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DOI 10.1016/0014-2999(91)90228-i

Медицинская библиотека · European journal of pharmacology · 1991

Comparison of pharmacodynamic effects of the non-competitive NMDA receptor antagonists MK-801 and ketamine in pigs.

Löscher W, Fredow G, Ganter M

Сравнительное исследованиеСтатьяПеревод в очереди

Аннотация

The non-competitive NMDA receptor antagonists MK-801 and ketamine were injected into pigs via chronically implanted intravenous catheters, and the animals were observed closely for alterations in general behaviour, heart rate, respiration and body temperature. MK-801 produced head shakes, sterotypies, 'psychotic' behaviour (e.g., hyperexcitation and screaming), and ketamine-like anesthetic effects in pigs at doses of 0.1-1.6 mg/kg. Almost the same behavioural pattern of effects was observed after i.v. injection of ketamine, 15mg/kg. Furthermore, both drugs reduced heart rate and increased respiration rate and body temperature. The most marked differences between MK-801 and ketamine were that MK-801 had a much longer duration of action and the catalepsy produced by MK-801 was much more pronounced. When animals were first anesthetized with pentobarbital, MK-801 did not alter the cardiovascular functions. In pigs genetically susceptible to induction of malignant hyperthermia by volatile anesthetics, MK-801 did not produce signs characteristic of fulminant malignant hyperthermia. The data show that MK-801 produces psychomotor and anesthetic effects that are almost indistinguishable from those observed after traditional dissociative anesthetics, such as phencyclidine and ketamine. With respect to the behavioural similarities between MK-801 and phencyclidine or ketamine, it seems unlikely that MK-801 will be useful clinically as an anticonvulsant or anxiolytic drug, but the data indicate that the drug may be suited as a long-acting dissociative anesthetic.

Для цитирования: Löscher W, Fredow G, Ganter M. Comparison of pharmacodynamic effects of the non-competitive NMDA receptor antagonists MK-801 and ketamine in pigs.. European journal of pharmacology. 1991. DOI: 10.1016/0014-2999(91)90228-i.

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