Biochemistry Department, Faculty of Pharmacy, Tanta University, El-Bahr Street, Tanta, El-Gharbia, 31527, Egypt.
Inflammopharmacology. 2018 Apr;26(2):551-559. doi: 10.1007/s10787-017-0373-9. Epub 2017 Jul 13.
Alternative medicine is widely accepted by public and becoming an attractive approach for treatment of various diseases. Glabridin (Gla), a major flavonoid present in licorice root, was reported to have antioxidant and anti-inflammatory properties.
The study aimed to investigate the possible protective role of Gla against dextran sulphate sodium (DSS)-induced ulcerative colitis (UC) in rats and to clarify the molecular mechanisms underlying Gla function.
Forty male Wistar rats were divided into control, colitis group (rats received 5% DSS in drinking water for 7 days), Gla group (50 mg/kg, orally, once daily), and sulfasalazine (SLZ) group (500 mg/kg, orally, once daily). Each of Gla and SLZ was administered 1 week ahead of DSS and parallel with its administration.
Gla ameliorated the inflammatory alterations induced by DSS. Gla group showed a reduction in colon concentration of tumor necrosis factor-alpha (TNF-α) and a decreased colon myeloperoxidase activity (MPO). Gla treatment downregulated inducible nitric oxide synthase (iNOS) gene expression in rat colon with a decreased content of nitric oxide (NO). Gla also increased cyclic AMP (cAMP) concentration in rat colon compared to colitis group. Such findings were comparable to or even better than those obtained by SLZ treatment. The histological features of UC such as ulceration and inflammatory cell infiltrations were improved in rat group treated by Gla.
Gla proved a potent anti-inflammatory role in UC through different mechanisms and, being a natural product, it could be safely used as a protective measure in inflammatory bowel diseases.
替代医学被公众广泛接受,并成为治疗各种疾病的一种有吸引力的方法。甘草素(Gla)是甘草根中主要的类黄酮,具有抗氧化和抗炎特性。
本研究旨在探讨 Gla 对葡聚糖硫酸钠(DSS)诱导的大鼠溃疡性结肠炎(UC)的可能保护作用,并阐明 Gla 作用的分子机制。
将 40 只雄性 Wistar 大鼠分为对照组、结肠炎组(大鼠饮用 5% DSS 水 7 天)、Gla 组(50mg/kg,口服,每天一次)和柳氮磺胺吡啶(SLZ)组(500mg/kg,口服,每天一次)。Gla 和 SLZ 分别在 DSS 之前 1 周开始给药,并与 DSS 同时给药。
Gla 改善了 DSS 诱导的炎症改变。Gla 组大鼠结肠肿瘤坏死因子-α(TNF-α)浓度降低,髓过氧化物酶(MPO)活性降低。Gla 治疗可下调大鼠结肠诱导型一氧化氮合酶(iNOS)基因表达,降低一氧化氮(NO)含量。与结肠炎组相比,Gla 还增加了大鼠结肠中环磷酸腺苷(cAMP)的浓度。这些发现与 SLZ 治疗相当,甚至更好。与结肠炎组相比,Gla 治疗组大鼠的 UC 组织学特征如溃疡和炎症细胞浸润得到改善。
Gla 通过不同的机制在 UC 中表现出强大的抗炎作用,并且作为一种天然产物,它可以作为炎症性肠病的一种安全保护措施。