The Journal of Practical Medicine >
Emodin upregulates the Sirt2 to attenuate LPS-induced oxidative stress response in RAW264.7 cells
Received date: 2023-12-25
Online published: 2024-07-09
Objective The aim of this study was to investigate the impact and mechanisms of emodin on oxidative stress response in lipopolysaccharide (LPS)-induced murine mononuclear macrophages (RAW264.7). Methods Involved the use of LPS, RAW264.7 cells, and emodin. Experimental groups included a control group, LPS(1 μg/mL) group, and LPS(1 μg/mL) + emodin (15 μmmol/L) pretreatment group. Aldehyde malondialdehyde (MDA) content, intracellular reactive oxygen species (ROS) levels, and silent information regulator 2(Sirt2) expression were evaluated at 6, 12, and 18 hours after LPS exposure. Additionally, RAW264.7 cells were pretreated with Sirt2 inhibitor AGK2 (20 μmol/L) followed by LPS stimulation, and the above-mentioned parameters were assessed at 6 hours. Results Compared to the control group, MDA content, ROS levels, Sirt2 mRNA, and protein expression in RAW264.7 cells in the LPS group increased at all time points (all P < 0.05). At 6 and 18 hours, MDA content and ROS levels in RAW264.7 cells in the LPS + emodin group decreased significantly (all P < 0.05), while at 12 hours, ROS levels were lower in the LPS group compared to the LPS + emodin group (P < 0.05). Sirt2 mRNA and protein levels significantly increased at all time points (all P < 0.05) compared to the LPS group. In the LPS + emodin + AGK2 group, Sirt2 mRNA and protein levels decreased, and MDA content and ROS levels increased compared to the LPS + emodin group (all P < 0.05). Conclusion LPS-induced oxidative stress in RAW264.7 cells and emodin attenuate LPS-induced oxidative stress in RAW264.7 cells through Sirt2.
Key words: sepsis; macrophages; oxidative stress; emodin; Sirt2
Chun LONG , Hongying BI , Changzhen YANG , Jiakai WANG , Yan TANG , Xu. LIU . Emodin upregulates the Sirt2 to attenuate LPS-induced oxidative stress response in RAW264.7 cells[J]. The Journal of Practical Medicine, 2024 , 40(13) : 1785 -1790 . DOI: 10.3969/j.issn.1006-5725.2024.13.004
| 1 | SINGER M, DEUTSCHMAN C S, SEYMOUR C W, et al. The third international consensus definitions for sepsis and septic shock (Sepsis-3)[J]. JAMA, 2016, 315(8): 801-810. doi:10.1001/jama.2016.0287 |
| 2 | RUDD K E, JOHNSON S C, AGESA K M, et al. Global, regional, and national sepsis incidence and mortality, 1990-2017: analysis for the Global Burden of Disease Study[J]. Lancet, 2020, 395(10219): 200-211. doi:10.1016/s0140-6736(19)32989-7 |
| 3 | VAN DER POLL T, SHANKAR-HARI M, WIERSINGA W J. The immunology of sepsis[J]. Immunity, 2021,54(11):2450-2464. doi:10.1016/j.immuni.2021.10.012 |
| 4 | DUGAR S, CHOUDHARY C, DUGGAL A. Sepsis and septic shock: Guideline-based management[J]. Cleve Clin J Med, 2020, 87(1): 53-64. doi:10.3949/ccjm.87a.18143 |
| 5 | GAWISH R, MARTINS R, B?HM B, et al. Triggering receptor expressed on myeloid cells‐2 fine‐tunes inflammatory responses in murine Gram‐negative sepsis[J]. FASEB J, 2015, 29(4): 1247-1257. doi:10.1096/fj.14-260067 |
| 6 | INOUE M, SHINOHARA M L.Cutting edge: Role of osteopontin and integrin alphav in T cell- mediated anti-inflammatory responses in endotoxemia[J]. Immunol, 2015,194:5595-5598. doi:10.4049/jimmunol.1500623 |
| 7 | 蒋龙元. 免疫紊乱在脓毒症中的作用[J]. 实用医学杂志, 2021, 37(6): 701-704. doi:10.3969/j.issn.1006-5725.2021.06.001 |
| 8 | KOROVESIS D, RUBIO-TOMáS T, TAVERNARAKIS N. Oxidative stress in age-related neurodegenerative diseases: An overview of recent tools and findings[J]. Antioxidants, 2023, 12(1): 131. doi:10.3390/antiox12010131 |
| 9 | CHEN J Y, ZHU G Y, SU X H,et al. 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling[J]. Oncotarget, 2017,8(33):55051-55063. doi:10.18632/oncotarget.19017 |
| 10 | 傅兴圣,陈菲,刘训红,等. 大黄化学成分与药理作用研究新进展[J]. 中国新药杂志, 2011,20(16):1534-1538. |
| 11 | CHEN G, ZHANG J, ZHANG H, et al. Anti-inflammatory effect of emodin on lipopolysaccharide-induced keratitis in Wistar rats[J]. Int J Clin Exp Med, 2015, 8(8): 12382. |
| 12 | YIN J T, WAN B, LIU D D, et al. Emodin alleviates lung injury in rats with sepsis[J]. J Sur Res, 2016, 202(2): 308-314. doi:10.1016/j.jss.2015.12.049 |
| 13 | 苏华. 大黄素对脓毒症急性肺损伤大鼠的保护作用及其分子作用机制研究[J]. 实用心脑肺血管病杂志, 2014,22(7):39-41. doi:10.3969/j.issn.1008-5971.2014.07.017 |
| 14 | QU Z A, MA X J, HUANG S B, et al. Sirt2 inhibits oxidative stress and inflammatory response in diabetic osteoarthritis[J]. Eur Rev Med Pharmacol Sci, 2020, 24(6):2855-2864. |
| 15 | LEMOS V, DE OLIVEIRA R M, NAIA L, et al. The NAD+-dependent deacetylase Sirt2 attenuates oxidative stress and mitochondrial dysfunction and improves insulin sensitivity in hepatocytes[J]. Hum Mol Genet,2017,26(21):4105-4117. doi:10.1093/hmg/ddx298 |
| 16 | KUMAR S, SAXENA J, SRIVASTAVA V K, et al. The Interplay of Oxidative Stress and ROS Scavenging: Antioxidants as a Therapeutic Potential in Sepsis[J]. Vaccines, 2022, 10(10):1575. doi:10.3390/vaccines10101575 |
| 17 | YANG H, LV H, LI H, et al. Oridonin protects LPS-induced acute lung injury by modulating Nrf2-mediated oxidative stress and Nrf2-independent NLRP3 and NF-κB pathways[J]. Cell Commun Signal, 2019, 17(1): 1-15. doi:10.1186/s12964-019-0366-y |
| 18 | REUTER S, GUPTA S C, CHATURVEDI M M, et al. Oxidative stress, inflammation, and cancer: how are they linked?[J]. Free Radic Biol Med, 2010, 49(11): 1603-1616. doi:10.1016/j.freeradbiomed.2010.09.006 |
| 19 | LIGUORI I, RUSSO G, CURCIO F, et al. Oxidative stress, aging, and diseases[J]. Clin Interv Aging, 2018,13: 757-772. doi:10.2147/cia.s158513 |
| 20 | 王慧,龚园其,周仪华,等. 青藤碱调控Nrf2/Keap1信号通路对脓毒症急性肺损伤的改善作用[J]. 实用医学杂志, 2022,38(15):1896-1900. doi:10.3969/j.issn.1006-5725.2022.15.009 |
| 21 | 胡莉芸,谭佳颖,沈隽,等. 大黄素对盲肠结扎穿孔脓毒症大鼠模型各器官氧化应激与炎症反应的保护作用[J]. 临床与病理杂志, 2019,39(7):1388-1395. doi:10.3978/j.issn.2095-6959.2019.07.002 |
| 22 | YU J, WU Y, YANG P. High glucose‐induced oxidative stress represses sirtuin deacetylase expression and increases histone acetylation leading to neural tube defects[J]. J Neurochem, 2016, 137(3): 371-383. doi:10.1111/jnc.13587 |
| 23 | QU Z A, MA X J, HUANG S B, et al. Sirt2 inhibits oxidative stress and inflammatory response in diabetic osteoarthritis[J]. Eur Rev Med Pharmacol Sci, 2020, 24(6):2855-2864. |
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