Effects of Dopamine Antagonists on Changes in Spontaneous EEG and Locomotor Activity in Ketamine-Treated Rats
YAMAMOTO M., Y. MIZUKI, M. SUETSUGI, Y. OZAWA, M. OOYAMA AND M. SUZUKI. Effects of dopamine antagonists on changes in spontaneous EEG and locomotor activity in ketamine-treated rats. PHARMACOL BIOCHEM BEHAV 57(1/2), 361–365, 1997.—We investigated the effects of dopamine antagonists on spontaneous co...
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Published in | Pharmacology, biochemistry and behavior Vol. 57; no. 1; pp. 361 - 365 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.05.1997
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Abstract | YAMAMOTO M., Y. MIZUKI, M. SUETSUGI, Y. OZAWA, M. OOYAMA AND M. SUZUKI.
Effects of dopamine antagonists on changes in spontaneous EEG and locomotor activity in ketamine-treated rats. PHARMACOL BIOCHEM BEHAV
57(1/2), 361–365, 1997.—We investigated the effects of dopamine antagonists on spontaneous cortical and hippocampal electroencephalographic (EEG) changes, and on hyperlocomotion in ketamine-treated rats. Ketamine (20–60 mg/kg IP) synchronized cortical EEG and desynchronized hippocampal EEG in a dose-dependent manner indicating that the drug induced a dissociation between the cortical and hippocampal EEG. These EEG changes were accompanied by an increase in spontaneous locomotor activity, which involved lack of focused direction, stereotypy, irritability and other abnormalities. Dopamine antagonists, such as haloperidol (0.3–1 mg/kg IP) and nemonapride (0.3–1 mg/kg IP), reversed the dissociation between the cortical and hippocampal EEG in ketamine (60 mg/kg IP)-treated rats. Ketamine-induced hyperlocomotion was also decreased by administration of haloperidol (0.3 and 1 mg/kg IP) or nemonapride (0.1–1 mg/kg IP). Thus, it was found that dopamine antagonists reversed the EEG alterations and behavioural changes in ketamine-treated rats. |
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AbstractList | YAMAMOTO M., Y. MIZUKI, M. SUETSUGI, Y. OZAWA, M. OOYAMA AND M. SUZUKI.
Effects of dopamine antagonists on changes in spontaneous EEG and locomotor activity in ketamine-treated rats. PHARMACOL BIOCHEM BEHAV
57(1/2), 361–365, 1997.—We investigated the effects of dopamine antagonists on spontaneous cortical and hippocampal electroencephalographic (EEG) changes, and on hyperlocomotion in ketamine-treated rats. Ketamine (20–60 mg/kg IP) synchronized cortical EEG and desynchronized hippocampal EEG in a dose-dependent manner indicating that the drug induced a dissociation between the cortical and hippocampal EEG. These EEG changes were accompanied by an increase in spontaneous locomotor activity, which involved lack of focused direction, stereotypy, irritability and other abnormalities. Dopamine antagonists, such as haloperidol (0.3–1 mg/kg IP) and nemonapride (0.3–1 mg/kg IP), reversed the dissociation between the cortical and hippocampal EEG in ketamine (60 mg/kg IP)-treated rats. Ketamine-induced hyperlocomotion was also decreased by administration of haloperidol (0.3 and 1 mg/kg IP) or nemonapride (0.1–1 mg/kg IP). Thus, it was found that dopamine antagonists reversed the EEG alterations and behavioural changes in ketamine-treated rats. We investigated the effects of dopamine antagonists on spontaneous cortical and hippocampal electroencephalographic (EEG) changes, and on hyperlocomotion in ketamine-treated rats. Ketamine (20-60 mg/kg IP) synchronized cortical EEG and desynchronized hippocampal EEG in a dose-dependent manner indicating that the drug induced a dissociation between the cortical and hippocampal EEG. These EEG changes were accompanied by an increase in spontaneous locomotor activity, which involved lack of focused direction, stereotypy, irritability and other abnormalities. Dopamine antagonists, such as haloperidol (0.3-1 mg/kg IP), and nemonapride (0.3-1 mg/kg IP), reversed the dissociation between the cortical and hippocampal EEG in ketamine (60 mg/kg IP)-treated rats. Ketamine-induced hyperlocomotion was also decreased by administration of haloperidol (0.3 and 1 mg/kg IP) or nemonapride (0.1-1 mg/kg IP). Thus, it was found that dopamine antagonists reversed the EEG alterations and behavioural changes in ketamine-treated rats. We investigated the effects of dopamine antagonists on spontaneous cortical and hippocampal electroencephalographic (EEG) changes, and on hyperlocomotion in ketamine-treated rats. Ketamine synchronized cortical EEG and desynchronized hippocampal EEG in a dose-dependent manner indicating that the drug induced a dissociation between the cortical and hippocampal EEG. These EEG changes were accompanied by an increase in spontaneous locomotor activity, which involved lack of focused direction, stereotypy, irritability and other abnormalities. Dopamine antagonists, such as haloperidol and nemonapride, reversed the dissociation between the cortical and hippocampal EEG in ketamine treated rats. Ketamine-induced hyperlocomotion was also decreased by administration of haloperidol or nemonapride. Thus, it was found that dopamine antagonists reversed the EEG alterations and behavioural changes in ketamine-treated rats. |
Author | Ooyama, M Ozawa, Y Yamamoto, M Suzuki, M Suetsugi, M Mizuki, Y |
Author_xml | – sequence: 1 givenname: M surname: Yamamoto fullname: Yamamoto, M organization: Clinical Pharmacology Res. Lab., Yamanouchi Pharmaceutical Co. Ltd., 1-1-8, Azusawa, Itabashi-ku, Tokyo 174 USA – sequence: 2 givenname: Y surname: Mizuki fullname: Mizuki, Y organization: Department of Neuropsychiatry, Yamaguchi University School of Medicine, 1144 Kogushi, Ube, Yamaguchi 755, Japan – sequence: 3 givenname: M surname: Suetsugi fullname: Suetsugi, M organization: Department of Neuropsychiatry, Yamaguchi University School of Medicine, 1144 Kogushi, Ube, Yamaguchi 755, Japan – sequence: 4 givenname: Y surname: Ozawa fullname: Ozawa, Y organization: Clinical Pharmacology Res. Lab., Yamanouchi Pharmaceutical Co. Ltd., 1-1-8, Azusawa, Itabashi-ku, Tokyo 174 USA – sequence: 5 givenname: M surname: Ooyama fullname: Ooyama, M organization: Clinical Pharmacology Res. Lab., Yamanouchi Pharmaceutical Co. Ltd., 1-1-8, Azusawa, Itabashi-ku, Tokyo 174 USA – sequence: 6 givenname: M surname: Suzuki fullname: Suzuki, M organization: Clinical Pharmacology Res. Lab., Yamanouchi Pharmaceutical Co. Ltd., 1-1-8, Azusawa, Itabashi-ku, Tokyo 174 USA |
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Keywords | Delirium Ketamine Dopamine antagonists EEG Haloperidol Nemonapride Locomotor activity Intraperitoneal administration Rat Dopamine receptor Toxicity Treatment efficiency Rodentia Electrophysiology Butyrophenone derivatives Electroencephalography Locomotion Vertebrata Chemotherapy Mammalia General anesthetic Animal Antagonist Mechanism of action |
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Snippet | YAMAMOTO M., Y. MIZUKI, M. SUETSUGI, Y. OZAWA, M. OOYAMA AND M. SUZUKI.
Effects of dopamine antagonists on changes in spontaneous EEG and locomotor activity in... We investigated the effects of dopamine antagonists on spontaneous cortical and hippocampal electroencephalographic (EEG) changes, and on hyperlocomotion in... |
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SubjectTerms | Analysis of Variance Animals Benzamides - pharmacology Biological and medical sciences Cerebral Cortex - drug effects Delirium Dopamine antagonists Dopamine Antagonists - pharmacology Drug Evaluation, Preclinical Drug toxicity and drugs side effects treatment EEG Electroencephalography - drug effects Haloperidol Haloperidol - pharmacology Hippocampus - drug effects Ketamine Ketamine - pharmacology Locomotor activity Male Medical sciences Miscellaneous (drug allergy, mutagens, teratogens...) Motor Activity - drug effects Nemonapride Pharmacology. Drug treatments Rats Rats, Wistar |
Title | Effects of Dopamine Antagonists on Changes in Spontaneous EEG and Locomotor Activity in Ketamine-Treated Rats |
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