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通过脂质体递送血管生成肽改善脑血流:¹⁸F-FDG PET 成像在缺血性脑卒中治疗中的应用潜力。

Improving Cerebral Blood Flow Through Liposomal Delivery of Angiogenic Peptides: Potential of ¹⁸F-FDG PET Imaging in Ischemic Stroke Treatment.

机构信息

Department of Nuclear Medicine, Molecular Imaging & Therapeutic Medicine Research Center, Cyclotron Research Center, Institute for Medical Sciences, Biomedical Research Institute, Chonbuk National University Medical School and Hospital, Jeonju, Jeonbuk, South Korea.

Department of Nuclear Medicine, Molecular Imaging & Therapeutic Medicine Research Center, Cyclotron Research Center, Institute for Medical Sciences, Biomedical Research Institute, Chonbuk National University Medical School and Hospital, Jeonju, Jeonbuk, South Korea

出版信息

J Nucl Med. 2015 Jul;56(7):1106-11. doi: 10.2967/jnumed.115.154443. Epub 2015 May 14.

Abstract

UNLABELLED

Strategies to promote angiogenesis can benefit cerebral ischemia. We determined whether liposomal delivery of angiogenic peptides with a known biologic activity of vascular endothelial growth factor benefitted cerebral ischemia. Also, the study examined the potential of (18)F-FDG PET imaging in ischemic stroke treatment.

METHODS

Male Sprague-Dawley rats (n = 40) underwent 40 min of middle cerebral artery occlusion. After 15 min of reperfusion, the rats (n = 10) received angiogenic peptides incorporated into liposomes. Animals receiving phosphate-buffered solution or liposomes without peptides served as controls. One week later, (18)F-FDG PET imaging was performed to examine regional changes in glucose utilization in response to the angiogenic therapy. The following day, (99m)Tc-hexamethylpropyleneamine oxime autoradiography was performed to determine changes in cerebral perfusion after angiogenic therapy. Corresponding changes in angiogenic markers, including von Willebrand factor and angiopoietin-1 and -2, were determined by immunostaining and polymerase chain reaction analysis, respectively.

RESULTS

A 40-min period of middle cerebral artery occlusion decreased blood perfusion in the ipsilateral ischemic cortex of the brain, compared with that in the contralateral cortex, as measured by (99m)Tc-hexamethylpropyleneamine oxime autoradiography. Liposomal delivery of angiogenic peptides to the ischemic hemisphere of the brain attenuated the cerebral perfusion defect compared with controls. Similarly, vascular density evidenced by von Willebrand factor-positive staining was increased in response to angiogenic therapy, compared with that of controls. This increase was accompanied by an early increase in angiopoietin-2 expression, a gene participating in angiogenesis. (18)F-FDG PET imaging measured at 7 d after treatment revealed that liposomal delivery of angiogenic peptides facilitated glucose utilization in the ipsilateral ischemic cortex of the brain, compared with that in the controls. Furthermore, the change in regional glucose utilization was correlated with the extent of improvement in cerebral perfusion (r = 0.742, P = 0.035).

CONCLUSION

Liposomal delivery of angiogenic peptides benefits cerebral ischemia. (18)F-FDG PET imaging holds promise as an indicator of the effectiveness of angiogenic therapy in cerebral ischemia.

摘要

目的

探讨促进血管生成的策略是否有益于脑缺血。我们确定了具有已知血管内皮生长因子生物学活性的血管生成肽的脂质体递送是否有益于脑缺血。此外,本研究还研究了(18)F-FDG PET 成像在缺血性脑卒中治疗中的应用潜力。

方法

雄性 Sprague-Dawley 大鼠(n=40)进行 40 分钟大脑中动脉闭塞。再灌注 15 分钟后,将血管生成肽包封在脂质体中的大鼠(n=10)接受治疗。接受磷酸盐缓冲液或不含肽的脂质体的动物作为对照。一周后,进行(18)F-FDG PET 成像以检查葡萄糖利用的区域变化,以响应血管生成治疗。次日,进行(99m)Tc-六甲基丙烯胺肟 Autoradiography 以确定血管生成治疗后脑灌注的变化。通过免疫染色和聚合酶链反应分析分别确定血管生成标志物,包括血管性血友病因子和血管生成素-1 和 -2 的相应变化。

结果

40 分钟大脑中动脉闭塞导致同侧缺血性大脑皮层的脑血流灌注减少,与对侧皮层相比,通过(99m)Tc-六甲基丙烯胺肟 Autoradiography 测量。与对照组相比,血管生成肽的脂质体递送至大脑缺血半球减轻了脑灌注缺陷。同样,血管密度由血管性血友病因子阳性染色证明,与对照组相比,血管生成治疗后增加。这种增加伴随着血管生成素-2 表达的早期增加,血管生成素-2 是参与血管生成的基因。治疗后 7 天进行的(18)F-FDG PET 成像测量显示,与对照组相比,血管生成肽的脂质体递送促进了同侧缺血性大脑皮层的葡萄糖利用。此外,区域葡萄糖利用的变化与脑灌注改善的程度相关(r=0.742,P=0.035)。

结论

血管生成肽的脂质体递送有益于脑缺血。(18)F-FDG PET 成像有望成为脑缺血血管生成治疗效果的指标。

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