The effects of ketamine-isomers on neuronal injury and regeneration in rat hippocampal neurons

Anesthesia and Analgesia

Volumn 83, Issue 3, 1996, Pages 505-512

  Himmelseher, Sabine ^a   Pfenninger, Ernst ^a   Georgieff, Michael ^a  

^a UNIVERSITY HOSPITAL ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DIZOCILPINE; KETAMINE;

ANIMAL CELL; ARTICLE; CELL SURVIVAL; CONTROLLED STUDY; DENDRITE; DRUG EFFECT; FETUS; HIPPOCAMPUS; ISOMER; NERVE CELL CULTURE; NERVE CELL LESION; NERVE FIBER TRANSECTION; NERVE REGENERATION; NONHUMAN; PRIORITY JOURNAL; RACEMIC MIXTURE; RAT;

EID: 0029818874     PISSN: 00032999     EISSN: None     Source Type: Journal    
DOI: 10.1213/00000539-199609000-00011     Document Type: Article

References (28)

1. White BC, Krause GS. Brain injury and repair mechanisms: the potential for pharmacologic therapy in closed-head trauma. Ann Emerg Med 1993;22:970-9.
2. Povlishock JT. Pathobiology of traumatically induced axonal injury in animals and man. Ann Emerg Med 1993;22:980-6.
3. Faden AI, Demediuk P, Panter SS, Vink R. The role of excitatory amino acids and NMDA receptors in traumatic brain injury. Science 1989;244:798-800.
4. Olney J, Price M, Salles S, et al. MK-801 powerfully protects against N-methyl-aspartate neurotoxicity. Eur J Pharmacol 1987;141:357-61.
5. Shapira Y, Yadid G, Cotev S, et al. Protective effect of MK801 in experimental brain injury. J Neurotrauma 1990;7:131-9.
6. Anis NA, Berry SC, Burton NR, Lodge D. The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N-methyl-D-aspartate. Br J Pharmacol 1983;79:565-75.
7. Church J, Lodge D. N-methyl-D-aspartate (NMDA) antagonism is central to the action of ketamine and other phencyclidine receptor ligands. In: Domino EF, ed. Status of ketamine in anesthesiology. Ann Arbor: NPP Books, 1990:501-12.
8. Choi DW. Ketamine reduces NMDA receptor mediated neurotoxicity in cortical cultures. In: Domino EF, ed. Status of ketamine in anesthesiology. Ann Arbor: NPP Books, 1990:549-55.
9. Shapira Y, Artru AA, Lam AM. Ketamine decreases cerebral infarct volume and improves neurological outcome following experimental head trauma in rats. J Neurosurg Anesthesiol 1992;4:231-40.
10. Óye I, Paulson O, Maurset A. Effects of ketamine on sensory perception: evidence for a role of N-methyl-aspartate receptors. J Pharmacol Exp Ther 1992;260:1209-13.
11. Lodge D, Anis NA, Burton NR. Effects of optical isomers of ketamine on excitation of cat and rat spinal neurones by amino acids and acetylcholine. Neurosci Lett 1982;29:281-6.
12. Zeilhofer HU, Swandulla D, Geisslinger G, Brune K. Differential effects of ketamine enantiomers on NMDA receptor currents in cultured neurons. Eur J Pharmacol 1992;213:155-8.
13. MacDonald JF, Bartlett MC, Mody I, et al. Actions of ketamine, phencyclidine, and MK-801 on NMDA receptor currents in cultured mouse hippocampal neurones. J Physiol (Lond) 1991;432:483-508.
14. Dotti CG, Sullivan CA, Banker GA. The establishment of polarity by hippocampal neurons in culture. J Neurosci 1988;8:1454-68.
15. Caceres A, Banker GA, Binder L. Immunocytochemical localization of tubulin and microtubule-associated protein 2 during the development of hippocampal neurons in culture. J Neurosci 1986;6:714-22.
16. Goslin KG, Banker G. Experimental observations on the development of polarity by hippocampal neurons in culture. J Cell Biol 1989;108:1507-16.
17. Cook JA, Mitchell JB. Viability measurements in mammalian cell systems. Anal Biochem 1989;179:1-7.
18. Dumuis A, Sebben M, Haynes L, et al. NMDA receptors activate the arachidonic acid cascade system in striatal neurons. Nature 1988;336:68-70.
19. Sanfeliu C, Hunt A, Patel AJ. Exposure to N-methyl-D-aspartate increases release of arachidonic acid in primary cultures of rat hippocampal neurons and not in astrocytes. Brain Res 1990;526:241-8.
20. Gole DJ, French J, Houser J, Domino EF. Plasma ketamine: relation to brain concentrations and the hippocampal electroencephalogram. In: Domino EF, ed. Status of ketamine in anesthesiology. Ann Arbor: NPP Books, 1990:297-304.
21. Cohen ML, Chan S-L, Way WL, et al. Distribution in the brain and metabolism of ketamine in the rat after intravenous administration. Anesthesiology 1973;39:370-6.
22. Jahr CE, Stevens CF. Calcium permeability of the N-methyl-D-aspartate receptor channel in hippocampal neurons in culture. Proc Natl Acad Sci USA 1993;90:11573-7.
23. Regehr WG, Tank DW. Postsynaptic NMDA receptor-mediated calcium accumulation in hippocampal CA1 pyramidal cell dendrites. Nature 1990;345:807-10.
24. Volterra A, Trott D, Cassutti P, et al. High sensitivity of glutamate uptake to extracellular free arachidonic acid levels in rat cortical synaptosomes and astrocytes. J Neurochem 1992;159:600-6.
25. Murphy T, Parikh A, Schnaar R, Coyle J. Arachidonic acid metabolism in glutamate neurotoxicity. Ann NY Acad Sci 1989;559:475-6.
26. Marini AM, Paul SM. N-Methyl-D-aspartate receptor-mediated neuroprotection in cerebellar granule cells requires new RNA and protein synthesis. Proc Natl Acad Sci USA 1992;89:6555-9.
27. Olney JW, Labruyere, Price MT. Pathological changes induced in cerebrocortical neurons by phencyclidine and related drugs. Science 1989;244:1360-2.
28. Kitagawa K, Matsumoto M, Niinobe M, et al. Microtubule-associated protein as a sensitive marker for cerebral ischemic damage-immunohistochemical investigation of dendritic damage. Neuroscience 1989;31:401-11.