Improving surgical wound healing with basic fibroblast growth factor after radiation

被引:40
作者
Hom, DB
Unger, GM
Pernell, KJ
Manivel, JC
机构
[1] Univ Minnesota, Sch Med, Dept Otolaryngol Head & Neck Surg, Div Facial Plast & Reconstruct Surg, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[3] Hennepin Cty Med Ctr, Minneapolis, MN 55415 USA
关键词
D O I
10.1097/01.mlg.0000157852.01402.12
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
Objectives/Hypothesis: Delayed wound healing in surgical patients who have received previous irradiation continues to be a significant problem. We investigated whether radiation decreases basic fibroblast growth factor (bFGF) production in skin and whether supplemental bFGF can improve irradiated postsurgical soft tissue healing. Study Design: Experimental study in the porcine skin flap model. Methods. Pigs were subjected to orthovoltage radiation (1,300 cGy). To test whether radiation alters bFGF production in skin, semiquantitation of bFGF message was compared in irradiated and nonirradiated skin by reverse transcription-polymerase chain reaction (RT-PCR). To determine whether supplemental bFGF can improve postsurgical soft tissue healing after radiation, bFGF was given intravenously or intracuticularly preoperatively. To investigate whether additional oxygen tissue levels would modify the effects of supplemental bFGF, one test group received hyperbaric oxygen. Six weeks later, 108 skin flaps (random and arterial) were created in 27 pigs and monitored over 2 weeks. Tissues were analyzed for flap viability, vascularity, endothelial cell apoptosis by caspase-3 activation, and histologic analysis. Results: Radiation statistically increased endothelial cell apoptosis in porcine skin by 650%. Radiation also significantly reduced bFGF message by 75% in porcine skin by RTPCR analysis. Supplemental intravenous bFGF in irradiated tissue significantly increased skin flap viability by 25% compared with controls (P <.001). Intravenous bFGF also significantly reduced gastrointestinal side effects from irradiation by 50% compared with controls. BFGF treatment induced a trend to decrease endothelial cell apoptosis in irradiated skin, but this was not statistically significant. Histologically, the intravenous bFGF-treated flaps had similar cellularity, fibroblasts, and extracellular acid mucopolysaccharides as controls. When bFGF was administered by intracuticular injection with and without hyperbaric oxygen, skin flap survival and flap vascularity were similar to controls. Conclusions: Decreased local levels of bFGF in skin may play an important role in the delayed healing of irradiated wounds. Radiation appears to decrease bFGF production by significantly reducing bFGF message in irradiated tissue. Supplemental intravenous bFGF reduced irradiated soft tissue injury and improved random skin flap viability in this porcine model. More studies are needed to investigate the effects of bFGF in the surgical healing of irradiated wounds.
引用
收藏
页码:412 / 422
页数:11
相关论文
共 59 条
[1]  
Abraham J. A., 1996, MOL CELLULAR BIOL WO, P195
[2]   RESPONSE OF SWINE SKIN MICROVASCULATURE TO ACUTE SINGLE EXPOSURES OF X-RAYS - QUANTIFICATION OF ENDOTHELIAL CHANGES [J].
ARCHAMBEAU, JO ;
INES, A ;
FAJARDO, LF .
RADIATION RESEARCH, 1984, 98 (01) :37-51
[3]  
Boykin JV, 1996, WOUNDS, V8, P183
[4]   Pharmacokinetics and pharmacodynamics of recombinant FGF-2 in a phase I trial in coronary artery disease [J].
Bush, MA ;
Samara, E ;
Whitehouse, MJ ;
Yoshizawa, C ;
Novicki, DL ;
Pike, M ;
Laham, RJ ;
Simons, M ;
Chronos, NA .
JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 41 (04) :378-385
[5]   Effects of basic fibroblast growth factor on irradiated porcine skin flaps [J].
Chang, HS ;
Hom, DB ;
Agarwal, RP ;
Pernell, K ;
Manivel, JC ;
Song, C .
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 1998, 124 (03) :307-312
[6]  
COLEMAN JJ, 1993, CLIN PLAST SURG, V20, P491
[7]   DETERMINATION OF ENDOGENOUS CYTOKINES IN CHRONIC WOUNDS [J].
COOPER, DM ;
YU, EZ ;
HENNESSEY, P ;
KO, F ;
ROBSON, MC .
ANNALS OF SURGERY, 1994, 219 (06) :688-692
[8]   Tumor growth and tumor radiosensitivity in mice given myeloprotective doses of fibroblast growth factors [J].
Ding, I ;
Huang, KD ;
Snyder, ML ;
Cook, J ;
Zhang, L ;
Wersto, N ;
Okunieff, P .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (19) :1399-1404
[9]   A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD [J].
Enari, M ;
Sakahira, H ;
Yokoyama, H ;
Okawa, K ;
Iwamatsu, A ;
Nagata, S .
NATURE, 1998, 391 (6662) :43-50
[10]   MICRO-ANGIOGRAPHY - A DETAILED TECHNIQUE OF PERFUSION [J].
EROL, OO ;
SPIRA, M ;
LEVY, B .
JOURNAL OF SURGICAL RESEARCH, 1980, 29 (05) :406-413