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非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂MK-801和氯胺酮对猪的药效学作用比较。

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

作者信息

Löscher W, Fredow G, Ganter M

机构信息

Department of Pharmacology, Toxicology and Pharmacy, School of Veterinary Medicine, Hanover, F.R.G.

出版信息

Eur J Pharmacol. 1991 Jan 17;192(3):377-82. doi: 10.1016/0014-2999(91)90228-i.

DOI:10.1016/0014-2999(91)90228-i
PMID:1829039
Abstract

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.

摘要

通过长期植入的静脉导管将非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂MK-801和氯胺酮注射到猪体内,密切观察动物的一般行为、心率、呼吸和体温变化。MK-801在剂量为0.1-1.6mg/kg时,可使猪出现摇头、刻板行为、“精神病性”行为(如过度兴奋和尖叫)以及类似氯胺酮的麻醉作用。静脉注射15mg/kg氯胺酮后,观察到几乎相同的行为效应模式。此外,两种药物均降低了心率,增加了呼吸频率和体温。MK-801和氯胺酮之间最显著的差异在于,MK-801的作用持续时间长得多,且由MK-801产生的僵住症更为明显。当动物先用戊巴比妥麻醉时,MK-801不会改变心血管功能。在对挥发性麻醉药诱导恶性高热敏感的猪中,MK-801未产生暴发性恶性高热的特征性体征。数据表明,MK-801产生的精神运动和麻醉作用与传统解离麻醉药(如苯环己哌啶和氯胺酮)后观察到的作用几乎无法区分。就MK-801与苯环己哌啶或氯胺酮之间的行为相似性而言,MK-801作为抗惊厥药或抗焦虑药在临床上似乎不太可能有用,但数据表明该药物可能适合作为长效解离麻醉药。

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