Glutamate, NMDA, and AMPA Induced Changes in Extracellular Space Volume and Tortuosity in the Rat Spinal Cord

Glutamate release, particularly in pathologic conditions, may result in cellular swelling. The authors studied the effects of glutamate, N-methyl-d-aspartate (NMDA), and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) on extracellular pH (pHe), extracellular potassium concentration ([K+]e), and changes in extracellular space (ECS) diffusion parameters (volume fraction α, tortuosity λ) resulting from cellular swelling. In the isolated spinal cord of 4-to 12-day-old rats, the application of glutamate receptor agonists induced an increase in [K+]e, alkaline-acid shifts, a substantial decrease in α, and an increase in λ. After washout of the glutamate receptor agonists, α either returned to or overshot normal values, whereas λ remained elevated. Pretreatment with 20 mmol/L Mg++, MK801, or CNQX blocked the changes in diffusion parameters, [K+]e and pHe evoked by NMDA or AMPA. However, the changes in diffusion parameters also were blocked in Ca2+-free solution, which had no effect on the [K+]e increase or acid shift. The authors conclude that increased glutamate release may produce a large, sustained and [Ca2+]e-dependent decrease in α and increase in λ. Repetitive stimulation and pathologic states resulting in glutamate release therefore may lead to changes in ECS volume and tortuosity, affecting volume transmission and enhancing glutamate neurotoxicity and neuronal damage.

[1]  K. Kaila,et al.  Modulation of pH by neuronal activity , 1992, Trends in Neurosciences.

[2]  S. Prokopová-Kubinová,et al.  Extracellular space diffusion and pathological states. , 2000, Progress in brain research.

[3]  H. Kimelberg,et al.  PHYSIOLOGICAL AND PATHOLOGICAL ASPECTS OF ASTROCYTIC SWELLING , 1986 .

[4]  M. Chesler The regulation and modulation of pH in the nervous system , 1990, Progress in Neurobiology.

[5]  U. Heinemann,et al.  Relations between slow extracellular potential changes, glial potassium buffering, and electrolyte and cellular volume changes during neuronal hyperactivity in cat brain , 1989, Glia.

[6]  A. Baba,et al.  l-Glutamate-induced swelling of cultured astrocytes is dependent on extracellular Ca2+ , 1991, Neuroscience Letters.

[7]  D. Choi,et al.  Neuroprotective effects of glutamate antagonists and extracellular acidity. , 1993, Science.

[8]  R. Bradley,et al.  Neural Circuits for Taste: Excitation, Inhibition, and Synaptic Plasticity in the Rostral Gustatory Zone of the Nucleus of the Solitary Tract a , 1998, Annals of the New York Academy of Sciences.

[9]  Eva Syková,et al.  Extracellular space volume changes in the rat spinal cord produced by nerve stimulation and peripheral injury , 1991, Brain Research.

[10]  H. Kimelberg,et al.  Furosemide- and bumetanide-sensitive ion transport and volume control in primary astrocyte cultures from rat brain , 1985, Brain Research.

[11]  J. Dubinsky,et al.  Changes in intracellular pH associated with glutamate excitotoxicity , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  O. Kempski,et al.  Glial Ion Transport and Volume Control , 1991, Annals of the New York Academy of Sciences.

[13]  M. Rice,et al.  Extracellular alkaline-acid pH shifts evoked by iontophoresis of glutamate and aspartate in turtle cerebellum , 1991, Neuroscience.

[14]  Z. Šimonová,et al.  K+ and pH homeostasis in the developing rat spinal cord is impaired by early postnatal X-irradiation , 1992, Brain Research.

[15]  L. Kaczmarek,et al.  Glutamate receptors in cortical plasticity: molecular and cellular biology. , 1997, Physiological reviews.

[16]  R. Duvoisin,et al.  The metabotropic glutamate receptors: Structure and functions , 1995, Neuropharmacology.

[17]  S. Heinemann,et al.  Cloned glutamate receptors. , 1994, Annual review of neuroscience.

[18]  E. Rubel,et al.  Extracellular potassium influences DNA and protein syntheses and glial fibrillary acidic protein expression in cultured glial cells , 1990, Glia.

[19]  Eva Syková,et al.  Diffusion barriers evoked in the rat cortex by reactive astrogliosis , 1999, Glia.

[20]  C. Nicholson,et al.  Extracellular space structure revealed by diffusion analysis , 1998, Trends in Neurosciences.

[21]  Eva Syková,et al.  Glial cells and volume transmission in the CNS , 2000, Neurochemistry International.

[22]  Eva Syková,et al.  The Extracellular Space in the CNS: Its Regulation, Volume and Geometry in Normal and Pathological Neuronal Function , 1997 .

[23]  W. Endres,et al.  Changes in extracellular pH during electrical stimulation of isolated rat vagus nerve , 1986, Neuroscience Letters.

[24]  H. Kennedy,et al.  Calcium–hydrogen exchange by the plasma membrane Ca-ATPase of voltage-clamped snail neurons , 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[25]  S. Waxman,et al.  Protection of the axonal cytoskeleton in anoxic optic nerve by decreased extracellular calcium , 1993, Brain Research.

[26]  H. Benveniste,et al.  Ischemic Damage in Hippocampal CA1 is Dependent on Glutamate Release and Intact Innervation from CA3 , 1989, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[27]  A. Chvátal,et al.  Extracellular Volume Fraction and Diffusion Characteristics during Progressive Ischemia and Terminal Anoxia in the Spinal Cord of the Rat , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[28]  C. Rose,et al.  Stimulus-evoked changes of extra- and intracellular pH in the leech central nervous system. II. Mechanisms and maintenance of pH homeostasis. , 1995, Journal of neurophysiology.

[29]  D. McAdoo,et al.  Neurotoxicity of glutamate at the concentration released upon spinal cord injury , 1999, Neuroscience.

[30]  A. Chvátal,et al.  Glial influence on neuronal signaling. , 2000, Progress in brain research.

[31]  C. Nicholson,et al.  Ion diffusion modified by tortuosity and volume fraction in the extracellular microenvironment of the rat cerebellum. , 1981, The Journal of physiology.

[32]  A. Lehmenkühler,et al.  Extracellular space parameters in the rat neocortex and subcortical white matter during postnatal development determined by diffusion analysis , 1993, Neuroscience.

[33]  P. Jendelová,et al.  Role of glia in K+ and pH homeostasis in the neonatal rat spinal cord , 1991, Glia.

[34]  H. Kimelberg,et al.  Anisotonic media and glutamate-induced ion transport and volume responses in primary astrocyte cultures. , 1987, Journal de physiologie.

[35]  H. Lassmann,et al.  Changes of extracellular space volume and tortuosity in the spinal cord of Lewis rats with experimental autoimmune encephalomyelitis. , 1996, Physiological research.

[36]  J. Olney,et al.  Excitotoxic neuronal damage and neuropsychiatric disorders. , 1993, Pharmacology & therapeutics.

[37]  Eva Syková,et al.  Glial swelling and astrogliosis produce diffusion barriers in the rat spinal cord , 1999, Glia.

[38]  L. Garcia-Segura,et al.  Neurosteroids modulate the reaction of astroglia to high extracellular potassium levels , 1996, Glia.

[39]  I. Vorisek,et al.  Ischemia-Induced Changes in the Extracellular Space Diffusion Parameters, K+, and pH in the Developing Rat Cortex and Corpus Callosum , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[40]  R. Thisted,et al.  Spreading depression increases immunohistochemical staining of glial fibrillary acidic protein , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[41]  M. Mayer,et al.  The physiology of excitatory amino acids in the vertebrate central nervous system , 1987, Progress in Neurobiology.

[42]  M. Norenberg,et al.  The role of K+ influx on glutamate induced astrocyte swelling: effect of temperature. , 1994, Acta neurochirurgica. Supplementum.

[43]  D. McAdoo,et al.  Considerations in the determination by microdialysis of resting extracellular amino acid concentrations and release upon spinal cord injury , 1998, Neuroscience.

[44]  Christian Steinhäuser,et al.  News on glutamate receptors in glial cells , 1996, Trends in Neurosciences.

[45]  M. Chesler,et al.  pH transients evoked by excitatory synaptic transmission are increased by inhibition of extracellular carbonic anhydrase. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[46]  W. Abraham,et al.  Metabotropic Glutamate Receptors Trigger Homosynaptic Protein Synthesis to Prolong Long-Term Potentiation , 2000, The Journal of Neuroscience.

[47]  K. Fuxe,et al.  Volume transmission in the CNS and its relevance for neuropsychopharmacology. , 1999, Trends in pharmacological sciences.

[48]  Ionic and Volume Changes in the Microenvironment of Nerve and Receptor Cells , 1992 .

[49]  P. Witkovsky,et al.  Glutamate receptors and circuits in the vertebrate retina , 1999, Progress in Retinal and Eye Research.

[50]  V. Gallo,et al.  Excitatory amino acid receptors in glia: Different subtypes for distinct functions? , 1995, Journal of neuroscience research.

[51]  A. Chvátal,et al.  Glutamate-, kainate- and NMDA-evoked membrane currents in identified glial cells in rat spinal cord slice. , 1998, Physiological research.

[52]  B. Johansson,et al.  Glutamate-induced swelling of single astroglial cells in primary culture , 1994, Neuroscience.

[53]  D. Kullmann,et al.  Extrasynaptic glutamate spillover in the hippocampus: evidence and implications , 1998, Trends in Neurosciences.

[54]  W. Walz,et al.  Glial swelling in ischemia: a hypothesis. , 1993, Developmental neuroscience.

[55]  Kimelberg Hk,et al.  Anisotonic media and glutamate-induced ion transport and volume responses in primary astrocyte cultures , 1987 .

[56]  M. Goldberg,et al.  Combined oxygen and glucose deprivation in cortical cell culture: calcium-dependent and calcium-independent mechanisms of neuronal injury , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[57]  E. Syková,et al.  Stimulation-evoked Changes in Extracellular Ph, Calcium and Potassium Activity in the Frog Spinal Cord * , 1988 .

[58]  Jiří Koryta ION-Selective Electrodes , 1986 .

[59]  C. Rose,et al.  pH regulation and proton signalling by glial cells , 1996, Progress in Neurobiology.

[60]  P. Vezina,et al.  Metabotropic glutamate receptors and the generation of locomotor activity: Interactions with midbrain dopamine , 1999, Neuroscience & Biobehavioral Reviews.

[61]  A. Baba,et al.  L-glutamate-induced swelling of cultured astrocytes. , 1992, Advances in experimental medicine and biology.

[62]  G. Gebhart,et al.  The glutamate synapse: a target in the pharmacological management of hyperalgesic pain states. , 1998, Progress in brain research.

[63]  D. Choi Excitotoxic cell death. , 1992, Journal of neurobiology.

[64]  Sylvia F. Chen,et al.  Effects of MK‐801 on glutamate‐induced swelling of astrocytes in primary cell culture , 1990, Journal of neuroscience research.

[65]  D. Attwell Brain uptake of glutamate: food for thought. , 2000, The Journal of nutrition.

[66]  V. Edgerton,et al.  Extracellular Glutamate in the Dorsal Horn of the Lumbar Spinal Cord in the Freely Moving Rat During Hindlimb Stepping , 1999, Pharmacology Biochemistry and Behavior.