Electrochemical detection of endogenous glutamate release from rat spinal cord organotypic slices as a real-time method to monitor excitotoxicity

Journal of Neuroscience Methods

Volumn 197, Issue 1, 2011, Pages 128-132

  Mazzone, Graciela L ^a   Nistri, Andrea ^a,b  

^a SISSA   (Italy)

^b IST   (Italy)

Author keywords

Cell death; Glutamate biosensor; Kainic acid; Spinal cord injury

Indexed keywords

GLUTAMIC ACID; KAINIC ACID;

ANIMAL TISSUE; ARTICLE; BIOSENSOR; CONTROLLED STUDY; ELECTROCHEMICAL ANALYSIS; EXCITOTOXICITY; NERVE CELL NECROSIS; NONHUMAN; PRIORITY JOURNAL; RAT; SPINAL CORD INJURY; SPINAL CORD VENTRAL HORN;

ANIMALS; BIOSENSING TECHNIQUES; ELECTROCHEMISTRY; GLUTAMIC ACID; KAINIC ACID; NEUROTOXINS; ORGAN CULTURE TECHNIQUES; PRESYNAPTIC TERMINALS; RATS; SPINAL CORD; TIME FACTORS;

EID: 79953043583     PISSN: 01650270     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jneumeth.2011.01.033     Document Type: Article

References (24)

1. Burmeister J.J., Gerhardt G.A. Self-referencing ceramic-based multisite microelectrodes for the detection and elimination of interferences from the measurement of l-glutamate and other analytes. Anal Chem 2001, 5:1037-1042.
2. Cater H.L., Gitterman D., Davis S.M., Benham C.D., Morrison B., Sundstrom L.E. Stretch-induced injury in organotypic hippocampal slice cultures reproduces in vivo post-traumatic neurodegeneration: role of glutamate receptors and voltage-dependent calcium channels. J Neurochem 2007, 2:434-447.
3. Dale N., Hatz S., Tian F., Llaudet E. Listening to the brain: microelectrode biosensors for neurochemicals. Trends Biotechnol 2005, 23:420-428.
4. Gourine A.V., Dale N., Korsak A., Llaudet E., Tian F., Huckstepp R., et al. Release of ATP and glutamate in the nucleus tractus solitarii mediate pulmonary stretch receptor (Breuer-Hering) reflex pathway. J Physiol 2008, 86:3963-3978.
5. Kuzhandaivel A., Nistri A., Mladinic M. Kainate-mediated excitotoxicity induces neuronal death in the rat spinal cord in vitro via a PARP-1 dependent cell death pathway (Parthanatos). Cell Mol Neurobiol 2010, 30:1001-1012.
6. Lau A., Tymianski M. Glutamate receptors, neurotoxicity and neurodegeneration. Pflugers Arch 2010, 460:525-542.
7. Liu D. An experimental model combining microdialysis with electrophysiology, histology, and neurochemistry for studying excitotoxicity in spinal cord injury. Effect of NMDA and kainate. Mol Chem Neuropathol 1994, 23:77-92.
8. Llaudet E., Hatz S., Droniou M., Dale N. Microelectrode biosensor for real-time measurement of ATP in biological tissue. Anal Chem 2005, 77:3267-3273.
9. Lossi L., Alasia S., Salio C., Merighi A. Cell death and proliferation in acute slices and organotypic cultures of mammalian CNS. Prog Neurobiol 2009, 4:221-245.
10. Magnuson D.S., Trinder T.C., ZhangYP, Burke D., Morassutti D.J., Shields C.B. Comparing deficits following excitotoxic and contusion injuries in the thoracic and lumbar spinal cord of the adult rat. Exp Neurol 1999, 56:191-204.
11. Margaryan G., Mattioli C., Mladinic M., Nistri A. Neuroprotection of locomotor networks after experimental injury to the neonatal rat spinal cord in vitro. Neuroscience 2010, 65:996-1010.
12. Mazzone G.L., Margaryan G., Kuzhandaivel A., Nasrabady S.E., Mladinic M., Nistri A. Kainate-induced delayed onset of excitotoxicity with functional loss unrelated to the extent of neuronal damage in the in vitro spinal cord. Neuroscience 2010, 168:451-462.
13. Mazzone G.L., Nistri A. Effect of the PARP-1 inhibitor PJ 34 on excitotoxic damage evoked by kainate on rat spinal cord organotypic slices. Cell Mol Neurobiol 2010, [Epub ahead of print].
14. McLamore E.S., Mohanty S., Shi J., Claussen J., Jedlicka S.S., Rickus J.L., et al. A self-referencing glutamate biosensor for measuring real time neuronal glutamate flux. J Neurosci Methods 2010, 189:14-22.
15. Milanese M., Zappettini S., Onofri F., Musazzi L., Tardito D., Bonifacino T., et al. Abnormal exocytotic release of glutamate in a mouse model of amyotrophic lateral sclerosis. J Neurochem 2010, [Epub ahead of print].
16. Nani F., Cifra A., Nistri A. Transient oxidative stress evokes early changes in the functional properties of neonatal rat hypoglossal motoneurons in vitro. Eur J Neurosci 2010, 6:951-966.
17. Oldenziel W.H., van der Zeyden M., Dijkstra G., Ghijsen W.E., Karst H., Cremers T.I., et al. Monitoring extracellular glutamate in hippocampal slices with a microsensor. J Neurosci Methods 2007, 1:37-44.
18. Park E., Velumian A.A., Fehlings M.G. The role of excitotoxicity in secondary mechanisms of spinal cord injury: a review with an emphasis on the implications for white matter degeneration. J Neurotrauma 2004, 21:754-774.
19. Rice M.E., Avshalumov M.V., Patel J.C. Hydrogen peroxide as a diffusible messenger: evidence from voltammetric studies of dopamine release in brain slices. Electrochemical methods for neuroscience, chapter 11 2007, CRC Press, Boca Raton (FL).
20. Robinson D.L., Hermans A., Seipel A.T., Wightman R.M. Monitoring rapid chemical communication in the brain. Chem Rev 2008, 108:2554-2584.
21. Taccola G., Margaryan G., Mladinic M., Nistri A. Kainate and metabolic perturbation mimicking spinal injury differentially contribute to early damage of locomotor networks in the in vitro neonatal rat spinal cord. Neuroscience 2008, 155:538-555.
22. Tian F., Gourine A.V., Huckstepp R.T., Dale N. A microelectrode biosensor for real time monitoring of l-glutamate release. Anal Chim Acta 2009, 645:86-91.
23. Wang Q., Yu S., Simonyi A., Sun G.Y., Sun A.Y. Kainic acid-mediated excitotoxicity as a model for neurodegeneration. Mol Neurobiol 2005, 31:3-16.
24. Wilson G.S., Johnson M.A. In-vivo electrochemistry: what can we learn about living systems?. Chem Rev 2008, 108:2462-2481.