Thalidomide Derivatives for the Treatment of Neuroinflammation

被引:12
作者
Contino-Pepin, Christiane [1 ]
Parat, Audrey [1 ]
Patinote, Cindy [1 ]
Roscoe, Wendi A. [2 ]
Karlik, Stephen J. [2 ]
Pucci, Bernard [1 ]
机构
[1] Univ Avignon & Pays de Vaucluse, Lab Chim Bioorgan & Syst Mol Vectoriels, Fac Sci, F-84000 Avignon, France
[2] Univ Western Ontario, Dept Med Imaging, LHSC UC, London, ON N6A 5A5, Canada
关键词
angiogenesis; multiple sclerosis; neuroinflammation; telomers; thalidomide; MULTIPLE-SCLEROSIS; ANGIOGENESIS; INHIBITION; TELOMERS; ANALOGS; COTELOMERS; TUMORS; ALPHA; RAT; SUPPRESSION;
D O I
10.1002/cmdc.201000326
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The precise mechanism-of-action of thalidomide remains uncertain and might differ between diseases and under different clinical condition. With implications in the treatment of a variety of inflammatory and autoimmune diseases, as well as for use as an anticancer agent, alone or in combination with established therapeutics, it is clear that thalidomide and its derivatives deserve further scrutiny. In particular, thalidomide was shown to be effective in a mouse model of multiple sclerosis (MS), an autoimmune inflammatory disorder, called experimental autoimmune encephalomyelitis (EAE). Herein, we describe the synthesis and preliminary biological evaluation of new macromolecular prodrugs of thalidomide bearing an aminoalkyl group on the phthalimide ring. The effectiveness of these compounds to limit EAE was investigated, and it was shown that, at 100 mg kg(-1) thalidomide-equivalent dose, they abrogated the clinical and pathological features of EAE.
引用
收藏
页码:2057 / 2064
页数:8
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