2013, Number 1
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Arch Neurocien 2013; 18 (1)
Variations on the suppression in Beta (13-30 Hz) frecuency band for tiopental –isofluorane, propofol and hydrocloride xylacine administration on healthy dogs (canis familiaris)
Rodríguez C, Ocampo L, López D, Solís H, Caballero S
Language: Spanish
References: 20
Page: 3-9
PDF size: 648.52 Kb.
ABSTRACT
The diagnostic value of electroencephalography (EEG) in clinical or experimental models are controversial. Because
the effects produced by chemical contention will alter its in diagnostic and investigative results.
Objective: this
essay was directed towards to recognize the effects of chemical contention on the EEG tracings and the background
activity.
Material and methods: two drugs and a drug combination were chosen for this study: hydrocloride of
xylazine, propofol, and thiopental-isoflurane. We work with three groups (n-15), at six times (t0, t1, t5, t10, t15,
t30) particular graphic artifacts of each drug were described and the relative power was quantified.
Results: each
group presents particular graphic artifacts on EEG record, we seems; in thiopental-isofluorano group, all channels
amplitude suppression when the isofluorano concentration was high. In propofol group we observe intermittent fast
activity in frontal electrodes, and xylacine group we describe acute spike on occipital electrodes. Finally, quantitative
analyses show that at t30 (thirty minutes) an equal BETA suppression was observed between the xylazine vs.propofol, and xylazine vs. thiopental-isoflurane groups (PÃ0.05).
Conclusions: each drug make a different EEG graphic
effect. Apparently the drug – receptor relationship make a particularly graphic artifact, but also we can observe
across these results that the BETA relative power in dogs is indistinguishable among these drugs, forward about
thirty minutes. This findings show that chemical contention for experimental or diagnostic EEG studies in dogs is a
limited factor, but with this, if we know the EEG drugs effects, we have better quality diagnostics or experimental
results.
REFERENCES
Bradford HF. Chemical neurobiology. WH. Freeman and company, New York. EUA. 1986.
Bufalary A, Short CE, Giannoni C, Vainio O. Comparative response to propofol anaesthesia alone and with 2-adrenergic medications in a canine model. Acta Veterinaria Scandinavia 1996;37, 187-201.
Fiset P, Paus T, Daloze T, Plourde G, Meuret P, Bonhomme V, Haji-Ali N, et al. Brain mechanism of Propofol-induced loss of conciousness in humans: a positron emission tomography study. J Neuroscien 1999;19:5506-13.
Hall LW, Chambers JP. A clinical trial of propofol infusion anaesthesia in dogs. J Small An Prac 1987;28,623-38.
Itamoto K, Taura Y, Wada N, Takuma T, Matsumura H, et al. Effect of medetomidine on electroencephalography and use of a quantitative electroencephalograph for evaluating sedation levels in dog. J Vet Med 2001;48:525-35.
Iversen S, Iversen L, Saper CB. Sistema nervioso autónomo e hipotálamo. en Kandel ER, Schwartz JH, Jessell TM. Principios de neurociencia. Cuarta edición, Ed. Mc Graw-Hill Interamericana. España. 2000;960-81.
Jaggy A, Bernardini M. Idiopatic epilepsy in 125 dogs: a long term study. Clinical and electroencephalographic findings. J Small An Prac 1998;39:23-9.
Jasper RD. Clinical Neurophysiology. 2nd edition. Oxford University Press. NY. U.S.A. 2002.
Jeserevics J, Viitmaa R, Cizinauskas S, Sainio K, Jokinen TS, et al. Electroencephalography findings in healthy and finnish spitz dogs with epilepsy: visual and background quantitative análisis. J Vet Intern Med 2007;21 (6):1299-306.
Joksovic PM, Weiergräber M, Lee W, Struck H, Schneider T, et al. Isofluorane-sensitive R-type calcium channels contribute to inhibitory synaptic transmission in the rat thalamus. J Neurosci 2009;4; 29 (5): 1434-45.
Knowles K. Idiophatic epilepsy. Clinical Techniques in Small Animal Practice 1998;13, 144-51.
Lejtien FSS, Teunissen NW, Wieneke GH, Knape JTA, Schobeen. Activation of interictal spiking in mesiotemporal lobe epilepsy by Propofol induced sleep. J Clin Neurophysiol 2001;18:291-8.
Moore MP, Greene SA, Keegan RD, Gallagher L. Quantitative electroencephalography in dogs anesthetized with 2.0% endtidal concentration of isoflurane anesthesia. Am J Vet Res 1991;52(4):551-60.
Pellegrino FC, Sica RE, Canine electroencephalographic recording technique: findings in normal and epileptic dogs. Clin Neurophysiol 2004;115(2):477-87.
Preobrazhenskaia LA. EEG dynamics during conditioning in symmetrical neocortical regions in dogs. Zh Vyssh Nerv Dejat Im Ip Pavlova 2002;52(4):441-9.
Scheller MS, Nakakimura K, Fleischer JE, Zornow MH. Cerebral effects of sevofluorane in the dog: comparison with isoflurane and enflurane. Br J Anaesth 1990;65(3):388-92.
Steiss JE. A survey of currents techniques in veterinary electrodiagnostics: EEG, spinal evoked and brainstem auditory evoked potential recording. Vet Res Cummunications 1988;124-5,281-8.
Tourai K, Senba H, Sasaki N, Tokuriki M. Developmental EEG of the Beagle Dog under Xylacine sedation. Jpn J Vet Sci 1985;47(3):459-63.
Watkins SB, Hall LW, Clarke KW. Propofol as an intravenous anaesthesic agent in dogs. Vet Record 1987;120,326-9.
Xiang Q, Tan L, Zhao YL, Wang JT. Isofluorane enhaces spontaneous Ca2+ oscillations in developing rat hippocampal neurons in vitro. Act Anaesthesiol Scand 2009;14.