Dutra-Tavares Ana Carolina, Couto Luciana Araújo, Souza Thainá P, Bandeira-Martins Anais, Silva Juliana Oliveira, Filgueiras Claudio C, Ribeiro-Carvalho Anderson, Manhães Alex C, Abreu-Villaça Yael
Departamento de Ciências Biomédicas e Saúde, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro (UERJ), Cabo Frio 28905-320, RJ, Brazil.
Laboratório de Neurofisiologia, Departamento de Ciências Fisiológicas, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro UERJ, Rio de Janeiro 20550-170, RJ, Brazil.
Brain Sci. 2024 Aug 25;14(9):855. doi: 10.3390/brainsci14090855.
Tobacco consumption in schizophrenia (SCHZ) patients is highly prevalent. Data support the occurrence of sequential events during comorbidity establishment, and both smoking first, SCHZ second and SCHZ first, smoking second sequences have been proposed. To investigate whether these two possibilities lead to distinct outcomes of comorbidity, we used a phencyclidine-induced SCHZ model and nicotine exposure as a surrogate of smoking. C57Bl/6 mice were submitted to a protocol that either began with 4 days of phencyclidine exposure or 4 days of nicotine exposure. This period was followed by 5 days of combined phencyclidine + nicotine exposure. Locomotor sensitization and pre-pulse inhibition (PPI) were assessed due to their well-known associations with SCHZ as opposed to rearing, an unrelated behavior. Nicotine priming potentiated phencyclidine-evoked sensitization. However, nicotine exposure after SCHZ modeling did not interfere with phencyclidine's effects. In the PPI test, nicotine after SCHZ modeling worsened the phencyclidine-evoked deficiency in males. In contrast, nicotine priming had no effects. Regarding rearing, nicotine priming failed to interfere with phencyclidine-mediated inhibition. Similarly, phencyclidine priming did not modify nicotine-mediated inhibition. The present results indicate that the sequence, either SCHZ-first or nicotine-first, differentially impacts comorbidity outcomes, a finding that is relevant for the identification of mechanisms of nicotine interference in the neurobiology of SCHZ.
精神分裂症(SCHZ)患者的烟草消费非常普遍。数据支持在共病形成过程中存在一系列事件,并且已经提出了先吸烟、后患精神分裂症以及先患精神分裂症、后吸烟这两种顺序。为了研究这两种可能性是否会导致共病的不同结果,我们使用苯环己哌啶诱导的精神分裂症模型,并将尼古丁暴露作为吸烟的替代物。将C57Bl/6小鼠按照以下方案进行处理:要么先进行4天的苯环己哌啶暴露,要么先进行4天的尼古丁暴露。在此期间之后,进行5天的苯环己哌啶+尼古丁联合暴露。由于运动致敏和前脉冲抑制(PPI)与精神分裂症有众所周知的关联,而与站立这种不相关行为不同,因此对其进行评估。尼古丁预处理增强了苯环己哌啶诱发的致敏作用。然而,在精神分裂症建模后进行尼古丁暴露并未干扰苯环己哌啶的作用。在PPI测试中,精神分裂症建模后给予尼古丁会使雄性小鼠中苯环己哌啶诱发的缺陷恶化。相比之下,尼古丁预处理没有影响。关于站立行为,尼古丁预处理未能干扰苯环己哌啶介导的抑制作用。同样,苯环己哌啶预处理也没有改变尼古丁介导的抑制作用。目前的结果表明,先患精神分裂症或先接触尼古丁的顺序会对共病结果产生不同影响,这一发现对于确定尼古丁干扰精神分裂症神经生物学机制具有重要意义。