Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE model

<p>Chronic Experimental Autoimmune Encephalomyelitis (EAE) was induced in rats to evaluate a new drug candidate (GEMSP) for the treatment of multiple sclerosis. This work is a part of preclinical studies on GEMSP, which is made up of fatty acids, vitamins and amino acids or their derivatives;...

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Main Author: A. Mangas, R. Cove&#241;as, D. Bodet, M. de Le&#243;n, S. Duleu, M. Geffard
Format: Article
Language:English
Published: Ivyspring International Publisher 2008-01-01
Series:International Journal of Biological Sciences
Online Access:http://www.biolsci.org/v04p0150.htm
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author A. Mangas, R. Cove&#241;as, D. Bodet, M. de Le&#243;n, S. Duleu, M. Geffard
author_facet A. Mangas, R. Cove&#241;as, D. Bodet, M. de Le&#243;n, S. Duleu, M. Geffard
author_sort A. Mangas, R. Cove&#241;as, D. Bodet, M. de Le&#243;n, S. Duleu, M. Geffard
collection DOAJ
description <p>Chronic Experimental Autoimmune Encephalomyelitis (EAE) was induced in rats to evaluate a new drug candidate (GEMSP) for the treatment of multiple sclerosis. This work is a part of preclinical studies on GEMSP, which is made up of fatty acids, vitamins and amino acids or their derivatives; all these compounds were linked to Poly-L-Lysine. In order to evaluate the effects of GEMSP, animals were divided into three experimental groups: 1) EAE rats treated with GEMSP; 2) EAE rats treated with NaCl; and 3) non-EAE rats. Using immunocytochemical techniques with a pan-leukocyte marker (anti-CD 45), differential leukocyte infiltration was compared in the central nervous systems of the different experimental groups. Antibodies directed against a component of GEMSP, the conjugated methionine, were used in all three groups. We found that: 1) GEMSP was effective in abolishing EAE. The crises and clinical scores were completely abolished in the animals of the first group, but not in the animals belonging to the second group; 2) the degree of leukocyte infiltration varied, depending on the different EAE stages, but was not related to the clinical score; and 3) after using anti-conjugated methionine antibodies, we observed immunoreactivity only in the motoneurons of the ventral horn of the spinal cord in the animals of the first group. This immunoreactivity was not found in the animals of the second or third groups. No methionine immunoreactivity was found in the brain. Our results suggest that GEMSP may be a potential drug candidate against the pathogenic processes involved in multiple sclerosis, inhibiting EAE episodes and brain leukocyte infiltration. Our results also show that one component of GEMSP, the methionine compound, is stored inside motoneurons. The possible physiological actions of GEMSP on spinal cord motoneurons are discussed.</p>
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spelling doaj.art-f02d285c88ef4585b3f06ecde412cd5a2022-12-21T18:44:11ZengIvyspring International PublisherInternational Journal of Biological Sciences1449-22882008-01-0143150160Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE modelA. Mangas, R. Cove&#241;as, D. Bodet, M. de Le&#243;n, S. Duleu, M. Geffard<p>Chronic Experimental Autoimmune Encephalomyelitis (EAE) was induced in rats to evaluate a new drug candidate (GEMSP) for the treatment of multiple sclerosis. This work is a part of preclinical studies on GEMSP, which is made up of fatty acids, vitamins and amino acids or their derivatives; all these compounds were linked to Poly-L-Lysine. In order to evaluate the effects of GEMSP, animals were divided into three experimental groups: 1) EAE rats treated with GEMSP; 2) EAE rats treated with NaCl; and 3) non-EAE rats. Using immunocytochemical techniques with a pan-leukocyte marker (anti-CD 45), differential leukocyte infiltration was compared in the central nervous systems of the different experimental groups. Antibodies directed against a component of GEMSP, the conjugated methionine, were used in all three groups. We found that: 1) GEMSP was effective in abolishing EAE. The crises and clinical scores were completely abolished in the animals of the first group, but not in the animals belonging to the second group; 2) the degree of leukocyte infiltration varied, depending on the different EAE stages, but was not related to the clinical score; and 3) after using anti-conjugated methionine antibodies, we observed immunoreactivity only in the motoneurons of the ventral horn of the spinal cord in the animals of the first group. This immunoreactivity was not found in the animals of the second or third groups. No methionine immunoreactivity was found in the brain. Our results suggest that GEMSP may be a potential drug candidate against the pathogenic processes involved in multiple sclerosis, inhibiting EAE episodes and brain leukocyte infiltration. Our results also show that one component of GEMSP, the methionine compound, is stored inside motoneurons. The possible physiological actions of GEMSP on spinal cord motoneurons are discussed.</p>http://www.biolsci.org/v04p0150.htm
spellingShingle A. Mangas, R. Cove&#241;as, D. Bodet, M. de Le&#243;n, S. Duleu, M. Geffard
Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE model
International Journal of Biological Sciences
title Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE model
title_full Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE model
title_fullStr Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE model
title_full_unstemmed Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE model
title_short Evaluation of the effects of a new drug candidate (GEMSP) in a chronic EAE model
title_sort evaluation of the effects of a new drug candidate gemsp in a chronic eae model
url http://www.biolsci.org/v04p0150.htm
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