Methamphetamine exposure can produce neuronal degeneration in mouse hippocampal remnants

Brain Research

Volumn 759, Issue 1, 1997, Pages 135-140

  Schmued, Larry C ^a   Bowyer, John F ^a  

^a Natl Ctr Toxicological Res F   (United States)

Author keywords

Catecholamine; Fluoro Jade; Glutamate; Hippocampal remnant; Indusium griseum; Methamphetamine; Neurodegeneration; Seizure

Indexed keywords

EXCITOTOXIN; METHAMPHETAMINE; PHENOBARBITAL;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BEHAVIOR; CELL DEATH; CONTROLLED STUDY; FRONTAL CORTEX; HIPPOCAMPUS; HYPERTHERMIA; MALE; MOUSE; NERVE CELL DEGENERATION; NEUROTOXICITY; NONHUMAN; PARIETAL LOBE; PRIORITY JOURNAL; PYRIFORM CORTEX; SEIZURE;

ANIMALS; BEHAVIOR, ANIMAL; CELL DEATH; FLUORESCENT DYES; HIPPOCAMPUS; LIMBIC SYSTEM; MALE; METHAMPHETAMINE; MICE; MICE, INBRED C57BL; NERVE DEGENERATION; NEURONS; PROSENCEPHALON; SEIZURES; SILVER; STAINING AND LABELING;

EID: 0030790961     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(97)00173-X     Document Type: Article

References (28)

1. Adamek G.A., Shipley M.T., Sanders M.S. The indusium griseum in the mouse: architecture, Timm's Histochemistry, and some afferent connections. Brain Res. Bull. 12:1984;657-668.
2. Ali S.F., Newport G.D., Holson R.R., Slikker W. Jr., Bowyer J.F. Low environmental temperatures or pharmacologic agents that produce hypothermia decrease methamphetamine neurotoxicity in mice. Brain Res. 658:1994;33-38.
3. J.F. Bowyer and R.R. Holson, Methamphetamine and amphetamine neurotoxicity, in: L.W. Chang and R.S. Dyer (Eds.), Handbook of Neurotoxicology, Vol. 2, Marcel Dekker Inc., New York, Basel, Hong Kong, 1995, pp. 845-870.
4. Callaway C.W., Clark R.F. Hyperthermia in psychostimulant overdose. Ann. Emerg. Med. 24:1994;68-76.
5. M.B. Carpenter, Human Neuroanatomy, 7th edn., Williams and Wilkins Co., Baltimore, 1976, 532 pp.
6. Cavazos J.E., Sutula T.P. Progressive neuronal loss induced by kindling: a possible mechanism for mossy fiber synaptic reorganization and hippocampal sclerosis. Brain Res. 527:1990;1-6.
7. Commins D.L., Seiden L.S. α-Methyltyrosine blocks methylamphetamine-induced degeneration in the rat somatosensory cortex. Brain Res. 365:1986;15-20.
8. de Olmos J.S., Beltramino C.A., de Olmos de Lorenzo S. Use of an amino-cupric-silver technique for the detection of early and semiacute neuronal degeneration caused by neurotoxicants hypoxia, and physical trauma. Neurotoxicol. Teratol. 16:1994;545-561.
9. Derlet R.W., Tseng J.C., Albertson T.E. Potentiation of cocaine and D-amphetamine toxicity with caffeine. Am. J. Emerg. Med. 10:1992;211-216.
10. Eisch A.J., Marshall, Slikker W. Jr., Schmued L.C. Methamphetamine-induced damage to cortical neurons is indicated by a newly-developed fluorescent tag. Soc. Neurosci. Abstr. 22:1996;1915.
11. Goddard G.V., McIntyre D., Leech C. A permanent change in brain function resulting from daily electrical stimulation. Exp. Neurol. 25:1969;295-330.
12. Hokfelt T., Johansson O., Fuxe K., Goldstein M., Park D. Immunohistochemical studies on the localization and distribution of monoamine neuron systems in the rat brain. II: Tyrosine hydroxylase in the telencephalon. Med. Biol. 55:1977;21-40.
13. Lothman E.W., Collins R.C. Kainic acid-induced limbic seizures: metabolic, behavioral, electroencephalographic, and neuropathological correlates. Brain Res. 218:1981;299-318.
14. 3H]AMPA binding sites in rat brain as determined by quantitative autoradiography. Brain Res. 324:1984;160-164.
15. Ottersen O.P., Storm-Mathisen J. Glutamate and GABA-containing neurons in the mouse and rat brain, as demonstrated with a new immunocytochemical technique. J. Comp. Neurol. 229:1984;374-392.
16. O'Callaghan J.P., Miller D.B. Neurotoxicity profiles of substitued amphetamines in the C57BL/6J mouse. J. Pharmacol. Exp. Ther. 270:1994;741-751.
17. Petralia R.S., Wenthold R.J. Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain. J. Comp. Neurol. 318:1992;329-354.
18. Petralia R.S., Yokotani N., Wenthold R.J. Light and electron microscopic distribution of the NMDA receptor subunit NMDAR1 in the rat nervous system using a selective anti-peptide antibody. J. Neurosci. 14:1994;667-696.
19. Ryan L.J., Linder Jean C., Martone M.E., Groves P.M. Histological and ultrastructrual evidence that D-amphetamine causes degeneration in the neostriatum and frontal cortex of rats. Brain Res. 518:1990;67-77.
20. Sato K., Mick G., Kiyama H., Tohyama M. Expression patterns of a glutamate-binding protein in the rat central nervous system: Comparison with N-methyl-D-asparate receptor subunit in the rat. Neuroscience. 64:1995;459-475.
21. L.S. Schmued, C. Albertson and W. Slikker Jr., Fluoro-Jade: A novel fluorochrome for the sensitive and reliable histochemical localization of neuronal degeneration, Brain Res., 751 (1997) 37-46.
22. L.S. Seiden and K.E. Sabol, Neurotoxicity of methamphetamine-related drugs and cocaine, in: L.W. Chang and R.S. Dyer (Eds.), Handbook of Neurotoxicology, Vol. 2, Marcel Dekker Inc., New York/Basel/Hong Kong, 1995, pp. 824-844.
23. Sonsalla P.K., Nicklas W.J., Heikkila R.E. Role for excitatory amino acids in methamphetamine-induced nigrostriatal dopaminergic toxicity. Science. 243:1989;398-400.
24. Sternberger L.A., Hardy P.H. Jr., Cuculis J.J., Meyer H.G. The unlabeled antibody-enzyme method of immunohistochemistry. Preparation and properties of soluable antigen-antibody complex (horseradish peroxidase-antihorseradish peroxidase) and its use in the identification of spirochetes. J. Histochem. Cytochem. 18:1970;315-333.
25. Swanson L.W., Hartman B.K. The central adrenergic system. An immunofluorescence study of the location of cell bodies and their efferent connections in the rat utilizing dopamine-β-hydroxylase as a marker. J. Comp. Neurol. 163:1975;467-505.
26. R.C. Switzer, J. de Olmos and L. Heimer, The olfactory system, in: G. Paxinos (Ed.), The Rat Nervous System, Academic Press, Sydney, 1985, pp. 19-20.
27. Torre E.R., Lothman E., Steward O. Glial response to neuronal activity: GFAP-mRNA and protein levels are transiently increased in the hippocampus after seizures. Brain Res. 631:1993;256-264.
28. Wyss J.M., Sripanidkulchai K. The indusium griseum and anterior hippocampal continuation in the rat. J. Comp. Neurol. 219:1983;251-272.