Schiavone Stefania, Camerino Giulia M, Mhillaj Emanuela, Zotti Margherita, Colaianna Marilena, De Giorgi Angelo, Trotta Antonello, Cantatore Francesco P, Conte Elena, Bove Maria, Tucci Paolo, Morgese Maria G, Trabace Luigia
Department of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy.
Department of Pharmacy and Drug Sciences, University of Bari Aldo Moro, Bari, Italy.
Front Pharmacol. 2017 Nov 8;8:787. doi: 10.3389/fphar.2017.00787. eCollection 2017.
Medication with neuroleptics has been associated with adipose tissue dysfunctions and, in particular, with increased visceral fat amount. However, several studies suggested that antipsychotic treatment might not be the main responsible of fat mass accumulation, as this has been also described in not treated psychotic patients. One of the most used "drug-free" rodent models of psychosis is the social isolation rearing of young adult rats, which provides a non-pharmacologic method of inducing long-term alterations reminiscent of symptoms seen in psychotic patients. Recent data highlighted a crucial role of redox imbalance in adipose tissue dysfunctions, in terms of decreased antioxidant defense and increased reactive oxygen species (ROS). Here, we investigated possible oxidative stress-related biomolecular alterations associated with visceral fat increase in 7 week isolated rats. To this purpose, we quantified total and visceral fat amount by using dual-energy X-ray (DEXA) absorptiometry. On visceral fat, we analyzed the expression of specific ROS-producer genes (), antioxidant enzymes ( and ) and oxidative stress-induced damage markers (, and ). The impact of oxidative stress on beta3-adrenergic receptors (), at both mRNA and protein level, was also assessed. We found that 7 weeks of social isolation induced an increase in total and visceral fat, associated with a decrease in (mRNA and protein) as well as mRNA levels and an enhanced expression of (mRNA and protein) and mRNA. No differences were detected in mRNA levels between grouped and isolated animals. Elevations in , , and expression in visceral fat of isolated animals accounted for oxidative stress-related damage in this tissue, further associated with a significant increase in mRNA and protein. Our results provide a novel understanding of the pathological link existing among psychosocial stress-induced psychosis, adipose tissue dysfunctions and redox imbalance, opening new therapeutic perspectives for the treatment of alterations in peripheral tissues associated with this mental disorder.
使用抗精神病药物与脂肪组织功能障碍有关,特别是与内脏脂肪量增加有关。然而,多项研究表明,抗精神病药物治疗可能不是脂肪量积累的主要原因,因为未接受治疗的精神病患者也存在这种情况。最常用的“无药物”啮齿动物精神病模型之一是对成年幼鼠进行社会隔离饲养,这提供了一种非药物方法来诱导长期变化,使人联想到精神病患者出现的症状。最近的数据强调了氧化还原失衡在脂肪组织功能障碍中的关键作用,表现为抗氧化防御能力下降和活性氧(ROS)增加。在此,我们研究了7周隔离大鼠内脏脂肪增加可能与氧化应激相关的生物分子改变。为此,我们使用双能X射线(DEXA)吸收法对总脂肪量和内脏脂肪量进行了量化。在内脏脂肪上,我们分析了特定ROS产生基因()、抗氧化酶(和)以及氧化应激诱导损伤标志物(、和)的表达。还评估了氧化应激对β3-肾上腺素能受体()在mRNA和蛋白质水平的影响。我们发现,7周的社会隔离导致总脂肪量和内脏脂肪量增加,同时(mRNA和蛋白质)以及mRNA水平降低,(mRNA和蛋白质)和mRNA表达增强。在分组动物和隔离动物之间,mRNA水平未检测到差异。隔离动物内脏脂肪中、和表达的升高说明了该组织中与氧化应激相关的损伤,这进一步与mRNA和蛋白质的显著增加有关。我们的研究结果为社会心理应激诱导的精神病、脂肪组织功能障碍和氧化还原失衡之间存在的病理联系提供了新的认识,为治疗与这种精神障碍相关的外周组织改变开辟了新的治疗前景。