静脉移植
- 网络vein graft;vein-graft
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PKC-αmRNA在兔自体静脉移植中的表达
Expression of PKC - α mRNA in autogenous vein graft in rabbits
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方法建立自体静脉移植模型,采用反转录聚合酶链反应(RTPCR)和免疫组织化学方法,对ECE、ET1和增殖细胞核抗原(proliferatingcellnuclearantigen,PCNA)在移植静脉的表达情况进行分析。
Methods A model of autogenous vein graft was established by interposition of the jugular vein into abdominal aorta in 80 Wistar rats . RT-PCR and immunohistochemistry were employed to test mRNA and protein level of ECE , ET-1 and proliferating cell nuclear antigen ( PCNA ) .
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大鼠自体静脉移植后增生内膜中α1(Ⅰ)和α1(Ⅲ)前胶原mRNA表达的定位研究
The expression of α 1 (ⅰ),α 1 (ⅲ) precollagen mRNA in intimal hyperplasia after autologous vein-to-artery transplantation in rats
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经静脉移植骨髓基质细胞治疗大鼠局灶性脑梗死Bcl-2蛋白表达的实验研究
Intravenous administration of bone marrow stromal cells after stroke in rats and the expression of Bcl-2 protein
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家兔静脉移植桥血管内膜c-myc蛋白的表达
Expression of c-myc protein in vascular smooth muscle cell of vein graft rabbits
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自体静脉移植术后血管平滑肌细胞内c-fos、c-myc和c-jun的表达
The study on the expression of immediate-early response gene c-fos , c-myc , c-jun , in VSMC after autogenous vein grafts
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结论经静脉移植骨髓基质细胞可明显改善大鼠局灶性脑梗死后神经功能恢复,并可上调脑内bcl-2蛋白表达水平。
Conclusion Intravenous administration of bone marrow stromal cells after stroke in rats can promote the recovery of the nervous functions and improve the expression of bcl-2 protein .
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结果:自体静脉移植后,Egr-1mRNA和Egr-1蛋白的表达具有双相变化。
Results : The expression of Egr-1 mRNA and Egr-1 protein had biphasic changes .
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p27~(kip1)基因在大鼠自体静脉移植中的表达
Expression of p27 ~ ( kip1 ) gene in autogenous vein grafts in rats
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方法将大鼠自体颈静脉移植于腹主动脉,分丹参组和对照组,丹参组于术前1d开始管饲丹参注射液[24g/(kg·d)]直至取材;
Methods Autologous jugular vein was grafted into abdominal artery in the rats . The rats were divided into two groups : RSM group and control group .
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方法建立100只Wistar大鼠自体颈静脉移植于肾下腹主动脉模型。
Methods A rat experimental model of autogenous graft vein was established by transplanting the right external jugular vein to infrarenal abdominal aorta in 100 Wistar rats .
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结论心肌梗死后1d经静脉移植的骨髓基质干细胞可以归巢至梗死心肌处,并且可以改善损伤的心功能。
Conclusion One day after MI , intravenously delivered mesenchymal stem cells can migrate into the damaged heart and improve the damaged cardiac function .
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大鼠心肌梗死后,静脉移植的EPCs能有效的向心肌梗死周边区归巢,形成新生血管,减少心肌梗死面积,促进心功能的恢复。
Intravenous implanted EPCs can effectively homing to the infarcted border zone , promote neovascularization , reduce infarct area and improve the cardiac function .
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静脉移植后7、28和90d取出静脉桥。
After 7 , 28 and 90 days of operation , vein grafts were harvested .
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另外,通过静脉移植的同种异体MSC,能在急性辐射损伤小鼠体内长期存活,并具有向特定的损伤部位进行迁移的能力,参与了急性辐射损伤后造血的重建。
Additionally , transplanted MSC can not only live inside the radiated mice , but also specially immigrate to the injured site , and participate the reconstitution of hemopoiesis after acute radiation injury .
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目的研究用外径1mm左右的自体小静脉移植修复小动脉和小静脉缺损在断指再植中的成功率。
Objective To evaluate the success rate of bridging defects of venule and arteriole by venule ( 1mm in diameter ) autograft in digital replantation .
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目的探讨内皮素1(endothelin1,ET1)及内源性内皮素转化酶(endothelinconvertingenzyme,ECE)在自体静脉移植术后内膜增生中的作用。
Objective To investigate changes of endothelin-1 ( ET-1 ) and endothelin-converting enzyme ( ECE ) in different time intervals after autograft vein implantation .
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目的探讨脐血间充质干细胞(MSCs)静脉移植治疗新生鼠缺氧缺血性脑损伤(HIBD)的可行性。
Objective To study the possibility of intravenous transplantation of the human umbilical blood mesenchymal stem cells ( MSCs ) after hypoxic-ischemic brain damage ( HIBD ) in neonatal rats .
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采用尾静脉移植K562细胞的方法在SCID小鼠建立白血病模型,接种第四周就可在外周血涂片中观察到白血病细胞。
The leukemic animal model ( SCID mouse ) was established by injecting K562 cells through tail vein . The leukemia cells were found on peripheral blood smear on the fourth week after inoculation .
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TGFβ1mRNA表达在静脉移植术后1周达467%,以后逐渐下降,但术后10周时,其阳性细胞仍达101%。
The expression of TGF β 1 mRNA peaked at 1 week and decreased gradually , but at 10 weeks , its positive cell percentage was still 10 1 % .
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[目的]探讨经静脉移植骨髓间充质干细胞(MSCs)对大鼠脊髓损伤(SCI)后胶质细胞源性神经营养因子(GDNF)表达的影响。
Objective To observe the effects of mesenchymal stem cells ( MSCs ) injection from tail-vein on the expression of glial cell line derived neurotrophic factor ( GDNF ) after the spinal cord injury ( SCI ) of rats .
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BMSCs静脉移植组大鼠运动功能改善,BBB评分高于对照组(P<0.05);
There was a significant improvement in neurological functions of rats treated with BMSCs transplantation and the scores of BBB in the BMSCs transplanted group were higher than those in the control group ( P < 0.05 ) .
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结果静脉移植后7、28和90d反义寡核苷酸可溶性支架组静脉桥内膜增生程度显著降低;
Results In the vein grafts of 7,28,90 days post-operation of soluble stent antisense-ODN group ① Intima hyperplasia were inhibited significantly compare with other four groups .
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骨髓间充质干细胞的诱导分化及GDNF基因修饰后对大鼠脊髓损伤修复的研究静脉移植骨髓间充质干细胞治疗脊髓
Study on the Differentiation of MSCs and Effect of MSCs with rAAV-GDNF on the Function Recovery of Spinal Cord after SCI in Rats Treatment of Spinal Cord Injury in Rat with Intravenous Administration of Bone Marrow Stromal Cells
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【方法】对近5年12例手术证实的闭合性股动脉损伤患者,采用端端吻合、静脉移植、ePTFE人工血管等方法治疗。
【 Methods 】 Twelve cases with close femoral arterial injuries confirmed by the clinical examination and Doppler were treated by end-to-end arterial anastomosis , blood vessel and ePTFE artificial blood vessel grafting .
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经尾静脉移植AD-MSC到CTX肌肉损伤模型小鼠和mdx小鼠(DMD动物模型)体内,通过RT-PCR和免疫荧光染色检测供体细胞的分布和分化情况,并进行统计分析。
The AD-MSCs were transplanted into CTX-injured mice model or mdx mice ( DMD animal model ) through tail vein ; the distribution and differentiation of AD-MSCs were detected by immunofluorescence staining and RT-PCR respectively , and statistic analysis was performed .
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目的:采用Brdu免疫组化标记技术观察经静脉移植人脐血间充质干细胞进入损伤脊髓组织的表达情况,探讨其促进损伤脊髓神经功能恢复的作用。
AIM : To observe the vein translated human umbilical cord blood ( hUCB ) mesenchymal stem cells infiltrating into the injured spinal cord tissues by Brdu immunohistochemical labeled technique and explore its role of improving neurological function recovery .
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血管修补缝合术、血管端端吻合术是主要修复方法,血管缺损2cm以上者应行自体静脉移植术;
The main renovations are repair and suture operation of blood vessel and end to end anastomosis , autotransplantation of venae should be adopted if the defects of blood vessels are over 2 cm .
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3例牛颈静脉移植法建立的模型,当内径≤1.5cm时,血流表现为层流,动脉瘤形态为梭形。
When the diameters of 3 models ' aneurysm were not more than 1.5 cm , the stream in the aneurysms was laminar flow .
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建立雌性小鼠CCl4肝损伤模型,静脉移植HGF处理后雄性小鼠外周血单个核细胞到其体内,4W后利用原位杂交技术检测新生肝组织中是否存在雄性细胞。
The peripheral blood nucleated cells of Ad-HGF treated male mice were intravenous administrated into these mice , and 4 weeks later , in situ hybridization for the sry gene was used to identify the implanted cells in the damaged tissues .