摘要
Background The regulation of t-PA gene is the essence and core of thrombosis. Therefore, the present study aimed to prepare nano t-PA gene coated stent and to observe its effect on coronary stent thrombosis in dogs.Methods Highly expressed t-PA gene plasmid was constructed and albumin nano t-PA gene coating stent was prepared. The major branch vessels of dog coronary artery were pre-expanded with a 3.0 mm×20 balloon with 8-10 atmospheric pressure. 10 dogs of the control group were implanted with bare metal stent; while 12 dogs of the experimental group were implanted with nano t-PA gene coating stent. Both groups were not given anti-coagulation treatments. Blood samples were taken for t-PA and D-dimer before the operation, at 1,2,4 and 8 weeks after operation. Pathological analysis found thrombosis in the cavity and the hyperplasia of the intima. t-PA expression was detected by immunohistochemical indirectly, and the thickness of the intima of the section cross was directly measured by morphometry. Liver, heart, kidneys and lung were taken for pathological observation. Results All experimental animals survived at postoperative 8 weeks. Vascular stent thrombosis was seen in 10 cases of the control group with the thrombosis rate of 100%; while was seen in 2 cases among 12 cases of the experimental group with the thrombosis rate was 16.67%（P=0.00087）. Immunohistochemical staining showed that the positive t-PA gene transfection of the experimental group was mainly distributed on the surface of hyperplasia intima, and vascular wall t-PA expression of the control group was negative. Positive t-PA signal was not found in the liver,heart, kidneys and lung. Conclusion Nano t-PA gene vector coating stent can effectively express t-PA in vascular wall and effectively prevents stent thrombosis.
Background The regulation of t-PA gene is the essence and core of thrombosis. Therefore, the present study aimed to prepare nano t-PA gene coated stent and to observe its effect on coronary stent thrombosis in dogs.Methods Highly expressed t-PA gene plasmid was constructed and albumin nano t-PA gene coating stent was prepared. The major branch vessels of dog coronary artery were pre-expanded with a 3.0 mm×20 balloon with 8-10 atmospheric pressure. 10 dogs of the control group were implanted with bare metal stent; while 12 dogs of the experimental group were implanted with nano t-PA gene coating stent. Both groups were not given anti-coagulation treatments. Blood samples were taken for t-PA and D-dimer before the operation, at 1,2,4 and 8 weeks after operation. Pathological analysis found thrombosis in the cavity and the hyperplasia of the intima. t-PA expression was detected by immunohistochemical indirectly, and the thickness of the intima of the section cross was directly measured by morphometry. Liver, heart, kidneys and lung were taken for pathological observation. Results All experimental animals survived at postoperative 8 weeks. Vascular stent thrombosis was seen in 10 cases of the control group with the thrombosis rate of 100%; while was seen in 2 cases among 12 cases of the experimental group with the thrombosis rate was 16.67%（P=0.00087）. Immunohistochemical staining showed that the positive t-PA gene transfection of the experimental group was mainly distributed on the surface of hyperplasia intima, and vascular wall t-PA expression of the control group was negative. Positive t-PA signal was not found in the liver,heart, kidneys and lung. Conclusion Nano t-PA gene vector coating stent can effectively express t-PA in vascular wall and effectively prevents stent thrombosis.
基金
supported by Basic research project of knowledge innovation program From Shenzhen Science and Technology Innovation Committee(No.JCYJ2015040209 4341903)
作者简介
Corresponding author： WANG Li- li, E-mail：1248532808 @qq.com
