Kryger Z, Zhang F, Dogan T, Cheng C, Lineaweaver W C, Buncke H J
Division of Plastic and Reconstructive Surgery, Stanford University Medical Center, Stanford, California, USA.
Br J Plast Surg. 2000 Apr;53(3):234-9. doi: 10.1054/bjps.1999.3315.
The purpose of the present study was to determine the effects of vascular endothelial growth factor (VEGF) on survival of a full thickness random pattern, McFarlane musculocutaneous flap in the rat. In addition, this study examined a number of different methods of VEGF delivery in an attempt to determine the most effective route of administration. A 2 x 8 cm full thickness dorsal flap with the pedicle remaining attached at the anterior end was elevated in 72 male Sprague-Dawley rats. The rats were randomised into six groups and immediately received the following treatment: Group I (n = 12): systemic VEGF injection into the femoral vein (50 microg/ml); Group II (n = 10): multiple systemic VEGF injections at 0, 24 and 48 h post flap elevation (50 microg/ml); Group III (n = 12): subdermal VEGF injection into the flap (1 microg/ml); Group IV (n = 12): subfascial VEGF injections into the recipient bed (1 microg/ml); Group V (n = 10): topical VEGF onto the recipient bed (1 microg/ml); Group VI (n = 16): control group with no treatment. Following 5 days recovery, the area of flap survival was measured. Mean flap survival ranged from 91% in Group II to 78% in Group V, and was significantly greater in all experimental groups (P< 0.001 for Groups I-IV and P< 0.05 for Group V) as compared to the control group (mean survival of 66%). The only significant difference between the experimental groups was between the mean survival in Group II and Group V (P< 0. 05). Histological analysis demonstrated a qualitatively greater amount of granulation tissue and neovascularisation in the experimental groups. These results support the notion that VEGF rescues tissue at risk of hypoxic damage by inducing angiogenesis, and the use of growth factors such as VEGF holds promise as a method of increasing skin viability.
本研究的目的是确定血管内皮生长因子(VEGF)对大鼠全层随意型麦克法兰肌皮瓣存活的影响。此外,本研究还考察了多种不同的VEGF递送方法,以确定最有效的给药途径。在72只雄性Sprague-Dawley大鼠中掀起一个2×8 cm的全层背部皮瓣,蒂部保留在前端。将大鼠随机分为六组,并立即给予以下治疗:第一组(n = 12):经股静脉全身注射VEGF(50微克/毫升);第二组(n = 10):在皮瓣掀起后0、24和48小时多次全身注射VEGF(50微克/毫升);第三组(n = 12):向皮瓣内皮下注射VEGF(1微克/毫升);第四组(n = 12):向受区床面筋膜下注射VEGF(1微克/毫升);第五组(n = 10):在受区床面局部应用VEGF(1微克/毫升);第六组(n = 16):未治疗的对照组。恢复5天后,测量皮瓣存活面积。皮瓣平均存活率从第二组的91%到第五组的78%不等,与对照组(平均存活率66%)相比,所有实验组的存活率均显著更高(第一至四组P<0.001,第五组P<0.05)。实验组之间唯一的显著差异是第二组和第五组的平均存活率之间(P<0.05)。组织学分析表明,实验组的肉芽组织和新血管形成在质量上更多。这些结果支持了这样一种观点,即VEGF通过诱导血管生成来挽救有缺氧损伤风险的组织,并且使用VEGF等生长因子有望作为一种提高皮肤存活率的方法。