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A synthetic heparin-mimicking polyanionic compound inhibits central nervous system inflammation
被引:28
作者:
Irony-Tur-Sinai, M
Vlodavsky, I
Ben-Sasson, SA
Pinto, F
Sicsic, C
Brenner, T
机构:
[1] Hadassah Univ Hosp, Lab Neuroimmunol, Dept Neurol, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Sch Med, IL-91120 Jerusalem, Israel
[3] Hadassah Univ Hosp, Dept Oncol, IL-91120 Jerusalem, Israel
[4] Hadassah Univ Hosp, Dept Expt Med & Canc Res, IL-91120 Jerusalem, Israel
关键词:
heparin-mimicking polyanionic compound (HMPAC);
CNS inflammation;
EAE;
multiple sclerosis;
immunomodulation;
heparanase;
D O I:
10.1016/S0022-510X(02)00318-0
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
The immunomodulating capacity of heparin led us to test the effect of the synthetic heparin-mimicking and low anticoagulant compound RG-13577 on the course of experimental autoimmune encephalomyelitis (EAE) and central nervous system (CNS) inflammation. EAE was induced in SJL mice by inoculation with whole mouse spinal cord homogenate. RG-13577, delivered intraperitoneally, inhibited the clinical signs of acute EAE and markedly ameliorated inflammation in the spinal cord, primarily by inhibiting heparanase activity in lymphocytes and astrocytes and thus impairing lymphocyte traffic. RG-13577 treatment was effective when started on day of disease induction or day 7 after induction. The low molecular weight heparin, enoxaparin, tested under the same conditions, exerted only a minor insignificant inhibitory effect. RG-13577 also inhibited the tyrosine phosphorylation of several proteins, particularly Erk1 and Erk2 of the MAP kinase signaling pathways associated with inflammation and cell proliferation. RG-13577 blocked the activity of sPLA(2) and inhibited CNS PGE(2) production both in vivo and in vitro. (C) 2002 Elsevier Science B.V. All rights reserved.
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页码:49 / 57
页数:9
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