Literature DB >> 9145812

Ion homeostasis in brain cells: differences in intracellular ion responses to energy limitation between cultured neurons and glial cells.

I A Silver1, J Deas, M Erecińska.   

Abstract

Intracellular concentrations of sodium, potassium and calcium together with membrane potentials were measured in cultured murine cortical neurons and glial cells under conditions which mimicked in vivo hypoxia, ischemia and hypoglycemia. These included; glucose omission with and without added pyruvate, addition of rotenone in the presence and absence of glucose and substitution of 2-deoxyglucose for glucose with and without rotenone. Cellular energy levels ([ATP], [ADP], [phosphocreatine], [creatine]) were measured in suspensions of C6 cells incubated in parallel under identical conditions. [Na+]i and [Ca2+]i rose while [K+]i fell and plasma membrane depolarized when energy production was limited. Intracellular acidification was observed when glycolysis was the sole source for ATP synthesis. There was a positive correlation between the extent of energy depletion in glial cells and the magnitude and velocity of alterations in ion levels. Neither glycolysis alone nor oxidative phosphorylation alone were able to ensure unaltered ion gradients. Since oxidative phosphorylation is much more efficient in generating ATP than glycolysis, this finding suggests a specific requirement of the Na pump for ATP generated by glycolysis. Changes in [Na+]i and [K+]i observed during energy depletion were gradual and progressive whereas those in [Ca2+]i were initially slow and moderate with large elevations occurring only as a late event. Increases in [Na+]i were usually smaller than reductions in [K+]i, particularly in the glia, suggestive of cellular swelling. Glia were less sensitive to identical insults than were neurons under all conditions. Results presented in this study lead to the conclusion that the response to energy deprivation of the two main types of brain cells, neurons and astrocytes, is a complex function of their capacity to produce ATP and the activities of various pathways which are involved in ion homeostasis.

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Year:  1997        PMID: 9145812     DOI: 10.1016/s0306-4522(96)00600-8

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  46 in total

1.  Exacerbated responses to oxidative stress by an Na(+) load in isolated nerve terminals: the role of ATP depletion and rise of [Ca(2+)](i).

Authors:  C Chinopoulos; L Tretter; A Rozsa; V Adam-Vizi
Journal:  J Neurosci       Date:  2000-03-15       Impact factor: 6.167

2.  Regulation of Na+,K+-ATPase by persistent sodium accumulation in adult rat thalamic neurones.

Authors:  V V Senatorov; P K Stys; B Hu
Journal:  J Physiol       Date:  2000-06-01       Impact factor: 5.182

3.  Increased adenine nucleotide translocator 1 in reactive astrocytes facilitates glutamate transport.

Authors:  Charles R Buck; Michael J Jurynec; Deepak K Gupta; Alick K T Law; Johannes Bilger; Douglas C Wallace; Robert J McKeon
Journal:  Exp Neurol       Date:  2003-06       Impact factor: 5.330

Review 4.  The Na-K-Cl Co-transporter in astrocyte swelling.

Authors:  Arumugam R Jayakumar; Michael D Norenberg
Journal:  Metab Brain Dis       Date:  2010-03-25       Impact factor: 3.584

5.  Calpain, not caspase, is the causative protease for hypoxic damage in cultured monkey retinal cells.

Authors:  Emi Nakajima; Katherine B Hammond; Jennifer L Rosales; Thomas R Shearer; Mitsuyoshi Azuma
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-09-01       Impact factor: 4.799

6.  Improvement of cerebral function by anti-amyloid precursor protein antibody infusion after traumatic brain injury in rats.

Authors:  Tatsuki Itoh; Takao Satou; Shozo Nishida; Masahiro Tsubaki; Shigeo Hashimoto; Hiroyuki Ito
Journal:  Mol Cell Biochem       Date:  2009-01-07       Impact factor: 3.396

7.  Differential hippocampal protection when blocking intracellular sodium and calcium entry during traumatic brain injury in rats.

Authors:  Xueren Zhao; Fredric A Gorin; Robert F Berman; Bruce G Lyeth
Journal:  J Neurotrauma       Date:  2008-10       Impact factor: 5.269

Review 8.  Role of connexin-based gap junction channels and hemichannels in ischemia-induced cell death in nervous tissue.

Authors:  Jorge E Contreras; Helmuth A Sánchez; Loreto P Véliz; Feliksas F Bukauskas; Michael V L Bennett; Juan C Sáez
Journal:  Brain Res Brain Res Rev       Date:  2004-12

Review 9.  Ion transporters and ischemic mitochondrial dysfunction.

Authors:  Yan Liu; Xiang-jun Liu; Dandan Sun
Journal:  Cell Adh Migr       Date:  2009-01-02       Impact factor: 3.405

10.  Oxygen/glucose deprivation in hippocampal slices: altered intraneuronal elemental composition predicts structural and functional damage.

Authors:  C P Taylor; M L Weber; C L Gaughan; E J Lehning; R M LoPachin
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

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