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Electroencephalographic Studies of Haloperidol

Electroencephalographic Studies of Haloperidol 1. Effects of haloperidol on EEG were examined in rabbits, curarizedand artificially respired. Twenty-five rabbits were used for studyingthe effect of acute administration and 25 rabbits for chronic administration.2. Haloperidol in doses of 1.5—4.0 mg/kg i.v. evoked two main changesin the EEG. Namely, a synchronization of cortical and subcorticalEEG patterns and a continuous desynchronized pattern in theolfactory bulb. In addition, the cortical EEG arousal reactions toclap and pain were blocked at 1.8 ± 0.8mg/kg and 2.9 ± 0.8 mg/kgrespectively. Hippocampal arousal reaction to these stimulations wasnot completely blocked.3. When more than 4.5 mg/kg was given, EEG activities of all the brainareas showed a continuous arousal pattern in 8 rabbits out of 15.4. There are two chief negative results. The chronic administration ofhaloperidol for 2—10 days did not significantly affect the per centtime distribution of arousal, mixed and resting patterns. Moreover,threshold voltages required to induce hippocampal seizure dischargesfollowing electrical stimulation of hippocampus were not significantlyraised with the acute administration of 1.5 mg/kg of haloperidol. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png International Pharmacopsychiatry Karger

Electroencephalographic Studies of Haloperidol

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Publisher
Karger
Copyright
© 1968 S. Karger AG, Basel
ISSN
0020-8272
eISSN
2504-2580
DOI
10.1159/000467926
Publisher site
See Article on Publisher Site

Abstract

1. Effects of haloperidol on EEG were examined in rabbits, curarizedand artificially respired. Twenty-five rabbits were used for studyingthe effect of acute administration and 25 rabbits for chronic administration.2. Haloperidol in doses of 1.5—4.0 mg/kg i.v. evoked two main changesin the EEG. Namely, a synchronization of cortical and subcorticalEEG patterns and a continuous desynchronized pattern in theolfactory bulb. In addition, the cortical EEG arousal reactions toclap and pain were blocked at 1.8 ± 0.8mg/kg and 2.9 ± 0.8 mg/kgrespectively. Hippocampal arousal reaction to these stimulations wasnot completely blocked.3. When more than 4.5 mg/kg was given, EEG activities of all the brainareas showed a continuous arousal pattern in 8 rabbits out of 15.4. There are two chief negative results. The chronic administration ofhaloperidol for 2—10 days did not significantly affect the per centtime distribution of arousal, mixed and resting patterns. Moreover,threshold voltages required to induce hippocampal seizure dischargesfollowing electrical stimulation of hippocampus were not significantlyraised with the acute administration of 1.5 mg/kg of haloperidol.

Journal

International PharmacopsychiatryKarger

Published: Jan 1, 2017

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