Nutritional Sciences Department.
Robert M Kerr Food and Agricultural Products Center.
J Nutr. 2019 Jul 1;149(7):1107-1115. doi: 10.1093/jn/nxz061.
A link between high-fat diet consumption and obesity-related diseases is the disruption of the gut bacterial population, which promotes local and systemic inflammation. Wheat germ (WG) is rich in bioactive components with antioxidant and anti-inflammatory properties.
The aim of this study was to investigate the effects of WG supplementation in modulating the gut bacterial population and local and systemic inflammatory markers of mice fed a high-fat, high-sucrose (HFS) diet.
Six-week-old male C57BL/6 mice were randomly assigned to 4 groups (n = 12/group) and fed a control (C; 10% kcal fat, 10% kcal sucrose) or HFS (60% kcal fat, 20% kcal sucrose) diet with or without 10% WG (wt:wt) for 12 wk. Cecal bacteria was assessed via 16S rDNA sequencing, fecal short-chain fatty acids by GC, small intestinal CD4+ lymphocytes using flow cytometry, and gut antimicrobial peptide genes and inflammatory markers by quantitative polymerase chain reaction. Statistical analyses included Kruskal-Wallis/Dunn's test and 2-factor ANOVA using HFS and WG as factors.
There was a 4-fold increase (P = 0.007) in the beneficial bacterial family, Lactobacillaceae, in the HFS + WG compared with the HFS group. Fecal propionic and n-butyric acids were elevated at least 2-fold in C + WG compared with the other groups (P < 0.0001). WG tended to increase (≥7%; P-trend = 0.12) small intestinal regulatory T cell:Th17 ratio, indicating a potential to induce an anti-inflammatory gut environment. WG elevated (≥35%) ileal gene expression of the anti-inflammatory cytokine Il10 compared to the unsupplemented groups (P = 0.038). Ileal gene expression of the antimicrobial peptides Reg3b and Reg3g was upregulated (≥95%) in the HFS + WG compared with other groups (P ≤ 0.040). WG reduced serum concentrations of the pro-inflammatory cytokines, interleukin (IL)-1B, IL-6, interferon-γ, and tumor necrosis factor-α (≥17%; P ≤ 0.012).
WG selectively increased gut Lactobacillaceae, upregulated ileal antimicrobial peptides, and attenuated circulating pro-inflammatory cytokines of C57BL/6 mice fed a HFS diet. These changes may be vital in preventing HFS diet-induced comorbidities.
高脂肪饮食消费与肥胖相关疾病之间的联系是肠道细菌群的破坏,这会促进局部和全身炎症。小麦胚芽(WG)富含具有抗氧化和抗炎特性的生物活性成分。
本研究旨在研究 WG 补充剂对高脂肪、高蔗糖(HFS)饮食喂养的小鼠肠道细菌群和局部及全身炎症标志物的调节作用。
将 6 周龄雄性 C57BL/6 小鼠随机分为 4 组(每组 n = 12),并分别给予对照(C;10%卡路里脂肪,10%卡路里蔗糖)或 HFS(60%卡路里脂肪,20%卡路里蔗糖)饮食,或给予 10% WG(wt:wt)补充 12 周。通过 16S rDNA 测序评估盲肠细菌,通过 GC 分析粪便短链脂肪酸,通过流式细胞术分析小肠 CD4+淋巴细胞,并通过定量聚合酶链反应分析肠道抗菌肽基因和炎症标志物。统计分析包括 Kruskal-Wallis/Dunn 检验和 2 因素方差分析,以 HFS 和 WG 为因素。
与 HFS 组相比,HFS+WG 组有益细菌家族乳杆菌科增加了 4 倍(P=0.007)。与其他组相比,C+WG 组粪便丙酸和正丁酸至少增加了 2 倍(P<0.0001)。WG 倾向于增加(≥7%;P 趋势=0.12)调节性 T 细胞:Th17 比值,表明其具有诱导抗炎肠道环境的潜力。与未补充组相比,WG 增加了回肠抗炎细胞因子 Il10 的基因表达(≥35%;P=0.038)。与其他组相比,HFS+WG 组回肠抗菌肽 Reg3b 和 Reg3g 的基因表达上调(≥95%;P≤0.040)。WG 降低了血清中促炎细胞因子白细胞介素(IL)-1B、IL-6、干扰素-γ和肿瘤坏死因子-α的浓度(≥17%;P≤0.012)。
WG 选择性地增加了肠道乳杆菌科,上调了回肠抗菌肽,并减轻了 C57BL/6 小鼠高脂肪饮食引起的循环促炎细胞因子。这些变化对于预防 HFS 饮食引起的合并症可能至关重要。