Erbaş Oytun, Akseki Hüseyin Serdar, Aktuğ Hüseyin, Taşkıran Dilek
Department of Physiology, Gaziosmanpaşa University, School of Medicine, Tokat, Turkey.
Metab Brain Dis. 2015 Jun;30(3):739-46. doi: 10.1007/s11011-014-9630-4. Epub 2014 Nov 21.
Schizophrenia is known to be associated with metabolic disturbances including diabetes mellitus, obesity and cardiovascular diseases. A growing body of evidence has suggested abnormal cytokine levels in schizophrenia. In the present study, we explored the effects of low-grade chronic inflammation on behavioral stereotypy in a rat model of non-alcoholic fatty liver disease (NAFLD). In order to induce NAFLD, rats were fed with either water enriched with 30 % fructose or plain tap water for 8 weeks. Following feeding period, behavioral stereotypy was evaluated with apomorphine-induced stereotypy test. Also, levels of tumor necrosis factor alpha (TNF-α), interleukin 2 (IL-2) and nuclear factor kappa B (NF-κB) in the liver and brain tissues were assessed biochemically. Brain homovanilic acid (HVA) was measured to evaluate the dopamine turnover. NAFLD rats showed significantly higher stereotypy score compared to controls (p = 0.016). TNF-α, IL-2, and NF-κB levels were significantly increased in NAFLD rats compared to control group. Brain HVA levels were elevated in NAFLD rats as well (p = 0.008). Moreover, NAFLD group prompted a considerable increase in brain IL-2 immunoexpression (p = 0.005). In conclusion, the present study demonstrates that low-grade chronic inflammation such as NAFLD may enhance apomorphine-induced stereotypic behavior via increasing dopaminergic activity in rats.
众所周知,精神分裂症与代谢紊乱有关,包括糖尿病、肥胖症和心血管疾病。越来越多的证据表明精神分裂症患者体内细胞因子水平异常。在本研究中,我们在非酒精性脂肪性肝病(NAFLD)大鼠模型中探讨了低度慢性炎症对行为刻板症的影响。为了诱导NAFLD,给大鼠喂食富含30%果糖的水或普通自来水,持续8周。喂食期结束后,用阿扑吗啡诱导的刻板症试验评估行为刻板症。此外,通过生化方法评估肝脏和脑组织中肿瘤坏死因子α(TNF-α)、白细胞介素2(IL-2)和核因子κB(NF-κB)的水平。测量脑内高香草酸(HVA)以评估多巴胺周转率。与对照组相比,NAFLD大鼠的刻板症评分显著更高(p = 0.016)。与对照组相比,NAFLD大鼠的TNF-α、IL-2和NF-κB水平显著升高。NAFLD大鼠的脑HVA水平也升高(p = 0.008)。此外,NAFLD组脑内IL-2免疫表达显著增加(p = 0.005)。总之,本研究表明,NAFLD等低度慢性炎症可能通过增加大鼠的多巴胺能活性来增强阿扑吗啡诱导的刻板行为。