Md. Kelland et al., BEHAVIORAL AND ELECTROPHYSIOLOGICAL COMPARISON OF KETAMINE WITH DIZOCILPINE IN THE RAT, Physiology & behavior, 54(3), 1993, pp. 547-554
We have compared the effects of MK 801 and ketamine on a measure of an
esthesia (loss of righting reflex) and two measures of basal ganglia d
opamine (DA) function: apomorphine (APO)-induced stereotypy and APO-in
duced excitation of type II globus pallidus (GP) neurons. As expected,
ketamine induced anesthesia. High-dose MK 801 administered IP induced
ataxia, but not anesthesia. When administered IV, high-dose MK 801 in
duced anesthesia in only three of five rats. Using a modified stereoty
py scale, it was found that pretreatment with MK 801 blocked APO-induc
ed stereotypic sniffing. Intravenous ketamine also blocked APO-induced
stereotypy, but IP ketamine did not. Similar results were observed in
neurophysiological studies; MK 801 altered the excitation of type II
GP neurons by APO. Intravenous ketamine (5 mg/kg) also altered the res
ponsiveness of these cells to APO, but ketamine anesthesia (150 mg/kg,
IP) had no effect. These findings suggest that MK 801 is not an effec
tive anesthetic in rats, and the method of administration of ketamine
plays a role in its ability to exert NMDA receptor blockade.