Palmer G C, Cregan E C, Borrelli A R, Harris E W, Stagnitto M L, Colombo P, Kaiser F C, Murray R J, Griffith R C, Strand J C
Astra Research Corporation, Rochester, New York, USA.
J Pharmacol Exp Ther. 1995 Aug;274(2):991-1000.
2-Amino-N-(1,2-diphenylethyl)-acetamide hydrochloride (FPL 13950) has been demonstrated to have good anticonvulsant efficacy and a relative lack of acute side effects in rodents. Similar in structure to remacemide hydrochloride, it was also shown to possess weak potency as an uncompetitive antagonist of N-methyl-D-aspartic acid (NMDA) receptors. In our study FPL 13950 was profiled preclinically as a potential neuroprotective agent with respect to lengthening the survival time of rodents exposed to hypoxia, as well as for ability to protect the vulnerable CA1 pyramidal neurons of the rat and dog from the consequences of global ischemia. Under conditions of hypoxia, pretreatment of rodents with FPL 13950 resulted in an extension in the time to loss of the righting reflex (rats) and mortality (rats and mice). This occurred whether the rats were maintained at ambient body temperature or made hyperthermic. When administered after 30 min of four-vessel occlusion global ischemia for periods of either 7 (b.i.d.) or 14 days (s.i.d.), FPL 13950 exhibited protection of the vulnerable CA1 hippocampal neurons in rat. In the 14-day treatment study the CA3 neurons were evaluated and FPL 13950 was found to prevent the lesser degree of ischemic-induced damage to this hippocampal region. In ischemic rats treated with FPL 13950 for 7 days, electrophysiological responses of CA1 neurons (orthodromic and antidromic population spikes, in vitro) were also preserved after FPL 13950 treatment. FPL 13950 was administered i.v. at 30 min after 8 min of clamping the ascending aorta in dogs, followed by a b.i.d./s.i.d. dosing regimen for 1 wk. Neuronal damage to CA1 was considerable in the saline-treated ischemic animals but significantly protected in dogs receiving FPL 13950. FPL 13950 continues to serve as a potential backup candidate for remacemide HCl which is currently in clinical trials for patients with stroke and epilepsy.
2-氨基-N-(1,2-二苯乙基)乙酰胺盐酸盐(FPL 13950)已被证明在啮齿动物中具有良好的抗惊厥疗效且相对缺乏急性副作用。它的结构与盐酸瑞马西胺相似,还被证明作为N-甲基-D-天冬氨酸(NMDA)受体的非竞争性拮抗剂,效力较弱。在我们的研究中,FPL 13950在临床前被作为一种潜在的神经保护剂进行评估,评估内容包括延长暴露于低氧环境下的啮齿动物的存活时间,以及保护大鼠和犬脆弱的CA1锥体神经元免受全脑缺血后果的影响。在低氧条件下,用FPL 13950预处理啮齿动物会导致翻正反射消失时间(大鼠)和死亡率(大鼠和小鼠)延长。无论大鼠是维持在环境体温还是处于体温过高状态,都会出现这种情况。在四动脉闭塞全脑缺血30分钟后给药,给药周期为7天(每日两次)或14天(每日一次),FPL 13950对大鼠脆弱的CA1海马神经元表现出保护作用。在为期14天的治疗研究中,对CA3神经元进行了评估,发现FPL 13950可防止该海马区域缺血性损伤程度较轻的情况发生。在用FPL 13950治疗7天的缺血大鼠中,FPL 13950治疗后CA1神经元的电生理反应(正向和逆向群体峰电位,体外)也得以保留。在犬类中,在升主动脉夹闭8分钟后30分钟静脉注射FPL 13950,随后按照每日两次/每日一次的给药方案给药1周。在接受生理盐水治疗的缺血动物中,CA1神经元损伤严重,但在接受FPL 13950治疗的犬类中受到显著保护。FPL 13950仍是盐酸瑞马西胺的潜在备用候选药物,盐酸瑞马西胺目前正在针对中风和癫痫患者进行临床试验。