Valin A, Cepeda C, Rey E, Naquet R
Electroencephalogr Clin Neurophysiol. 1981 Dec;52(6):647-51. doi: 10.1016/0013-4694(81)91439-5.
The action of lorazepam was studied in photosensitive baboons. Animals were either naturally very photosensitive or rendered photosensitive by a previous injection of allylglycine. Intravenous administration of varying doses, from 0.05 to 0.5 mg/kg, of lorazepam blocked the myoclonus induced by intermittent light stimulation in all the animals. However, in the naturally photosensitive baboon the injection of lorazepam favoured the appearance of spontaneous myoclonus with no important EEG modification. This myoclonus is different from that induced by intermittent light stimulation, which is always preceded by spike-wave cortical discharges. Lorazepam-induced myoclonus appears during the period when the animal is not photosensitive and its origin is probably in the medulla or in the brain stem.
研究了劳拉西泮在光敏狒狒中的作用。动物要么天生对光非常敏感,要么通过先前注射烯丙基甘氨酸而变得对光敏感。静脉注射0.05至0.5mg/kg不同剂量的劳拉西泮,可阻断所有动物因间歇性光刺激诱发的肌阵挛。然而,在天生光敏的狒狒中,注射劳拉西泮有利于自发性肌阵挛的出现,且脑电图无重要改变。这种肌阵挛与间歇性光刺激诱发的肌阵挛不同,后者总是先有皮层棘波放电。劳拉西泮诱发的肌阵挛出现在动物无光敏性的时期,其起源可能在延髓或脑干。