O'Sullivan David, Green Laura, Stone Sarrabeth, Zareie Pirooz, Kharkrang Marie, Fong Dahna, Connor Bronwen, La Flamme Anne Camille
School of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Department of Pharmacology and Clinical Pharmacology, Centre for Brain Research, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
PLoS One. 2014 Aug 12;9(8):e104430. doi: 10.1371/journal.pone.0104430. eCollection 2014.
Recent studies have demonstrated that atypical antipsychotic agents, which are known to antagonize dopamine D2 and serotonin 5-HT2a receptors, have immunomodulatory properties. Given the potential of these drugs to modulate the immune system both peripherally and within the central nervous system, we investigated the ability of the atypical anti-psychotic agent, risperidone, to modify disease in the animal model of multiple sclerosis (MS)4, experimental autoimune encephalomyelitis (EAE). We found that chronic oral administration of risperidone dose-dependently reduced the severity of disease and decreased both the size and number of spinal cord lesions. Furthermore, risperidone treatment substantially reduced antigen-specific interleukin (IL)-17a, IL-2, and IL-4 but not interferon (IFN)-γ production by splenocytes at peak disease and using an in vitro model, we show that treatment of macrophages with risperidone alters their ability to bias naïve T cells. Another atypical antipsychotic agent, clozapine, showed a similar ability to modify macrophages in vitro and to reduce disease in the EAE model but this effect was not due to antagonism of the type 1 or type 2 dopamine receptors alone. Finally, we found that while risperidone treatment had little effect on the in vivo activation of splenic macrophages during EAE, it significantly reduced the activation of microglia and macrophages in the central nervous system. Together these studies indicate that atypical antipsychotic agents like risperidone are effective immunomodulatory agents with the potential to treat immune-mediated diseases such as MS.
最近的研究表明,已知能拮抗多巴胺D2和5-羟色胺5-HT2a受体的非典型抗精神病药物具有免疫调节特性。鉴于这些药物在外周和中枢神经系统中调节免疫系统的潜力,我们研究了非典型抗精神病药物利培酮在多发性硬化症(MS)的动物模型——实验性自身免疫性脑脊髓炎(EAE)中改善疾病的能力。我们发现,长期口服利培酮可剂量依赖性地降低疾病严重程度,并减少脊髓损伤的大小和数量。此外,利培酮治疗在疾病高峰期可显著降低脾细胞产生的抗原特异性白细胞介素(IL)-17a、IL-2和IL-4,但不影响干扰素(IFN)-γ的产生。并且,利用体外模型我们发现,用利培酮处理巨噬细胞会改变其使未成熟T细胞产生偏向性的能力。另一种非典型抗精神病药物氯氮平在体外显示出类似的改变巨噬细胞的能力,并在EAE模型中减轻疾病,但这种作用并非仅由对1型或2型多巴胺受体的拮抗作用所致。最后,我们发现,虽然利培酮治疗对EAE期间脾巨噬细胞的体内激活作用不大,但它能显著降低中枢神经系统中小胶质细胞和巨噬细胞的激活。这些研究共同表明,像利培酮这样的非典型抗精神病药物是有效的免疫调节药物,具有治疗如MS等免疫介导疾病的潜力。