Monte Aline Santos, Mello Bruna Stefânia Ferreira, Borella Vládia Célia Moreira, da Silva Araujo Tatiane, da Silva Francisco Eliclécio Rodrigues, Sousa Francisca Cléa F de, de Oliveira Antônio Carlos Pinheiro, Gama Clarissa Severino, Seeman Mary V, Vasconcelos Silvânia Maria Mendes, Lucena David Freitas De, Macêdo Danielle
Drug Research and Development Center, Department of Physiology and Pharmacology, Universidade Federal do Ceará, Fortaleza, CE, Brazil.
Department of Pharmacology and Department of Physiology - ICB, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.
Behav Brain Res. 2017 Jul 28;331:30-37. doi: 10.1016/j.bbr.2017.04.057. Epub 2017 May 17.
Schizophrenia is considered to be a developmental disorder with distinctive sex differences. Aiming to simulate the vulnerability of the third trimester of human pregnancy to the developmental course of schizophrenia, an animal model was developed, using neonatal poly(I:C) as a first-hit, and peripubertal stress as a second-hit, i.e. a two-hit model. Since, to date, there have been no references to sex differences in the two-hit model, our study sought to determine sex influences on the development of behavior and brain oxidative change in adult rats submitted to neonatal exposure to poly(I:C) on postnatal days 5-7 as well as peripubertal unpredictable stress (PUS). Our results showed that adult two-hit rats present sex-specific behavioral alterations, with females showing more pronounced deficits in prepulse inhibition of the startle reflex and hyperlocomotion, while males showing more deficits in social interaction. Male and female animals exhibited similar working memory deficits. The levels of the endogenous antioxidant, reduced glutathione, were decreased in the prefrontal cortex (PFC) of both male and female animals exposed to both poly(I:C) and poly(I:C)+PUS. Only females presented decrements in GSH levels in the striatum. Nitrite levels were increased in the PFC of male and in the striatum of female poly(I:C)+PUS rats. Increased lipid peroxidation was observed in the PFC of females and in the striatum of males and females exposed to poly(I:C) and poly(I:C)+PUS. Thus, the present study presents evidence for sex differences in behavior and oxidative brain change induced by a two-hit model of schizophrenia.
精神分裂症被认为是一种具有明显性别差异的发育障碍。为了模拟人类妊娠晚期对精神分裂症发展过程的易感性,开发了一种动物模型,以新生期聚肌苷酸胞苷酸(poly(I:C))作为首次打击,青春期前应激作为第二次打击,即双打击模型。由于迄今为止,尚未有关于双打击模型中性别差异的参考文献,我们的研究旨在确定性别对成年大鼠行为发育和脑氧化变化的影响,这些成年大鼠在出生后第5 - 7天接受新生期聚肌苷酸胞苷酸暴露以及青春期前不可预测应激(PUS)。我们的结果表明,成年双打击大鼠表现出性别特异性行为改变,雌性大鼠在惊吓反射的前脉冲抑制和运动亢进方面表现出更明显的缺陷,而雄性大鼠在社交互动方面表现出更多缺陷。雄性和雌性动物表现出相似的工作记忆缺陷。在暴露于聚肌苷酸胞苷酸和聚肌苷酸胞苷酸 + PUS的雄性和雌性动物的前额叶皮质(PFC)中,内源性抗氧化剂还原型谷胱甘肽的水平均降低。只有雌性大鼠纹状体中的谷胱甘肽水平下降。在雄性聚肌苷酸胞苷酸 + PUS大鼠的PFC和雌性大鼠的纹状体中,亚硝酸盐水平升高。在暴露于聚肌苷酸胞苷酸和聚肌苷酸胞苷酸 + PUS的雌性大鼠的PFC以及雄性和雌性大鼠的纹状体中,观察到脂质过氧化增加。因此,本研究为精神分裂症双打击模型诱导的行为和脑氧化变化中的性别差异提供了证据。