de Queiroz Ronaldo Bezerra, de Carvalho Fabíola Lélis, Fonsêca Diogo Vilar da, Barbosa-Filho José Maria, Salgado Paula Regina Rodrigues, Paulo Luciano Leite, de Queiroz Ana Bárbara Maroja, Pordeus Liana Clébia de Morais, de Souza Severino Araújo, Souza Helivaldo Diogenes da Silva, Lira Bruno Freitas, de Athayde-Filho Petrônio Filgueiras
Center for Health Sciences, Federal University of Paraiba, João Pessoa PB 58059-900, Brazil.
Department of Chemistry, Federal University of Paraiba, João Pessoa PB 58059-900, Brazil.
Molecules. 2015 Jan 8;20(1):974-86. doi: 10.3390/molecules20010974.
Imidazolidine derivatives, or hydantoins, are synthetic compounds with different therapeutic applications. Many imidazolidine derivatives have psychopharmacological properties, such as phenytoin, famous for its anticonvulsant efficacy, but also effective in the treatment of neuropathic pain. The hydantoin, 3-phenyl-5-(4-ethylphenyl)-imidazolidine-2,4-dione (IM-3), synthesized from the amino acid, glycine, was selected for psychopharmacological studies in mice on the basis of its chemical and structural similarity with phenytoin. The first step of this study was to define the LD50, which determined the doses of 50, 100 and 200 mg/kg for subsequent tests. The results obtained from the behavioral screening indicated that IM-3 produces decreased ambulation and analgesia in mice. Motor coordination and anxiety behavior were not affected by treatment with IM-3, as observed in the rotarod and elevated plus-maze tests, respectively. Regarding its antinociceptive properties, IM-3 showed efficacy in the acetic acid-induced writhing test by increasing the latency of the first writhe and reducing the number of writhes, as well as reducing the paw licking time in the second phase of the formalin test. The behavior of treated animals exposed to the hot plate test, however, did not differ from that of the control group. These data suggest that IM-3 has antinociceptive effects in mice, which is probably mediated by anti-inflammatory mechanisms.
咪唑烷衍生物或乙内酰脲是具有不同治疗用途的合成化合物。许多咪唑烷衍生物具有精神药理学特性,例如苯妥英,它以其抗惊厥功效而闻名,但也可有效治疗神经性疼痛。基于其与苯妥英在化学和结构上的相似性,从氨基酸甘氨酸合成的乙内酰脲3-苯基-5-(4-乙基苯基)-咪唑烷-2,4-二酮(IM-3)被选用于小鼠的精神药理学研究。本研究的第一步是确定半数致死量(LD50),这确定了后续试验中50、100和200mg/kg的剂量。行为筛选获得的结果表明,IM-3会使小鼠的活动减少并产生镇痛作用。分别在转棒试验和高架十字迷宫试验中观察到,IM-3处理对运动协调性和焦虑行为没有影响。关于其抗伤害感受特性,IM-3在乙酸诱导的扭体试验中显示出功效,它增加了首次扭体的潜伏期并减少了扭体次数,同时在福尔马林试验的第二阶段减少了舔爪时间。然而,接受热板试验的处理动物的行为与对照组没有差异。这些数据表明,IM-3在小鼠中具有抗伤害感受作用,这可能是由抗炎机制介导的。