Abstract
The effects of N6-(L-2-phenylisopropyl)-adenosine (L-PIA), an A1 agonist, were measured on both spontaneous locomotor activity and electroencephalographic (EEG) measures of sleep in rats. L-PIA strongly inhibited motor activity at 100 μg/kg intraperitoneally (IP), a dose which had no statistically significant effects on EEG-defined sleep. A higher dose of L-PIA (200 μg/kg) increased the latency to sleep initiation and inhibited later REM sleep. These results demonstrate that L-PIA can produce a state of apparent behavioral quiescence in the presence of EEG-defined arousal.
Original language | English (US) |
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Pages (from-to) | 507-510 |
Number of pages | 4 |
Journal | Pharmacology, Biochemistry and Behavior |
Volume | 34 |
Issue number | 3 |
DOIs | |
State | Published - Nov 1989 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Toxicology
- Pharmacology
- Clinical Biochemistry
- Biological Psychiatry
- Behavioral Neuroscience
Keywords
- Adenosine agonist
- Electroencephalogram
- Locomotor activity
- N-(L-2-phenylisopropyl)-adenosine (L-PIA)
- REM
- Sedation
- Sleep