4.2 Article

GEMSP exerts a myelin-protecting role in the rat optic nerve

Journal

NEUROLOGICAL RESEARCH
Volume 35, Issue 9, Pages 903-911

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1179/1743132813Y.0000000233

Keywords

Demyelination; Experimental autoimmune encephalomyelitis (EAE); Multiple sclerosis (MS); Optic nerve

Funding

  1. GEMACBIO (St Jean d'Illac, France)
  2. Institut pour le Developpement de la Recherche en Pathologie Humaine et Therapeutique (IDRPHT) (Talence, France)
  3. Red de Terapia Celular de Castilla y Leon (Spain)
  4. Consejeria de Educacion de la Junta de Castilla y Leon (Spain) [SA099A08]
  5. INCYL-Federacion de Cajas de Ahorro de Castilla y Leon (Spain)
  6. Ministerio de Educacion y Ciencia (Spain) [SA F2007-62060]
  7. Grupos Consolidados del Gobierno Vasco
  8. RETICS Red Patologia Ocular [RD07/0062, BIOEF08/ER/006]

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Objectives: Chronic experimental autoimmune encephalomyelitis (EAE) was induced in rats to evaluate the potential protective effect of GEMSP, a mixture made up of fatty acids (FA), vitamins, and amino acids or their derivatives, linked to Poly-L-Lysine, on the myelin sheath of the optic nerve. Methods: To evaluate the effects of GEMSP on the optic nerve, animals were divided into three experimental groups: (1) EAE rats treated with GEMSP; (2) EAE rats treated with 0.9% NaCl; and (3) control, non-EAE rats. Using electron microscopy, we investigated the possibility that this new drug candidate has a myelin-protective role. Results: A marginally significant reduction in the thickness of the myelin around optic nerve medium-size axons (diameter between 0.8-1.3 mu m) was found in EAE rats. Treatment of EAE rats with GEMSP ameliorated myelin damage. Significantly increased myelin thickness was found when animals in groups 2 and 3 were compared. However, the number of myelinated axons studied was not altered in groups 1 or 2 when compared to controls. Discussion: Our results suggest that in a model of demyelination, GEMSP protects and enhances the formation of the myelin sheath of the optic nerve and therefore could be a potential drug candidate to reduce optic nerve pathogenesis in multiple sclerosis (MS).

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