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1.
Article in English | WPRIM | ID: wpr-110760

ABSTRACT

We induced percutaneous spinal cord injuries (SCI) using a balloon catheter in 45 rats and transplanted human umbilical cord blood derived mesenchymal stem cells (hUCB-MSCs) at the injury site. Locomotor function was significantly improved in hUCB-MSCs transplanted groups. Quantitative ELISA of extract from entire injured spinal cord showed increased expression of brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF) and neurotrophin-3 (NT-3). Our results show that treatment of SCI with hUCB-MSCs can improve locomotor functions, and suggest that increased levels of BDNF, NGF and NT-3 in the injured spinal cord were the main therapeutic effect.


Subject(s)
Animals , Humans , Rats , Brain-Derived Neurotrophic Factor/genetics , Cord Blood Stem Cell Transplantation , Enzyme-Linked Immunosorbent Assay , Gene Expression Profiling , Gene Expression Regulation , Locomotion , Nerve Growth Factor/genetics , Spinal Cord Injuries/therapy
2.
Article in English | WPRIM | ID: wpr-92897

ABSTRACT

Here, percutaneous spinal cord injury (SCI) methods using a balloon catheter in adult rats are described. A balloon catheter was inserted into the epidural space through the lumbosacral junction and then inflated between T9-T10 for 10min under fluoroscopic guidance. Animals were divided into three groups with respect to inflation volume: 20 microL (n = 18), 50 microL (n = 18) and control (Fogarty catheter inserted but not inflated; n = 10). Neurological assessments were then made based on BBB score, magnetic resonance imaging and histopathology. Both inflation volumes produced complete paralysis. Gradual recovery of motor function occurred when 20 microL was used, but not after 50 microL was applied. In the 50 microL group, all gray and white matter was lost from the center of the lesion. In addition, supramaximal damage was noted, which likely prevented spontaneous recovery. This percutaneous spinal cord compression injury model is simple, rapid with high reproducibility and the potential to serve as a useful tool for investigation of pathophysiology and possible protective treatments of SCI in vivo.


Subject(s)
Animals , Male , Rats , Balloon Embolectomy/methods , Disease Models, Animal , Rats, Sprague-Dawley , Spinal Cord Compression/therapy
3.
Article in English | WPRIM | ID: wpr-43055

ABSTRACT

The use of human umbilical cord blood-derived mesenchymal stem cells for cell transplantation therapy holds great promise for repairing spinal cord injury. Here we report the first clinical trial transplantation of human umbilical cord (hUCB)-derived mesenchymal stem cells (MSCs) into the spinal cord of a dog suspected to have fibrocartilaginous embolic myelopathy (FCEM) and that experienced a loss of deep pain sensation. Locomotor functions improved following transplantation in a dog. Based on our findings, we suggest that transplantation of hUCB-derived MSCs will have beneficial therapeutic effects on FCEM patients lacking deep pain sensation.


Subject(s)
Animals , Dogs , Female , Humans , Cartilage Diseases/etiology , Cord Blood Stem Cell Transplantation/veterinary , Dog Diseases/etiology , Embolism/etiology , Mesenchymal Stem Cells/cytology , Spinal Cord Diseases/etiology , Treatment Outcome
4.
Article in English | WPRIM | ID: wpr-104701

ABSTRACT

We evaluated the biological scaffold properties of canine small intestinal submucosa (SIS) compared to a those of polypropylene mesh in growing rats with full-thickness abdominal defects. SIS is used to repair musculoskeletal tissue while promoting cell migration and supporting tissue regeneration. Polypropylene mesh is a non-resorbable synthetic material that can endure mechanical tension. Canine SIS was obtained from donor German shepherds, and its porous collagen fiber structure was identified using scanning electron microscopy (SEM). A 2.50-cm2 section of canine SIS (SIS group) or mesh (mesh group) was implanted in Sprague-Dawley rats. At 1, 2, 4, 12, and 24 weeks after surgery, the implants were histopathologically examined and tensile load was tested. One month after surgery, CD68+ macrophage numbers in the SIS group were increased, but the number of CD8+ T cells in this group declined more rapidly than that in rats treated with the mesh. In the SIS group, few adhesions and well-developed autologous abdominal muscle infiltration into the SIS collagen fibers were observed. No significant differences in the tensile load test results were found between the SIS and mesh groups at 24 weeks. Canine SIS may therefore be a suitable replacement for artificial biological scaffolds in small animals.


Subject(s)
Animals , Dogs , Female , Rats , Abdominal Wall/surgery , Biocompatible Materials/therapeutic use , Intestinal Mucosa/cytology , Intestine, Small/cytology , Polypropylenes/therapeutic use , Rats, Sprague-Dawley , Tensile Strength , Tissue Adhesions , Tissue Scaffolds , Transplantation, Heterologous/methods , Wound Healing
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