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西尼莫德是否在中枢神经系统中发挥直接作用?

Does Siponimod Exert Direct Effects in the Central Nervous System?

机构信息

Institute of Anatomy, Rostock University Medical Center, Gertrudenstrasse 9, 18057 Rostock, Germany.

出版信息

Cells. 2020 Jul 24;9(8):1771. doi: 10.3390/cells9081771.

DOI:10.3390/cells9081771
PMID:32722245
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7463861/
Abstract

The modulation of the sphingosine 1-phosphate receptor is an approved treatment for relapsing multiple sclerosis because of its anti-inflammatory effect of retaining lymphocytes in lymph nodes. Different sphingosine 1-phosphate receptor subtypes are expressed in the brain and spinal cord, and their pharmacological effects may improve disease development and neuropathology. Siponimod (BAF312) is a novel sphingosine 1-phosphate receptor modulator that has recently been approved for the treatment of active secondary progressive multiple sclerosis (MS). In this review article, we summarize recent evidence suggesting that the active role of siponimod in patients with progressive MS may be due to direct interaction with central nervous system cells. Additionally, we tried to summarize our current understanding of the function of siponimod and discuss the effects observed in the case of MS.

摘要

鞘氨醇 1-磷酸受体的调节是复发性多发性硬化症的一种已批准的治疗方法,因为它具有抗炎作用,可以将淋巴细胞保留在淋巴结中。不同的鞘氨醇 1-磷酸受体亚型在大脑和脊髓中表达,其药理作用可能改善疾病的发展和神经病理学。西尼莫德(BAF312)是一种新型的鞘氨醇 1-磷酸受体调节剂,最近已被批准用于治疗活跃的继发进展性多发性硬化症(MS)。在这篇综述文章中,我们总结了最近的证据,表明西尼莫德在进展性 MS 患者中的积极作用可能是由于其与中枢神经系统细胞的直接相互作用。此外,我们还试图总结我们对西尼莫德功能的现有认识,并讨论在 MS 病例中观察到的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0e/7463861/9c40a0ca7812/cells-09-01771-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0e/7463861/c957a6db259e/cells-09-01771-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0e/7463861/a3e07196ccb2/cells-09-01771-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0e/7463861/9c40a0ca7812/cells-09-01771-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0e/7463861/c957a6db259e/cells-09-01771-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0e/7463861/a3e07196ccb2/cells-09-01771-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0e/7463861/9c40a0ca7812/cells-09-01771-g003.jpg

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引用本文的文献

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Investigating the Mitoprotective Effects of S1P Receptor Modulators Ex Vivo Using a Novel Semi-Automated Live Imaging Set-Up.使用新型半自动活细胞成像系统研究 S1P 受体调节剂的线粒体保护作用。
Int J Mol Sci. 2023 Dec 23;25(1):261. doi: 10.3390/ijms25010261.
3
The Benefits and Risks of Switching from Fingolimod to Siponimod for the Treatment of Relapsing-Remitting and Secondary Progressive Multiple Sclerosis.

本文引用的文献

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In vivo Characterization of Four F-Labeled S1PR1 Tracers for Neuroinflammation.体内评价四种 F 标记的 S1PR1 示踪剂用于神经炎症。
Mol Imaging Biol. 2020 Oct;22(5):1362-1369. doi: 10.1007/s11307-020-01514-8.
2
Mfsd2a and Spns2 are essential for sphingosine-1-phosphate transport in the formation and maintenance of the blood-brain barrier.Mfsd2a和Spns2在血脑屏障的形成和维持过程中对1-磷酸鞘氨醇的转运至关重要。
Sci Adv. 2020 May 29;6(22):eaay8627. doi: 10.1126/sciadv.aay8627. eCollection 2020 May.
3
Imaging Mechanisms of Disease Progression in Multiple Sclerosis: Beyond Brain Atrophy.
从芬戈莫德转换为西尼莫德治疗复发缓解型和继发进展型多发性硬化症的获益与风险。
Drugs R D. 2023 Dec;23(4):331-338. doi: 10.1007/s40268-023-00434-6. Epub 2023 Aug 28.
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Anti-inflammatory Effects of Siponimod in a Mouse Model of Excitotoxicity-Induced Retinal Injury.西尼莫德在兴奋性毒性诱导的视网膜损伤小鼠模型中的抗炎作用。
Mol Neurobiol. 2023 Dec;60(12):7222-7237. doi: 10.1007/s12035-023-03535-0. Epub 2023 Aug 5.
5
The impact of disease modifying therapies on cognitive functions typically impaired in multiple sclerosis patients: a clinician's review.疾病修饰疗法对多发性硬化症患者典型受损认知功能的影响:临床医生综述
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First fluorine-19 magnetic resonance imaging of the multiple sclerosis drug siponimod.首例多发性硬化症药物西尼莫德的氟-19 磁共振成像研究。
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