Preliminary of molecule mechanism of rat's infarct brain With VEGF165 gene therapy
Ming-Jun Hu
Abstract
Ming-Jun Hu
Abstract
Objective To observe the expression of certain molecule in brain of MCAO rats in VEGF 165 gene therapy to provide some molecule evidence for clinical cerebral infarct research.Methods To establish a rat's permanent model of MCAO by nylon suture embolization, VEGF 165 gene was directly injected through skull into the ischemia area,after seven days, the rats were killed,immunohistochemistry was used to show the expression of HSP70 AND VEGF proteins in rats brain.Results There was a significant increase at level of HSP70 and VEGF's expression.Conclusion Ischemic brain tissue could take in and express the VEGF 165 gene, and VEGF 165 gene could induce HSP70 protein.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To observe the expression of certain molecule in brain of MCAO rats in VEGF 165 gene therapy to provide some molecule evidence for clinical cerebral infarct research.Methods To establish a rat's permanent model of MCAO by nylon suture embolization, VEGF 165 gene was directly injected through skull into the ischemia area,after seven days, the rats were killed,immunohistochemistry was used to show the expression of HSP70 AND VEGF proteins in rats brain.Results There was a significant increase at level of HSP70 and VEGF's expression.Conclusion Ischemic brain tissue could take in and express the VEGF 165 gene, and VEGF 165 gene could induce HSP70 protein.
Key concepts: Hsp70, Immunohistochemistry, VEGF receptors, Genetic enhancement, Medicine, Gene expression, Gene, Angiogenesis