TY - JOUR
T1 - Use of a combination strategy to improve neuroprotection and neuroregeneration in a rat model of acute spinal cord injury
AU - García, Elisa
AU - Rodríguez-Barrera, Roxana
AU - Buzoianu-Anguiano, Vinnitsa
AU - Flores-Romero, Adrian
AU - Malagón-Axotla, Emanuel
AU - Guerrero-Godinez, Marco
AU - De La Cruz-Castillo, Estefanía
AU - Castillo-Carvajal, Laura
AU - Rivas-Gonzalez, Monserrat
AU - Santiago-Tovar, Paola
AU - Morales, Ivis
AU - Borlongan, Cesar
AU - Ibarra, Antonio
N1 - Publisher Copyright:
© E-Flow Wolters Kluwer Medknow Publications 2019. All rights reserved.
PY - 2019/6/1
Y1 - 2019/6/1
N2 - Spinal cord injury is a very common pathological event that has devastating functional consequences in patients. In recent years, several research groups are trying to find an effective therapy that could be applied in clinical practice. In this study, we analyzed the combination of different strategies as a potential therapy for spinal cord injury. Immunization with neural derived peptides (INDP), inhibition of glial scar formation (dipyridyl: DPY), as well as the use of biocompatible matrix (fibrin glue: FG) impregnated with bone marrow mesenchymal stem cells (MSCs) were combined and then its beneficial effects were evaluated in the induction of neuroprotection and neuroregeneration after acute SCI. Sprague-Dawley female rats were subjected to a moderate spinal cord injury and then randomly allocated into five groups: 1) phosphate buffered saline; 2) DPY; 3) INDP + DPY; 4) DPY+ FG; 5) INDP + DPY + FG + MSCs. In all rats, intervention was performed 72 hours after spinal cord injury. Locomotor and sensibility recovery was assessed in all rats. At 60 days after treatment, histological examinations of the spinal cord (hematoxylin-eosin and Bielschowsky staining) were performed. Our results showed that the combination therapy (DPY+ INDP + FG + MSCs) was the best strategy to promote motor and sensibility recovery. In addition, significant increases in tissue preservation and axonal density were observed in the combination therapy group. Findings from this study suggest that the combination theapy (DPY+ INDP + FG + MSCs) exhibits potential effects on the protection and regeneration of neural tissue after acute spinal cord injury. All procedures were approved by the Animal Bioethics and Welfare Committee (approval No. 178544; CSNBTBIBAJ 090812960) on August 15, 2016.
AB - Spinal cord injury is a very common pathological event that has devastating functional consequences in patients. In recent years, several research groups are trying to find an effective therapy that could be applied in clinical practice. In this study, we analyzed the combination of different strategies as a potential therapy for spinal cord injury. Immunization with neural derived peptides (INDP), inhibition of glial scar formation (dipyridyl: DPY), as well as the use of biocompatible matrix (fibrin glue: FG) impregnated with bone marrow mesenchymal stem cells (MSCs) were combined and then its beneficial effects were evaluated in the induction of neuroprotection and neuroregeneration after acute SCI. Sprague-Dawley female rats were subjected to a moderate spinal cord injury and then randomly allocated into five groups: 1) phosphate buffered saline; 2) DPY; 3) INDP + DPY; 4) DPY+ FG; 5) INDP + DPY + FG + MSCs. In all rats, intervention was performed 72 hours after spinal cord injury. Locomotor and sensibility recovery was assessed in all rats. At 60 days after treatment, histological examinations of the spinal cord (hematoxylin-eosin and Bielschowsky staining) were performed. Our results showed that the combination therapy (DPY+ INDP + FG + MSCs) was the best strategy to promote motor and sensibility recovery. In addition, significant increases in tissue preservation and axonal density were observed in the combination therapy group. Findings from this study suggest that the combination theapy (DPY+ INDP + FG + MSCs) exhibits potential effects on the protection and regeneration of neural tissue after acute spinal cord injury. All procedures were approved by the Animal Bioethics and Welfare Committee (approval No. 178544; CSNBTBIBAJ 090812960) on August 15, 2016.
KW - Fibrin glue
KW - Glial scar
KW - Mesenchymal stem cells
KW - Neural derived peptides
KW - Neural regeneration
KW - Protective autoimmunity
UR - http://www.scopus.com/inward/record.url?scp=85061834903&partnerID=8YFLogxK
U2 - 10.4103/1673-5374.250627
DO - 10.4103/1673-5374.250627
M3 - Artículo
AN - SCOPUS:85061834903
SN - 1673-5374
VL - 14
SP - 1060
EP - 1068
JO - Neural Regeneration Research
JF - Neural Regeneration Research
IS - 6
ER -