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An In Vitro Study of the Influence of Curcuma longa Extracts on the Microbiota Modulation Process In Patients with Hypertension

机译:姜黄提取物对高血压患者微生物群调节过程影响的体外研究

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摘要

The multiple causes of cardiovascular diseases signify a major incidence and developmental risk of this pathology. One of the processes accountable for this pathologic development is the instauration of dysbiosis and its connection with an inflammatory process. Low antioxidant colonic protection encourages the progression of inflammation, with cardiovascular dysfunctions being a secondary consequence of the dysbiosis. Curcumin is one of the bioactive compounds displaying promising results for the reduction of an inflammatory process. The present study aims at demonstrating the capacity of three extracts drawn from Curcuma (C.) longa through an in vitro simulation process, for microbiota modulation in patients with hypertension. The acidic pH in the extraction process determined a high curcumin content in the extracts. The major phenolic compound identified was curcumin III, 622 ± 6.88 µg/mL for the ethanol/water/acetic acid extract. Low EC50 values were associated (0.2 µg/mL for DPPH scavenging activity) with the presence of curcumin isomers. A metabolic pattern became evident because the relationship between the short-chain fatty acids acted as a clinical biomarker. The curcumin present stimulated the formation of butyric and propionic acids. Microbiota activity control included a high degree of curcumin degradation and biotransformation in the other phenolic compounds. This developmental process was supported by the progression in the enterobacteria with a corresponding escalation in the pH level. The metabolomic pattern demonstrated a performance similar to the administration of dietary fibre, with the positive effects being dose-dependent.
机译:心血管疾病的多种原因表明该病理的主要发病率和发展风险。导致这种病理发展的过程之一是恢复性失调及其与炎性过程的联系。较低的抗氧化结肠保护作用会促进炎症的发展,心血管功能障碍是营养不良的继发后果。姜黄素是一种生物活性化合物,在减少炎症过程中显示出令人鼓舞的结果。本研究旨在证明通过体外模拟过程从姜黄提取的三种提取物对高血压患者微生物群的调节作用。提取过程中的酸性pH值确定了提取物中姜黄素含量高。鉴定出的主要酚类化合物为姜黄素III,乙醇/水/乙酸提取物的浓度为622±6.88 µg / mL。低的EC50值与姜黄素异构体的存在有关(DPPH清除活性为0.2 µg / mL)。由于短链脂肪酸之间的关系充当了临床生物标记,因此代谢模式变得明显。存在的姜黄素刺激了丁酸和丙酸的形成。微生物群活性的控制包括姜黄素的高度降解和其他酚类化合物的生物转化。肠杆菌的生长和相应的pH值升高支持了这种发育过程。代谢组学模式显示出与膳食纤维施用相似的性能,其积极作用是剂量依赖性的。

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