과제정보
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MOE) (No. 2017R1D1A3B03031863).
참고문헌
- Kim TY, Kim DU, Kang Y. New insight of the needs for standardization on the processing of herbal medicines: Concentrated on standard terminology. Korean Herb Med Inf. 2019 ; 7(1) : 41-69. https://doi.org/10.22674/KHMI-7-1-4
- Kim IR. Studies about the origin, storage, cutting, processing and decokting methods of medicinal herbs. Seoul : Korea Institute of Oriental Medicine. 1998 : 1-3.
- Kim IR. A research on the origin and daily dose of Gardeniae Fructus in Shanghanlun. Kor J Herbol. 2011 ; 26(4) : 155-61. https://doi.org/10.6116/KJH.2011.26.4.155
- Shin YW, Kim DH, Kim NJ. Studies on the processing of crude drugs(7) - On the constituents and biological activities of Gardeniae Fructus by processing. Kor J Pharmacogn. 2003 ; 34(1) : 45-54.
- Alavizadeh SH, Hosseinzadeh H. Bioactivity assessment and toxicity of crocin: a comprehensive review. Food Chem Toxicol. 2014 ; 64 : 65-80. https://doi.org/10.1016/j.fct.2013.11.016
- Xiao W, Li S, Wang S, Ho CT. Chemistry and bioactivity of Gardenia jasminoides. J Food Drug Anal. 2017 ; 25(1) : 43-61. https://doi.org/10.1016/j.jfda.2016.11.005
- Kim KH, Kim SM, Shin SH, Lee YJ, Baek WS. Quality monitoring of specification standard of Gardeniae Fructus in the Korean pharmacopoeia and studies HPLC standard chromatogram. Kor J Herbol. 2017 ; 32(2) : 97-105. https://doi.org/10.6116/KJH.2017.32.2.97
- Lee JH, Lee DU, Jeong CS. Gardenia jasminoides Ellis ethanol extract and its constituents reduce the risks of gastritis and reverse gastric lesions in rats. Food Chem Toxicol. 2009 ; 47(6) : 1127-31. https://doi.org/10.1016/j.fct.2009.01.037
- Mahajan L, Verma PK, Raina R, Pankaj NK, Sood S, Singh M. Alteration in thiols homeostasis, protein and lipid peroxidation in renal tissue following subacute oral exposure of imidacloprid and arsenic in Wistar rats. Toxicol Rep. 2018 ; 5 : 1114-9. https://doi.org/10.1016/j.toxrep.2018.11.003
- Poli G, Leonarduzzi G, Biasi F, Chiarpotto E. Oxidative stress and cell signalling. Curr Med Chem. 2004 ; 11(9) : 1163-82. https://doi.org/10.2174/0929867043365323
- Fulda S, Gorman A, Hori O, Samali A. Cellular stress responses: Cell survival and cell death. Int J Cell Biol. 2010 ; 2010 : 214074.
- Han L, Xia X, Xiang X, Huang F, Zhang Z. Protective effects of canolol against hydrogen peroxide-induced oxidative stress in AGS cells. RSC Adv. 2017 ; 7 : 42826-32. https://doi.org/10.1039/C7RA08524A
- Davies GR, Simmonds NJ, Stevens TR, Sheaff MT, Banatvala N, Laurenson IF, Blake DR, Rampton DS. Helicobacter pylori stimulates antral mucosal reactive oxygen metabolite production in vivo. Gut. 1994 ; 35 : 179-85. https://doi.org/10.1136/gut.35.2.179
- Hussar P. Apoptosis regulators Bcl-2 and caspase-3. Encyclopedia. 2022 ; 2 : 1624-36. https://doi.org/10.3390/encyclopedia2040111
- Mates JM, Sanchez-Jimenez FM. Role of reactive oxygen species in apoptosis: implications for cancer therapy. Int J Biochem Cell Biol. 2000 ; 32 : 157-70. https://doi.org/10.1016/S1357-2725(99)00088-6
- Simon HU, Haj-Yehia A, Levi-Schaffer F. Role of reactive oxygen species (ROS) in apoptosis induction. Apoptosis. 2000 ; 5 : 415-8. https://doi.org/10.1023/a:1009616228304
- Crane D, Haussinger D, Graf P, Sies H. Decreased flux through pyruvate dehydrogenase by thiol oxidation during t-butyl hydroperoxide metabolism in perfused rat liver. Hoppe Seylers Z Physiol Chem. 1983 ; 364(8) : 977-87. https://doi.org/10.1515/bchm2.1983.364.2.977
- An I, Kim SC, Byun SH, Lee JR, Park SJ. Antiinflammatory effect of the processed Gardeniae Fructus in LPS-induced macrophages. Herb Formula Sci. 2019 ; 27(4) : 245-55. https://doi.org/10.14374/HFS.2019.27.4.245
- Selvakumar GP, Manivasagam T, Rekha KR, Jayaraj RL, Elangovan N. Escin, a novel triterpene, mitigates chronic MPTP/p-induced dopaminergic toxicity by attenuating mitochondrial dysfunction, oxidative stress, and apoptosis. J Mol Neurosci. 2015 ; 55 : 184-97. https://doi.org/10.1007/s12031-014-0303-x
- Imberti R, Nieminen AL, Herman B, Lemasters JJ. Mitochondrial and glycolytic dysfunction in lethal injury to hepatocytes by t-butylhydroperoxide: protection by fructose, cyclosporin A and trifluoperazine. J Pharmacol Exp Ther. 1993 ; 265(1) : 392-400.
- Marsden VS, Ekert PG, Delft MV, Vaux DL, Adams JM, Strasser A. Bcl-2-regulated apoptosis and cytochrome c release can occur independently of both caspase-2 and caspase-9. J Cell Biol. 2004 ; 65(6) : 775-80. https://doi.org/10.1083/jcb.200312030
- Brunelle JK, Letai A. Control of mitochondrial apoptosis by the Bcl-2 family. J Cell Sci. 2009 ; 122 : 437-41. https://doi.org/10.1242/jcs.031682
- Noh GP, Byun SH, Lee JR, Park SJ, Kim SC. Protective effect of Citrus unshiu peel on the cadmium-induced apoptosis in HepG2 cells. Kor J Herbol. 2021 ; 36(1) : 41-9. https://doi.org/10.6116/KJH.2021.36.1.41.
- Circu ML, Aw TY. Reactive oxygen species, cellular redox systems, and apoptosis. Free Radic Biol Med. 2010 ; 48(6) : 749-62. https://doi.org/10.1016/j.freeradbiomed.2009.12.022
- Lee JY, Yu BP, Chung HY. Activation mechanisms of endothelial NF-kappa B, IKK, and MAP kinase by tert-butyl hydroperoxide. Free Radic Res. 2005 ; 39(4) : 399-409. https://doi.org/10.1080/1071576040002870
- Pober JS, Min W, Bradley JR. Mechanisms of endothelial dysfunction, injury, and death. Annu Rev Pathol. 2009 ; 4 : 71-95. https://doi.org/10.1146/annurev.pathol.4.110807.092155
- Wu YT, Xie LP, Hua Y, Xu HL, Chen GH, Han X, Tan ZB, Fan HJ, Chen HM, Li J, Liu B, Zhou YC. Tanshinone I inhibits oxidative stress-induced cardiomyocyte injury by modulating Nrf2 signaling. Front Pharmacol. 2021 ; 12 : 644116.
- Zhao W, Feng H, Sun W, Liu K, Lu JJ, Chen X. Tert-butyl hydroperoxide (t-BHP) induced apoptosis and necroptosis in endothelial cells: Roles of NOX4 and mitochondrion. Redox Biol. 2017 ; 11 : 524-34. https://doi.org/10.1016/j.redox.2016.12.036