Pharmacology and Toxicology Department, Faculty of Pharmacy, Misr International University (MIU), Cairo, Egypt.
Pharmacology and Toxicology Department, Faculty of Pharmacy, Badr University in Cairo (BUC), Cairo, Egypt.
Food Chem Toxicol. 2022 Jul;165:113146. doi: 10.1016/j.fct.2022.113146. Epub 2022 May 18.
Nod-like receptor pyrin domain-1 containing 3 (NLRP3) inflammasome/tumor necrosis factor alpha (TNFα)/nuclear factor kappa B (NFκB) inflammatory pathway is known to be involved in the pathogenesis of ulcerative colitis (UC). Inversely, miRNA-223 can exert counter-regulatory effect on NLRP3 expression. The mulberry tree (Morus macroura) fruit is attaining increased importance for its antioxidant and anti-inflammatory activity in addition to its high safety profile. Accordingly, we attempted to explore the possible protective effect of mulberry fruit extract (MFE) in acetic acid (AA)-induced UC rat model. Phytochemical constituents of MFE were characterized using high performance liquid chromatography coupled to mass spectrometry (HPLC-MS). In the in vivo study, three doses of MFE were orally given for seven days before intra-rectal induction of UC by AA on day eight. Screening study revealed that MFE (300 mg/kg) significantly reduced macroscopic and microscopic UC scores. Biochemically, MFE ameliorated oxidative stress, levels of TNFR1, NLRP3, p-NFκB p65, TNFα, IL-1β, and IL-18, caspase-1 activity, but enhanced miRNA-223 expression. In conclusion, our study provided a novel protective impact for MFE against UC, in which miRNA-223 and TNFα/NFκB/NLRP3 pathway are involved. These results provide a promising step that might encourage further investigations of MFE as a protective agent in UC patients.
核苷酸结合寡聚结构域样受体热蛋白结构域 3(NLRP3)包含炎症小体/肿瘤坏死因子-α(TNFα)/核因子-κB(NFκB)炎症通路,已知其参与溃疡性结肠炎(UC)的发病机制。相反,miRNA-223 可以对 NLRP3 表达发挥反向调节作用。桑树(Morus macroura)果实因其抗氧化和抗炎活性以及高安全性而日益受到重视。因此,我们试图探讨桑果提取物(MFE)在乙酸(AA)诱导的 UC 大鼠模型中的可能保护作用。采用高效液相色谱-质谱联用(HPLC-MS)对 MFE 的化学成分进行了表征。在体内研究中,在第 8 天通过 AA 直肠内诱导 UC 之前,MFE 以三个剂量口服给药 7 天。筛选研究表明,MFE(300mg/kg)可显著降低 UC 的宏观和微观评分。生化分析表明,MFE 改善了氧化应激、TNFR1、NLRP3、p-NFκB p65、TNFα、IL-1β 和 IL-18、半胱天冬酶-1 活性,但增强了 miRNA-223 的表达。总之,我们的研究为 MFE 防治 UC 提供了新的保护作用,其中 miRNA-223 和 TNFα/NFκB/NLRP3 通路参与其中。这些结果为 MFE 作为 UC 患者的保护剂提供了有希望的一步,可能鼓励进一步研究。