Khanna Savita, Venojarvi Mika, Roy Sashwati, Sharma Nidhi, Trikha Prashant, Bagchi Debasis, Bagchi Manashi, Sen Chandan K
Department of Surgery, Heart and Lung Research Institute, The Ohio State University Medical Center, Columbus, OH 43210, USA.
Free Radic Biol Med. 2002 Oct 15;33(8):1089-96. doi: 10.1016/s0891-5849(02)00999-1.
Angiogenesis plays a central role in wound healing. Among many known growth factors, vascular endothelial growth factor (VEGF) is believed to be the most prevalent, efficacious, and long-term signal that is known to stimulate angiogenesis in wounds. The wound site is rich in oxidants, such as hydrogen peroxide, mostly contributed by neutrophils and macrophages. We proposed that oxidants in the wound microenvironment support the repair process. Proanthocyanidins or condensed tannins are a group of biologically active polyphenolic bioflavonoids that are synthesized by many plants. Previously we have reported that a grape seed proanthycyanidin extract containing 5000 ppm resveratrol (GSPE) potently upregulates oxidant and tumor necrosis factor-alpha inducible VEGF expression in human keratinocytes (Free Radic. Biol. Med. 31:38-42, 2001). Our current objective was to follow up on that finding and test whether GSPE influences dermal wound healing in vivo. First, using a VEGF promoter-driven luciferase reporter construct we observed that the potentiating effect of GSPE on inducible VEGF expression is at the transcriptional level. The reporter assay showed that GSPE alone is able to drive VEGF transcription. Next, two dermal excisional wounds were inflicted on the back of mice and the wounds were left to heal by secondary intention. Topical application of GSPE accelerated wound contraction and closure. GSPE treatment was associated with a more well-defined hyperproliferative epithelial region, higher cell density, enhanced deposition of connective tissue, and improved histological architecture. GSPE treatment also increased VEGF and tenascin expression in the wound edge tissue. Tissue glutathione oxidation and 4-hydroxynonenal immunostaining results supported that GSPE application enhanced the oxidizing environment at the wound site. Oxidants are known to promote both VEGF as well as tenascin expression. In summary, our current study provides firm evidence to support that topical application of GSPE represents a feasible and productive approach to support dermal wound healing.
血管生成在伤口愈合过程中起着核心作用。在众多已知的生长因子中,血管内皮生长因子(VEGF)被认为是最普遍、最有效且能长期刺激伤口血管生成的信号。伤口部位富含氧化剂,如过氧化氢,主要由中性粒细胞和巨噬细胞产生。我们提出伤口微环境中的氧化剂有助于修复过程。原花青素或缩合单宁是一类由多种植物合成的具有生物活性的多酚类生物黄酮。此前我们报道过,一种含有5000 ppm白藜芦醇的葡萄籽原花青素提取物(GSPE)能有效上调人角质形成细胞中氧化剂和肿瘤坏死因子-α诱导的VEGF表达(《自由基生物学与医学》31:38 - 42, 2001)。我们当前的目标是跟进这一发现,并测试GSPE是否会影响体内皮肤伤口的愈合。首先,使用VEGF启动子驱动的荧光素酶报告基因构建体,我们观察到GSPE对诱导型VEGF表达的增强作用是在转录水平。报告基因检测表明,单独的GSPE就能驱动VEGF转录。接下来,在小鼠背部造成两个皮肤切除伤口,让伤口通过二期愈合自行愈合。局部应用GSPE加速了伤口收缩和闭合。GSPE治疗与更明确的上皮细胞过度增殖区域、更高的细胞密度、结缔组织沉积增加以及组织学结构改善相关。GSPE治疗还增加了伤口边缘组织中VEGF和腱生蛋白的表达。组织谷胱甘肽氧化和4 - 羟基壬烯醛免疫染色结果支持了GSPE的应用增强了伤口部位的氧化环境。已知氧化剂能促进VEGF以及腱生蛋白的表达。总之,我们当前的研究提供了确凿证据,支持局部应用GSPE是一种支持皮肤伤口愈合的可行且有效的方法。