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Acute and delayed implantation of positively charged 2-hydroxyethyl methacrylate scaffolds in spinal cord injury in the rat
Ales Hejcl, Lucie Urdzikova, Jiri Sedy, Petr Lesny, Martin Pradny, Jiri Michalek, Martin Burian, Milan Hajek, Josef Zamecnik, Pavla Jendelova, Eva Sykova
Language English Country United States
Document type Comparative Study
Grant support
1A8697
MZ0
CEP Register
PubMed
18173349
DOI
10.3171/spi-08/01/067
Knihovny.cz E-resources
- MeSH
- Axons physiology pathology MeSH
- Biocompatible Materials chemistry therapeutic use MeSH
- Time Factors MeSH
- Cysts pathology MeSH
- Financing, Organized MeSH
- Wound Healing physiology MeSH
- Hydrogels chemistry therapeutic use MeSH
- Rats MeSH
- Methacrylates chemistry therapeutic use MeSH
- Spinal Cord blood supply pathology MeSH
- Disease Models, Animal MeSH
- Neurofibrils ultrastructure MeSH
- Paraplegia physiopathology MeSH
- Connective Tissue pathology MeSH
- Spinal Cord Injuries surgery MeSH
- Rats, Wistar MeSH
- Nerve Regeneration physiology MeSH
- Guided Tissue Regeneration MeSH
- Schwann Cells pathology MeSH
- Tissue Scaffolds MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Comparative Study MeSH
OBJECT: Hydrogels are nontoxic, chemically inert synthetic polymers with a high water content and large surface area that provide mechanical support for cells and axons when implanted into spinal cord tissue. METHODS: Macroporous hydrogels based on 2-hydroxyethyl methacrylate (HEMA) were prepared by radical copolymerization of monomers in the presence of fractionated NaCl particles. Male Wistar rats underwent complete spinal cord transection at the T-9 level. To bridge the lesion, positively charged HEMA hydrogels were implanted either immediately or 1 week after spinal cord transection; control animals were left untreated. Histological evaluation was performed 3 months after spinal cord transection to measure the volume of the pseudocyst cavities and the ingrowth of tissue elements into the hydrogels. RESULTS: The hydrogel implants adhered well to the spinal cord tissue. Histological evaluation showed ingrowth of connective tissue elements, blood vessels, neurofilaments, and Schwann cells into the hydrogels. Morphometric analysis of lesions showed a statistically significant reduction in pseudocyst volume in the treated animals compared with controls and in the delayed treatment group compared with the immediate treatment group (p < 0.001 and p < 0.05, respectively). CONCLUSIONS: Positively charged HEMA hydrogels can bridge a posttraumatic spinal cord cavity and provide a scaffold for the ingrowth of regenerating axons. The results indicate that delayed implantation can be more effective than immediate reconstructive surgery.
Center for Cell Therapy and Tissue Repair 2nd Faculty of Medicine Charles University
Department of Neurosurgery Masaryk Hospital Usti nad Labem Czech Republic
Institute of Clinical and Experimental Medicine Prague
Institute of Experimental Medicine Academy of Sciences of the Czech Republic Czech Republic
Institutes of Experimental Medicine Academy of Sciences of the Czech Republic
Macromolecular Chemistry Academy of Sciences of the Czech Republic
Pathology and Molecular Medicine 2nd Faculty of Medicine Charles University
References provided by Crossref.org
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- $a OBJECT: Hydrogels are nontoxic, chemically inert synthetic polymers with a high water content and large surface area that provide mechanical support for cells and axons when implanted into spinal cord tissue. METHODS: Macroporous hydrogels based on 2-hydroxyethyl methacrylate (HEMA) were prepared by radical copolymerization of monomers in the presence of fractionated NaCl particles. Male Wistar rats underwent complete spinal cord transection at the T-9 level. To bridge the lesion, positively charged HEMA hydrogels were implanted either immediately or 1 week after spinal cord transection; control animals were left untreated. Histological evaluation was performed 3 months after spinal cord transection to measure the volume of the pseudocyst cavities and the ingrowth of tissue elements into the hydrogels. RESULTS: The hydrogel implants adhered well to the spinal cord tissue. Histological evaluation showed ingrowth of connective tissue elements, blood vessels, neurofilaments, and Schwann cells into the hydrogels. Morphometric analysis of lesions showed a statistically significant reduction in pseudocyst volume in the treated animals compared with controls and in the delayed treatment group compared with the immediate treatment group (p < 0.001 and p < 0.05, respectively). CONCLUSIONS: Positively charged HEMA hydrogels can bridge a posttraumatic spinal cord cavity and provide a scaffold for the ingrowth of regenerating axons. The results indicate that delayed implantation can be more effective than immediate reconstructive surgery.
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