Valin A, Bryere P, Naquet R
Neurosci Lett. 1986 May 15;66(2):210-4. doi: 10.1016/0304-3940(86)90192-8.
The effects of Ro 5-4864, a 1,4-benzodiazepine with a high affinity for the peripheral-type benzodiazepine (Bz) binding site, were investigated in the baboon (Papio papio), which is genetically predisposed to epilepsy. A proconvulsant effect of low doses (1-3 mg/kg, i.v.) of Ro 5-4864 was observed by studying its effect on the photic responses induced by intermittent light stimulation in non-photosensitive baboons. Higher doses of Ro 5-4864 (10 mg/kg, i.v.) were overtly convulsant. The Bzs clonazepam and diazepam blocked these convulsant actions of Ro 5-4864 whereas neither Ro 15-1788, an antagonist of central Bz binding sites, nor PK 11 195, an antagonist of peripheral Bz binding sites, had any effect. It thus appeared that the convulsant effect of Ro 5-4864 was not mediated by Bz binding sites of either the central or the peripheral type. It is possible that Ro 5-4864 exerts its convulsant action at the picrotoxin site of the central Bz receptor - gamma-aminobutyric acid receptor-chloride ionophore complex.
研究了对周围型苯二氮䓬(Bz)结合位点具有高亲和力的1,4-苯二氮䓬Ro 5-4864对狒狒(豚尾狒狒)的作用,该狒狒具有癫痫遗传易感性。通过研究低剂量(1-3毫克/千克,静脉注射)的Ro 5-4864对非光敏狒狒间歇性光刺激诱导的光反应的影响,观察到了其惊厥作用。更高剂量的Ro 5-4864(10毫克/千克,静脉注射)具有明显的惊厥作用。苯二氮䓬类药物氯硝西泮和地西泮可阻断Ro 5-4864的这些惊厥作用,而中枢Bz结合位点拮抗剂Ro 15-1788和周围Bz结合位点拮抗剂PK 11 195均无任何作用。因此,Ro 5-4864的惊厥作用似乎不是由中枢或周围型Bz结合位点介导的。Ro 5-4864可能在中枢Bz受体-γ-氨基丁酸受体-氯离子通道复合物的印防己毒素位点发挥其惊厥作用。