Functional and Structural Assessment of the Effect of Human Umbilical Cord Blood Mesenchymal Stem Cells in Doxorubicin-Induced Cardiotoxicity

被引:14
作者
Abd Allah, Somia H. [1 ]
Hussein, Samia [1 ]
Hasan, Mai M. [2 ]
Deraz, Raghda H. A. [3 ]
Hussein, Wafaa F. [3 ]
Sabik, Laila M. E. [3 ]
机构
[1] Zagazig Univ, Dept Med Biochem & Mol Biol, Fac Med, Zagazig, Egypt
[2] Zagazig Univ, Dept Med Physiol, Fac Med, Zagazig, Egypt
[3] Zagazig Univ, Dept Forens Med & Clin Toxicol, Fac Med, Zagazig, Egypt
关键词
MESENCHYMAL STEM CELLS; DOXORUBICIN-INDUCED CARDIOTOXICITY; RATS; STROMAL CELLS; THERAPY; MODEL; MICE;
D O I
10.1002/jcb.26168
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2017 Wiley Periodicals, Inc.
引用
收藏
页码:3119 / 3129
页数:11
相关论文
共 51 条
  • [1] Comparison of adipose tissue- and bone marrow- derived mesenchymal stem cells for alleviating doxorubicin-induced cardiac dysfunction in diabetic rats
    Ammar, Hania Ibrahim
    Sequiera, Glen Lester
    Nashed, Mira B.
    Ammar, Rasha I.
    Gabr, Hala M.
    Elsayed, Hany E.
    Sareen, Niketa
    Rub, Ejlal Abu-El
    Zickri, Maha B.
    Dhingra, Sanjiv
    [J]. STEM CELL RESEARCH & THERAPY, 2015, 6
  • [2] Nesfatin-1 as a novel cardiac peptide: identification, functional characterization, and protection against ischemia/reperfusion injury
    Angelone, T.
    Filice, E.
    Pasqua, T.
    Amodio, N.
    Galluccio, M.
    Montesanti, G.
    Quintieri, A. M.
    Cerra, M. C.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2013, 70 (03) : 495 - 509
  • [3] Protective effect of bilberry (Vaccinium myrtillus) against doxorubicin-induced oxidative cardiotoxicity in rats
    Ashour, Osama M.
    Elberry, Ahmed A.
    Alahdal, Abdulrahman M.
    Al Mohamadi, Ameen M.
    Nagy, Ayman A.
    Abdel-Naim, Ashraf B.
    Abdel-Sattar, Essam A.
    Mohamadin, Ahmed M.
    [J]. MEDICAL SCIENCE MONITOR, 2011, 17 (04): : BR110 - BR115
  • [4] Mesenchymal stromal cells as universal donor cells
    Atoui, Rony
    Chiu, Ray C. J.
    [J]. EXPERT OPINION ON BIOLOGICAL THERAPY, 2012, 12 (10) : 1293 - 1297
  • [5] Comparison of proliferative and multilineage differentiation potential of human mesenchymal stem cells derived from umbilical cord and bone marrow
    Baksh, Dolores
    Yao, Raphael
    Tuan, Rocky S.
    [J]. STEM CELLS, 2007, 25 (06) : 1384 - 1392
  • [6] The modulatory effect of lithium on doxorubicin-induced cardiotoxicity in rat
    Balaei, Maryam Rahimi
    Momeny, Majid
    Babaeikelishomi, Rohollah
    Mehr, Shahram Ejtemaei
    Tavangar, Seyed Mohammad
    Dehpour, Ahmad Reza
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 641 (2-3) : 193 - 198
  • [7] Bancroft JD, 2008, THEORY PRACTICE HIST, pp138
  • [8] Patient-specific pluripotent stem cells in doxorubicin cardiotoxicity: A new window into personalized medicine
    Bernstein, Daniel
    Burridge, Paul
    [J]. PROGRESS IN PEDIATRIC CARDIOLOGY, 2014, 37 (1-2) : 23 - 27
  • [9] Differential levels of soluble endoglin (CD105) in myeloid malignancies
    Calabrò, L
    Fonsatti, E
    Bellomo, G
    Alonci, A
    Colizzi, F
    Sigalotti, L
    Altomonte, M
    Musolino, C
    Maio, M
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 194 (02) : 171 - 175
  • [10] Therapeutic effects of ivabradine on hemodynamic parameters and cardiotoxicity induced by doxorubicin treatment in rat
    Colak, M. C.
    Parlakpinar, H.
    Tasdemir, S.
    Samdanci, E.
    Kose, E.
    Polat, A.
    Sarihan, E.
    Acet, A.
    [J]. HUMAN & EXPERIMENTAL TOXICOLOGY, 2012, 31 (09) : 945 - 954