228 Edward R Madigan Lab, Department Food Science, and Human Nutrition, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Benson Hill Company, St. Louis, MO 63132, USA.
Int J Mol Sci. 2023 Aug 3;24(15):12396. doi: 10.3390/ijms241512396.
Soybean compounds have been established to modulate inflammation, but less is known about how whole soybean compositions work together after digestion. The objective was to evaluate and compare the anti-inflammatory responses of different soybean varieties under simulated gastrointestinal digestion, with additional consideration of the glycinin:β-conglycinin ratio (GBR). Soybean colonic digests (SCD) inhibited cyclooxygenase (COX)-2 (25-82%), 5-lipoxidase (LOX) (18-35%), and inducible nitric oxide (iNOS) (8-61%). Varieties 88, GN3, and 93 were the most effective inhibitors. SCD (1 mg/mL) of varieties 81 and GN1 significantly ( < 0.05) reduced nitrite production by 44 and 47%, respectively, compared to lipopolysaccharide (LPS)-stimulated macrophages. SCD effectively reduced pro-inflammatory cytokine interleukin (IL)-6 (50 and 80% for 96 and GN1, respectively). Western blot results showed a decrease in the expression of iNOS, p65, and p50. The GBR was in the range of 0.05-1.57. Higher ratio correlated with higher production of IL-1β (r = 0.44) and tumor necrosis factor-alpha (TNF-α, r = 0.56). Inflammatory microarray results showed a significant decrease in expression of markers granulocyte-macrophage colony-stimulating factor (GM-CSF) and IL-6 in cells treated with GN1 SCD compared to LPS. The results suggested that SCD exerted its anti-inflammatory potential through nuclear factor kappa B (NF-κΒ) pathway inhibition by decreasing the levels of NF-κB-dependent cytokines and subunits, and inhibition of pro-inflammatory enzyme activity.
大豆化合物已被证实可调节炎症,但对于消化后大豆整体成分如何协同作用知之甚少。本研究旨在评价和比较不同大豆品种在模拟胃肠道消化条件下的抗炎反应,并进一步考虑伴大豆球蛋白:β-伴大豆球蛋白比值(GBR)的影响。大豆结肠消化物(SCD)可抑制环氧化酶(COX)-2(25-82%)、5-脂氧合酶(LOX)(18-35%)和诱导型一氧化氮合酶(iNOS)(8-61%)。品种 88、GN3 和 93 是最有效的抑制剂。与脂多糖(LPS)刺激的巨噬细胞相比,品种 81 和 GN1 的 SCD(1mg/mL)分别显著(<0.05)降低 44%和 47%的亚硝酸盐生成。SCD 可有效降低促炎细胞因子白细胞介素(IL)-6(品种 96 和 GN1 分别降低 50%和 80%)。Western blot 结果显示,iNOS、p65 和 p50 的表达减少。GBR 范围为 0.05-1.57。比值越高,IL-1β(r = 0.44)和肿瘤坏死因子-α(TNF-α,r = 0.56)的产生越高。炎症微阵列结果显示,与 LPS 相比,GN1 SCD 处理的细胞中粒细胞-巨噬细胞集落刺激因子(GM-CSF)和 IL-6 标志物的表达显著降低。结果表明,SCD 通过降低 NF-κB 依赖性细胞因子和亚基的水平以及抑制促炎酶活性,抑制核因子κB(NF-κΒ)通路来发挥其抗炎潜力。