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Cardiac troponin-I, brain natriuretic peptide and endothelin-1 levels in a rat model of doxorubicin-induced cardiac injury

机译:阿霉素致心脏损伤大鼠模型中的心肌肌钙蛋白-I,脑钠肽和内皮素-1水平

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Background: Cardiotoxicity, during or after therapy, is the most serious side effect of doxorubicin (DXR). The risk of developing cardiac impairment increases concomitantly with an increase in the cumulative dose of DXR. Aim: The aim was to evaluate the levels of cardiac troponin-I (cTnI), brain natriuretic peptide (BNP) and endothelin-1 (ET-1) in DXR induced cardiac injury. Materials and Methods: Thirty-nine Wistar albino rats were divided into three groups; a control group and two-study groups that received low-dose DXR (LDD) and high-dose DXR (HDD) in a weekly schedule for reaching a cumulative dose. Results: Serum cTnI level was significantly increased in both LDD and HDD-treated groups. Although serum BNP was not significantly increased either LDD or HDD-treated groups, ET-1 levels was significantly increased in only HDD-treated groups. Histopathologic injury was more evident in HDD-treated group. Conclusions: Serum cTnI was increased even in LDD and parallel to it low cardiac injury induced by DXR. In the low-dose group, BNP and ET-1 levels were not elevated significant as cTnI despite cardiac injury. Thus, cTnI may be a predictive marker in of DXR-induced cardiotoxicity.
机译:背景:在治疗期间或之后,心脏毒性是阿霉素(DXR)最严重的副作用。随着DXR累积剂量的增加,发生心脏损害的风险也随之增加。目的:目的是评估DXR诱发的心脏损伤中心肌肌钙蛋白I(cTnI),脑利钠肽(BNP)和内皮素1(ET-1)的水平。材料与方法:39只Wistar白化病大鼠分为三组。对照组和两个研究组,每周接受低剂量DXR(LDD)和高剂量DXR(HDD),以达到累积剂量。结果:LDD和HDD治疗组的血清cTnI水平均显着升高。尽管LDD或HDD治疗组的血清BNP均未显着升高,但仅HDD治疗组的ET-1水平显着升高。 HDD治疗组的组织病理学损伤更为明显。结论:即使在LDD中,血清cTnI也升高,与之平行,而DXR可引起低心脏损伤。在低剂量组中,尽管有心脏损伤,但BNP和ET-1水平并未像cTnI那样显着升高。因此,cTnI可能是DXR诱导的心脏毒性的预测指标。

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