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Effect of Preventive and Curative Fingolimod Treatment Regimens on Microglia Activation and Disease Progression in a Rat Model of Multiple Sclerosis

机译:芬戈莫德预防和治疗方案对多发性硬化大鼠模型中小胶质细胞活化和疾病进展的影响

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摘要

Fingolimod was the first oral drug approved for multiple sclerosis treatment. Its principal mechanism of action is blocking of lymphocyte trafficking. In addition, recent studies have shown its capability to diminish microglia activation. The effect of preventive and curative fingolimod treatment on the time-course of neuroinflammation was investigated in the experimental autoimmune encephalomyelitis rat model for multiple sclerosis. Neuroinflammatory progression was followed in Dark Agouti female rats after immunization. Positron-Emission tomography (PET) imaging with (R)-[11C]PK11195 was performed on day 11, 15, 19, 27, 29 and 34 during normal disease progression, preventive and curative treatments with fingolimod (1 mg/kg/day). Additionally, bodyweight and clinical symptoms were determined. Preventive treatment diminished bodyweight loss and inhibited the appearance of neurological symptoms. In non-treated rats, PET showed that neuroinflammation peaked in the brainstem at day 19, whereas the imaging signal was decreased in cortical regions. Both preventive and curative treatment reduced neuroinflammation in the brainstem at day 19. Eight days after treatment withdrawal, neuroinflammation had flared-up, especially in cortical regions. Preventive treatment with fingolimod suppressed clinical symptoms and neuroinflammation in the brainstem. After treatment withdrawal, clinical symptoms reappeared together with neuroinflammation in cortical regions, suggesting a different pathway of disease progression.Electronic supplementary materialThe online version of this article (doi:10.1007/s11481-017-9741-x) contains supplementary material, which is available to authorized users.
机译:芬戈莫德是第一种被批准用于多发性硬化症治疗的口服药物。其主要作用机制是阻断淋巴细胞运输。另外,最近的研究表明其减少小胶质细胞活化的能力。在实验性多发性硬化的自身免疫性脑脊髓炎大鼠模型中研究了芬戈莫德预防性和治疗性治疗对神经炎症时程的影响。免疫后,Dark Agouti雌性大鼠追踪神经炎症进展。在疾病进展正常的第11、15、19、27、29和34天,使用(R)-[ 11 C] PK11195进行正电子发射断层扫描(PET)成像,并进行预防和治疗芬戈莫德(1 mg / kg /天)。另外,确定体重和临床症状。预防性治疗可减少体重减轻并抑制神经系统症状的出现。在未经治疗的大鼠中,PET显示在第19天,脑干的神经炎症达到高峰,而在皮层区域的成像信号则下降。预防性和治疗性治疗均在第19天减少了脑干的神经炎症。停药八天后,神经炎症开始发作,尤其是在皮质区域。芬戈莫德预防性治疗可抑制脑干的临床症状和神经炎症。停药后,皮质区域会再次出现临床症状并伴发神经炎症,提示疾病发展的途径不同。电子补充材料本文的在线版本(doi:10.1007 / s11481-017-9741-x)包含补充材料,可以通过以下途径获得给授权用户。

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