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炎症相关抑郁的治疗策略。

Therapeutic Strategies for Treatment of Inflammation-related Depression.

机构信息

Department of Molecular Biology and Endocrinology, VINCA Institute of Nuclear Sciences, University of Belgrade, Serbia.

Clinic for Psychiatry, Clinical Centre of Serbia, Pasterova 2, 11000, Belgrade, Serbia.

出版信息

Curr Neuropharmacol. 2018 Jan 30;16(2):176-209. doi: 10.2174/1570159X15666170828163048.

Abstract

BACKGROUND

Mounting evidence demonstrates enhanced systemic levels of inflammatory mediators in depression, indicating that inflammation may play a role in the etiology and course of mood disorders. Indeed, proinflammatory cytokines induce a behavioral state of conservation- withdrawal resembling human depression, characterized by negative mood, fatigue, anhedonia, psychomotor retardation, loss of appetite, and cognitive deficits. Neuroinflammation also contributes to non-responsiveness to current antidepressant (AD) therapies. Namely, response to conventional AD medications is associated with a decrease in inflammatory biomarkers, whereas resistance to treatment is accompanied by increased inflammation.

METHODS

In this review, we will discuss the utility and shortcomings of pharmacologic AD treatment strategies focused on inflammatory pathways, applied alone or as an adjuvant component to current AD therapies.

RESULTS

Mechanisms of cytokine actions on behavior involve activation of inflammatory pathways in the brain, resulting in changes of neurotransmitter metabolism, neuroendocrine function, and neuronal plasticity. Selective serotonin reuptake inhibitors exhibit the most beneficial effects in restraining the inflammation markers in depression. Different anti-inflammatory agents exhibit AD effects via modulating neurotransmitter systems, neuroplasticity markers and glucocorticoid receptor signaling. Anti-inflammatory add-on therapy in depression highlights such treatment as a candidate for enhancement strategy in patients with moderate-to-severe depression.

CONCLUSION

The interactions between the immune system and CNS are not only involved in shaping behavior, but also in responding to therapeutics. Even though, substantial evidence from animal and human research support a beneficial effect of anti-inflammatory add-on therapy in depression, further research with special attention on safety, particularly during prolonged periods of antiinflammatory co-treatments, is required.

摘要

背景

越来越多的证据表明,抑郁症患者体内的炎症介质水平升高,这表明炎症可能在心境障碍的病因和病程中起作用。事实上,促炎细胞因子会诱发一种类似于人类抑郁症的保护-撤退行为状态,其特征是情绪低落、疲劳、快感缺失、精神运动迟缓、食欲不振和认知功能障碍。神经炎症也导致对当前抗抑郁(AD)治疗的反应不足。即,对常规 AD 药物的反应与炎症生物标志物的减少相关,而对治疗的抵抗则伴随着炎症的增加。

方法

在这篇综述中,我们将讨论针对炎症途径的 AD 治疗策略的应用及其优缺点,这些策略单独或作为当前 AD 治疗的辅助成分。

结果

细胞因子对行为的作用机制涉及到大脑中炎症途径的激活,导致神经递质代谢、神经内分泌功能和神经元可塑性的变化。选择性 5-羟色胺再摄取抑制剂在抑制抑郁症中的炎症标志物方面显示出最有益的效果。不同的抗炎剂通过调节神经递质系统、神经可塑性标志物和糖皮质激素受体信号来发挥 AD 作用。在抑郁症中添加抗炎治疗强调了这种治疗方法作为中度至重度抑郁症患者增强策略的候选方法。

结论

免疫系统和中枢神经系统之间的相互作用不仅参与了行为的形成,也参与了对治疗的反应。尽管来自动物和人类研究的大量证据支持在抑郁症中添加抗炎治疗的有益效果,但仍需要进一步的研究,特别要注意安全性,尤其是在抗炎联合治疗的延长期间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/5883379/c9d67a753b32/CN-16-176_F1.jpg

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