Naik S R, Naid P R, Sheth U K
Psychopharmacology (Berl). 1978 Apr 14;57(1):103-7. doi: 10.1007/BF00426965.
The effects of methaqualone on isonicotinic acid hydrazide, 6-mercapto propionic acid, picrotoxin, and strychnine-induced convulsion were studied in mice and the results compared with diazepam. Methaqualone, like diazepam, was found to be a selective antagonist of isoniazid-induced convulsion and a much less effective inhibitor of strychnine convulsion. Methaqualone elicits muscle-relaxant, sedative, and anticonvulsant effects at different dose levels. At low, nonsedative doses the drug produces anticonvulsant effects, and at higher doses, muscle-relaxant and sedative effects. It appears that the mechanism(s) of action of methaqualone in on GABA deficiency or receptor blockade, rather than on glycine receptors.
研究了甲喹酮对异烟肼、6-巯基丙酸、印防己毒素和士的宁诱导的小鼠惊厥的影响,并将结果与地西泮进行比较。发现甲喹酮与地西泮一样,是异烟肼诱导惊厥的选择性拮抗剂,而对士的宁惊厥的抑制作用则弱得多。甲喹酮在不同剂量水平下会产生肌肉松弛、镇静和抗惊厥作用。在低剂量、无镇静作用时,该药物产生抗惊厥作用,而在高剂量时,则产生肌肉松弛和镇静作用。甲喹酮的作用机制似乎在于γ-氨基丁酸(GABA)缺乏或受体阻断,而非作用于甘氨酸受体。