Zugno Alexandra I, Canever Lara, Heylmann Alexandra S, Wessler Patrícia G, Steckert Amanda, Mastella Gustavo A, de Oliveira Mariana B, Damázio Louyse S, Pacheco Felipe D, Calixto Octacílio P, Pereira Flávio P, Macan Tamires P, Pedro Thayara H, Schuck Patrícia F, Quevedo João, Budni Josiane
Laboratório de Neurociências, Programa de Pós-Graduação em Ciências da Saúde, Unidade Acadêmica de Ciências da Saúde, Universidade do Extremo Sul Catarinense, Criciúma, SC, Brazil.
Laboratório de Neurociências, Programa de Pós-Graduação em Ciências da Saúde, Unidade Acadêmica de Ciências da Saúde, Universidade do Extremo Sul Catarinense, Criciúma, SC, Brazil.
J Psychiatr Res. 2016 Oct;81:23-35. doi: 10.1016/j.jpsychires.2016.06.013. Epub 2016 Jun 16.
Recent studies have shown benefits for the supplementation of folic acid in schizophrenic patients. The aim of this study was to evaluate the effects of folic acid addition on adult rats, over a period of 7 or 14 days. It also sets out to verify any potential protective action using an animal model of schizophrenia induced by ketamine, in behavioral and biochemical parameters. This study used two protocols (acute and chronic) for the administration of ketamine at a dose of 25 mg/kg (i.p.). The folic acid was given by oral route in doses of 5, 10 and 50 mg/kg, once daily, for 7 and/or 14 days in order to compare the protective effects of folic acid. Thirty minutes after the last administration of ketamine, the locomotor and social interaction activities were evaluated, and immediately the brain structure were removed for biochemical analysis. In this study, ketamine was administered in a single dose or in doses over the course of 7 days increasing the animal's locomotion. This study showed that the administration of folic acid over 7 days was unable to prevent hyper locomotion. In contrast, folic acid (10 and 50 mg/kg) administrated over a period of 14 days, was able to partially prevent the hyper locomotion. Our data indicates that both acute and chronic administrations of ketamine increased the time to first contact between the animals, while the increased latency for social contact was completely prevented by folic acid (5, 10 and 50 mg/kg). Chronic and acute administrations of ketamine also increased lipid peroxidation and protein carbonylation in brain. Folic acid (10 and 50 mg/kg) supplements showed protective effects on the oxidative damage found in the different brain structures evaluated. All together, the results indicate that nutritional supplementation with folic acid provides promising results in an animal model of schizophrenia induced by ketamine.
近期研究表明,补充叶酸对精神分裂症患者有益。本研究的目的是评估在7天或14天的时间里,添加叶酸对成年大鼠的影响。研究还着手使用氯胺酮诱导的精神分裂症动物模型,在行为和生化参数方面验证叶酸的任何潜在保护作用。本研究采用两种方案(急性和慢性)以25mg/kg(腹腔注射)的剂量给予氯胺酮。叶酸通过口服途径给药,剂量分别为5mg/kg、10mg/kg和50mg/kg,每日一次,持续7天和/或14天,以比较叶酸的保护作用。在最后一次给予氯胺酮30分钟后,评估运动和社交互动活动,并立即取出脑结构进行生化分析。在本研究中,氯胺酮以单次剂量或在7天内多次给药,增加了动物的运动能力。本研究表明,连续7天给予叶酸无法预防运动亢进。相比之下,连续14天给予叶酸(10mg/kg和50mg/kg)能够部分预防运动亢进。我们的数据表明,急性和慢性给予氯胺酮均增加了动物之间首次接触的时间,而叶酸(5mg/kg、10mg/kg和50mg/kg)完全预防了社交接触潜伏期的增加。急性和慢性给予氯胺酮还增加了脑中的脂质过氧化和蛋白质羰基化。叶酸补充剂(10mg/kg和50mg/kg)对所评估的不同脑结构中的氧化损伤具有保护作用。总之,结果表明,在氯胺酮诱导的精神分裂症动物模型中,补充叶酸营养具有良好前景。