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作为多发性硬化症和缺血性中风恢复增强疗法的C-藻蓝蛋白和藻蓝胆素:临床前视角

C-Phycocyanin and Phycocyanobilin as Remyelination Therapies for Enhancing Recovery in Multiple Sclerosis and Ischemic Stroke: A Preclinical Perspective.

作者信息

Pentón-Rol Giselle, Marín-Prida Javier, Falcón-Cama Viviana

机构信息

Center for Genetic Engineering and Biotechnology (CIGB), Ave. 31 e/158 y 190, Cubanacan, P.O. Box 6162, Playa, Havana 10600, Cuba.

Center for Research and Biological Evaluations (CEIEB), Institute of Pharmacy and Food, University of Havana, Ave. 23 e/214 y 222, La Lisa, PO Box 430, Havana 13600, Cuba.

出版信息

Behav Sci (Basel). 2018 Jan 18;8(1):15. doi: 10.3390/bs8010015.

DOI:10.3390/bs8010015
PMID:29346320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5791033/
Abstract

Myelin loss has a crucial impact on behavior disabilities associated to Multiple Sclerosis (MS) and Ischemic Stroke (IS). Although several MS therapies are approved, none of them promote remyelination in patients, limiting their ability for chronic recovery. With no available therapeutic options, enhanced demyelination in stroke survivors is correlated with a poorer behavioral recovery. Here, we show the experimental findings of our group and others supporting the remyelinating effects of C-Phycocyanin (C-PC), the main biliprotein of and its linked tetrapyrrole Phycocyanobilin (PCB), in models of these illnesses. C-PC promoted white matter regeneration in rats and mice affected by experimental autoimmune encephalomyelitis. Electron microscopy analysis in cerebral cortex from ischemic rats revealed a potent remyelinating action of PCB treatment after stroke. Among others biological processes, we discussed the role of regulatory T cell induction, the control of oxidative stress and pro-inflammatory mediators, gene expression modulation and COX-2 inhibition as potential mechanisms involved in the C-PC and PCB effects on the recruitment, differentiation and maturation of oligodendrocyte precursor cells in demyelinated lesions. The assembled evidence supports the implementation of clinical trials to demonstrate the recovery effects of C-PC and PCB in these diseases.

摘要

髓鞘丢失对与多发性硬化症(MS)和缺血性中风(IS)相关的行为障碍具有至关重要的影响。尽管有几种MS疗法已获批准,但它们都不能促进患者的髓鞘再生,限制了患者慢性恢复的能力。由于没有可用的治疗选择,中风幸存者中髓鞘脱失的加重与行为恢复较差相关。在这里,我们展示了我们小组和其他研究小组的实验结果,这些结果支持藻蓝蛋白(C-PC)及其连接的四吡咯藻蓝胆素(PCB)在这些疾病模型中的髓鞘再生作用,C-PC是蓝藻的主要双蛋白。C-PC促进了受实验性自身免疫性脑脊髓炎影响的大鼠和小鼠的白质再生。对缺血大鼠大脑皮层的电子显微镜分析显示,中风后PCB治疗具有强大的髓鞘再生作用。在其他生物学过程中,我们讨论了调节性T细胞诱导、氧化应激和促炎介质的控制、基因表达调节以及COX-2抑制作为潜在机制,这些机制参与了C-PC和PCB对脱髓鞘病变中少突胶质前体细胞的募集、分化和成熟的影响。综合证据支持开展临床试验,以证明C-PC和PCB在这些疾病中的恢复作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/5791033/d3ef72a42786/behavsci-08-00015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/5791033/773b311e31b1/behavsci-08-00015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/5791033/a3e996092e1a/behavsci-08-00015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/5791033/d3ef72a42786/behavsci-08-00015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/5791033/773b311e31b1/behavsci-08-00015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/5791033/a3e996092e1a/behavsci-08-00015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/5791033/d3ef72a42786/behavsci-08-00015-g003.jpg

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