Pickich Matthew B, Hargrove Mark W, Phillips C Niles, Healy James C, Moore Angelique N, Roberts Michael D, Martin Jeffrey S
Department of Cell Biology and Physiology, Edward Via College of Osteopathic Medicine-Auburn Campus, Auburn, AL, 36832, USA.
School of Kinesiology, Auburn University, Auburn, AL, 36849, USA.
BMC Res Notes. 2019 Aug 9;12(1):496. doi: 10.1186/s13104-019-4540-5.
We recently reported that curcumin supplementation in a metabolically (i.e., Western diet [WD]) and chemically (i.e., CCl) induced female rat model of non-alcoholic steatohepatitis (NASH) was associated with lower liver pathology scores and molecular markers of inflammation. This occurred when curcumin was given during induction of disease (preventative arm; 8-week WD with or without curcumin [8WD + C vs. 8WD]) as well as when given after disease development (treatment arm; 12-week WD with or without curcumin during weeks 9-12 [12WD + C vs. 12WD]). Herein, we sought to extend our findings from that study by determining the effects of curcumin supplementation on cytokine/chemokine expression in serum collected from these same rats.
24 cytokines/chemokines were assayed. IL-2 (+ 80%) and IL-13 (+ 83%) were greater with curcumin supplementation in the prevention arm. IL-2 (+ 192%), IL-13 (+ 87%), IL-17A (+ 81%) and fractalkine (+ 121%) were higher while RANTES was lower (- 22%) with curcumin supplementation in the treatment arm (p < 0.05 for all). RANTES concentrations also correlated significantly with hepatic pathology scores of inflammation (r = 0.417, p = 0.008). Select serum cytokines/chemokines were affected with curcumin supplementation in this female rat model of NASH. Moreover, curcumin's effect(s) on RANTES and its association with liver disease pathogenesis and progression may warrant further investigation.
我们最近报道,在代谢性(即西式饮食[WD])和化学性(即四氯化碳[CCl])诱导的非酒精性脂肪性肝炎(NASH)雌性大鼠模型中补充姜黄素与较低的肝脏病理评分和炎症分子标志物相关。当在疾病诱导期间给予姜黄素时(预防组;8周WD饮食,有或没有姜黄素[8WD+C与8WD])以及在疾病发展后给予姜黄素时(治疗组;9至12周期间为12周WD饮食,有或没有姜黄素[12WD+C与12WD]),均出现这种情况。在此,我们试图通过确定补充姜黄素对从这些相同大鼠收集的血清中细胞因子/趋化因子表达的影响来扩展该研究的结果。
检测了24种细胞因子/趋化因子。在预防组中,补充姜黄素后白细胞介素-2(IL-2)增加了80%,白细胞介素-13(IL-13)增加了83%。在治疗组中,补充姜黄素后IL-2增加了192%,IL-13增加了87%,IL-17A增加了81%, fractalkine增加了121%,而调节激活正常T细胞表达和分泌的趋化因子(RANTES)降低了22%(所有p均<0.05)。RANTES浓度也与肝脏炎症病理评分显著相关(r = 0.417,p = 0.008)。在这个NASH雌性大鼠模型中,补充姜黄素会影响特定血清细胞因子/趋化因子。此外,姜黄素对RANTES的作用及其与肝病发病机制和进展的关联可能值得进一步研究。