Löscher W, Lehmann H
Department of Pharmacology, Toxicology and Pharmacy, School of Veterinary Medicine, Hannover, Germany.
J Pharmacol Exp Ther. 1996 Jun;277(3):1410-7.
L-Deprenyl (selegiline), a selective inhibitor of monoamine oxidase type B, has recently been shown to exert anticonvulsant and antiepileptogenic effects in the kindling model of partial (focal) epilepsy. In the present study, we examined if L-deprenyl exerts anticonvulsant effects in standard rodent models of generalized seizures. In addition to anticonvulsant activity, behavioral effects induced by L-deprenyl were monitored closely. To assess the stereoselectivity of anticonvulsant and behavioral effects of deprenyl, the D-enantiomer was included in the studies. Furthermore, the antiepileptic drug phenobarbital was used for comparison. The following tests were performed in mice: 1) the threshold for tonic electroconvulsions; 2) the maximal electroshock seizure test with fixed supramaximal (suprathreshold) stimulation; 3) the threshold for myoclonic, clonic and tonic seizures in response to i.v. infusion of pentylenetetrazole (PTZ); 4) the s.c. PTZ seizure test, with a fixed dose of PTZ (80 microgram/kg) for seizure induction; 5) the rotarod and chimney tests for determination of motor impairment. Furthermore, animals were observed in cage and open field for stereotyped behavior and other behavioral abnormalities. L-Deprenyl, tested at doses of 1 to 40 microgram/kg i.p., significantly increased myoclonic and clonic PTZ thresholds and the threshold for tonic electroconvulsions, whereas D-deprenyl was either ineffective or exhibited a lower anticonvulsant potency than L-deprenyl. Both drugs were ineffective in the maximal electroshock seizure and s.c. PTZ seizure tests. In contrast to the higher anticonvulsant potency of L-deprenyl in seizure threshold tests, D-deprenyl was more potent than L-deprenyl to induce behavioral abnormalities, such as hyperlocomotion. The data indicate that L-deprenyl exerts anticonvulsant activity against different seizure types. This anticonvulsant activity and the previously reported neuroprotective and cognition-enhancing action of L-deprenyl offer a unique combination of drug effects which might be of clinical benefit in patients with epilepsy.
L-司来吉兰(Selegiline),一种单胺氧化酶B型的选择性抑制剂,最近已显示在部分(局灶性)癫痫的点燃模型中具有抗惊厥和抗癫痫发作作用。在本研究中,我们检测了L-司来吉兰在全身性癫痫发作的标准啮齿动物模型中是否具有抗惊厥作用。除了抗惊厥活性外,还密切监测了L-司来吉兰诱导的行为效应。为了评估司来吉兰抗惊厥和行为效应的立体选择性,研究中纳入了D-对映体。此外,使用抗癫痫药物苯巴比妥作为对照。在小鼠中进行了以下试验:1)强直电惊厥阈值;2)固定超强(阈上)刺激的最大电休克惊厥试验;3)静脉注射戊四氮(PTZ)后肌阵挛、阵挛和强直惊厥阈值;4)皮下注射PTZ惊厥试验,使用固定剂量的PTZ(80微克/千克)诱导惊厥;5)用于测定运动障碍的转棒试验和烟囱试验。此外,在笼内和旷场中观察动物的刻板行为和其他行为异常。腹腔注射剂量为1至40微克/千克的L-司来吉兰显著提高了肌阵挛和阵挛性PTZ阈值以及强直电惊厥阈值,而D-司来吉兰要么无效,要么表现出比L-司来吉兰更低的抗惊厥效力。两种药物在最大电休克惊厥试验和皮下注射PTZ惊厥试验中均无效。与L-司来吉兰在惊厥阈值试验中较高的抗惊厥效力相反,D-司来吉兰比L-司来吉兰更易诱导行为异常,如活动亢进。数据表明,L-司来吉兰对不同类型的癫痫发作具有抗惊厥活性。这种抗惊厥活性以及先前报道的L-司来吉兰的神经保护和认知增强作用提供了独特的药物效应组合,这可能对癫痫患者具有临床益处。