Graduate Program in Pharmaceutical Sciences, Federal University of Espirito Santo - UFES, Vitória, Brazil.
Graduate Program in Pharmaceutical Sciences, Federal University of Espirito Santo - UFES, Vitória, Brazil; Department of Pharmaceutical Sciences, Federal University of Espirito Santo - UFES, Vitória, Brazil.
Life Sci. 2020 Sep 1;256:117977. doi: 10.1016/j.lfs.2020.117977. Epub 2020 Jun 27.
Silibinin is the major component of flavonolignans complex mixture (Silymarin), which is obtained from Silybum marianum (L.) Gaertn. Despite several reports about silibinin, little is known about its effects on gastric diseases. Then, the present study aims to evaluate the silibinin effect against Helicobacter pylori infection, gastric tumor cells and immunomodulation.
The anti-H. pylori effect was performed on 43504 and 43629 strains by minimum inhibitory concentration (MIC) determination, observing morphological alterations by scanning electron microscopy and in silico evaluation by molecular docking. Immunomodulatory activity (Interleukins-6 and 10, TNF-α and NO inhibition) was determined in H. pylori-stimulated macrophages and the cytotoxic activity on gastric adenocarcinoma cells prior and after metabolization by S9 fraction.
Silibinin showed anti-H. pylori activity with MIC of 256 μg/mL, promoted important morphological changes in the bacterial cell wall, as blebs and clusters, suggesting interaction with Penicillin Binding Protein (PBP) subunits. Immunomodulatory potential was observed at 50 μg/mL with the inhibition of produced cytokines and NO by H. pylori-stimulated macrophages of 100% for TNF-ɑ, 56.83% for IL-6, and 70.29% for IL-10 and 73.33% for NO. Moreover, silibinin demonstrated significant cytotoxic activity on adenocarcinoma cells (CI: 60.17 ± 0.95 μg/mL) with a higher selectivity index (SI: 1.52) compared to cisplatin. After metabolization silibinin showed an increase of cytotoxicity with a CI six-fold decrease (10.46 ± 0.25).
The use of silibinin may become an important alternative tool in the prevention and treatment of H. pylori infection and, consequently, in gastric cancer.
水飞蓟宾是从水飞蓟(Silybum marianum(L.)Gaertn)中提取的黄酮木脂素复合物(水飞蓟素)的主要成分。尽管有几项关于水飞蓟宾的报道,但对其在胃部疾病方面的影响知之甚少。因此,本研究旨在评估水飞蓟宾对幽门螺杆菌感染、胃肿瘤细胞和免疫调节的作用。
通过最小抑菌浓度(MIC)测定,对 43504 和 43629 株菌进行抗幽门螺杆菌作用,通过扫描电子显微镜观察形态学改变,并通过分子对接进行计算机模拟评估。在幽门螺杆菌刺激的巨噬细胞中测定免疫调节活性(白细胞介素-6 和 10、TNF-α 和 NO 抑制),并测定 S9 馏分代谢前后对胃腺癌细胞的细胞毒性。
水飞蓟宾对幽门螺杆菌具有抗活性,MIC 为 256μg/ml,导致细菌细胞壁出现重要的形态学变化,如泡状和簇状,提示与青霉素结合蛋白(PBP)亚基相互作用。在 50μg/ml 时观察到免疫调节潜力,幽门螺杆菌刺激的巨噬细胞产生的细胞因子和 NO 抑制率分别为 TNF-α 100%、IL-6 56.83%、IL-10 70.29%和 NO 73.33%。此外,与顺铂相比,水飞蓟宾对腺癌细胞具有显著的细胞毒性(CI:60.17±0.95μg/ml),选择性指数(SI)更高(1.52)。代谢后,水飞蓟宾的细胞毒性增加,CI 值降低了六倍(10.46±0.25μg/ml)。
水飞蓟宾的使用可能成为预防和治疗幽门螺杆菌感染,进而预防胃癌的重要手段。