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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >The Endogenous Lusitropic and Chronotropic Agent, B-Type Natriuretic Peptide, Limits Cardiac Troponin Release in Cancer Patients with an Early Impairment of Myocardial Relaxation Induced by Anthracyclines
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The Endogenous Lusitropic and Chronotropic Agent, B-Type Natriuretic Peptide, Limits Cardiac Troponin Release in Cancer Patients with an Early Impairment of Myocardial Relaxation Induced by Anthracyclines

机译:内源性血管疏水剂和时铬肽,B型利可钠肽,限制癌症患者的心肌肌钙蛋白释放,其早期受蒽环植物诱导的心肌松弛损害

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We have reported that cancer patients treated with anthracycline-based or nonanthracycline chemotherapy developed an early impairment of myocardial relaxation at echocardiography or persistent elevations of the cardiac hormone B-type natriuretic peptide (BNP). Post-hoc pharmacologic analyses showed that BNP elevations were induced by impaired relaxation and caused positive lusitropic effects that maintained normal relaxation. High BNP levels and impaired relaxation were therefore characterized as mutually exclusive manifestations of diastolic dysfunction, but high BNP levels resulted in positive chronotropism and inappropriate tachycardia. Some patients developed increased circulating levels of cardiac troponin I isoform (cTnI), a marker of cardiomyocyte necrosis. Here we have characterized whether cTnI elevations correlated with diastolic dysfunction that manifested as impaired relaxation or a high level of BNP. The effects of high BNP levels on cTnI elevations were also characterized. We show that impaired relaxation or high BNP levels were significantly more frequent in patients with cTnI elevations. High BNP levels diminished the plasma peak and area under the curve of cTnI, but this result was accompanied by inappropriate tachycardia. cTnI elevations occurred only in patients treated with anthracyclines; moreover, the association of impaired relaxation or high BNP levels with cTnI elevations was significantly more frequent in doxorubicin-treated patients compared with patients treated with its analog, epirubicin. These findings describe cause-and-effect relations between impaired relaxation and cardiomyocyte necrosis, illuminate the role of anthracycline analogs, denote that the beneficial effects of BNP in relieving impaired relaxation and cardiomyocyte necrosis are counterbalanced by inappropriate tachycardia. Patients showing troponin elevations and impaired relaxation or high BNP levels should be treated with lusitropic drugs that lack a positive chronotropism.
机译:我们据报道,癌症患者治疗的基于蒽环或非蒽环化疗的患者在心动脉造影或心脏激素B型Natrietic肽(BNP)的超声心动图或持续升高中产生了早期的心肌弛豫损伤。后HOC药理分析表明,BNP升高被损伤诱导,导致正常松弛的正挫伤效应。因此,高BNP水平和缓解受损的是舒张性功能障碍的相互独家表现,但高BNP水平导致阳性正常性和不适当的心动过速。有些患者开发了增加的循环水平的心肌肌钙蛋白I同种型(CTNI),心肌细胞坏死的标志物。在这里,我们表征了CTNI升高是否与舒张功能障碍相关,表现为弛豫损害或高水平的BNP。还表征了高BNP水平对CTNI升高的影响。在CTNI升高的患者中表明,在CTNI升高的患者中表明损害或高BNP水平显着更频繁。高BNP水平降低了CTNI曲线下的等离子体峰和面积,但这种结果伴随着不适当的心动过速。 CTNI升高仅发生在用蒽环植物治疗的患者中;此外,与用IDS的患者相比,在多柔比蛋白治疗的患者中,在多柔比蛋白治疗的患者中,患有损伤或高BNP水平的关联或高BNP水平的关系显着更频繁。这些发现描述了损害缓释和心肌细胞坏死之间的原因和效应关系,阐明了蒽环类类似物的作用,表示BNP在缓解缓解缓解和心肌细胞坏死中的有益效果通过不适当的心动过速抵消。表现出肌钙蛋白升高和损伤或高BNP水平的患者应用缺乏阳性正调性的杀菌药物治疗。

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