalis. Whole-cell patch clamp recordings of calcium currents (ICa) and fura-2 microfluorimetric recordings of intracellular free Ca2+ concentration ([Ca2+]i) were made simultaneously. 2. Depolarization from -60 to 0 mV elicited ICa and a gradual increase in [Ca2+]i. After repolarization, ICa terminated in 0.7 ms, and [Ca2+]i recovered to control exponentially (1-5 s). 3. Both ICa and the transient [Ca2+]i increase in response to step depolarizations, were abolished in Ca2+ free extracellular solution and in Cd(2+)-containing solution. 4. Depolarizations from -90 mV to membrane potentials less negative than -40 mV induced ICa and an increase in [Ca2+]i. Depolarization to 0 mV elicited the maximum ICa, and produced the largest increase in [Ca2+]i. There was a parallel relationship between the [Ca2+]i increase and the magnitude of the ICa. 5. The [Ca2+]i increase was associated with an increase in total Ca2+ influx when the duration of the step depolarization was varied. The relationship between the total Ca2+ influx and the peak of [Ca2+]i transient reached an asymptote as total Ca2+ influx exceeded 200 pC. A similar finding was made when more than thirty action potentials were used in increasing [Ca2+]i. 6. The process of the [Ca2+]i recovery was slowed down by lowering the temperature, by an intracellular dialysis with vanadate, by extracellular application of a mitochondrial inhibitor, carbonyl cyanide m-chlorophenyl-hydrazone (CCCP), and by Na(+)-free external solution. It was unaffected by membrane potential (-50 to -130 mV). 7. When pipette solution contained a high concentration of fura-2 (200 microM), the [Ca2+]i increase per 1 pC of Ca2+ influx decreased, and the [Ca2+]i recovery was slowed. 8. The results indicate that the ICa through voltage-dependent Ca2+ channels elevates [Ca2+]i. The neurones possess a large capacity for Ca2+ buffering, and the recovery of [Ca2+]i requires both the Ca2+ pump and membrane Na(+)-Ca2+ exchange.
An Inconvenient Truth: Calcium Sensors Are Calcium Buffers.
McMahon S, Jackson M Trends Neurosci. 2018; 41(12):880-884.
PMID: 30287084 PMC: 6252283. DOI: 10.1016/j.tins.2018.09.005.
Nutraceuticals against Neurodegeneration: A Mechanistic Insight.
Dadhania V, Trivedi P, Vikram A, Tripathi D Curr Neuropharmacol. 2016; 14(6):627-40.
PMID: 26725888 PMC: 4981739. DOI: 10.2174/1570159x14666160104142223.
Tatsumi H, Toyota M, Furuichi T, Sokabe M Plant Signal Behav. 2015; 9(8):e29099.
PMID: 25763612 PMC: 4203510. DOI: 10.4161/psb.29099.
Endogenous calcium buffering capacity of substantia nigral dopamine neurons.
Foehring R, Zhang X, Lee J, Callaway J J Neurophysiol. 2009; 102(4):2326-33.
PMID: 19675297 PMC: 2775382. DOI: 10.1152/jn.00038.2009.
Altered neuronal excitability in cerebellar granule cells of mice lacking calretinin.
Gall D, Roussel C, Susa I, DAngelo E, Rossi P, Bearzatto B J Neurosci. 2003; 23(28):9320-7.
PMID: 14561859 PMC: 6740583.