TY - JOUR
T1 - Reversal of akinesia and release of festination by morphine or GABA applied focally to the nucleus reticularis tegmenti pontis
AU - Chesire, R. M.
AU - Cheng, J. T.
AU - Teilbaum, P.
PY - 1984
Y1 - 1984
N2 - Focal application of 5 μg of morphine sulfate to the nucleus reticularis tegmenti pontis (NRTP) in rats reversed the akinesia induced by 5 mg/kg systemic haloperidol or 40 mg/kg systemic morphine and released festinating forward locomotion. γ-Aminobutyric acid (200 μg) applied to this nucleus also reversed such kinesia. Intraventricular naloxone (10μg) or picrotoxin (0.1μg), respectively, blocked the effects of such focally applied drugs. Thus, morphine and γ-aminobutyric acid appear to act physiologically on the cells of the NRTP. The results suggest that suystemic morphine, in addition to producing immobility, simultaneously facilitates a readiness for locomotion by inactivating a final common inhibitory system in the region of the NRTP.
AB - Focal application of 5 μg of morphine sulfate to the nucleus reticularis tegmenti pontis (NRTP) in rats reversed the akinesia induced by 5 mg/kg systemic haloperidol or 40 mg/kg systemic morphine and released festinating forward locomotion. γ-Aminobutyric acid (200 μg) applied to this nucleus also reversed such kinesia. Intraventricular naloxone (10μg) or picrotoxin (0.1μg), respectively, blocked the effects of such focally applied drugs. Thus, morphine and γ-aminobutyric acid appear to act physiologically on the cells of the NRTP. The results suggest that suystemic morphine, in addition to producing immobility, simultaneously facilitates a readiness for locomotion by inactivating a final common inhibitory system in the region of the NRTP.
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U2 - 10.1037/0735-7044.98.4.739
DO - 10.1037/0735-7044.98.4.739
M3 - Article
C2 - 6466446
AN - SCOPUS:0021636040
SN - 0735-7044
VL - 98
SP - 739
EP - 742
JO - Behavioral Neuroscience
JF - Behavioral Neuroscience
IS - 4
ER -