高选择性A(1) -腺苷激动剂(2-氯- n6 -环戊基腺苷)和减少大鼠脂肪皮肤皮瓣坏死。

Head & Neck Pub Date : 2012-08-01 Epub Date: 2011-10-29 DOI:10.1002/hed.21869
Andreas K Dacho, Stefan Lyutenski, Gabriela Aust, Andreas Dietz
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引用次数: 2

摘要

背景:2-氯- n6 -环戊基腺苷(CCPA)被证实是心肌缺血再灌注损伤的保护因子,并能减小心肌梗死面积。本研究的目的是确定静脉给药CCPA是否可以减少皮瓣坏死。方法:56只雄性Wistar大鼠分为4个实验组。术后第5天,用平面测量软件评估各组皮瓣坏死面积。结果:对照组皮瓣坏死率明显低于缺血对照组(p < 0.05)。非缺血CCPA组皮瓣坏死率明显低于非缺血对照组(p < 0.05)。CCPA缺血组下皮瓣坏死率显著高于缺血对照组(p < 0.0001)。结论:我们的数据显示,静脉给药CCPA可以减少皮瓣坏死,无论是有缺血期还是没有缺血期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Highly selective A(1) -adenosine-agonist (2-chloro-N6-cyclopentyladenosine) and reduction of flap necrosis in adipocutaneous flaps in rats.

Background: The 2-chloro-N6-cyclopentyladenosine (CCPA) was proven to be a protective factor in ischemic reperfusion injury in myocardium and to reduce the infarct size in the heart. The purpose of this study was to determine whether flap necrosis could be reduced by intravenous administration of CCPA.

Methods: Fifty-six male Wistar rats were divided into 4 experimental groups. An epigastric adipocutaneous flap was raised, and the area of flap necrosis was assessed for all groups on the fifth postoperative day with planimetry software.

Results: The control group had a significantly lower rate of flap necrosis than the ischemic control group (p < .05). The nonischemic CCPA group had a significantly lower rate of flap necrosis than the nonischemic control group (p < .05). The ischemic CCPA group had a highly significant (p < .0001) rate of lower flap necrosis than the ischemic control group.

Conclusion: Our data show that reduction of flap necrosis can be achieved both with and without ischemic periods by intravenous administration of CCPA.

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