Abd Allah Somia H, Hussein Samia, Hasan Mai M, Deraz Raghda H A, Hussein Wafaa F, Sabik Laila M E
Faculty of Medicine, Department of Medical Biochemistry and Molecular Biology, Zagazig University, Zagazig, Egypt.
Faculty of Medicine, Department of Medical Physiology, Zagazig University, Zagazig, Egypt.
J Cell Biochem. 2017 Oct;118(10):3119-3129. doi: 10.1002/jcb.26168. Epub 2017 Jun 19.
Cardiomyopathy induced by doxorubicin (DOX) was recognized at an early stage and also several years after drug administration. Mesenchymal stem cells (MSCs) have many properties that make them suitable for preventive and/or regenerative therapies. In this study, we evaluated the effect of MSCs in the functional and the structural improvement of DOX-induced cardiomyopathy in rats. Ninety adult male albino rats were randomly divided into three equal groups of thirty rats each: Group I (control): rats received normal saline. Group II (DOX- group): rats received DOX. Group III (DOX-MSCs group): rats received DOX for 2 weeks then human umbilical cord blood mesenchymal stem cells (hUCB-MSCs). Rats in all groups were evaluated for: physical condition, electrocardiography (ECG), and hemodynamic parameters. Serum cardiac troponin I (cTnI), malondialdehyde (MDA), total antioxidant capacity (TAC), and DNA fragmentation on heart tissue isolated DNA were estimated for evaluation of the mechanism and the extent of the damage. Hearts were examined histopathologically for detection of MSCs homing, structural evaluation, with counting of the collagen fibers for evaluation of fibrosis. DOX-administered rats showed significant functional and structural deterioration. DOX-MSCs treated rats (group III) showed improved functional and structural criteria with restoration of all biochemical indicators of cardiac damage and reactive oxygen species (ROS) to normal, as well. In Conclusion, hUCB-MSCs significantly ameliorated the cardiotoxic manifestations as shown by biochemical, functional, and structural cardiac improvement. J. Cell. Biochem. 118: 3119-3129, 2017. © 2017 Wiley Periodicals, Inc.
阿霉素(DOX)诱导的心肌病在给药早期以及给药数年之后均可被识别。间充质干细胞(MSCs)具有许多特性,使其适用于预防性和/或再生性治疗。在本研究中,我们评估了间充质干细胞对阿霉素诱导的大鼠心肌病功能和结构改善的影响。90只成年雄性白化大鼠被随机分为三组,每组30只:第一组(对照组):大鼠接受生理盐水。第二组(DOX组):大鼠接受阿霉素。第三组(DOX-MSCs组):大鼠接受2周阿霉素治疗,然后接受人脐带血间充质干细胞(hUCB-MSCs)。对所有组的大鼠进行以下评估:身体状况、心电图(ECG)和血流动力学参数。测定血清心肌肌钙蛋白I(cTnI)、丙二醛(MDA)、总抗氧化能力(TAC)以及从心脏组织分离的DNA上的DNA片段化情况,以评估损伤的机制和程度。对心脏进行组织病理学检查,以检测间充质干细胞归巢、进行结构评估,并对胶原纤维进行计数以评估纤维化情况。接受阿霉素治疗的大鼠表现出明显的功能和结构恶化。接受DOX-MSCs治疗的大鼠(第三组)显示功能和结构标准有所改善,心脏损伤和活性氧(ROS)的所有生化指标也恢复正常。总之,如生化、功能和心脏结构改善所示,hUCB-MSCs显著改善了心脏毒性表现。《细胞生物化学杂志》118: 3119 - 3129, 2017。© 2017威利期刊公司