참고문헌
- Kim DW, Lee SH, Shin MJ, Kim K, Ku SK, Youn JK, Cho SB, Park JH, Lee CH, Son O, et al. PEP-1-FK506BP inhibits alkali burn-induced corneal inflammation on the rat model of corneal alkali injury. BMB Rep 2015;48:618-23. https://doi.org/10.5483/BMBRep.2015.48.11.041
- Hwang SH, Lee BH, Choi SH, Kim HJ, Won KJ, Lee HM, Rhim H, Kim HC, Nah SY. Effects of gintonin on the proliferation, migration, and tube formation of human umbilical-vein endothelial cells: involvement of lysophosphatidic-acid receptors andvascular-endothelial-growth-factor signaling. J Ginseng Res 2016;40:325-33. https://doi.org/10.1016/j.jgr.2015.10.002
- Watelet JB, Bachert C, Gevaert P, van Cauwenberge P. Wound healing of the respiratory mucosa: a review. Am J Rhinol 2002;16:77-84. https://doi.org/10.1177/194589240201600202
- Hosemann W, Wigand ME, Gode U, Langer F, Dunker I. Normal wound healing of the paranasal sinuses: clinical and experimental investigations. Eur Arch Otorhinolaryngol 1991;248:390-4. https://doi.org/10.1007/BF01463560
- Li J, Zhang YP, Kirsner RS. Angiogenesis in wound repair: angiogenic growth factors and the extracellular matrix. Microsc Res Tech 2003;60:107-14. https://doi.org/10.1002/jemt.10249
- Lee CS, Ghim J, Song P, Suh PG, Ryu SH. Loss of phospholipase D2 impairs VEGF-induced angiogenesis. BMB Rep 2016;49:191-6. https://doi.org/10.5483/BMBRep.2016.49.3.219
-
Choi SW, Lee KS, Lee JH, Kang HJ, Lee MJ, Kim HY, Park KI, Kim SL, Shin HK, Seo WD. Suppression of Akt-HIF-
$1{\alpha}$ signaling axis by diacetyl atractylodiol inhibits hypoxia-induced angiogenesis. BMB Rep 2016;49:508-13. https://doi.org/10.5483/BMBRep.2016.49.9.069 - Keck PJ, Hauser SD, Krivi G, Sanzo K, Warren T, Feder J, Connolly DT. Vascular permeability factor, an endothelial cell mitogen related to PDGF. Science 1989;246:1309-12. https://doi.org/10.1126/science.2479987
- Senger DR, Ledbetter SR, Claffey KP, Papadopoulos-Sergiou A, Peruzzi CA, Detmar M. Stimulation of endothelial cell migration by vascular permeability factor/vascular endothelial growth factor through cooperative mechanisms involving the alphavbeta3 integrin, osteopontin, and thrombin. Am J Pathol 1996;149:293-305.
-
Baek SH, Kim KI. Regulation of HIF-
$1{\alpha}$ stability by lysine methylation. BMB Rep 2016;49:245-6. https://doi.org/10.5483/BMBRep.2016.49.5.053 - Nissen NN, Polverini PJ, Koch AE, Volin MV, Gamelli RL, DiPietro LA. Vascular endothelial growth factor mediates angiogenic activity during the proliferative phase of wound healing. Am J Pathol 1998;152:1445-52.
- Schweigerer L, Neufeld G, Friedman J, Abraham JA, Fiddes J, Gospodarowicz D. Capillary endothelial cells express basic fibroblast growth factor, a mitogen that promotes their own growth. Nature 1987;325:257-9. https://doi.org/10.1038/325257a0
- Montesano R, Vassalli JD, Baird A, Guillemin R, Orci L. Basic fibroblast growth factor induces angiogenesis in vitro. Proc Natl Acad Sci USA 1986;83:7297-301. https://doi.org/10.1073/pnas.83.19.7297
- Pepper MS, Ferrara N, Orci L, Montesano R. Potent synergism between vascular endothelial growth factor and basic fibroblast growth factor in the induction of angiogenesis in vitro. Biochem Biophys Res Commun 1992;189:824-31. https://doi.org/10.1016/0006-291X(92)92277-5
- Goto F, Goto K, Weindel K, Folkman J. Synergistic effects of vascular endothelial growth factor and basic fibroblast growth factor on the proliferation and cord formation of bovine capillary endothelial cells within collagen gels. Lab Invest 1993;69:508-17.
- Ha JM, Baek SH, Kim YH, Jin SY, Lee HS, Kim SJ, Shin HK, Lee DH, Song SH, Kim CD, et al. Regulation of retinal angiogenesis by phospholipase C-b3 signaling pathway. Exp Mol Med 2016;48:e240. https://doi.org/10.1038/emm.2016.39
- Yang EY, Moses HL. Transforming growth factor beta 1-induced changes in cell migration, proliferation, and angiogenesis in the chicken chorioallantoic membrane. J Cell Biol 1990;111:731-41. https://doi.org/10.1083/jcb.111.2.731
- Madri JA, Pratt BM, Tucker AM. Phenotypic modulation of endothelial cells by transforming growth factor-beta depends upon the composition and organization of the extracellular matrix. J Cell Biol 1988;106:1375-84. https://doi.org/10.1083/jcb.106.4.1375
- Sankar S, Mahooti-Brooks N, Bensen L, McCarthy TL, Centrella M, Madri JA. Modulation of transforming growth factor beta receptor levels on microvascular endothelial cells during in vitro angiogenesis. J Clin Invest 1996;97:1436-46. https://doi.org/10.1172/JCI118565
- Case MA, Flinn KM, Jancaitis J, Alley A, Paxton A. Declining abundance of American ginseng (Panax quinquefolius L.) documented by herbarium specimens. Biol Conserv 2007;134:22-30. https://doi.org/10.1016/j.biocon.2006.07.018
- Kong BR, Park MJ, Min JW, Kim HB, Kim SH, Kim SY, Yang DC. Physicochemical characteristics of white, fermented and red ginseng extracts. J Ginseng Res 2008;32:238-43. https://doi.org/10.5142/JGR.2008.32.3.238
- Park JY, Choi P, Kim HK, Kang KS, Ham J. Increase in apoptotic effect of Panax ginseng by microwave processing in human prostate cancer cells: in vitro and in vivo studies. J Ginseng Res 2016;40:62-7. https://doi.org/10.1016/j.jgr.2015.04.007
- Choi KT. Botanical characteristics, pharmacological effects and medicinal components of Korean Panax ginseng C. A. Meyer. Acta Pharmacol Sin 2008;29:1109-18. https://doi.org/10.1111/j.1745-7254.2008.00869.x
- Shin BK, Kwon SW, Park JH. Chemical diversity of ginseng saponins from Panax ginseng. J Ginseng Res 2015;39:287-98. https://doi.org/10.1016/j.jgr.2014.12.005
- Han MS, Han IH, Lee D, An JM, Kim SN, Shin MS, Yamabe N, Hwang GS, Yoo HH, Choi SJ, et al. Beneficial effects of fermented black ginseng and its ginsenoside 20(S)-Rg3 against cisplatin-induced nephrotoxicity in LLC-PK1 cells. J Ginseng Res 2016;40:135-40. https://doi.org/10.1016/j.jgr.2015.06.006
- Roh SS, Park JH. The effects of ginseng radix preparata extract on antithrombotic activity. J East-West Med 2008;33:47-61.
-
Bak MJ, Jeong WS, Kim KB. Detoxifying effect of fermented black ginseng on
$H_{2}O_{2}$ -induced oxidative stress in HepG2 cells. Int J Mol Med 2014;34:1516-22. https://doi.org/10.3892/ijmm.2014.1972 - Singer AJ, Clark RA. Cutaneous wound healing. N Engl J Med 1999;341:738-46. https://doi.org/10.1056/NEJM199909023411006
- Watelet JB, Demetter P, Claeys C, Cauwenberge P, Cuvelier C, Bachert C. Wound healing after paranasal sinus surgery: neutrophilic inflammation influences the outcome. Histopathology 2006;48:174-81. https://doi.org/10.1111/j.1365-2559.2005.02310.x
- Plouet J, Schilling J, Gospodarowicz D. Isolation and characterization of a newly identified endothelial cell mitogen produced by AtT-20 cells. Embo J 1989;8:3801-6. https://doi.org/10.1002/j.1460-2075.1989.tb08557.x
- Shin EY, Kim SY, Kim EG. c-Jun N-terminal kinase is involved in motility of endothelial cell. Exp Mol Med 2001;33:276-83. https://doi.org/10.1038/emm.2001.45
- Lee J, Song J, Kwon ES, Jo S, Kang MK, Kim YJ, Hwang Y, Bae H, Kang TH, Chang S, et al. CTHRC1 promotes angiogenesis by recruiting Tie2-expressing monocytes to pancreatic tumors. Exp Mol Med 2016;48:e261. https://doi.org/10.1038/emm.2016.87
피인용 문헌
- Rg6, a rare ginsenoside, inhibits systemic inflammation through the induction of interleukin-10 and microRNA-146a vol.9, pp.None, 2018, https://doi.org/10.1038/s41598-019-40690-8
- Inhibitory effects of protopanaxatriol type ginsenoside fraction (Rgx365) on particulate matter-induced pulmonary injury vol.82, pp.5, 2018, https://doi.org/10.1080/15287394.2019.1596183
- Black Ginseng and Its Saponins: Preparation, Phytochemistry and Pharmacological Effects vol.24, pp.10, 2018, https://doi.org/10.3390/molecules24101856
- Pulmonary Protective Functions of Rare Ginsenoside Rg4 on Particulate Matter-induced Inflammatory Responses vol.24, pp.3, 2018, https://doi.org/10.1007/s12257-019-0096-4
- $ \text{Rg}\text{x}365$ , a Rare Protopanaxatriol-Type Ginsenoside Fraction from Black Ginseng, Suppresses Inflammatory Gene iNOS via the Iinhibition of p-STAT-1 and NF- $ \kappa $ B vol.48, pp.5, 2018, https://doi.org/10.1142/s0192415x20500536
- Panax ginseng Pharmacopuncture: Current Status of the Research and Future Challenges vol.10, pp.1, 2020, https://doi.org/10.3390/biom10010033
- Protective effects of phenolic acid extract from ginseng on vascular endothelial cell injury induced by palmitate via activation of PI3K/Akt/eNOS pathway vol.85, pp.3, 2020, https://doi.org/10.1111/1750-3841.15071
- In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-O-Glucoside and Quercetin 3-O-Glucoside Isolated from Salicornia herbacea vol.9, pp.3, 2018, https://doi.org/10.3390/pr9030483
- Identification of Phytoconstituents as Potent Inhibitors of Casein Kinase-1 Alpha Using Virtual Screening and Molecular Dynamics Simulations vol.13, pp.12, 2021, https://doi.org/10.3390/pharmaceutics13122157
- Characteristics of Black Ginseng (Panax ginseng C.A. Mayer) Production Using Ginseng Stored at Low Temperature after Harvest vol.11, pp.2, 2018, https://doi.org/10.3390/metabo11020098