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硝普盐类一氧化氮供体的比较研究:精脒硝普盐是最适合用于血管生成的一氧化氮供体。

A comparative study of NONOate based NO donors: spermine NONOate is the best suited NO donor for angiogenesis.

机构信息

Vascular Biology Lab, AU-KBC Research Centre, Anna University, Chennai, India.

Department of Pharmacology, C.L. Baid Metha College of Pharmacy, Chennai, India.

出版信息

Nitric Oxide. 2014 Jan 30;36:76-86. doi: 10.1016/j.niox.2013.12.002. Epub 2013 Dec 12.

Abstract

Nitric oxide (NO) is a known modulator of angiogenesis. The NONOate subfamily of NO donors has long been used in experimental and clinical studies to promote angiogenesis. However, no studies have been conducted yet to compare the angiogenesis potential of these NO donors in respect to their pattern of NO release. We hypothesize that having different pattern of NO release, each of the NO donors in NONOate subfamily can promote key stages of angiogenesis in differential manner. To verify our hypothesis, NO donors with half life ranging from seconds to several hours and having very different pattern of NO release were selected to evaluate their efficacy in modulating angiogenesis. Endothelial tube formation using EAhy926 cells was maximally increased by Spermine NONOate (SP) treatment. SP treatment maximally induced both ex vivo and in vivo angiogenesis using egg yolk and cotton plug angiogenesis models respectively. Experiment using chick embryo partial ischemia model revealed SP as the best suited NO donor to recover ischemia driven hampered angiogenesis. The present study elaborated that differential release pattern of NO by different NO donors can modulate angiogenesis differentially and also suggested that SP have a unique pattern of NO release that best fits for angiogenesis.

摘要

一氧化氮(NO)是已知的血管生成调节剂。NO 供体的 NONOate 亚家族长期以来一直被用于实验和临床研究以促进血管生成。然而,目前还没有研究比较这些 NO 供体在其 NO 释放模式方面的血管生成潜力。我们假设,由于具有不同的 NO 释放模式,NONOate 亚家族中的每种 NO 供体都可以以不同的方式促进血管生成的关键阶段。为了验证我们的假设,选择半衰期从几秒钟到几个小时不等且具有非常不同的 NO 释放模式的 NO 供体来评估它们调节血管生成的功效。使用 EAhy926 细胞进行的内皮管形成最大程度地增加了 spermine NONOate(SP)处理。SP 处理分别使用蛋黄和棉塞血管生成模型最大程度地诱导了体外和体内血管生成。使用鸡胚部分缺血模型的实验表明 SP 是最适合恢复缺血驱动的血管生成障碍的 NO 供体。本研究阐述了不同 NO 供体通过不同的 NO 释放模式可以不同地调节血管生成,并表明 SP 具有最适合血管生成的独特的 NO 释放模式。

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