Literature DB >> 33415464

Therapeutic approach for global myocardial injury using bone marrow-derived mesenchymal stem cells by cardiac support device in rats.

Ziwei Liu1, Muhammad Naveed1,2, Mirza Muhammad Faran Ashraf Baig3, Reyaj Mikrani1, Cuican Li1, Muhammad Saeed4, Qin Zhang1, Muhammad Asim Farooq5, Hafiz Muhammad Zubair6, Zhou Xiaohui7,8,9.   

Abstract

Bone marrow-derived mesenchymal stem cells (BMSCs) have been considered a promising therapeutic approach to cardiovascular disease. This study intends to compare the effect of BMSCs through a standard active cardiac support device (ASD) and intravenous injection on global myocardial injury induced by isoproterenol. BMSCs were cultured in vitro, and the transplanted cells were labeled with a fluorescent dye CM-Dil. Isoproterenol (ISO) was injected into the rats; 2 weeks later, the labeled cells were transplanted into ISO-induced heart-jury rats through the tail vein or ASD device for 5 days. The rats were sacrificed on the first day, the third day, and the fifth day after transplantation to observe the distribution of cells in the myocardium by fluorescence microscopy. The hemodynamic indexes of the left ventricle were measured before sacrificing. H&E staining and Masson's trichrome staining were used to evaluate the cardiac histopathology. In the ASD groups, after 3 days of transplantation, there were a large number of BMSCs on the epicardial surface, and after 5 days of transplantation, BMSCs were widely distributed in the ventricular muscle. But in the intravenous injection group, there were no labeled-BMSCs distributed. In the ASD + BMSCs-three days treated group and ASD + BMSCs -five days-treated group, left ventricular systolic pressure (LVSP), the maximum rate of left ventricular pressure rise (+dP/dt), the maximum rate of left ventricular pressure decline (-dP/dt) increased compared with model group and intravenous injection group (P < 0.05). By giving BMSCs through ASD device, cells can rapidly and widely distribute in the myocardium and significantly improve heart function.

Entities:  

Keywords:  Active cardiac support device (ASD); BMSCs; Epicardial delivery; Global myocardial injury; Stem cell treatment

Year:  2021        PMID: 33415464     DOI: 10.1007/s10544-020-00538-9

Source DB:  PubMed          Journal:  Biomed Microdevices        ISSN: 1387-2176            Impact factor:   2.838


  2 in total

1.  Cardioprotective effect of silicon-built restraint device (ASD), for left ventricular remodeling in rat heart failure model.

Authors:  Waqas Nawaz; Muhammad Naveed; Jing Zhang; Sobia Noreen; Muhammad Saeed; Kiganda Raymond Sembatya; Awais Ullah Ihsan; Imran Shair Mohammad; Gang Wang; Xiaohui Zhou
Journal:  J Mater Sci Mater Med       Date:  2022-05-10       Impact factor: 4.727

Review 2.  Cardiac Differentiation of Mesenchymal Stem Cells: Impact of Biological and Chemical Inducers.

Authors:  Saravanan Ramesh; Kavitha Govarthanan; Serge Ostrovidov; Haiguang Zhang; Qingxi Hu; Gulden Camci-Unal; Rama S Verma; Murugan Ramalingam
Journal:  Stem Cell Rev Rep       Date:  2021-04-16       Impact factor: 5.739

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.