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Oral Supplementation with Non-Absorbable Antibiotics or Curcumin Attenuates Western Diet-Induced Atherosclerosis and Glucose Intolerance in LDLR−/− Mice – Role of Intestinal Permeability and Macrophage Activation

机译:口服补充不可吸收的抗生素或姜黄素可减轻LDLR-/-小鼠中西方饮食诱发的动脉粥样硬化和葡萄糖耐量–肠道通透性和巨噬细胞活化的作用

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摘要

Association between circulating lipopolysaccharide (LPS) and metabolic diseases (such as Type 2 Diabetes and atherosclerosis) has shifted the focus from Western diet-induced changes in gut microbiota per se to release of gut bacteria-derived products into circulation as the possible mechanism for the chronic inflammatory state underlying the development of these diseases. Under physiological conditions, an intact intestinal barrier prevents this release of LPS underscoring the importance of examining and modulating the direct effects of Western diet on intestinal barrier function. In the present study we evaluated two strategies, namely selective gut decontamination and supplementation with oral curcumin, to modulate Western-diet (WD) induced changes in intestinal barrier function and subsequent development of glucose intolerance and atherosclerosis. LDLR−/− mice were fed WD for 16 weeks and either received non-absorbable antibiotics (Neomycin and polymyxin) in drinking water for selective gut decontamination or gavaged daily with curcumin. WD significantly increased intestinal permeability as assessed by in vivo translocation of FITC-dextran and plasma LPS levels. Selective gut decontamination and supplementation with curcumin significantly attenuated the WD-induced increase in plasma LPS levels (3.32 vs 1.90 or 1.51 EU/ml, respectively) and improved intestinal barrier function at multiple levels (restoring intestinal alkaline phosphatase activity and expression of tight junction proteins, ZO-1 and Claudin-1). Consequently, both these interventions significantly reduced WD-induced glucose intolerance and atherosclerosis in LDLR−/− mice. Activation of macrophages by low levels of LPS (50 ng/ml) and its exacerbation by fatty acids is likely the mechanism by which release of trace amounts of LPS into circulation due to disruption of intestinal barrier function induces the development of these diseases. These studies not only establish the important role of intestinal barrier function, but also identify oral supplementation with curcumin as a potential therapeutic strategy to improve intestinal barrier function and prevent the development of metabolic diseases.
机译:循环脂多糖(LPS)与代谢性疾病(例如2型糖尿病和动脉粥样硬化)之间的关联已将重点从西方饮食引起的肠道菌群本身变化转移到释放肠道细菌衍生产品进入循环中,将其作为可能的机制。这些疾病发展的慢性炎症状态。在生理条件下,完整的肠屏障可防止LPS的这种释放,从而强调了检查和调节西餐对肠屏障功能的直接作用的重要性。在本研究中,我们评估了两种策略,即选择性肠道净化和口服姜黄素的补充,以调节Western-diet(WD)引起的肠屏障功能的改变以及随后的葡萄糖耐量和动脉粥样硬化的发展。 LDLR-/-小鼠接受WD喂养16周,并在饮用水中接受不可吸收的抗生素(新霉素和多粘菌素)以进行选择性肠道去污或每天用姜黄素进行灌胃。通过FITC-葡聚糖的体内易位和血浆LPS水平评估,WD显着提高了肠道通透性。选择性肠净化和姜黄素补充可显着减轻WD诱导的血浆LPS水平升高(分别为3.32 vs 1.90或1.51 EU / ml),并在多个水平上改善肠屏障功能(恢复肠碱性磷酸酶活性和紧密连接蛋白的表达) ,ZO-1和Claudin-1)。因此,这两种干预措施均显着降低了LDLR-/-小鼠中WD诱发的葡萄糖耐受不良和动脉粥样硬化。低水平的LPS(50 ng / ml)激活巨噬细胞并被脂肪酸加重可能是由于肠屏障功能破坏导致微量LPS释放进入循环的机制。这些研究不仅确立了肠屏障功能的重要作用,而且确定了口服姜黄素补充剂是改善肠屏障功能和预防代谢性疾病发展的潜在治疗策略。

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