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载粒细胞集落刺激因子的可生物降解明胶水凝胶微球治疗腿部缺血。

Treatment of leg ischemia with biodegradable gelatin hydrogel microspheres incorporating granulocyte colony-stimulating factor.

机构信息

Department of Cardiology, Gifu University Graduate School of Medicine, Gifu, Japan.

出版信息

J Cardiovasc Pharmacol. 2011 Apr;57(4):416-23. doi: 10.1097/FJC.0b013e31820c9776.

Abstract

Granulocyte colony-stimulating factor (G-CSF) is a potent angiogenic factor. We hypothesized that G-CSF-immersed gelatin hydrogel microspheres (G-CSF-GHMs) injected into the ischemic legs might continuously release a small amount of G-CSF to locally stimulate angiogenesis without unfavorable systemic effects. Just after ligation of the right femoral artery of BALB/c mice, recombinant human G-CSF (100-μg/kg)-immersed GHM was injected into the right hindlimb muscles; the controls included a saline-injected group, an intramuscularly injected G-CSF group, a subcutaneously injected G-CSG group, and an empty GHM-injected group. Eight weeks later, improvement of blood perfusion to the ischemic limb was significantly augmented in the G-CSF-GHM group compared with any of the control groups. Despite there being no increase in the serum concentration of G-CSF, in peripheral granulocytes, or in circulating endothelial progenitor cells, not only capillary but also arteriolar density was significantly increased in this group. Next, we started treatment with G-CSF-GHM 4 weeks after ligation to examine whether the treatment is effective if performed during the chronic stage of ischemia. The late treatment was also found to effectively improve blood flow in the ischemic leg. In conclusion, G-CSF-GHM administration is suggested to be a promising and readily usable approach to treating peripheral artery disease, applicable even during the chronic stage.

摘要

粒细胞集落刺激因子 (G-CSF) 是一种有效的血管生成因子。我们假设,将浸润 G-CSF 的明胶水凝胶微球 (G-CSF-GHM) 注射到缺血肢体中,可能会持续释放少量 G-CSF,从而在不产生不利全身影响的情况下局部刺激血管生成。在 BALB/c 小鼠右侧股动脉结扎后,立即将重组人 G-CSF(100μg/kg)浸润的 GHM 注入右侧后肢肌肉;对照组包括盐水注射组、肌肉内注射 G-CSF 组、皮下注射 G-CSG 组和空 GHM 注射组。8 周后,与任何对照组相比,G-CSF-GHM 组缺血肢体的血液灌注改善明显增强。尽管血清 G-CSF 浓度、外周粒细胞或循环内皮祖细胞没有增加,但该组不仅毛细血管而且小动脉密度均显著增加。接下来,我们在结扎后 4 周开始用 G-CSF-GHM 进行治疗,以检查在缺血的慢性阶段进行治疗是否有效。结果发现,晚期治疗也能有效改善缺血肢体的血流。总之,G-CSF-GHM 给药被认为是一种有前途且易于使用的治疗外周动脉疾病的方法,即使在慢性阶段也适用。

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