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人体心脏内源性阿片类物质和降钙素基因相关肽的心肌更新以及脊髓刺激对起搏诱导型心绞痛的影响。

Myocardial turnover of endogenous opioids and calcitonin-gene-related peptide in the human heart and the effects of spinal cord stimulation on pacing-induced angina pectoris.

作者信息

Eliasson T, Mannheimer C, Waagstein F, Andersson B, Bergh C H, Augustinsson L E, Hedner T, Larson G

机构信息

Multidisciplinary Pain Center, Department of Medicine, Ostra University Hospital, Göteborg, Sweden.

出版信息

Cardiology. 1998 Mar;89(3):170-7. doi: 10.1159/000006783.

Abstract

Earlier studies have shown that spinal cord stimulation (SCS) has antianginal and anti-ischemic effects in severe coronary artery disease. In the present study, 14 patients were subjected to right-sided atrial catheterization and atrial pacing. The patients were paced to angina during a control session and during spinal cord stimulation. Myocardial extraction of beta-endorphin (BE) during control pacing (8 +/- 22%) changed to release at the maximum pacing rate during treatment (-21 +/- 47%, a negative value representing release). Furthermore, the results indicate local myocardial turnover of leuenkephalin, BE and calcitonin-gene-related peptide. In addition, it is implied that SCS may induce myocardial release of BE which could explain the beneficial effects in myocardial ischemia.

摘要

早期研究表明,脊髓刺激(SCS)对严重冠状动脉疾病具有抗心绞痛和抗缺血作用。在本研究中,14例患者接受了右侧心房导管插入术和心房起搏。在对照期和脊髓刺激期间,对患者进行起搏诱发心绞痛。对照起搏期间β-内啡肽(BE)的心肌摄取率为(8±22%),在治疗期间以最大起搏率时转变为释放(-21±47%,负值表示释放)。此外,结果表明亮脑啡肽、BE和降钙素基因相关肽在心肌局部存在更新。另外,这意味着SCS可能诱导BE从心肌释放,这可以解释其对心肌缺血的有益作用。

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