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Regeneration Effects of Lespedeza cuneata Ethanol Extract on Experimental Open Wound in Rat

흰쥐의 외과적 창상에 대한 야관문 에탄올 추출물의 피부재생 효과

  • Kim, Dae-Ik (Oriental Medicine Industry Support Center) ;
  • Kim, Hye-Jeong (Dept. of Biomedical Laboratory Science, Kyungwoon University)
  • 김대익 ((재)대구테크노파크 한방산업지원센터) ;
  • 김혜정 (경운대학교 임상병리학과)
  • Received : 2013.12.04
  • Accepted : 2014.02.18
  • Published : 2014.04.30

Abstract

The purpose of this study was to examine the skin regeneration ability of Lespedeza cuneata extract (LC) as well as verify its wound healing effects on an open wound in rats. Rats were divided into six groups (NO, saline treated group; CO, 1% carboxy methyl cellulose (CMC) treated group; PC, fucidin treated group; LCL, 1% LC treated group; LCM, 3% LC treated group; LCH, 5% LC treated group), and the experimental material was applied for 5 weeks. Elastase inhibition rate of the LCM group was 2.7% lower than that of butylated hydroxy anisole (BHA), which is an antioxidant. Futher, the collagenase inhibition rate of the LCM showed 7% higher activity than that of BHA. The left wound areas in the LCL group, LCM group, and LCH group after the 21st day were noticeably reduced in wound area by 54.2%, 53.5%, and 48.7%, respectively, compared to the CO group. This suggests that Lespedeza cuneata extract has healing effects on surgical wounds by promoting regeneration of skin epithelial tissue and synthesis of collagen.

야관문 추출물의 피부재생능력을 알아보고, 창상을 유발한 실험동물 모델에서 창상 치유 효과를 검증하고자 6개 군(NO, CO, PC, LCL, LCM, LCH)으로 나누어 5주간 실험하였다. Elastase 저해 활성을 평가한 결과 LCM군에서 항산화제인 BHA보다 2.7%($52.39{\pm}4.52$ vs $53.88{\pm}1.85$) 낮은 수치를 나타내었으며, collagenase 저해 활성을 평가한 결과 LCM군에서 BHA보다 7%($37.68{\pm}2.91$ vs $35.19{\pm}7.80$) 더 높은 활성을 나타내었다. 창상유발 21일에 LCL군, LCM군 및 LCH군의 왼쪽 창상 면적은 CO군과 비교하여 각각 54.2%, 53.5% 및 48.7% 현저한 창상면적 감소를 보였다. 이로서 야관문 추출물은 피부상피조직의 재생과 교원질의 합성을 도와 외과적 창상에 치료 효과가 있는 것으로 판단된다.

Keywords

References

  1. Muralidhar A, Sudhakar Babu K, Ravi Sankar T, Reddanna P, Latha J. 2011. Evaluation of wound healing properties of bioactive fractions from the extract of Butea monosperma (lam) stem bark. Int J Phytomed 3: 41-49.
  2. Odimegwu DC, Ibezim EC, Esimone CO, Nworu CS, Okoye FBC. 2008. Wound healing and antibacterial activities of the extract of Dissotis theifolia (Melastomataceae) stem formulated in a simple ointment base. J Med Plants Res 2:11-16.
  3. Gopalakrishnan S, Rajameena R. 2012. Evaluation of ethanol extract of Desmodium gyrans DC leaves on wound healing activity in rats. Pharm Anal Acta 3: 169.
  4. Buckley A, Davidson JM, Kamerath CD, Wolt TB, Woodward SC. 1985. Sustained release of epidermal growth factor accelerates wound repair. Proc Natl Acad Sci 82: 7340-7344. https://doi.org/10.1073/pnas.82.21.7340
  5. Karodi R. 2009. Evaluation of the wound healing activity of a crude extract of Rubia cordifolia L. (Indian madder) in mice. IJARNP 2: 12-18.
  6. Han SK. 2011. Wound coverage using advanced technology in Korea. J Korean Med Assoc 54: 594-603. https://doi.org/10.5124/jkma.2011.54.6.594
  7. Kim DI. 2010. Healing effects of ginsenoside Rg1 on experimental open wound in rat. J Korean Soc Food Sci Nurt 39: 1452-1458. https://doi.org/10.3746/jkfn.2010.39.10.1452
  8. Sharma B, Kumar P. 2009. Extraction and pharmacological evaluation of some extracts of Tridax procumbens and Capparis decidua. IJARNP 1: 5-12.
  9. Moon KH, Park HJ. 2010. Wound healing effects of Allium cepa L. in dogs. J Vet Clin 27: 382-385.
  10. Kim HJ, Kim KS, Kim DI. 2012. Inhibitory effects of Lespedeza cuneata ethanol extract on ultraviolet-induced photo aging. J Korean Soc Food Sci Nutr 41: 1540-1545. https://doi.org/10.3746/jkfn.2012.41.11.1540
  11. Numata A, Hokimoto K, Shimada A, Yamaguchi H, Takaishi K. 1979. Plant constituents biologically active to insect. I. Feeding stimulants for the larvae of the yellow butterfly, Eurema hecabe mandarina (1). Chem Pharm Bull 27: 602-608. https://doi.org/10.1248/cpb.27.602
  12. Kim YH, Ryu SN. 2008. Antioxidant activity of methanol extract from aerial parts in Lespedeza cuneata G. Don. Korean J Crop Sci 53: 121-123.
  13. James AEK, Timothy DW, Gorden L. 1996. Inhibition of human leukocyte and porcin pancreatic elastase by homologues of bovine pancreatic tyrosin inhibitors. Biochemistry 35: 9090-9096. https://doi.org/10.1021/bi953013b
  14. Sawabe Y, Yamasaki K, Iwagami S, Kajimura K, Nakagomi K. 1998. Inhibitory effects of natural medicines on the enzymes related to the skin. Yakugaku Zasshi 118: 423-429.
  15. Iwona M, Edyta GD. 2011. Proangiogenic activity of plant extracts in accelerating wound healing - a new face of old phytomedicines. Acta Biochimica Polonica 58: 449-460.
  16. Lewis JS, Lee JA, Underwood JC, Harris AL, Lewis CE. 1999. Macrophage responses to hypoxia: relevance to disease mechanisms. J Leukoc Biol 66: 889-900.
  17. Kurkinen M, Vaheri A, Roberts PJ, Stenman S. 1980. Sequential appearance of fibronectin and collagen in experimental granulation tissue. Lab Invest 43: 47-51.
  18. Woodley DT, O'Keefe EJ, Prunieras M. 1985. Cutaneous wound healing: a model for cell-matrix interactions. J Am Acad Dermatol 112: 420-433.
  19. Booth BA, Polak KL, Uitto J. 1980. Collagen biosynthesis by human skin fibroblasts: I. Optimization of the culture conditions for synthesis of type I and type III procollagens. Biochim Biophys Acta 607: 145-160. https://doi.org/10.1016/0005-2787(80)90228-2
  20. Abercrombie M, Flint MH, James DW. 1956. Wound contraction in relation to collagen formation in scorbutic guinea pigs. J Embryol Exp Morph 4: 167-175.
  21. Brody GS, Peng ST, Landel RF. 1981. The etiollogy of hypertrophic scaicontracture another view. Plast Reconstr Surg 67: 673-684. https://doi.org/10.1097/00006534-198105000-00021
  22. Lim HJ, Kim HT, Oh EJ, Choi JH, Ghim HD, Pyun DG, Lee SB, Chung DJ, Chung HY. 2010. Effect of newly developed pectin/CMC dressing materials on three different types of wound model. Polymer (Korea) 34: 363-368.
  23. Hasan W, Zhang R, Lin M, Warn JD, Smith PG. 2000. Coordinate expression of NGF and alpha-smooth muscle actin mRNA and protein in cutaneous wound tissue of developing and adult rats. Cell Tissue Res 300: 97-109.
  24. Sayah DN, Soo C, Shaw WW, Watson J, Messadi D, Longaker MT, Zhang X, Ting K. 1999. Downregulation of apoptosis-related genes in keloid tissues. J Surg Res 87:209-216. https://doi.org/10.1006/jsre.1999.5761
  25. Bae TH, Kim WS, Kim HK, Kim MK. 2009. Effect of verapamil on scar formation in early wound scarring of the rabbit ear. J Korean Soc Plast Reconstr Surg 36: 11-18.
  26. Hiroshi U, Haruo Y, Ichiro T, Naoki K, Mitsunobu M, Masahiro O, Tsuyoshi K, Toru F. 1999. Accelerating effects of chitosan for healing at early phase of experimental open wound in dogs. Biomaterials 20: 1407-1414. https://doi.org/10.1016/S0142-9612(99)00046-0
  27. Lim AK, Kim KS, Park SJ, Hong JH, Choi HJ, Kim DI. 2010. Healing effects of ginsenoside Rg1 on experimental open wound in rat. J Korean Soc Food Sci Nutr 39: 1452-1458. https://doi.org/10.3746/jkfn.2010.39.10.1452
  28. Sen CK, Khanna S, Gordillo G, Bagchi D, Bagchi M, Roy S. 2002. Oxygen, oxidants, and antioxidants in wound healing: an emerging paradigm. Ann N Y Acad Sci 957: 239-249. https://doi.org/10.1111/j.1749-6632.2002.tb02920.x

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