최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기Journal of clinical medicine, v.9 no.1, 2020년, pp.59 -
Kang, Min Cheol (College of Pharmacy, Gachon University 191, Hambakmoero, Yeonsu-gu, Incheon 21936, Korea) , Yumnam, Silvia (mincjf07@gmail.com (M.C.K.)) , Park, Woo Sung (silviayumnam@gmail.com (S.Y.)) , So, Hae Min (College of Pharmacy, Gachon University 191, Hambakmoero, Yeonsu-gu, Incheon 21936, Korea) , Kim, Ki Hyun (mincjf07@gmail.com (M.C.K.)) , Shin, Meong Cheol (silviayumnam@gmail.com (S.Y.)) , Ahn, Mi-Jeong (College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, Jinju 52828, Korea) , Kim, Sun Yeou (pws8822@gmail.com (W.S.P.))
Ulmus parvifolia is one of the medicinal plants used traditionally for treatment of wounds. We intended to investigate the wound healing effect of the powder of Ulmus parvifolia (UP) root bark in a mouse wound healing model. We also determined the mechanisms of effects of U. parvifolia in skin and s...
1. Takeo M. Lee W. Ito M. Wound healing and skin regeneration Cold Spring Harb. Perspect. Med. 2015 5 a023267 10.1101/cshperspect.a023267 25561722
2. Martin P. Wound healing―Aiming for perfect skin regeneration Science 1997 276 75 81 10.1126/science.276.5309.75 9082989
3. Barrientos S. Stojadinovic O. Golinko M.S. Brem H. Tomic-Canic M. Growth factors and cytokines in wound healing Wound Repair Regen. 2008 16 585 601 10.1111/j.1524-475X.2008.00410.x 19128254
5. Olczyk P. Mencner L. Komosinska-Vassev K. The role of the extracellular matrix components in cutaneous wound healing BioMed Res. Int. 2014 2014 747584 10.1155/2014/747584 24772435
6. Wathoni N. Motoyama K. Higashi T. Okajima M. Kaneko T. Arima H. Enhancement of curcumin wound healing ability by complexation with 2-hydroxypropyl-gamma-cyclodextrin in sacran hydrogel film Int. J. Biol. Macromol. 2017 98 268 276 10.1016/j.ijbiomac.2017.01.144 28161536
7. Tasic-Kostov M. Arsic I. Pavlovic D. Stojanovic S. Najman S. Naumovic S. Tadic V. Towards a modern approach to traditional use: In vitro and in vivo evaluation of Alchemilla vulgaris L. gel wound healing potential J. Ethnopharmacol. 2019 238 111789 10.1016/j.jep.2019.03.016 30904703
8. Jun C.D. Pae H.O. Kim Y.C. Jeong S.J. Yoo J.C. Lee E.J. Choi B.M. Chae S.W. Park R.K. Chung H.T. Inhibition of nitric oxide synthesis by butanol fraction of the methanol extract of Ulmus davidiana in murine macrophages J. Ethnopharmacol. 1998 62 129 135 10.1016/S0378-8741(98)00063-4 9741885
9. Yang H.J. Ko B.S. Kwon D.Y. Lee H.W. Kim M.J. Ryuk J. Kang S. Kim D.S. Park S. Asian Elm tree inner bark prevents articular cartilage deterioration in ovariectomized obese rats with monoiodoacetate-induced osteoarthritis Menopause 2016 23 197 208 10.1097/GME.0000000000000521 26506502
10. Gardiner P. Kemper K.J. Herbs in pediatric and adolescent medicine Pediatr. Rev. 2000 21 44 57 10.1542/pir.21-2-44 10660631
11. Lee Y. Park H. Ryu H.S. Chun M. Kang S. Kim H.S. Effects of elm bark ( Ulmus davidiana var. japonica) extracts on the modulation of immunocompetence in mice J. Med. Food 2007 10 118 125 10.1089/jmf.2006.078 17472475
12. Mina S.A. Melek F.R. Adeeb R.M. Hagag E.G. LC/ESI-MS/MS profiling of Ulmus parvifolia extracts and evaluation of its anti-inflammatory, cytotoxic, and antioxidant activities Z. Naturforschung 2016 71 415 421 10.1515/znc-2016-0057 27197132
13. Moon Y.H. Rim G.R. Studies on the constituents of Ulmus parvifolia Korean J. Pharmacogn. 1995 26 1 7
14. Kim S.P. Lee S.J. Nam S.H. Friedman M. Elm Tree ( Ulmus parvifolia ) Bark Bioprocessed with Mycelia of Shiitake ( Lentinus edodes ) Mushrooms in Liquid Culture: Composition and Mechanism of Protection against Allergic Asthma in Mice J. Agric. Food Chem. 2016 64 773 784 10.1021/acs.jafc.5b04972 26807923
15. Cho S.K. Lee S.G. Kim C.J. Anti-inflammatory and analgesic activities of water extract of root bark of Ulmus parvifolia Korean J. Pharmacogn. 1996 27 274 281
17. Gould L. Abadir P. Brem H. Carter M. Conner-Kerr T. Davidson J. DiPietro L. Falanga V. Fife C. Gardner S. Chronic wound repair and healing in older adults: Current status and future research J. Am. Geriatr. Soc. 2015 63 427 438 10.1111/jgs.13332 25753048
18. Ghatnekar A.V. Elstrom T. Ghatnekar G.S. Kelechi T. Novel wound healing powder formulation for the treatment of venous leg ulcers J. Am. Coll. Certif. Wound Spec. 2011 3 33 41 10.1016/j.jcws.2011.09.004
19. Bylka W. Znajdek-Awizen P. Studzinska-Sroka E. Brzezinska M. Centella asiatica in cosmetology Postep. Dermatol. Alergol. 2013 30 46 49 10.5114/pdia.2013.33378
20. Zhao X. Yang Z. Gai G. Yang Y. Effect of superfine grinding on properties of ginger powder J. Food Eng. 2009 91 217 222 10.1016/j.jfoodeng.2008.08.024
21. Mehrtash M. Mohammadi R. Hobbenaghi R. Effect of adipose derived nucleated cell fractions with chitosan biodegradable film on wound healing in rats Wound Med. 2015 10 1 8 10.1016/j.wndm.2015.09.001
22. Fray M.J. Dickinson R.P. Huggins J.P. Occleston N.L. A potent, selective inhibitor of matrix metalloproteinase-3 for the topical treatment of chronic dermal ulcers J. Med. Chem. 2003 46 3514 3525 10.1021/jm0308038 12877590
23. Koshikawa N. Giannelli G. Cirulli V. Miyazaki K. Quaranta V. Role of cell surface metalloprotease MT1-MMP in epithelial cell migration over laminin-5 J. Cell Biol. 2000 148 615 624 10.1083/jcb.148.3.615 10662785
24. Sudbeck B.D. Pilcher B.K. Welgus H.G. Parks W.C. Induction and repression of collagenase-1 by keratinocytes is controlled by distinct components of different extracellular matrix compartments J. Biol. Chem. 1997 272 22103 22110 10.1074/jbc.272.35.22103 9268353
25. Salo T. Makela M. Kylmaniemi M. Autio-Harmainen H. Larjava H. Expression of matrix metalloproteinase-2 and -9 during early human wound healing Lab. Investig. 1994 70 176 182 8139259
26. Mulholland B. Tuft S.J. Khaw P.T. Matrix metalloproteinase distribution during early corneal wound healing Eye 2005 19 584 588 10.1038/sj.eye.6701557 15332107
27. Hattori N. Mochizuki S. Kishi K. Nakajima T. Takaishi H. D’Armiento J. Okada Y. MMP-13 plays a role in keratinocyte migration, angiogenesis, and contraction in mouse skin wound healing Am. J. Pathol. 2009 175 533 546 10.2353/ajpath.2009.081080 19590036
28. Nardini J.T. Chapnick D.A. Liu X. Bortz D.M. Modeling keratinocyte wound healing dynamics: Cell-cell adhesion promotes sustained collective migration J. Theor. Biol. 2016 400 103 117 10.1016/j.jtbi.2016.04.015 27105673
29. Eming S.A. Martin P. Tomic-Canic M. Wound repair and regeneration: Mechanisms, signaling, and translation Sci. Transl. Med. 2014 6 265sr266 10.1126/scitranslmed.3009337
30. Blakytny R. Jude E. The molecular biology of chronic wounds and delayed healing in diabetes Diabet. Med. 2006 23 594 608 10.1111/j.1464-5491.2006.01773.x 16759300
31. Heimler D. Mittempergher L. Buzzini P. Boddi V. Quantitative HPTLC separation of flavonoid glycosides in the taxonomy of elm (Ulmus spp.) Chromatographia 1990 29 16 20 10.1007/BF02261132
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
오픈액세스 학술지에 출판된 논문
※ AI-Helper는 부적절한 답변을 할 수 있습니다.