人组织激肽激酶基因转移预防糖尿病性微血管病变

C. Emanueli, M. Salis, A. Pinna, Tiziana Stacca, A. Milia, A. Spano, J. Chao, L. Chao, L. Sciola, P. Madeddu
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引用次数: 83

摘要

背景:微血管功能不全是糖尿病患者终末器官衰竭的主要原因。方法与结果:在链脲佐菌素诱导的糖尿病小鼠中,我们评估了人组织激肽肽(hTK)基因作为外周微血管病变的唯一治疗方法的潜力。hTK基因的局部递送通过抑制细胞凋亡阻止后肢骨骼肌微血管稀疏的进展,从而确保在血管闭塞的情况下改善血流动力学恢复。hTK的治疗作用不需要补充胰岛素。基因治疗在微血管病变阶段的应用刺激了血管再生。结论:我们的研究表明,hTK可能是治疗糖尿病微血管并发症的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevention of Diabetes-Induced Microangiopathy by Human Tissue Kallikrein Gene Transfer
Background—Microvascular insufficiency represents a major cause of end-organ failure among diabetics. Methods and Results—In streptozotocin-induced diabetic mice, we evaluated the potential of human tissue kallikrein (hTK) gene as a sole therapy against peripheral microangiopathy. Local delivery of hTK gene halted the progression of microvascular rarefaction in hindlimb skeletal muscle by inhibiting apoptosis, thus ensuring an improved hemodynamic recovery in case of supervening vascular occlusion. The curative action of hTK did not necessitate insulin supplementation. Application of gene therapy at a stage of established microangiopathy stimulated vascular regeneration. Conclusions—Our studies indicate that hTK may represent a useful tool for the treatment of microvascular complications in diabetics.
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