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芬戈莫德的心血管效应:一篇综述文章。

Cardiovascular effects of fingolimod: A review article.

作者信息

Behjati Mohaddeseh, Etemadifar Masoud, Abdar Esfahani Morteza

机构信息

Department of Cardiology, School of Medicine, Cardiovascular Research Center AND Heart Failure Research Center, Isfahan Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Neurology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Iran J Neurol. 2014 Jul 4;13(3):119-26.

PMID:25422729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4240927/
Abstract

Multiple sclerosis (MS) is a chronic auto-immune disease. Most therapeutic strategies for treatment of this disease direct immune modulation and control of inflammatory processes. First-line therapeutic agents showed moderate efficacy and frequent side-effects with moderate efficacy in trials. Their parental administration and limited long-term adherence restrict their efficacy compared with second-line therapies. Fingolimod as a second-line therapeutic agent has been shown to reduce annualized relapse rate, risk of disability progression and inflammatory activity of relapsing MS. Safety and efficacy FTY720: Safety and efficacy issues are the main metrics for judgment of drug efficacy. In this article, we focus on cardiovascular effects of FTY720 treatment. Effect of FTY720 on rate and rhythm, impact of FTY720 on endothelial cells, its atheroprotective effects, its effects on cardiac transplantation outcomes, vascular complications of FTY720, effects of FTY720 on endocrine functions and interaction of FTY720 with cardioactive agents are explained in this review article.

摘要

多发性硬化症(MS)是一种慢性自身免疫性疾病。治疗该疾病的大多数治疗策略都旨在进行免疫调节和控制炎症过程。一线治疗药物在试验中显示出中等疗效且副作用频繁。与二线疗法相比,它们的肠胃外给药方式以及有限的长期依从性限制了其疗效。芬戈莫德作为二线治疗药物已被证明可降低复发型MS的年化复发率、残疾进展风险和炎症活动。FTY720的安全性和有效性:安全性和有效性问题是判断药物疗效的主要指标。在本文中,我们重点关注FTY720治疗的心血管效应。本文综述了解释了FTY720对心率和节律的影响、FTY720对内皮细胞的影响、其动脉粥样硬化保护作用、其对心脏移植结果的影响、FTY720的血管并发症、FTY720对内分泌功能的影响以及FTY720与心脏活性药物的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc99/4240927/2e1f7b286037/IJNL-13-119-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc99/4240927/2e1f7b286037/IJNL-13-119-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc99/4240927/2e1f7b286037/IJNL-13-119-g001.jpg

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本文引用的文献

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The molecular study of IFNβ pleiotropic roles in MS treatment.IFNβ在多发性硬化症治疗中的多效性作用的分子研究。
Iran J Neurol. 2013;12(4):149-56.
2
Factors affecting bone mineral density in multiple sclerosis patients.影响多发性硬化症患者骨密度的因素。
Iran J Neurol. 2013;12(1):19-22.
3
How does fingolimod (gilenya(®)) fit in the treatment algorithm for highly active relapsing-remitting multiple sclerosis?那非利莫德(商品名:吉兰泰)在治疗高度活跃的复发缓解型多发性硬化症的治疗算法中是如何发挥作用的?
精油对多发性硬化症的铜离子螯合剂诱导大鼠模型胼胝体脱髓鞘的预防作用。
Avicenna J Phytomed. 2023 Nov-Dec;13(6):675-687. doi: 10.22038/AJP.2023.22784.
4
A Theranostic Small-Molecule Prodrug Conjugate for Neuroendocrine Prostate Cancer.一种用于神经内分泌前列腺癌的诊疗小分子前药缀合物。
Pharmaceutics. 2023 Feb 1;15(2):481. doi: 10.3390/pharmaceutics15020481.
5
Updates and advances in multiple sclerosis neurotherapeutics.多发性硬化症神经治疗学的最新进展。
Neurodegener Dis Manag. 2023 Feb;13(1):47-70. doi: 10.2217/nmt-2021-0058. Epub 2022 Oct 31.
6
Sphingosine 1 phosphate promotes hypertension specific memory T cell trafficking in response to repeated hypertensive challenges.鞘氨醇-1-磷酸促进高血压特异性记忆T细胞在反复高血压刺激下的迁移。
Front Physiol. 2022 Sep 7;13:930487. doi: 10.3389/fphys.2022.930487. eCollection 2022.
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The impact of SARS-CoV-2 treatment on the cardiovascular system: an updated review.新型冠状病毒 2 型治疗对心血管系统的影响:最新综述。
Inflammopharmacology. 2022 Aug;30(4):1143-1151. doi: 10.1007/s10787-022-01009-8. Epub 2022 Jun 14.
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ST-2191, an Anellated Bismorpholino Derivative of Oxy-Fingolimod, Shows Selective S1P Agonist and Functional Antagonist Potency In Vitro and In Vivo.ST-2191,一种氧芬戈莫德的稠合双吗啉衍生物,在体外和体内显示出选择性 S1P 激动剂和功能拮抗剂活性。
Molecules. 2021 Aug 24;26(17):5134. doi: 10.3390/molecules26175134.
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Fingolimod (FTY720) Preserves High Energy Phosphates and Improves Cardiac Function in Heterotopic Heart Transplantation Model.芬戈莫德(FTY720)可保存高能磷化合物并改善异位心脏移植模型的心脏功能。
Int J Mol Sci. 2020 Sep 8;21(18):6548. doi: 10.3390/ijms21186548.
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