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Leuprolide acetate induces structural and functional recovery of injured spinal cord in rats
Authors:Carmen Díaz Galindo  Beatriz Gómez-González  Eva Salinas  Denisse Calderón-Vallejo  Irma Hernández-Jasso  Eduardo Bautista  J Luis Quintanar
Affiliation:1.Laboratory of Neurophysiology, Department of Physiology and Pharmacology, Universidad Autónoma de Aguascalientes, Aguascalientes, México;2.Area of Neuroscience, Department of Reproductive Biology, CBS, Universidad Autónoma Metropolitana, Unidad Iztapalapa, México;3.Laboratory of Immunology, Department of Microbiology, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes, Aguascalientes, México
Abstract:Gonadotropin-releasing hormone (GnRH) and its synthetic analog leuprolide acetate, a GnRH agonist, have neurotrophic properties. This study was designed to determine whether administration of leuprolide acetate can improve locomotor behavior, gait, micturition reflex, spinal cord morphology and the amount of microglia in the lesion epicenter after spinal cord injury in rats. Rats with spinal cord compression injury were administered leuprolide acetate or saline solution for 5 weeks. At the 5th week, leuprolide acetate-treated rats showed locomotor activity recovery by 38%, had improvement in kinematic gait and exhibited voiding reflex recovery by 60%, as compared with the 1st week. By contrast, saline solution-treated rats showed locomotor activity recovery only by 7%, but voiding reflex did not recover. More importantly, leuprolide acetate treatment reduced microglial immunological reaction and induced a trend towards greater area of white and gray matter in the spinal cord. Therefore, leuprolide acetate has great potential to repair spinal cord injury.
Keywords:nerve regeneration   spinal cord injury   leuprolide acetate   gonadotropin-releasing hormone   neurotrophic factor   microglia   micturition reflex   gait   inflammation   neural regeneration
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