Glutamate, NMDA, and AMPA induced changes in extracellular space volume and tortuosity in the rat spinal cord
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- 6-Cyano-7-nitroquinoxaline-2,3-dione pharmacology MeSH
- Excitatory Amino Acid Agonists pharmacology MeSH
- Excitatory Amino Acid Antagonists pharmacology MeSH
- Cell Death drug effects MeSH
- Chelating Agents pharmacology MeSH
- Diffusion MeSH
- Dizocilpine Maleate pharmacology MeSH
- Potassium metabolism MeSH
- Edema pathology MeSH
- Egtazic Acid pharmacology MeSH
- Extracellular Space drug effects metabolism MeSH
- Gliosis metabolism pathology MeSH
- Magnesium pharmacology MeSH
- Hydrogen-Ion Concentration MeSH
- Rats MeSH
- alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid pharmacology MeSH
- Glutamic Acid pharmacology MeSH
- Spinal Cord drug effects metabolism pathology MeSH
- N-Methylaspartate pharmacology MeSH
- Rats, Wistar MeSH
- In Vitro Techniques MeSH
- Calcium pharmacology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 6-Cyano-7-nitroquinoxaline-2,3-dione MeSH
- Excitatory Amino Acid Agonists MeSH
- Excitatory Amino Acid Antagonists MeSH
- Chelating Agents MeSH
- Dizocilpine Maleate MeSH
- Potassium MeSH
- Egtazic Acid MeSH
- Magnesium MeSH
- alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid MeSH
- Glutamic Acid MeSH
- N-Methylaspartate MeSH
- Calcium MeSH
Glutamate release, particularly in pathologic conditions, may result in cellular swelling. The authors studied the effects of glutamate, N-methyl-D-aspartate (NMDA), and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) on extracellular pH (pH(e)), extracellular potassium concentration ([K(+)](e)), and changes in extracellular space (ECS) diffusion parameters (volume fraction alpha, tortuosity lambda) 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 alpha, and an increase in lambda. After washout of the glutamate receptor agonists, alpha either returned to or overshot normal values, whereas lambda remained elevated. Pretreatment with 20 mmol/L Mg(++), MK801, or CNQX blocked the changes in diffusion parameters, [K(+)](e) and pH(e) evoked by NMDA or AMPA. However, the changes in diffusion parameters also were blocked in Ca(2+)-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 [Ca(2+)](e)-dependent decrease in alpha and increase in lambda. 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.
References provided by Crossref.org
Diffusion in brain extracellular space