Urbanska Aleksandra Malgorzata, Paul Arghya, Bhathena Jasmine, Prakash Satya
Biomedical Technology and Cell Therapy Research Laboratory, Departments of Biomedical Engineering and Physiology, Artificial Cells and Organs Research Center, Faculty of Medicine, McGill University, 3775 University Street, Montreal, QC, Canada H3A 2B4.
Int J Inflam. 2010 Oct 31;2010:894972. doi: 10.4061/2010/894972.
The objective of this study was to examine the ability of a novel microencapsulated probiotic yogurt formulation to suppress the intestinal inflammation. We assessed its anticancer activity by screening interleukin-1, 6, and 12 (IL-1, 6, 12), secretory levels of tumor necrosis factor-alpha (TNF-α), interferon-gamma (IFN-γ), prostaglandin E(2) (PGE(2)), and thromboxane B2 in the digesta obtained from the duodenum, jejunum, proximal, and distal segments of the ileum of C57BL/6J-Apc(Min)/J mice. Formulation-receiving animals showed consistently lower proinflammatory cytokines' levels when compared to control group animals receiving empty alginate-poly-L-lysine-alginate (APA) microcapsules suspended in saline. The concentrations of IL-12 found in serum in control and treatment group animals were significant: 46.58 ± 16.96 pg/mL and 158.58 ± 28.56 pg/mL for control and treatment animals, respectively. We determined a significant change in plasma C-reactive protein: 81.04 ± 23.73 ng/mL in control group and 64.21 ± 16.64 ng/mL in treatment group. Western blots showed a 71% downregulation of cyclooxygenase-2 (COX-2) protein in treatment group animals compared to control. These results point to the possibility of using this yogurt formulation in anticancer therapies, in addition to chronic gut diseases such as Crohn's disease, irritable bowel syndrome (IBS), and inflammatory bowel disease (IBD) thanks to its inflammation lowering properties.
本研究的目的是检验一种新型微囊化益生菌酸奶制剂抑制肠道炎症的能力。我们通过筛选白细胞介素-1、6和12(IL-1、6、12)、肿瘤坏死因子-α(TNF-α)、干扰素-γ(IFN-γ)、前列腺素E(2) (PGE(2))以及血栓素B2在C57BL/6J-Apc(Min)/J小鼠十二指肠、空肠、回肠近端和远端肠段食糜中的分泌水平,评估了其抗癌活性。与接受悬浮于生理盐水中的空藻酸盐-聚-L-赖氨酸-藻酸盐(APA)微胶囊的对照组动物相比,接受该制剂的动物体内促炎细胞因子水平持续较低。对照组和治疗组动物血清中IL-12的浓度差异显著:对照组为46.58±16.96 pg/mL,治疗组为158.58±28.56 pg/mL。我们测定了血浆C反应蛋白的显著变化:对照组为81.04±23.73 ng/mL,治疗组为64.21±16.64 ng/mL。蛋白质印迹法显示,与对照组相比,治疗组动物体内环氧化酶-2(COX-2)蛋白下调了71%。这些结果表明,除了用于治疗克罗恩病、肠易激综合征(IBS)和炎症性肠病(IBD)等慢性肠道疾病外,这种酸奶制剂因其降低炎症的特性,还具有用于抗癌治疗的可能性。