Quantification of S-adenosylmethionine-induced tremors: A possible tremor model for Parkinson's disease

Citation
Ns. Lamango et al., Quantification of S-adenosylmethionine-induced tremors: A possible tremor model for Parkinson's disease, PHARM BIO B, 65(3), 2000, pp. 523-529
Citations number
20
Categorie Soggetti
Neurosciences & Behavoir
Journal title
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
ISSN journal
00913057 → ACNP
Volume
65
Issue
3
Year of publication
2000
Pages
523 - 529
Database
ISI
SICI code
0091-3057(200003)65:3<523:QOSTAP>2.0.ZU;2-6
Abstract
Tremor is the most visible symptom of Parkinson's Disease (PD), and should be the appropriate parameter in models for its evaluation. Lack of reliable PD tremor models and methods to distinguish tremors from nontremor movemen ts means that nontremor behavior such as rotation following basal ganglia d amage are mostly used. Our laboratory has shown that S-adenosylmethionine ( SAM) injections into the brain of rats reliably produced tremors, rigidity, hypokinesia, and abnormal posture. Thus. SAM-induced tremors, when disting uished from nontremor activities, has the potential as a model for testing anti-PD agents. Tremor Monitor-recorded activity profiles of the rats injec ted with SAM showed low-amplitude signals interlaced with high-amplitude bu rsts of tremor episodes. Control activities were of low-medium amplitudes w ith no such patterns. The number of real and apparent episodes detected ove r 20 min were 92 +/- 12 and 84 +/- 14 lasting 470 +/- 50 and 210 +/- 50 s, indicating mean durations of 5.1, and 2.4 s, frequencies of 12 +/- 0.1 and 11 +/- 0.2 Hz, cycles (waves) per episode of 54 +/- 6 and 19 +/- 2 and ampl itudes of 42.3 +/- 5 and 19.8 +/- 1 for the SAM-treated and control rats, r espectively. The nontremor activities of rats injected with phosphate-buffe red saline were distinguished and eliminated by raising the minimum amplitu de and number of cycles to 20. This procedure is being enhanced for screeni ng antitremor agents and for elucidating the possible mechanism for Parkins onism. (C) 2000 Elsevier Science Inc.