Dermal wound healing properties of redox-active grape seed proanthocyanidins

被引:147
作者
Khanna, S
Venojarvi, M
Roy, S
Sharma, N
Trikha, P
Bagchi, D
Bagchi, M
Sen, CK
机构
[1] Ohio State Univ, Med Ctr, Mol Med Lab, Heart & Lung Res Inst 512,Dept Surg, Columbus, OH 43210 USA
[2] Univ Kuopio, Dept Physiol, FIN-70211 Kuopio, Finland
[3] Creighton Univ, Med Ctr, Sch Pharm & Hlth Profess, Omaha, NE USA
关键词
wound healing; angiogenesis; skin; redox; tannins; oxidant;
D O I
10.1016/S0891-5849(02)00999-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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-a 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. (C) 2002 Elsevier Science Inc.
引用
收藏
页码:1089 / 1096
页数:8
相关论文
共 41 条
[1]
Basal layer of epithelium expresses tenascin mRNA during healing of incisional skin wounds [J].
Aukhil, I ;
Sahlberg, C ;
Thesleff, I .
JOURNAL OF PERIODONTAL RESEARCH, 1996, 31 (02) :105-112
[2]
[3]
Protective effects of grape seed proanthocyanidins and selected antioxidants against TPA-induced hepatic and brain lipid peroxidation and DNA fragmentation, and peritoneal macrophage activation in mice [J].
Bagchi, D ;
Garg, A ;
Krohn, RL ;
Bagchi, M ;
Bagchi, DJ ;
Balmoori, J ;
Stohs, SJ .
GENERAL PHARMACOLOGY, 1998, 30 (05) :771-776
[4]
Bagchi D, 1997, RES COMMUN MOL PATH, V95, P179
[5]
Protective effects of antioxidants against smokeless tobacco-induced oxidative stress and modulation of Bcl-2 and p53 genes in human oral keratinocytes [J].
Bagchi, M ;
Kuszynski, CA ;
Balmoori, J ;
Joshi, SS ;
Stohs, SJ ;
Bagchi, D .
FREE RADICAL RESEARCH, 2001, 35 (02) :181-194
[6]
Smokeless tobacco, oxidative stress, apoptosis, and antioxidants in human oral keratinocytes [J].
Bagchi, M ;
Balmoori, J ;
Bagchi, D ;
Ray, SD ;
Kuszynski, C ;
Stohs, SJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (7-8) :992-1000
[7]
Bancroft J.D., 1990, THEORY PRACTICE HIST, V3rd
[8]
Barrett B, 2001, WMJ, V100, P20
[9]
Electron paramagnetic resonance studies of radical species of proanthocyanidins and gallate esters [J].
Bors, W ;
Michel, C ;
Stettmaier, K .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 374 (02) :347-355
[10]
BOUKAMP P, 1988, J CELL BIOL, V106, P161