과제정보
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (NRF-2017M3A9E4057926).
참고문헌
- Zajaczkowska R, Kocot-Kepska M, Leppert W, Wrzosek A, Mika J, Wordliczek J. Mechanisms of chemotherapy-induced peripheral neuropathy. Int J Mol Sci. 2019;20:1451. https://doi.org/10.3390/ijms20061451
- Boyette-Davis JA, Hou S, Abdi S, Dougherty PM. An updated understanding of the mechanisms involved in chemotherapy-induced neuropathy. Pain Manag. 2018;8:363-375. https://doi.org/10.2217/pmt-2018-0020
- Starobova H, Vetter I. Pathophysiology of chemotherapy-induced peripheral neuropathy. Front Mol Neurosci. 2017;10:174. https://doi.org/10.3389/fnmol.2017.00174
- Kerckhove N, Collin A, Conde S, Chaleteix C, Pezet D, Balayssac D. Long-term effects, pathophysiological mechanisms, and risk factors of chemotherapy-induced peripheral neuropathies: a comprehensive literature review. Front Pharmacol. 2017;8:86. https://doi.org/10.3389/fphar.2017.00086
- Choi HM, Jung Y, Park J, Kim HL, Youn DH, Kang J, Jeong MY, Lee JH, Yang WM, Lee SG, Ahn KS, Um JY. Cinnamomi cortex (Cinnamomum verum) suppresses testosterone-induced benign prostatic hyperplasia by regulating 5α-reductase. Sci Rep. 2016;6:31906. https://doi.org/10.1038/srep31906
- Hayashi K, Imanishi N, Kashiwayama Y, Kawano A, Terasawa K, Shimada Y, Ochiai H. Inhibitory effect of cinnamaldehyde, derived from Cinnamomi cortex, on the growth of influenza A/PR/8 virus in vitro and in vivo. Antiviral Res. 2007;74:1-8. https://doi.org/10.1016/j.antiviral.2007.01.003
- Chae HK, Kim W, Kim SK. Phytochemicals of Cinnamomi Cortex: cinnamic acid, but not cinnamaldehyde, attenuates oxaliplatin-induced cold and mechanical hypersensitivity in rats. Nutrients. 2019;11:432. https://doi.org/10.3390/nu11020432
- Kim C, Lee JH, Kim W, Li D, Kim Y, Lee K, Kim SK. The suppressive effects of Cinnamomi Cortex and its phytocompound coumarin on oxaliplatin-induced neuropathic cold allodynia in rats. Molecules. 2016;21:1253. https://doi.org/10.3390/molecules21091253
- Perfumi M, Mattioli L. Adaptogenic and central nervous system effects of single doses of 3% rosavin and 1% salidroside Rhodiola rosea L. extract in mice. Phytother Res. 2007;21:37-43. https://doi.org/10.1002/ptr.2013
- Chiang HM, Chen HC, Wu CS, Wu PY, Wen KC. Rhodiola plants: chemistry and biological activity. J Food Drug Anal. 2015;23:359-369. https://doi.org/10.1016/j.jfda.2015.04.007
- Park JS, Choi J, Kwon JY, Jung KA, Yang CW, Park SH, Cho ML. A probiotic complex, rosavin, zinc, and prebiotics ameliorate intestinal inflammation in an acute colitis mouse model. J Transl Med. 2018;16:37. https://doi.org/10.1186/s12967-018-1410-1
- Panossian AG, Efferth T, Shikov AN, Pozharitskaya ON, Kuchta K, Mukherjee PK, Banerjee S, Heinrich M, Wu W, Guo DA, Wagner H. Evolution of the adaptogenic concept from traditional use to medical systems: pharmacology of stress- and aging-related diseases. Med Res Rev. 2021;41:630-703. https://doi.org/10.1002/med.21743
- Stancheva SL, Mosharrof A. Effect of the extract of Rhodiola rosea L. on the content of the brain biogenic monamines. Med Physiol. 1987;40:85-87.
- Chen QG, Zeng YS, Qu ZQ, Tang JY, Qin YJ, Chung P, Wong R, Hagg U. The effects of Rhodiola rosea extract on 5-HT level, cell proliferation and quantity of neurons at cerebral hippocampus of depressive rats. Phytomedicine. 2009;16:830-838. https://doi.org/10.1016/j.phymed.2009.03.011
- Lishmanov IuB, Trifonova ZhV, Tsibin AN, Maslova LV, Dement'eva LA. [Plasma beta-endorphin and stress hormones in stress and adaptation]. Biull Eksp Biol Med. 1987;103:422-424. Russian.
- Montiel-Ruiz RM, Gonzalez-Trujano ME, Deciga-Campos M. Synergistic interactions between the antinociceptive effect of Rhodiola rosea extract and B vitamins in the mouse formalin test. Phytomedicine. 2013;20:1280-1287. https://doi.org/10.1016/j.phymed.2013.07.006
- Millan MJ. Descending control of pain. Prog Neurobiol. 2002;66:355-474. https://doi.org/10.1016/S0301-0082(02)00009-6
- Nguyen LM, Rhondali W, De la Cruz M, Hui D, Palmer L, Kang DH, Parsons HA, Bruera E. Frequency and predictors of patient deviation from prescribed opioids and barriers to opioid pain management in patients with advanced cancer. J Pain Symptom Manage. 2013;45:506-516. https://doi.org/10.1016/j.jpainsymman.2012.02.023
- Zimmermann M. Ethical guidelines for investigations of experimental pain in conscious animals. Pain. 1983;16:109-110. https://doi.org/10.1016/0304-3959(83)90201-4
- Li D, Lee JH, Choi CW, Kim J, Kim SK, Kim W. The analgesic effect of venlafaxine and its mechanism on oxaliplatin-induced neuropathic pain in mice. Int J Mol Sci. 2019;20:1652. https://doi.org/10.3390/ijms20071652
- Li D, Lee Y, Kim W, Lee K, Bae H, Kim SK. Analgesic effects of Bee Venom derived phospholipase A2 in a mouse model of oxaliplatin-induced neuropathic pain. Toxins (Basel). 2015;7:2422-2434. https://doi.org/10.3390/toxins7072422
- Li D, Chung G, Kim SK. The involvement of central noradrenergic pathway in the analgesic effect of bee venom acupuncture on vincristine-induced peripheral neuropathy in rats. Toxins (Basel). 2020;12:775. https://doi.org/10.3390/toxins12120775
- Nakagawa T, Minami M, Katsumata S, Ienaga Y, Satoh M. Suppression of naloxone-precipitated withdrawal jumps in morphine-dependent mice by stimulation of prostaglandin EP3 receptor. Br J Pharmacol. 1995;116:2661-2666. https://doi.org/10.1111/j.1476-5381.1995.tb17223.x
- Choi S, Chae HK, Heo H, Hahm DH, Kim W, Kim SK. Analgesic effect of melittin on oxaliplatin-induced peripheral neuropathy in rats. Toxins (Basel). 2019;11:396. https://doi.org/10.3390/toxins11070396
- Sung SH, Kim JW, Han JE, Shin BC, Park JK, Lee G. Animal venom for medical usage in pharmacopuncture in Korean medicine: current status and clinical implication. Toxins (Basel). 2021;13:105. https://doi.org/10.3390/toxins13020105
- Kwon JY, Lee SH, Jhun J, Choi J, Jung K, Cho KH, Kim SJ, Yang CW, Park SH, Cho ML. The combination of probiotic complex, rosavin, and zinc improves pain and cartilage destruction in an osteoarthritis rat model. J Med Food. 2018;21:364-371. https://doi.org/10.1089/jmf.2017.4034
- Deciga-Campos M, Gonzalez-Trujano ME, Ventura-Martinez R, Montiel-Ruiz RM, Angeles-Lopez GE, Brindis F. Antihyperalgesic activity of Rhodiola rosea in a diabetic rat model. Drug Dev Res. 2016;77:29-36. https://doi.org/10.1002/ddr.21289
- Polter AM, Li X. 5-HT1A receptor-regulated signal transduction pathways in brain. Cell Signal. 2010;22:1406-1412. https://doi.org/10.1016/j.cellsig.2010.03.019
- Otoshi CK, Walwyn WM, Tillakaratne NJ, Zhong H, Roy RR, Edgerton VR. Distribution and localization of 5-HT1A receptors in the rat lumbar spinal cord after transection and deafferentation. J Neurotrauma. 2009;26:575-584. https://doi.org/10.1089/neu.2008.0640
- Oyama T, Ueda M, Kuraishi Y, Akaike A, Satoh M. Dual effect of serotonin on formalin-induced nociception in the rat spinal cord. Neurosci Res. 1996;25:129-135. https://doi.org/10.1016/0168-0102(96)01034-6
- Lee JH, Min D, Lee D, Kim W. Zingiber officinale roscoe rhizomes attenuate oxaliplatin-induced neuropathic pain in mice. Molecules. 2021;26:548. https://doi.org/10.3390/molecules26030548
- Liu Z, Li X, Simoneau AR, Jafari M, Zi X. Rhodiola rosea extracts and salidroside decrease the growth of bladder cancer cell lines via inhibition of the mTOR pathway and induction of autophagy. Mol Carcinog. 2012;51:257-267. https://doi.org/10.1002/mc.20780
- Udintsev SN, Shakhov VP. [Decrease in the growth rate of Ehrlich's tumor and Pliss' lymphosarcoma with partial hepatectomy]. Vopr Onkol. 1989;35:1072-1075. Russian.