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Effects of metabolic blockade on the regulation of intracellular calcium in dissociated mouse sensory neurones.
Author(s) -
Duchen M R,
Valdeolmillos M,
O'Neill S C,
Eisner D A
Publication year - 1990
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1990.sp018074
Subject(s) - extracellular , intracellular , biophysics , depolarization , chemistry , calcium , cytoplasm , calcium in biology , fura 2 , cytosol , biochemistry , microbiology and biotechnology , medicine , endocrinology , biology , organic chemistry , enzyme
1. Impaired intracellular Ca2+ concentration ([Ca2+]i) regulation may underlie alterations in neuronal function during hypoxia or hypoglycaemia and may initiate cell damage. We have used the Ca2(+)‐sensitive fluorophore, Fura‐2, to study the regulation of [Ca2+]i in neurones isolated from mouse dorsal root ganglia. Mean resting [Ca2+]i was 163 +/‐ 11 nM (mean +/‐ S.E.M., n = 38). 2. Depolarization by exposure to 20 or 30 mM‐K+ caused a rapid Co2(+)‐ and Cd2(+)‐sensitive rise in [Ca2+]i, which subsequently declined with a time course usually fitted by the sum of two exponential functions. 3. Interference with mitochondrial function (by CN‐ or FCPP) or with glycolysis (by glucose removal) all raised [Ca2+]i by up to 220%. Addition of FCCP in the presence of CN‐ further increased [Ca2+]i. The response to CN‐ was still seen in the absence of extracellular Ca2+, although it attenuated rapidly, indicating release from an intracellular store. 4. Either CN‐ or glucose removal increased the rise in [Ca2+]i induced by K+ 2‐ to 3‐fold and slowed recovery, suggesting interference with sequestration or extrusion of [Ca2+]i. 5. Resting [Ca2+]i rose when external Na+ was replaced by Li+ or N‐methyl‐D‐glucamine, demonstrating the presence of a Na(+)‐Ca2+ exchange process. However, Na+ replacement had only a slight effect on the handling of a Ca2+ load. 6. We conclude that (i) Ca2+ is released into the cytoplasm from intracellular organelles when energy supplies are reduced: (ii) that the extrusion or sequestration of Ca2+ entering the cell during electrical activity is rapidly impaired by interference with mitochondrial metabolism: and (iii) Na(+)‐Ca2+ exchange makes only a small contribution to intracellular Ca2+ homeostasis. 7. [Ca2+]i would thus be expected to rise in vivo during hypoxia or hypoglycaemia and may initiate alterations in neuronal function. However, if a rise in Ca2+ is an important cause of cell damage in cerebral hypoxaemia, the combination of excitation and hypoxia will lead to the largest increases in [Ca2+]i, while hypoxia alone appears to cause only a small increase in [Ca2+]i in quiescent cells.