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Therapeutic potential of statins in multiple sclerosis: immune modulation, neuroprotection and neurorepair.他汀类药物在多发性硬化症中的治疗潜力:免疫调节、神经保护和神经修复
Future Neurol. 2008 Mar 1;3(2):153. doi: 10.2217/14796708.3.2.153.
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Statins as potential therapeutic agents in neuroinflammatory disorders.他汀类药物作为神经炎症性疾病的潜在治疗药物。
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Statins--a cure-all for the brain?他汀类药物——大脑的万灵药?
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Atorvastatin added to interferon beta for relapsing multiple sclerosis: 12-month treatment extension of the randomized multicenter SWABIMS trial.阿托伐他汀联合β-干扰素治疗复发型多发性硬化症:随机多中心SWABIMS试验的12个月治疗延长期
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Stimulation of osteoclast formation by RANKL requires interferon regulatory factor-4 and is inhibited by simvastatin in a mouse model of bone loss.RANKL 刺激破骨细胞形成需要干扰素调节因子 4,并且在骨质流失的小鼠模型中被辛伐他汀抑制。
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Human TH17 lymphocytes promote blood-brain barrier disruption and central nervous system inflammation.人类辅助性T细胞17淋巴细胞会促进血脑屏障破坏和中枢神经系统炎症。
Nat Med. 2007 Oct;13(10):1173-5. doi: 10.1038/nm1651. Epub 2007 Sep 9.
2
Lovastatin suppresses erythropoietin receptor surface expression through dual inhibition of glycosylation and geranylgeranylation.洛伐他汀通过对糖基化和香叶基香叶基化的双重抑制作用来抑制促红细胞生成素受体的表面表达。
Biochem Pharmacol. 2007 Aug 15;74(4):590-600. doi: 10.1016/j.bcp.2007.04.028. Epub 2007 May 5.
3
Simvastatin and atorvastatin improve behavioral outcome, reduce hippocampal degeneration, and improve cerebral blood flow after experimental traumatic brain injury.辛伐他汀和阿托伐他汀可改善实验性创伤性脑损伤后的行为结果,减少海马体退化,并改善脑血流量。
Exp Neurol. 2007 Jul;206(1):59-69. doi: 10.1016/j.expneurol.2007.03.031. Epub 2007 Apr 27.
4
Autoimmune inflammation from the Th17 perspective.从辅助性T细胞17的角度看自身免疫性炎症
Autoimmun Rev. 2007 Jan;6(3):169-75. doi: 10.1016/j.autrev.2006.10.002. Epub 2006 Nov 14.
5
Post-trauma Lipitor treatment prevents endothelial dysfunction, facilitates neuroprotection, and promotes locomotor recovery following spinal cord injury.创伤后使用立普妥治疗可预防内皮功能障碍,促进神经保护,并促进脊髓损伤后的运动功能恢复。
J Neurochem. 2007 Apr;101(1):182-200. doi: 10.1111/j.1471-4159.2006.04354.x. Epub 2007 Jan 8.
6
CNS myeloid DCs presenting endogenous myelin peptides 'preferentially' polarize CD4+ T(H)-17 cells in relapsing EAE.在复发型实验性自身免疫性脑脊髓炎中,呈递内源性髓磷脂肽的中枢神经系统髓样树突状细胞“优先”使CD4 + T(H)-17细胞极化。
Nat Immunol. 2007 Feb;8(2):172-80. doi: 10.1038/ni1430. Epub 2007 Jan 7.
7
The role of T helper cells in neuroprotection and regeneration.辅助性T细胞在神经保护和再生中的作用。
J Neuroimmunol. 2007 Mar;184(1-2):100-12. doi: 10.1016/j.jneuroim.2006.11.019. Epub 2007 Jan 2.
8
Bcl-2 upregulation and neuroprotection in guinea pig brain following chronic simvastatin treatment.慢性辛伐他汀治疗后豚鼠脑内Bcl-2上调与神经保护作用
Neurobiol Dis. 2007 Feb;25(2):438-45. doi: 10.1016/j.nbd.2006.10.004. Epub 2006 Dec 6.
9
IL-10 inhibits lipopolysaccharide-induced CD40 gene expression through induction of suppressor of cytokine signaling-3.白细胞介素-10通过诱导细胞因子信号传导抑制因子3来抑制脂多糖诱导的CD40基因表达。
J Immunol. 2006 Dec 1;177(11):7761-71. doi: 10.4049/jimmunol.177.11.7761.
10
3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitor Atorvastatin mediated effects depend on the activation status of target cells in PLP-EAE.3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂阿托伐他汀介导的效应取决于实验性自身免疫性脑脊髓炎中靶细胞的激活状态。
J Autoimmun. 2006 Dec;27(4):251-65. doi: 10.1016/j.jaut.2006.09.006. Epub 2006 Nov 3.

他汀类药物在多发性硬化症中的治疗潜力:免疫调节、神经保护和神经修复

Therapeutic potential of statins in multiple sclerosis: immune modulation, neuroprotection and neurorepair.

作者信息

Markovic-Plese Silva, Singh Avtar K, Singh Inderjit

机构信息

University of North Carolina at Chapel Hill, Department of Neurology, Department of Microbiology & Immunology, Chapel Hill, NC, USA, Tel.: +1 919 966 3701;

出版信息

Future Neurol. 2008 Mar 1;3(2):153. doi: 10.2217/14796708.3.2.153.

DOI:10.2217/14796708.3.2.153
PMID:20107624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2811338/
Abstract

Statins as inhibitors of 3-hydroxy-3-methyl glutaryl coenzyme A reductase are widely used as cholesterol-lowering drugs. Recent studies provide evidence that the anti-inflammatory activity of statins, which is independent of their cholesterol-lowering effects, may have potential therapeutic implications for neuroinflammatory diseases such as multiple sclerosis (MS), Alzheimer's disease and brain tumors, as well as traumatic spinal cord and brain injuries. Studies with animal models of MS suggest that, in addition to immunomodulatory activities similar to the ones observed with approved MS medications, statin treatment also protects the BBB, protects against neurodegeneration and may also promote neurorepair. Although the initial human studies on statin treatment for MS are encouraging, prospective randomized clinical studies will be required to evaluate their efficacy in the larger patient population.

摘要

他汀类药物作为3-羟基-3-甲基戊二酰辅酶A还原酶的抑制剂,被广泛用作降胆固醇药物。最近的研究表明,他汀类药物的抗炎活性与其降胆固醇作用无关,可能对多发性硬化症(MS)、阿尔茨海默病和脑肿瘤等神经炎症性疾病以及创伤性脊髓和脑损伤具有潜在的治疗意义。对MS动物模型的研究表明,除了具有与已批准的MS药物类似的免疫调节活性外,他汀类药物治疗还能保护血脑屏障,预防神经退行性变,还可能促进神经修复。尽管最初关于他汀类药物治疗MS的人体研究令人鼓舞,但仍需要进行前瞻性随机临床研究,以评估其在更大患者群体中的疗效。