| خلاصه مقاله | Background and Aim: Despite the emergence of novel therapeutic
advances regarding MI, ischemic heart disease is conceived as a
major cause of global mortality and morbidity. it made investigators to
develop novel re-vascularization techniques that specifically target the
microvasculature in ischemic myocardium. Several studies have recently
reported promising results by modifying and enhancing cell-mediated
ischemic myocardial repair and regeneration. In this study, we aimed to
investigate the effect of alginate-gelatin encapsulation on the viability
and dynamic of rat cardiomyoblasts in vitro.
Methods: Rat cardiomyoblasts cell line H9C2 were encapsulated by
alginate-gelatin solution and incubated for 7 days, and the control group
was rat cardiomyoblasts from the same cell line without encapsulation
while incubated for 7 days as like the encapsulated group. The level of
extracellular enzymes as like SGPT, SGOT, CPK, and LDH were detected
in supernatants from both groups. The level of intracellular enzymes as
like SOD, GPx, and TAC was measured by biochemical analyses in cell
lysates. To the examination of cell viability, we used MTT method.
Results: We found that encapsulation was able to increase the viability
of rat cardiomyocytes after 7 days. The increased level of intracellular
enzymes including SOD, GPx, and TAC was identified compared to the
control cells (P>0.05). No significant differences were found regarding
the level of SGPT and CPK while the level of LDH and SGOT as
extracellular enzymes showed decreasing compared to the control nontreated
cells (P>0.05).
Conclusion: The results of this investigation showed that encapsulation
of rat cardiomyoblasts with alginate-gelatin microspheres improves the
cell's dynamic and viability. |