Negative pressure wound therapy accelerates rats diabetic wound by promoting agenesis

被引:1
作者
Li, Xiaoqiang [1 ]
Liu, Jiaqi [1 ]
Liu, Yang [1 ]
Hu, Xiaolong [1 ]
Dong, Maolong [1 ]
Wang, Hongtao [1 ]
Hu, Dahai [1 ]
机构
[1] Fourth Mil Med Univ, Dept Burn & Cutaneous Surg, Burn Ctr PLA, Xijing Hosp, Xian 710032, Peoples R China
关键词
Negative pressure wound therapy; diabetic wound; angiogenesis; wound healing; ENDOTHELIAL GROWTH-FACTOR; VACUUM-ASSISTED CLOSURE; OF-THE-LITERATURE; MICROVESSEL DENSITY; EXPRESSION; VASCULARIZATION; ANGIOPOIETINS; MELLITUS; TUMORS;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Negative Pressure Wound Therapy (NPWT) has become widely adopted to several wound treatment over the last 15 years, including diabetic foot ulcer (DFU). Much of the existing evidence supports that NPWT increase in blood flow, reduce in edema, decrease bacterial proliferation and accelerate granulation-tissue formation. However, the accurate mechanism is not clear till now. The aim of the present study was to further elucidate the effects of NPWT on angiogenesis of diabetic wound model. As result, our data showed: 1) NPWT promoted the wound healing and blood perfusion on both diabetic and normal wound compared with control, 2) The NPWT increased wound vessel density, and the wound treated with NPWT showed well developed and more functional vessels at day 7 post operation compared with control 3) NPWT up regulated the expression of VEGF at day 3 and Ang1 at day 7 on RNA and protein level. 4) Ang2 was up regulated in diabetic rats but NPWT attenuated this affection. Our data indicated that NPWT increased vessel density and promoted the maturation of neovascular over the potential mechanism of up regulated VEGF and Ang1 and down regulated of Ang2.
引用
收藏
页码:3506 / 3513
页数:8
相关论文
共 22 条
[1]   Vacuum-assisted closure: A new method for wound control and treatment: Clinical experience [J].
Argenta, LC ;
Morykwas, MJ .
ANNALS OF PLASTIC SURGERY, 1997, 38 (06) :563-576
[2]   Negative pressure wound therapy after partial diabetic foot amputation: a multicentre, randomised controlled trial [J].
Armstrong, DG ;
Lavery, LA .
LANCET, 2005, 366 (9498) :1704-1710
[3]  
Bitar MS, 1998, AM J PATHOL, V152, P547
[4]  
Borgquist O, 2011, OSTOMY WOUND MANAG, V57, P44
[5]   Cellular and molecular basis of wound healing in diabetes [J].
Brem, Harold ;
Tomic-Canic, Marjana .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (05) :1219-1222
[6]  
Broadley K N, 1989, Biotechnol Ther, V1, P55
[7]   Inhibition of Protein Tyrosine Phosphatase Improves Angiogenesis via Enhancing Ang-1/Tie-2 Signaling in Diabetes [J].
Chen, Jian-Xiong ;
Tuo, Qinhui ;
Liao, Duan-Fang ;
Zeng, Heng .
EXPERIMENTAL DIABETES RESEARCH, 2012,
[8]  
Chen Shao-Zong, 2005, Asian J Surg, V28, P211, DOI 10.1016/S1015-9584(09)60346-8
[9]   Angiogenesis in Wounds Treated by Microdeformational Wound Therapy [J].
Erba, Paolo ;
Ogawa, Rei ;
Ackermann, Maximilian ;
Adini, Avner ;
Miele, Lino F. ;
Dastouri, Pouya ;
Helm, Doug ;
Mentzer, Steven J. ;
D'Amato, Robert J. ;
Murphy, George F. ;
Konerding, Moritz A. ;
Orgill, Dennis P. .
ANNALS OF SURGERY, 2011, 253 (02) :402-409
[10]   The use of microvessel density in assessing human urological tumours [J].
Goddard, JC ;
Sutton, CD ;
Berry, DP ;
O'Byrne, KJ ;
Kockelbergh, RC .
BJU INTERNATIONAL, 2001, 87 (09) :866-875