首页> 外文会议>Institute of Electrical and Electronics Engineers International Conference on Medical Imaging Physics and Engineering >Evaluation of the therapeutic effects of mesenchymal stem cell transplantation in rat model of Parkinson#039;s disease using 1.5T MRS
【24h】

Evaluation of the therapeutic effects of mesenchymal stem cell transplantation in rat model of Parkinson#039;s disease using 1.5T MRS

机译:用1.5吨MRS评价帕金森病大鼠大鼠帕金森病大鼠模型的治疗效果

获取原文

摘要

Purpose: Using 1.5 T proton magnetic resonance spectroscopy (1H-MRS) with high resolution 23mm special coil in vivo to monitor the metabolic changes of the nerves in the striatum of Parkinson's disease (PD) rat before and after mesenchymal stem cells (MSCs) transplantation, in result to explore the value of 1.5T clinical MR spectral analysis in evaluating the therapeutic effects of MSCs transplantation. Materials and methods: Thirty cases of normal rats were treated as Parkinson's disease models with unilateral symptom by taking 6-hydroxydopamine (6-OHDA) to enforce unilateral (right) lesion, and 26 cases were successful. 1H-MRS was performed in the vivo rats using Philips 1.5T two gradients clinical MR machine with high resolution 23mm special coil on the three weeks point after lesion establishment, and on the three, six and nine weeks points after MSCs and serum-free medium injected respectively. The changes of NAA/Cr, Cho/Cr ratio in the bilateral striatum were analyzed. Meanwhile, the rat behavior was detected. The expression characteristics of tyrosine hydroxylase (TH) were checked in substantia nigra and the migration of the transplanted cells were observed using immunocytochemical and immunofluorescent methods. Results: At 6 weeks and 9 weeks points after MSCs transplanted, NAA/Cr ratios increased gradually in striatum of the damage side (right) comparing with the control group, and significant difference was showed between them (P<0.05). At nine-week point after MSCs transplantation, NAA/Cr ratio was higher than that at six weeks point (P<0.05). Cho/Cr ratios on the damaged side in MSCs transplantation group was lower than control group at 3, 6, 9 weeks points respectively (P<0.05), but no significant difference was shown among 3, 6, 9 weeks points (P> 0.05). NAA/Cr ratios and Cho/Cr ratios in damaged side of MSCs transplantation group decreased comparing with their opposite parts respectively (P<0.05. The number o- rat's full rotations at 6 weeks and 9 weeks points after MSCs transplanted gradually showed a significant reduction compared with other rats (P<0.05). The survival rates of TH-positive cells in the damage side striatum among two injected groups were no significant difference (P>0.05). However, by immunofluorescence staining, a part of BrdU labeled MSCs showed GFAP-positive, which conduced to the function of nerves repairing. Conclusion: As a non-invasive examination method in vivo, 1.5T 1H-MRS can be used to monitor the metabolic changes dynamically in the striatum of PD rat model after MSCs transplantation, that was able to evaluate the therapeutic effects efficiently.
机译:目的:使用1.5 T质子磁共振光谱(1H-MRS),具有高分辨率23mm特殊线圈,在间充质干细胞(MSCs)移植之前和之后,监测帕金森病(PD)大鼠纹状体(Pd)大鼠纹状体中神经的代谢变化结果,探讨了1.5T临床MR光谱分析评估MSCs移植治疗效果的值。材料和方法:通过服用6-羟基多胺(6-OHDA)来实施单方面(右)病变的单侧症状,治疗帕金森病模型,达到帕金森病模型,26例成功。在体内大鼠中使用Philips 1.5T两种梯度临床MR机器进行了高分辨率23mm特殊线圈在病变建立后的高分辨率23mm特殊线圈中进行,在MSC和无血清培养基之后的三个星期点和三个,六个和九周点分别注入。分析了双侧纹状体中NAA / Cr,CHO / Cr比的变化。同时,检测到大鼠的行为。在Commina NIGRA中检查酪氨酸羟化酶(TH)的表达特征,使用免疫细胞化学和免疫荧光方法观察移植细胞的迁移。结果:在MSCs移植后6周和9周点,与对照组比较的损伤侧(右侧)的纹状体逐渐增加NAA / Cr比率,并在它们之间显示显着差异(P <0.05)。在MSCs移植后九周点,NAA / Cr比率高于六周点(P <0.05)。在MSCs移植组的受损侧的CHO / CR比分别低于对照组,分别低于对照组(P <0.05),但在3,6,9周点中没有显示显着差异(P> 0.05 )。 MSCS移植组受损侧的NAA / CR比率和CHO / CR比分别与其相反的部件相比减少了(P <0.05。在MSCs移植的MSC移植后6周和9周点的数量的全旋转逐渐显示出显着减少与其他大鼠相比(P <0.05)。两种注射基团损伤侧纹状体中Th阳性细胞的存活率无显着差异(P> 0.05)。但是,通过免疫荧光染色,Brdu标记的MSCs的一部分显示出来GFAP阳性,导致神经修复的功能。结论:作为体内的非侵入性检查方法,1.5T 1H-MRS可用于在MSC移植后PD大鼠模型的纹状体动态地监测代谢变化,这能够有效地评估治疗效果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号