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Role of calcitonin gene-related peptide in ischaemic preconditioning in diabetic rat hearts.

机译:降钙素基因相关肽在糖尿病大鼠心脏缺血预处理中的作用。

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1. It has been suggested that calcitonin gene-related peptide (CGRP) is involved in the protection provided by ischaemic preconditioning in rat hearts and that ischaemic preconditioning is absent in diabetic rat hearts. 2. In the present study, we tested the relationship between sensory nerve function and ischaemic preconditioning in diabetic rats. 3. In 4- and 8-week diabetic rats and age-matched non- diabetic controls, 30 min global ischaemia and 40 min reperfusion caused a significant decrease in cardiac function and a marked increase in creatine kinase (CK) release. Ischaemic preconditioning, by three cycles of 5 min ischaemia and 5 min reperfusion, improved the recovery of cardiac function and decreased CK release during reperfusion in 4-week diabetic rat hearts. However, the cardioprotection afforded by ischaemic preconditioning was lost in 8-week diabetic rat hearts. Pretreatment with CGRP for 5 min also significantly improved the recovery of cardiac function and decreased CK release in rats subjected to 4 or 8 weeks of diabetes. 4. The content of CGRP in the coronary effluent during ischaemic preconditioning was significantly increased in 4-week diabetic rat hearts (P < 0.05). However, only a slight increase in the release of CGRP was shown in 8-week diabetic rat hearts (P > 0.05). 5. In summary, the present results suggest that the protection afforded by ischaemic preconditioning is attenuated in diabetic rats and that the change may be related to the reduction in CGRP release in diabetic rat hearts.
机译:1.已表明降钙素基因相关肽(CGRP)参与大鼠心脏缺血预处理提供的保护作用,而糖尿病大鼠心脏不存在缺血预处理。 2.在本研究中,我们测试了糖尿病大鼠感觉神经功能与缺血预处理之间的关系。 3.在4周和8周的糖尿病大鼠和年龄匹配的非糖尿病对照组中,30分钟的全脑缺血和40分钟的再灌注导致心脏功能显着下降,并且肌酸激酶(CK)释放显着增加。缺血预处理,通过5分钟局部缺血和5分钟再灌注的三个周期,改善了4周糖尿病大鼠心脏在再灌注过程中的心脏功能恢复并降低了CK释放。但是,缺血性预处理提供的心脏保护作用在8周的糖尿病大鼠心脏中消失了。在患有糖尿病4或8周的大鼠中,用CGRP预处理5分钟还可以显着改善心脏功能的恢复并降低CK释放。 4.在糖尿病预处理大鼠的心脏中,缺血预处理期间冠状流出物中的CGRP含量显着增加(P <0.05)。但是,在8周的糖尿病大鼠心脏中,CGRP的释放仅略有增加(P> 0.05)。 5.总而言之,目前的结果表明在糖尿病大鼠中缺血预处理提供的保护作用减弱,并且该变化可能与糖尿病大鼠心脏中CGRP释放的减少有关。

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