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Combination of simvastatin administration and EPC transplantation enhances angiogenesis and protects against apoptosis for hindlimb ischemia.

Authors :
Hu, Zhengli
Zhang, Fumin
Yang, Zhijian
Yang, Naiquan
Zhang, Dingguo
Zhang, Jinying
Cao, Kejiang
Source :
Journal of Biomedical Science. Jul2008, Vol. 15 Issue 4, p509-517. 9p. 1 Color Photograph, 6 Graphs.
Publication Year :
2008

Abstract

The aim of this present study is to investigate the impacts of combinatorial simvastatin administration and endothelial progenitor cell (EPC) transplantation on therapeutic angiogenesis in an athymic nude mouse model of hind limb ischemia. Athymic nude mice were divided into four groups ( n = 10/group): vehicle administration plus PBS injection (control), simvastatin administration plus PBS injection (simvastatin), vehicle administration plus EPC transplantation (EPC), and simvastatin administration plus EPC transplantation (combination). The combination therapy had the greatest laser Doppler blood perfusion imager (LDPI) index and capillary density among the four groups. Importantly, this combination therapy significantly reduced apoptosis of ischemic skeletal muscle cells in part through downregulation of Bax and upregulation of Bcl-2 compared with the other groups. Moreover, the combination therapy exhibited the highest efficacy of increasing the ratio of phospho-Akt to Akt among the four groups. Taken together, the simvastatin and EPC combination therapy promotes powerful angiogenesis in hindlimb ischemia. The combination therapy not only inhibites apoptosis of ischemic skeletal muscle cells partially via downregulation of Bax and upregulation of Bcl-2, but also activates Akt phosphorylation significantly. These efficacies may be mediated by the angiogenic potency of simvastatin, EPCs, and by the beneficial effects of simvastatin on transplanted EPCs as well. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10217770
Volume :
15
Issue :
4
Database :
Academic Search Index
Journal :
Journal of Biomedical Science
Publication Type :
Academic Journal
Accession number :
32484504
Full Text :
https://doi.org/10.1007/s11373-008-9243-1