Feng Burong, Zhao Xiuye, Zhao Wei, Jiang Huiwei, Ren Zijing, Chen Yingfu, Yuan Ye, Du Zhimin
Institute of Clinical Pharmacy, The Second Affiliated Hospital of Harbin Medical University (The University Key Laboratory of Drug Research, Heilongjiang Province), Harbin, China.
Department of Clinical Pharmacology, College of Pharmacy, Harbin Medical University, Harbin, China.
Front Pharmacol. 2021 Nov 8;12:719822. doi: 10.3389/fphar.2021.719822. eCollection 2021.
Aloe-emodin widely possesses antibacterial, anti-inflammatory, antioxidant, antiviral, and anti-infectious properties. This study investigated the effect of ethyl 2-succinate-anthraquinone (Luhui derivative, LHD) on inflammation. , a THP-1 macrophage inflammation model, made by 100 ng/ml phorbol-12-myristate-13-acetate (PMA) and 1 μg/ml LPS for 24 h, was constructed. The LHD group (6.25 μmol/L, 12.5 μmol/L, 25 μmol/L, 50 μmol/L) had no effect on THP-1 cell activity, and the expression of IL-6 mRNA was down-regulated in a concentration-dependent manner, of which the 25 μmol/L group had the best inhibitory effect. The migration of THP-1 macrophages induced by LPS was decreased by the LHD. Moreover, the LHD suppressed ROS fluorescence expression by inhibiting MDA expression and increasing SOD activity. , we revealed that the LHD, in different doses (6.25 mg/kg, 12.5 mg/kg, 25 mg/kg, 50 mg/kg), has a protective effect on stress physiological responses by assessing the body temperature of mice. Interestingly, acute lung injury (e.g., the structure of the alveoli disappeared and capillaries in the alveolar wall were dilated and congested) and liver damage (e.g., hepatocyte swelling, neutrophil infiltration, and hepatocyte apoptosis) were obviously improved at the same condition. Furthermore, we initially confirmed that the LHD can down-regulate the expression of NLRP3, IL-1β, and caspase-1 proteins, thereby mediating the NLRP3 inflammasome signaling pathway to produce anti-inflammatory effects. In conclusion, our results indicate that the LHD exerts anti-inflammatory activity via regulating the NLRP3 signaling pathway, inhibition of oxidative stress, and THP-1 macrophage migration.
芦荟大黄素具有广泛的抗菌、抗炎、抗氧化、抗病毒和抗感染特性。本研究调查了2-琥珀酸乙酯蒽醌(芦荟衍生物,LHD)对炎症的影响。构建了由100 ng/ml佛波酯-12-肉豆蔻酸酯-13-乙酸酯(PMA)和1 μg/ml脂多糖(LPS)作用24小时制成的THP-1巨噬细胞炎症模型。LHD组(6.25 μmol/L、12.5 μmol/L、25 μmol/L、50 μmol/L)对THP-1细胞活性无影响,白细胞介素-6(IL-6)mRNA的表达呈浓度依赖性下调,其中25 μmol/L组的抑制作用最佳。LHD可降低LPS诱导的THP-1巨噬细胞的迁移。此外,LHD通过抑制丙二醛(MDA)表达和增加超氧化物歧化酶(SOD)活性来抑制活性氧(ROS)荧光表达。通过评估小鼠体温,我们发现不同剂量(6.25 mg/kg、12.5 mg/kg、25 mg/kg、50 mg/kg)的LHD对应激生理反应具有保护作用。有趣的是,在相同条件下,急性肺损伤(如肺泡结构消失、肺泡壁毛细血管扩张和充血)和肝损伤(如肝细胞肿胀、中性粒细胞浸润和肝细胞凋亡)明显改善。此外,我们初步证实LHD可下调NLRP3、白细胞介素-1β(IL-1β)和半胱天冬酶-1(caspase-1)蛋白的表达,从而介导NLRP3炎性小体信号通路产生抗炎作用。总之,我们的结果表明,LHD通过调节NLRP3信号通路、抑制氧化应激和THP-1巨噬细胞迁移发挥抗炎活性。