Marescaux C, Micheletti G, Vergnes M, Rumbach L, Warter J M
Eur J Pharmacol. 1985 Jul 11;113(1):19-24. doi: 10.1016/0014-2999(85)90338-3.
Wistar rats in our laboratory breeding colony spontaneously present petit mal-like, non-convulsive, epileptic seizures. In these rats, as in other animal petit mal models, GABAmimetics, agonists of GABA-A receptors such as 4, 5, 6, 7 tetrahydroisooxazolo (5,4-c) pyridin-3-ol (THIP), or inhibitors of GABA catabolism such as gamma-vinyl GABA (GVG) or L-cycloserine (CYC), aggravated the seizures. Diazepam not only abolished the spontaneous seizures but also completely blocked the effects of the GABAmimetics, totally suppressing seizures in rats given THIP, GVG or CYC. These findings show that the mode of action of benzodiazepines is not comparable to a non-specific potentiation of GABA transmission, and suggest that the anti-absence effects of the benzodiazepines could depend on interactions with neurotransmitter systems other than GABA.
我们实验室繁殖群体中的Wistar大鼠会自发出现小发作样、非惊厥性癫痫发作。在这些大鼠中,与其他动物小发作模型一样,GABA模拟物,如GABA - A受体激动剂4, 5, 6, 7 - 四氢异恶唑并(5,4 - c)吡啶 - 3 - 醇(THIP),或GABA分解代谢抑制剂,如γ - 乙烯基GABA (GVG)或L - 环丝氨酸(CYC),会加重癫痫发作。地西泮不仅消除了自发发作,还完全阻断了GABA模拟物的作用,完全抑制了给予THIP、GVG或CYC的大鼠的癫痫发作。这些发现表明,苯二氮卓类药物的作用方式与GABA传递的非特异性增强不可比,并表明苯二氮卓类药物的抗失神发作作用可能取决于与GABA以外的神经递质系统的相互作用。