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利钠肽在心肌缺血/再灌注治疗中的应用

Natriuretic peptides as therapy in cardiac ischaemia/reperfusion.

作者信息

Kousholt Birgitte Saima

机构信息

Department of Cardiothoracic and Vascular Surgery, T-research, Aarhus University Hospital, Brendstrupgaardvej 100, 8200 Aarhus N, Denmark.

出版信息

Dan Med J. 2012 Jun;59(6):B4469.

Abstract

Natriuretic peptides elicit vasodilation, increased sodium excretion and concomitant diuresis, and counteract the RAAS. In the heart itself, natriuretic peptides may also act anti-inflammatory and antifibrotic. This has led to the pursuit of natriuretic peptides and chemically modified peptides as adjunctive therapy in myocardial ischaemia. However, natriuretic peptide infusion may also influence the endogenous natriuretic peptide response and lipid accumulation. We hypothesised that a) natriuretic peptide infusion (BNP and CD-NP) is cardiomyocyte protective, b) affects the endogenous response, and c) facilitate cardiac lipid accumulation. We examined these effects in a minimally invasive porcine model of regional cardiac ischaemia and reperfusion. The studies were supplemented by a 48-hour porcine model of ischemia and reperfusion as well as an in vitro study of BNP administered in a HL-1 cell model of "ischaemia/reperfusion". Infarct size was determined by TTC staining, plasma troponin T release, and total RNA integrity in cardiac tissue samples. The endogenous response was assessed by a processing-independent proANP immunoassay and mRNA quantitation. Lipids in plasma and myocardial tissue were determined by TLC. The studies show that natriuretic peptides decrease cardiomyocyte damage, possibly partly through indirect mechanisms. Furthermore, BNP infusion completely inverts the endogenous response, whereas CD-NP infusion does not. Finally, both natriuretic peptides increase plasma free fatty acids, which is associated with an increased cardiac lipid accumulation in non-ischaemic myocardium. In conclusion, the studies suggest that natriuretic peptides are beneficial in terms of reduced cardiac injury. In addition, the endogenous natriuretic peptide response is inverted. The results advocate for pursuing natriuretic peptide treatment in ischaemia/reperfusion damage. However, the metabolic consequences in a cardiac tissue challenged by ischaemia should be pursued before testing the peptides in patients.

摘要

利钠肽可引起血管舒张、增加钠排泄及随之而来的利尿作用,并拮抗肾素 - 血管紧张素 - 醛固酮系统(RAAS)。在心脏本身,利钠肽还可能具有抗炎和抗纤维化作用。这促使人们寻求将利钠肽和化学修饰肽作为心肌缺血的辅助治疗方法。然而,输注利钠肽也可能影响内源性利钠肽反应和脂质蓄积。我们推测:a)输注利钠肽(脑钠肽[BNP]和环化二肽[CD - NP])具有心肌保护作用;b)会影响内源性反应;c)会促进心脏脂质蓄积。我们在区域心脏缺血再灌注的微创猪模型中研究了这些作用。通过48小时猪缺血再灌注模型以及在“缺血/再灌注”的HL - 1细胞模型中给予BNP的体外研究对这些研究进行补充。通过TTC染色、血浆肌钙蛋白T释放以及心脏组织样本中的总RNA完整性来确定梗死面积。通过一种不依赖处理过程的前心钠素原免疫测定法和mRNA定量来评估内源性反应。通过薄层层析法测定血浆和心肌组织中的脂质。研究表明,利钠肽可减少心肌细胞损伤,可能部分是通过间接机制。此外,输注BNP完全逆转了内源性反应,而输注CD - NP则没有。最后,两种利钠肽均增加血浆游离脂肪酸,这与非缺血心肌中心脏脂质蓄积增加有关。总之,这些研究表明利钠肽在减少心脏损伤方面是有益的。此外,内源性利钠肽反应被逆转。这些结果支持在缺血/再灌注损伤中采用利钠肽治疗。然而,在对患者进行肽类测试之前,应先研究缺血心脏组织中的代谢后果。

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