참고문헌
- Gesler WM. Therapeutic landscapes: medical issues in light of the new cultural geography. Soc Sci Med 1992;34:735-46. https://doi.org/10.1016/0277-9536(92)90360-3
- Wojcikowski K, Johnson DW, Gobe G. Medicinal herbal extracts-renal friend or foe?: Part two. Herbal extracts with potential renal benefits. Nephrology 2004;9:400-5. https://doi.org/10.1111/j.1440-1797.2004.00355.x
- Ceylan-Isik AF, Fliethman RM, Wold LE, Ren J. Herbal and traditional Chinese medicine for the treatment of cardiovascular complications in diabetes mellitus. Curr Diabetes Rev 2008;4:320-8. https://doi.org/10.2174/157339908786241142
- Li X, Hassoun HT, Santora R, Rabb H. Organ crosstalk: the role of the kidney. Curr Opin Crit Care 2009;15:481-7. https://doi.org/10.1097/MCC.0b013e328332f69e
- Forbes JM, Coughlan MT, Cooper ME. Oxidative stress as a major culprit in kidney disease in diabetes. Diabetes 2008;57:1446-54. https://doi.org/10.2337/db08-0057
- Nistala R, Whaley-Connell A, Sowers JR. Redox control of renal function and hypertension. Antioxid Redox Signal 2008;10:2047-89. https://doi.org/10.1089/ars.2008.2034
- Heyman SN, Rosen S, Rosenberger C. A role for oxidative stress. Contrib Nephrol 2011;174:138-48.
- Manucha W, Valles PG. Apoptosis modulated by oxidative stress and inflammation during obstructive nephropathy. Inflamm Allergy Drug Targets 2012;11:303-12. https://doi.org/10.2174/187152812800958997
- Ozbek E. Induction of oxidative stress in kidney. Int J Nephrol 2012;2012:465897.
- Li JM, Shah AM. ROS generation by nonphagocytic NADPH oxidase: potential relevance in diabetic nephropathy. J Am Soc Nephrol 2003;14:S221-6. https://doi.org/10.1097/01.ASN.0000077406.67663.E7
- Gokhan SH. Endoplasmic reticulum stress and the inflammatory basis of metabolic disease. Cell 2010;140:900-17. https://doi.org/10.1016/j.cell.2010.02.034
-
Chung HW, Lim JH, Kim MY, Shin SJ, Chung S, Choi BS, Kim HW, Kim YS, Park CW, Chang YS. High-fat diet-induced renal cell apoptosis and oxidative stress in spontaneously hypertensive rat are ameliorated by fenofibrate through the
$PPAR{\alpha}-FoxO3a-PGC-1{\alpha}$ pathway. Nephrol Dial Transplant 2012;27:2213-25. https://doi.org/10.1093/ndt/gfr613 - Lim JH, Kim EN, Kim MY, Chung S, Shin SJ, Kim HW, Yang CW, Kim YS, Chang YS, Park CW, et al. Age-associated molecular changes in the kidney in aged mice. Oxid Med Cell Longev 2012;2012:171383.
- Mathushima H, Yonemura K, Ohishi K, Hishida A. The role of oxygen free radicals in cisplatin-induced acute renal failure in rats. J Lab Clin Med 1998;131:518-26. https://doi.org/10.1016/S0022-2143(98)90060-9
- Kaushal GP, Kaushal V, Hong X, Shah SV. Role and regulation of activation of caspases in cisplatin-induced injury to renal tubular epithelial cells. Kidney Int 2001;60:1726-36. https://doi.org/10.1046/j.1523-1755.2001.00026.x
- Basnakian AG, Apostolov EO, Yin X, Napirei M, Mannherz HG, Shah SV. Cisplatin nephrotoxicity is mediated by deoxyribonuclease I. J Am Soc Nephrol 2005;16:697-702. https://doi.org/10.1681/ASN.2004060494
- Mitazaki S, Honma S, Suto M, Kato N, Hiraiwa K, Yoshida M, Abe S. Interleukin-6 plays a protective role in development of cisplatin-induced acute renal failure through upregulation of anti-oxidative stress factors. Life Sci 2011;88:1142-8. https://doi.org/10.1016/j.lfs.2011.04.016
- Yang F, Long W, Xuechuan H, Xueqin L, Hongyun M, Yonghui D. Upregulation of Fas in epithelial ovarian cancer reverses the development of resistance to cisplatin. BMB Rep 2015;48:30-5. https://doi.org/10.5483/BMBRep.2015.48.1.042
- Kitagawa I, Taniyama T, Shibuya H, Noda T, Yoshikawa M. Chemical studies on crude drug processing: V. On the constituents of ginseng radix rubra (2): comparison of the constituents of white ginseng and red ginseng prepared from the same Panax ginseng root. Yakugaku Zasshi 1987;107:495-505. https://doi.org/10.1248/yakushi1947.107.7_495
- Wang CZ, Zhang B, Song WX, Wang A, Ni M, Luo X, Aung HH, Xie JT, Tong R, He TC, et al. Steamed American ginseng berry: ginsenoside analyses and anticancer activities. J Agric Food Chem 2006;54:9936-42. https://doi.org/10.1021/jf062467k
- Kang KS, Kim HY, Baek SH, Yoo HH, Park JH, Yokozawa T. Study on the hydroxyl radical scavenging activity changes of ginseng and ginsenoside-Rb2 by heat processing. Biol Pharm Bull 2007;30:724-8. https://doi.org/10.1248/bpb.30.724
-
Bak MJ, Jeong WS, Kim KB. Detoxifying effect of fermented black ginseng on
$H_2O_2$ -induced oxidative stress in HepG2 cells. Int J Mol Med 2014;34:1516-22. https://doi.org/10.3892/ijmm.2014.1972 - Lee W, Park SH, Lee S, Chung BC, Song MO, Song KI, Ham J, Kim SN, Kang KS. Increase in antioxidant effect of ginsenoside Reealanine mixture by Maillard reaction. Food Chem 2012;135:2430-5. https://doi.org/10.1016/j.foodchem.2012.06.108
- Kaneko H, Nakanishi K. Proof of the mysterious efficacy of ginseng; basic and clinical trials: clinical effects of medical ginseng, Korean red ginseng: specifically, its anti-stress action for prevention of disease. J Pharmacol Sci 2004;95:158-62. https://doi.org/10.1254/jphs.FMJ04001X5
- Kang KS, Yamabe N, Kim HY, Park JH, Yokozawa T. Therapeutic potential of 20(S)-ginsenoside Rg3 against streptozotocin-induced diabetic renal damage in rats. Eur J Pharmacol 2008;591:266-72. https://doi.org/10.1016/j.ejphar.2008.06.077
- Byeon SE, Lee J, Kim JH, Yang WS, Kwak YS, Kim SY, Choung ES, Rhee MH, Cho JY. Molecular mechanism of macrophage activation by red ginseng acidic polysaccharide from Korean red ginseng. Mediators Inflamm 2012;2012:732860.
- Ramesh T, Kim SW, Hwang SY, Sohn SH, Yoo SK, Kim SK. Panax ginseng reduces oxidative stress and restores antioxidant capacity in aged rats. Nutr Res 2012;32:718-26. https://doi.org/10.1016/j.nutres.2012.08.005
- Park HJ, Shim HS, Kim KS, Shim I. The protective effect of black ginseng against transient focal ischemia-induced neuronal damage in rats. Korean J Physiol Pharmacol 2011;15:333-8. https://doi.org/10.4196/kjpp.2011.15.6.333
- Lee HS, Kim MR, Park Y, Park HJ, Chang UJ, Kim SY, Suh HJ. Fermenting red ginseng enhances its safety and efficacy as a novel skin care anti-aging ingredient: in vitro and animal study. J Med Food 2012;15:1015-23. https://doi.org/10.1089/jmf.2012.2187
- Singleton VL, Orthofer R, Lamuela-Raventos RM. Analysis of total phenols and other oxidation substrates and antioxidants by means of FolineCiocalteu reagent. Methods Enzymol 1999;299:152-78.
- Hatano T, Edamatsu R, Hiramatsu M, Mori A, Fujita Y, Yasuhara T, Yoshida T, Okuda T. Effects of the interaction of tannins with co-existing substances: VI. Effects of tannins and related polyphenols on superoxide anion radical, and on 1,1-diphenyl-2-picrylhydrazyl radical. Chem Pharm Bull 1989;37:2016-21. https://doi.org/10.1248/cpb.37.2016
- Park JY, Choi P, Kim T, Ko H, Kim HK, Kang KS, Ham J. Protective effects of processed ginseng and its active ginsenosides on cisplatin-induced nephrotoxicity: in vitro and in vivo studies. J Agric Food Chem 2015;63:5964-9. https://doi.org/10.1021/acs.jafc.5b00782
- 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 2017;42(2):135-40.
- Oh JS, Lee SR, Hwang KT, Ji GE. The anti-obesity effects of the dietary combination of fermented red ginseng with levan in high fat diet mouse model. Phytother Res 2014;28(4):617-22. https://doi.org/10.1002/ptr.5042
- Takeda H, Sadakane C, Hattori T, Katsurada T, Ohkawara T, Nagai K, Asaka M. Rikkunshito, an herbal medicine, suppresses cisplatin-induced anorexia in rats via 5-HT2 receptor antagonism. Gastroenterology 2008;134:2004-13. https://doi.org/10.1053/j.gastro.2008.02.078
- Kang KS, Ham J, Kim YJ, Park JH, Cho EJ, Yamabe N. Heat-processed Panax ginseng and diabetic renal damage: active components and action mechanism. J Ginseng Res 2013;37:379-88. https://doi.org/10.5142/jgr.2013.37.379
- Yamabe N, Kim YJ, Lee S, Cho EJ, Park SH, Ham J, Kim HY, Kang KS. Increase in antioxidant and anticancer effects of ginsenoside Reelysine mixture by Maillard reaction. Food Chem 2013;138:876-83. https://doi.org/10.1016/j.foodchem.2012.12.004
- 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
- Zhu QY, Hackman RM, Ensunsa JL, Holt RR, Keen CL. Antioxidant activities of oolong tea. J Agric Food Chem 2002;50:6929-34. https://doi.org/10.1021/jf0206163
- Cai Y, Luo Q, Sun M, Corke H. Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer. Life Sci 2004;74:2157-84. https://doi.org/10.1016/j.lfs.2003.09.047
- Tortorici MA, Nolin TD. Kidney function assessment and its role in drug development, review and utilization. Expert Rev Clin Pharmacol 2014;7:523-32. https://doi.org/10.1586/17512433.2014.922865
- Bratton SB, Cohen GM. Apoptotic death sensor: an organelle's alter ego? Trends Pharmacol Sci 2001;22:306-15. https://doi.org/10.1016/S0165-6147(00)01718-1
- Razzaque MS. Cisplatin nephropathy: is cytotoxicity avoidable? Nephrol Dial Transplant 2007;22:2112-6. https://doi.org/10.1093/ndt/gfm378
- Domitrovic R, Cvijanovic O, Pugel EP, Zagorac GB, Mahmutefendic H, Skoda M. Luteolin ameliorates cisplatin-induced nephrotoxicity in mice through inhibition of platinum accumulation, inflammation and apoptosis in the kidney. Toxicology 2013;310:115-23. https://doi.org/10.1016/j.tox.2013.05.015
피인용 문헌
- Stimulation of Innate Immune Function by Panax ginseng after Heat Processing vol.66, pp.18, 2017, https://doi.org/10.1021/acs.jafc.8b00152
- Protective Role of Natural Products in Cisplatin-Induced Nephrotoxicity vol.19, pp.14, 2019, https://doi.org/10.2174/1389557519666190320124438
- Ameliorative effect of selenium nanoparticles and fish oil on cisplatin and gamma irradiation-induced nephrotoxicity in male albino rats vol.42, pp.1, 2019, https://doi.org/10.1080/01480545.2018.1497050
- All-trans retinoic acid prevents cisplatin-induced nephrotoxicity in rats vol.392, pp.2, 2017, https://doi.org/10.1007/s00210-018-01603-0
- Black Ginseng and Its Saponins: Preparation, Phytochemistry and Pharmacological Effects vol.24, pp.10, 2017, https://doi.org/10.3390/molecules24101856
- Ginsenoside Rb3 provides protective effects against cisplatin‐induced nephrotoxicity via regulation of AMPK‐/mTOR‐mediated autophagy and inhibition of apoptosis in vitro and in vivo vol.52, pp.4, 2017, https://doi.org/10.1111/cpr.12627
- Coleus amboinicus extract increases transforming growth factor-1β expression in Wistar rats with cisplatin-induced nephropathy vol.12, pp.8, 2017, https://doi.org/10.14202/vetworld.2019.1346-1351
- Antiviral Effect of Ginsenoside Rb2 and Rb3 Against Bovine Viral Diarrhea Virus and Classical Swine Fever Virus in vitro vol.8, pp.None, 2017, https://doi.org/10.3389/fvets.2021.764909
- The cardio and renoprotective role of ginseng against epinephrine-induced myocardial infarction in rats: Involvement of angiotensin II type 1 receptor/protein kinase C vol.8, pp.None, 2021, https://doi.org/10.1016/j.toxrep.2021.04.008
- Endoplasmic Reticulum Stress-Activated PERK-eIF2α-ATF4 Signaling Pathway is Involved in the Ameliorative Effects of Ginseng Polysaccharides against Cisplatin-Induced Nephrotoxicity in Mice vol.6, pp.13, 2017, https://doi.org/10.1021/acsomega.0c06339