CRC Scotland & London, Eccleston Square, London. United Kingdom.
2Department of Psychiatry, Deakin University, Geelong. Australia.
CNS Neurol Disord Drug Targets. 2017;16(3):266-278. doi: 10.2174/1871527315666161122144659.
In this article the emerging biological overlaps of CNS disorders and psychiatric conditions are reviewed. Recent work has highlighted how immune-inflammatory processes and their interactions with oxidative and nitrosative stress, couple to drive changes in neuroregulatory tryptophan catabolites, with consequences for serotonin availability, including as a precursor for the melatonergic pathways. Subsequent alterations in the regulation of local melatonin synthesis are likely to have direct impacts on the reactivity of immune cells, both centrally and systemically. These inflammatory processes also lead to the activation of wider immune processes. Such wider processes can include the production of immunoglobulin (Ig)A and IgM antibody responses, including to tryptophan catabolites, emphasizing the importance of immune responses, and their interactions with inflammatory processes, in the etiology and course of an array of medical conditions, including CNS disorders and psychiatric conditions. Such work poses questions as to the validity and utility of current, non-biologically based classification systems for psychiatric and CNS disorders. In this article, the biological underpinnings of CNS disorders and psychiatric conditions are reviewed in the context of how recent data, in reconceptualizing key processes in these classically-conceived brain-associated disorders, provides scope for novel, and hopefully more clinically useful, treatments. These processes are looked at in detail in Alzheimer's disease and major depressive disorder. One important treatment target is the gut. Alterations in the gut, including gut permeability and the composition of the microbiome, have now become an important target for treatment across an array of medical conditions, emphasizing the importance of targeting regulators of the immune system in developing novel treatments that are based on a more comprehensive and 'wholistic' understanding of currently poorly managed medical conditions, particularly psychiatric and CNS disorders.
本文综述了中枢神经系统疾病和精神疾病之间新出现的生物学重叠。最近的研究强调了免疫炎症过程及其与氧化和硝化应激的相互作用,如何导致神经调节色氨酸分解产物的变化,从而影响 5-羟色胺的供应,包括作为褪黑素途径的前体。随后,局部褪黑素合成调节的改变可能直接影响免疫细胞的反应性,包括中枢和全身的免疫细胞。这些炎症过程也会导致更广泛的免疫过程的激活。更广泛的过程可能包括免疫球蛋白 (Ig)A 和 IgM 抗体的产生反应,包括对色氨酸分解产物的反应,这强调了免疫反应及其与炎症过程的相互作用在一系列医学疾病(包括中枢神经系统疾病和精神疾病)的病因和病程中的重要性。此类研究提出了关于当前非生物学为基础的精神和中枢神经系统疾病分类系统的有效性和实用性的问题。本文综述了中枢神经系统疾病和精神疾病的生物学基础,以及最近的数据如何重新概念化这些经典脑相关疾病的关键过程,为新的、有希望更具临床应用价值的治疗方法提供了可能性。这些过程在阿尔茨海默病和重度抑郁症中进行了详细研究。一个重要的治疗靶点是肠道。肠道的改变,包括肠道通透性和微生物组的组成,现在已成为一系列医学疾病治疗的重要靶点,强调了靶向免疫系统调节剂在开发基于更全面和“整体”理解的新型治疗方法中的重要性目前管理不善的医学疾病,特别是精神和中枢神经系统疾病。