Luszczki Jarogniew J, Swiader Mariusz J, Swiader Katarzyna, Paruszewski Ryszard, Turski Waldemar A, Czuczwar Stanislaw J
Department of Pathophysiology, Medical University of Lublin, Jaczewskiego 8, PL 20-090 Lublin, Poland.
Fundam Clin Pharmacol. 2008 Feb;22(1):69-74. doi: 10.1111/j.1472-8206.2007.00547.x. Epub 2007 Nov 15.
The objective of this study was to evaluate the anticonvulsant properties of picolinic acid 2-fluoro-benzylamide (Pic-2F-BZA) in numerous experimental seizure models [maximal electroshock (MES), bicuculline (BIC), pentylenetetrazole (PTZ), pilocarpine (PILO), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), kainic acid (KA) and N-methyl-D-aspartic acid (NMDA)-induced seizures]. Moreover, the acute adverse-effect profile of the agent with respect to impairment of motor performance was assessed in animals subjected to the chimney test. Results indicate that Pic-2F-BZA in time- and dose-dependent manners produced both the anti-electroshock action and acute adverse effects in the MES and chimney tests in mice respectively. The experimentally derived median effective dose (ED(50) value) in the MES test was 24.2 mg/kg (at 5 min after i.p. administration), whereas the median toxic dose (TD(50) value) in the chimney test was 71.7 mg/kg. Furthermore, Pic-2F-BZA produced clear-cut antiseizure effects in all chemically induced seizure models and its ED(50) values amounted to 19.9 mg/kg for KA-, 39.5 mg/kg for AMPA-, 56.2 mg/kg for PTZ-, 76.4 mg/kg for BIC-, 160.1 mg/kg for PILO- and 165.2 mg/kg for NMDA-induced seizures. Based on this study, one can conclude that Pic-2F-BZA, because of its broad spectrum of anticonvulsant action and the short time to peak of its maximum anticonvulsant effects (5 min after its i.p. administration), deserves more attention as a potential antiepileptic drug for status epilepticus patients.
本研究的目的是评估吡啶甲酸2-氟苄酰胺(Pic-2F-BZA)在多种实验性癫痫模型[最大电休克(MES)、荷包牡丹碱(BIC)、戊四氮(PTZ)、毛果芸香碱(PILO)、α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)、 kainic酸(KA)和N-甲基-D-天冬氨酸(NMDA)诱导的癫痫发作]中的抗惊厥特性。此外,在进行烟囱试验的动物中评估了该药物对运动性能损害的急性不良反应情况。结果表明,Pic-2F-BZA在小鼠的MES和烟囱试验中分别以时间和剂量依赖性方式产生抗电休克作用和急性不良反应。在MES试验中实验得出的半数有效剂量(ED50值)为24.2mg/kg(腹腔注射给药后5分钟),而在烟囱试验中的半数中毒剂量(TD50值)为71.7mg/kg。此外,Pic-2F-BZA在所有化学诱导的癫痫模型中均产生明显的抗癫痫作用,其KA诱导癫痫发作的ED50值为19.9mg/kg,AMPA诱导癫痫发作的为39.5mg/kg,PTZ诱导癫痫发作的为56.2mg/kg,BIC诱导癫痫发作的为76.4mg/kg,PILO诱导癫痫发作的为160.1mg/kg,NMDA诱导癫痫发作的为165.2mg/kg。基于本研究,可以得出结论,Pic-2F-BZA由于其广泛的抗惊厥作用谱以及最大抗惊厥作用达到峰值的时间短(腹腔注射给药后5分钟),作为癫痫持续状态患者的潜在抗癫痫药物值得更多关注。