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Effect of glucocorticoid on inflammatory cytokines and miRNA-122a in septic shock |
Sang Zhen-zhen, Gao Jie, Jia Chun-mei, Li Yong |
Department of Emergency, Cangzhou Central Hospital, Cangzhou 061000, China |
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Abstract Objective To observe the effect of hydrocortisone on inflammatory cytokines and miRNA-122a in patients with septic shock. Methods Total of 125 septic shock patients admitted to the emergency intensive care unit (EICU) of Cangzhou central hospital from Dec. 2016 to Dec. 2018 were divided into two groups: conventional treatment group (65 cases), Hydrocortisone treatment group (60 cases).The conventional treatment group received basic treatment, while the Hydrocortisone treatment group on the basis comprehensive treatment were given intravenous infusion of hydrocortisone (200 mg, every day) for consecutive 7 days. The serum levels of tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), High mobility family protein B-1 (HMGB-1) were determined by enzyme-linked immunosorbent (ELISA) before and after 3 and 7d of treatment. The expression level of serum miRNA-122a was detected by real-time PCR. The APACHEⅡ score, SOFA score, liver function, vasoactive drug use time, EICU treatment time and 28d death rate were compared between the two groups. Results Before treatment, there were no significant difference in serum TNF-α, IL-6, HMGB-1 and miRNA-122a levels between the two groups (P>0.05). After treatment, the above indexes were lower than those before treatment, and all indexes in the hydrocortisone treatment group were lower than those in the conventional treatment group[TNF-α(pg/mL): 3 d 146.29±19.34 vs. 165.26±16.45, 7 d 118.63±20.48 vs. 125.83±16.87; IL-6(pg/mL): 3 d 150.73±15.36 vs. 237.62±18.45, 7 d 124.35±16.28 vs. 149.94±19.64;HMGB-1(ng/mL): 3 d 7.78±1.06 vs. 11.72±1.25, 7 d 2.49±0.50 vs. 3.87±0.64;miRNA-122a: 3 d 1.42±0.46 vs. 1.95±0.37, 7 d 0.86±0.15 vs. 1.18±0.29;P<0.01]. Compared with the conventional treatment group, the liver function improved obviously[ALT(U/L): 3 d 77(120.3) vs. 72.8(112.4), 7 d 69(28.2) vs. 62.5(20.9);AST(U/L): 3 d 80.4(118.5) vs. 76.7(105.8), 7 d 73.6(29.7) vs. 65.9(26.7);TBIL(mg/dL): 3 d 1.7(3.4) vs. 1.6(2.7), 7 d 1.5(0.9) vs. 1.4(0.8);P<0.01], and EICU treatment time(d:15.4±6.5 vs. 10.7±5.3)were significantly shortened, and the differences were statistically significant (P<0.05). However, there was no statistically significant difference in the 28-day mortality between the two groups (P>0.05). Conclusion Hydrogenation can significantly reduce the expression level of serum miRNA-122a of patients with septic shock and reduce the levels of inflammatory cytokines, thus reducing liver injury and shortening the treatment time of EICU, but it cannot reduce the 28-day mortality of patients with septic shock.
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Corresponding Authors:
Li Yong, E-mail: sangzhenzhen@163.com
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[1]Singer M, Deutschman CS, Seymour CW, et al. The third international consensus definitions for sepsis and septic shock(sepsis-3.0)[J]. JAMA, 2016, 315(8):801-810.
[2]Rahmel T, Sch fer ST, Frey UH, et al. Increased circulating microRNA-122 is a biomarker for discrimination and risk stratification in patients defined by sepsis-3 criteria[J]. PLoS One, 2018, 13(5):e0 197 637.
[3]Ani C, Farshidpanah S, Bellinghausen Stewart A, et al. Variations in organism-specific severe sepsis mortality in the United States:1999-2008[J]. Crit Care Med, 2015, 43(1):65-77.
[4]Nastos C, Kalimeris K, Papoutsidakis N, et al. Global consequences of liver ischemia /reperfusion injury[J]. Oxid Med Cell Longev, 2014, 2014: 906 965.
[5]Mobergslien A, Sioud M. Exosome-derived miRNAs and cellular miRNAs activate innate immunity[J]. J Innate Immun, 2014, 6(1): 105-110.
[6]Friedrich K, Baumann C, Wannhoff A, et al. Serum miRNA-122 is an independent biomarker of survival in patients with primary sclerosing cholangitis[J]. J Gastrointestin Liver Dis, 2018, 27(2):145-150.
[7]Yang F, Li L, Yang R, et al. Identification of serum microRNAs as potential toxicological biomarkers for toosendanin-induced liver injury in mice[J]. Phytomedicine, 2019, 58:152 867.
[8]Jia YX, Pan CS, Yang JH, et al. Altered L-arginine/nitric oxide synthase/nitric oxide pathway in the vascular adventitia of rats with sepsis[J]. Clin Exp Pharmacol Physiol, 2006, 33(12):1202-1208.
[9]殷杰,杨晓燕,虞佳,等. miR-122表达载体的构建及其对Bcl-x L,Bcl-2 基因的抑制作用[J]. 中南医学科学杂志, 2013, 41(1):13-16.
[10]Rahmel T, Rump K, Adamzik M, et al. Increased circulating microRNA-122 is associated with mortality and acute liver injury in the acute respiratory distress syndrome[J]. BMC Anesthesiol, 2018,18(1):75.
[11]Kim SJ, Park JS, Lee DW, et al. Trichostatin a protects liver against septic injury through inhibiting toll-like receptor signaling[J]. Biomol ther (seoul), 2016, 24(4):387-394.
[12]Weber MD, Frank MG, Tracey KJ, et al. Stress induces the danger-associated molecular pattern HMGB-1 in the hippocampus of male sprague dawley rats: a priming stimulus of microglia and the NLRP3 inflammasome[J]. J Neuro, 2015, 35(1):316-324.
[13]Zheng Y, Xiong S, Jiang P, et al. Glucocorticoids inhibit lipopolysaccharide-mediated inflammatory response by downregulating microRNA-155:a novel anti-inflammation mechanism[J]. Free Radic Biol Med, 2012, 52(8): 1307-1317.
[14]Minneci PC, Deans KJ, Banks SM, et al. Meta-analysis: the effect of steroids on survival and shock during sepsis depends on the dose[J]. Ann Intern Med, 2004, 141(1): 47-56. |
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