Chen Weijia, Zhang Feng, Chen Michael B, Lineaweaver William C
Division of Plastic Surgery, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
J Surg Res. 2007 Jun 1;140(1):45-9. doi: 10.1016/j.jss.2006.10.046. Epub 2007 Apr 9.
Ischemia of muscle flaps is a significant problem in reconstructive surgery. Administration of either recombinant vascular endothelium growth factor (VEGF) protein or gene transfers has been conducted to improve the survival of ischemic tissue. These biophysiological functions of VEGF are mediated through its receptor. In this study the changes of expression in VEGF receptor mRNA in muscle flaps with acute ischemia were examined in a rat gracilis muscle flap model.
Twenty-four Sprague Dawley rats were used. The ischemia of the flap was induced by clamping its vascular pedicle. At 3-, 6-, and 18-h intervals, the flaps were biopsied for histology and examination of VEGFR-2 mRNA gene expression. The muscle flap without ischemia was used as the control.
The results showed that the VEGFR-2 mRNA level was significantly increased 3 h after ischemia was induced and then attenuated to the baseline at 6 and 18 h ischemia.
This study delineated the changes in expression of VEGFR-2 receptor in muscle flap in several postischemic intervals and provided a timeframe for the clinical application of VEGF.