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首页> 外文期刊>Theranostics >Screening for in-vivo regional contractile defaults to predict the delayed Doxorubicin Cardiotoxicity in Juvenile Rat
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Screening for in-vivo regional contractile defaults to predict the delayed Doxorubicin Cardiotoxicity in Juvenile Rat

机译:筛选体内区域收缩违约,以预测幼年大鼠的延迟多柔比星心毒性

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Anthracyclines are key chemotherapeutic agents used in various adult and pediatric cancers, however, their clinical use is limited due to possible congestive heart failure (HF) caused by acute and irreversible cardiotoxicity. Currently, there is no method to predict the future development of the HF in these patients. In order to identify early biomarkers to predict anthracycline cardiotoxicity in long-term survivors of childhood cancer, this longitudinal study aimed to analyze early and late in-vivo regional myocardial anthracycline-induced cardiotoxicity, related to in-vitro cardiac myocytes dysfunction, in a juvenile rat model. Methods: Young male Wistar rats (4 weeks-old) were treated with different cumulative doses of doxorubicin (7.5, 10 or 12.5 mg/kg) or NaCl (0.9%) once a week for 6 weeks by intravenous injection. Cardiac function was evaluated in-vivo by conventional (left ventricular ejection fraction, LVEF) and regional two-dimensional (2D) speckle tracking echocardiography over the 4 months after the last injection. The animals were assigned to preserved (pEF) or reduced EF (rEF) groups at the end of the protocol and were compared to controls. Results: We observed a preferential contractile dysfunction of the base of the heart, further altered in the posterior segment, even in pEF group. The first regional alterations appeared 1 month after chemotherapy. Functional investigation of cardiomyocytes isolated from the LV base 1 month after doxorubicin treatment showed that early in-vivo contractile alterations were associated with both decreased myofilament Ca 2 sensitivity and length-dependent activation. Changes in post-translational modifications (phosphorylation; S-glutathionylation) and protein degradation of the cardiac myosin binding protein-C may contribute to these alterations. Conclusion: Our data suggest that screening of the contractile defaults of the base of the heart by regional 2D strain echocardiography is useful to detect subclinical myocardial dysfunction prior to the development of delayed anthracycline-induced cardiomyopathy in pediatric onco-cardiology.? The author(s).
机译:蒽环类是各种成人和儿科癌症中使用的主要化学治疗剂,然而,由于急性和不可逆的心脏毒性引起的可能充血性心力衰竭(HF),它们的临床用途受到限制。目前,没有方法可以预测这些患者在这些患者中的未来发展。为了鉴定早期生物标志物预测儿童癌症的长期幸存者中的蒽环类心脏毒性,这项纵向研究旨在分析早期和晚期的内部区域心肌蒽环素诱导的心脏毒性,与少年有关的体外心肌细胞功能障碍。大鼠模型。方法:每周用不同累积剂量的多柔比星(7.5,10或12.5mg / kg)或NaCl(0.9%)治疗幼小雄性Wistar大鼠(4周龄)。通过静脉注射,每周持续6周。通过常规(左心室喷射部分,LVEF)和地区二维(2D)在最后一次注射后4个月内通过常规(左心室喷射分数,LVEF)和区域二维(2D)斑点跟踪超声心动图进行了表现。将动物分配给在方案结束时保存(PEF)或减少EF(REF)基团,并与对照进行比较。结果:我们观察到心脏碱的优先收缩功能障碍,即使在PEF组中也会进一步改变后部。化疗后,第一个区域改变效果1个月。多柔比蛋白治疗后1个月的LV基碱分离的心肌细胞的功能性研究表明,早期的体内收缩改变与降低的纤细CA 2敏感性和长度依赖性活化有关。翻译后修饰的变化(磷酸化; S-谷胱甘肽)和心肌肌苷结合蛋白-c的蛋白质降解可能有助于这些改变。结论:我们的数据表明,通过区域2D菌株超声心动图筛查心脏基部的收缩违约是有助于检测在儿科onco-cardiology的延迟蒽环素诱导的心肌病症之前检测亚临床心肌功能障碍。作者。

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