Literature DB >> 17492904

Evaluation of atorvastatin and simvastatin for treatment of multiple sclerosis.

Oliver Neuhaus1, Hans-Peter Hartung.   

Abstract

Atorvastatin and simvastatin (members of the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor family) are widely prescribed as cholesterol-lowering agents. As they have been shown to exhibit potent immunomodulatory effects, they may become a future treatment option for autoimmune disease in general and multiple sclerosis (MS) in particular. Several recent reports have demonstrated that statins prevent and reverse chronic and relapsing experimental autoimmune encephalomyelitis, an animal model of MS. An open-label clinical trial assessing simvastatin in MS revealed a significant decrease in the number and volume of new MRI lesions and a favorable safety profile. The results of a large multicenter, placebo-controlled clinical trial assessing atorvastatin in patients with clinically isolated syndrome (a disease that predisposes to development MS) are expected soon. However, prospective placebo-controlled trials of atorvastatin or simvastatin in definite MS are difficult to perform due to ethical and financial objections. In this review, we discuss the backgrounds, mechanisms of action and future perspectives of atorvastatin and simvastatin as putative future treatment options in MS.

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Year:  2007        PMID: 17492904     DOI: 10.1586/14737175.7.5.547

Source DB:  PubMed          Journal:  Expert Rev Neurother        ISSN: 1473-7175            Impact factor:   4.618


  7 in total

1.  Simvastatin stimulates production of the antiapoptotic protein Bcl-2 via endothelin-1 and NFATc3 in SH-SY5Y cells.

Authors:  Tammy A Butterick; Urule Igbavboa; Gunter P Eckert; Grace Y Sun; Gary A Weisman; Walter E Müller; W Gibson Wood
Journal:  Mol Neurobiol       Date:  2010-04-06       Impact factor: 5.590

2.  Lp-PLA2: inflammatory biomarker of vascular risk in multiple sclerosis.

Authors:  Zohara Sternberg; Alison Drake; Daniel S Sternberg; Ralph H B Benedict; Fan Li; David Hojnacki; Bianca Weinstock-Guttmann; Frederick E Munschauer
Journal:  J Clin Immunol       Date:  2012-01-13       Impact factor: 8.317

3.  Atorvastatin Protects NSC-34 Motor Neurons Against Oxidative Stress by Activating PI3K, ERK and Free Radical Scavenging.

Authors:  Seok-Ho Lee; Na-Young Choi; Hyun-Jeung Yu; Jinse Park; Hojin Choi; Kyu-Yong Lee; Yong-Min Huh; Young Joo Lee; Seong-Ho Koh
Journal:  Mol Neurobiol       Date:  2015-01-11       Impact factor: 5.590

Review 4.  Statins and neuroprotection: a prescription to move the field forward.

Authors:  W Gibson Wood; Gunter P Eckert; Urule Igbavboa; Walter E Müller
Journal:  Ann N Y Acad Sci       Date:  2010-06       Impact factor: 5.691

5.  Atorvastatin does not alter serum levels of sCD95 and sCD95L in multiple sclerosis.

Authors:  J Sellner; I Greeve; O Findling; D Grandgirard; S L Leib; H P Mattle
Journal:  Clin Exp Immunol       Date:  2008-03-12       Impact factor: 4.330

6.  Hyperlipidemia and statins affect neurological outcome in lumbar spine injury.

Authors:  Wu-Fu Chung; Shih-Wei Liu; Peng-Yuan Chang; Feng-Shu Lin; Li-Fu Chen; Jau-Ching Wu; Yu-Chun Chen; Laura Liu; Wen-Cheng Huang; Henrich Cheng; Su-Shun Lo
Journal:  Int J Environ Res Public Health       Date:  2015-01-05       Impact factor: 3.390

7.  Collision cross sections obtained with ion mobility mass spectrometry as new descriptor to predict blood-brain barrier permeation by drugs.

Authors:  Armin Sebastian Guntner; Bernhard Thalhamer; Christian Klampfl; Wolfgang Buchberger
Journal:  Sci Rep       Date:  2019-12-16       Impact factor: 4.379

  7 in total

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