降钙素基因相关肽预适应对在体大鼠心肌缺血/再灌注损伤的保护作用
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Calcitonin Gene-Related Peptide-Induced Preconditioning Protects Against Ischemia-Reperfusion Injury in Intact Rat Heart
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    摘要:

    为探讨降钙素基因相关肽预适应对在体大鼠心肌缺血/再灌注损伤模型是否具有保护作用,用36只SD大鼠随机分为三组:对照组、缺血预适应组和降钙素基因相关肽组。后组持续缺血前20min静脉注射降钙素基因相关肽(10μg/kg)。所有动物均接受30min缺血/2h再灌注。预适应方案由3次5min缺血/再灌注组成。梗塞大小由硝基四唑氮兰染色判定,并以坏死区占危险区的百分数表示。结果发现,缺血预适应和降钙素基因相关肽预适应均能显著地降低缺血和再灌注所致的室性心动过速或心室纤维性颤动的发生。缺血预适应(15.7%,P<0.01)和降钙素基因相关肽预适应(28.8%,P<0.01)也均能较对照组(54.0%)显著降低缺血/再灌注后的心肌梗塞面积。本研究结果证实降钙素基因相关肽预适应在在体大鼠模型中也具有心肌保护作用。

    Abstract:

    Aim Calcitonin gene-related peptide (CGRP), a princlpal transmitter in cardiac and vascular sensory nerves, is released from the heart during ischemia,which protected the myocardium against ischemia-reperfusion injury in isolated rat hearts. The purpose of this study was to investigate whether CGRP-induced preconditioning has cardioprotective effects in intact rat hearts.Methods 36 SD rats were at random divided into three groups of control, ischemic preconditioning (IPC) and CGRP. CGRP (10 μg/kg) was given 20min before 30 min ischemia. All animals were .sub-jected to 30 min of regional ischemia followed by 2 h of reperfusion. The preconditioning protocol consisted of 3 cycles of 5 min regional ischemia and 3 cycles of 5min of reperfusion. Infarct size as a percentage of the area at risk was determined with nitro blue tetrazoli-um.Results Both of IPC and CGRP-induced precondi-tioning markedly reduced the incidences of ventricular arrhythmias during ischemia and reperfusion. Both ofIPC (15. 7%, P< 0. 01) and CGRP-induced precondi-tioning (28. 8%, P<0.01) also resulted in a signifi-cant reduction in infarct size when compared to control(54. 0%).Conclusion These results support the hypothesis that CGRP-induced preconditioning has cardoprotective effects in intact rat hearts.

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欧阳伟,钱学贤,付向阳,李志梁,王素华.降钙素基因相关肽预适应对在体大鼠心肌缺血/再灌注损伤的保护作用[J].中国动脉硬化杂志,1998,6(3):228~232.

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  • 收稿日期:1998-05-30
  • 最后修改日期:1998-08-12
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