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运动训练可减轻幼年大鼠模型中蒽环类药物引起的慢性心脏毒性。

Exercise training mitigates anthracycline-induced chronic cardiotoxicity in a juvenile rat model.

机构信息

School of Sport and Exercise Science and the Rocky Mountain Cancer Rehabilitation Institute, University of Northern Colorado, Greeley, Colorado 80639, USA.

出版信息

Pediatr Blood Cancer. 2012 Jul 15;59(1):149-54. doi: 10.1002/pbc.23392. Epub 2011 Nov 2.

Abstract

BACKGROUND

Childhood cancer survivors are at greater risk of cardiovascular complications once they reach adulthood. Anthracyclines may be a major contributor to these delayed-onset complications, yet their use continues because of favorable clinical outcomes. Exercise has been shown to protect against anthracycline cardiotoxicity, yet it is unclear whether exercise can protect against delayed-onset cardiotoxicity when treatment is initiated in childhood. The aim of the present study was to determine if exercise training provides cardioprotection in a juvenile rat model of delayed-onset anthracycline cardiotoxicity.

PROCEDURE

At 25 days of age, male Sprague-Dawley rat pups were subjected to a treatment regimen with the anthracycline doxorubicin (DOX). Pups received DOX at 2 mg/kg on 7 consecutive days (cumulative dose 14 mg/kg) or saline as a control. At the time DOX treatment began, pups remained sedentary or were allowed to voluntarily exercise. Ten weeks after the initiation of exercise, cardiac function was assessed both in vivo and ex vivo.

RESULTS

DOX treatment stunted normal growth and significantly impaired cardiac function. While voluntary exercise did not offset changes in the growth curve, it did provide significant cardioprotection against DOX-induced cardiotoxicity.

CONCLUSIONS

Exercise training, initiated at the time treatment begins, can protect against delayed-onset anthracycline-induced cardiotoxicity in adult rats that were treated with anthracyclines as juveniles.

摘要

背景

儿童癌症幸存者成年后患心血管并发症的风险更高。蒽环类药物可能是这些迟发性并发症的主要原因,但由于临床疗效良好,它们仍在使用。运动已被证明可以预防蒽环类药物的心脏毒性,但尚不清楚在儿童期开始治疗时,运动是否可以预防迟发性心脏毒性。本研究的目的是确定运动训练是否在蒽环类药物迟发性心脏毒性的幼年大鼠模型中提供心脏保护。

过程

在 25 天大时,雄性 Sprague-Dawley 幼鼠接受了蒽环类药物多柔比星(DOX)的治疗方案。幼鼠在连续 7 天内接受 2 mg/kg 的 DOX(累积剂量 14 mg/kg)或生理盐水作为对照。在开始 DOX 治疗时,幼鼠保持静止或允许自愿运动。在开始运动 10 周后,在体内和体外评估心脏功能。

结果

DOX 治疗阻碍了正常生长并显著损害了心脏功能。虽然自愿运动并没有改变生长曲线,但它确实对 DOX 引起的心脏毒性提供了显著的心脏保护。

结论

在青少年时期接受蒽环类药物治疗的成年大鼠中,在开始治疗时开始进行运动训练可以预防蒽环类药物引起的迟发性心脏毒性。

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