Abstract
Animal models of experimental allergic encephalomyelitis (EAE) are the most commonly used animal models for studying the pathogenesis of human multiple sclerosis (MS) as well as for target validation and compound characterization in pharmacology. By using an EAE model in Lewis rats, we focus on its neuroimmunological characterization with special attention to disease-involved cytokines, chemokines, and adhesion molecules. Furthermore, we used MR imaging to investigate macrophage infiltration and ICAM-1 expression in lesional spinal cord. Overall, due to its inflammatory character, this model is suggested to be used in early drug discovery particularly directed against acute inflammatory processes.
MeSH terms
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Acute Disease
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Animals
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Chemokines / metabolism
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Chemotaxis, Leukocyte / immunology
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Cytokines / metabolism
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Disease Models, Animal
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Encephalomyelitis, Autoimmune, Experimental / immunology*
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Encephalomyelitis, Autoimmune, Experimental / metabolism
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Encephalomyelitis, Autoimmune, Experimental / pathology
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Female
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Intercellular Adhesion Molecule-1 / metabolism
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Macrophages / immunology
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Macrophages / metabolism
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Magnetic Resonance Imaging
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Multiple Sclerosis / immunology*
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Multiple Sclerosis / metabolism
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Multiple Sclerosis / pathology
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Myelitis / immunology*
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Myelitis / metabolism
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Myelitis / pathology
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Neural Cell Adhesion Molecules / metabolism
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Rats
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Rats, Inbred Lew
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Spinal Cord / immunology*
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Spinal Cord / metabolism
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Spinal Cord / pathology
Substances
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Chemokines
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Cytokines
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Neural Cell Adhesion Molecules
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Intercellular Adhesion Molecule-1