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Metabolomics analysis of herb-partitioned moxibustion treatment on rats with diarrhea-predominant irritable bowel syndrome

机译:腹泻为主的肠易激综合征大鼠中药分区灸的代谢组学分析

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Irritable bowel syndrome (IBS) is a common functional gastrointestinal disorder, which is commonly treated with antidiarrhoeal, antispasmodics, serotonergic agents or laxative agents. These treatments provide relief for IBS symptoms but may also lead to undesired side effects. Previously, herb-partitioned moxibustion (HPM) treatment has been demonstrated to be effective in ameliorating symptoms of IBS. However, the underlying mechanism of this beneficial treatment is yet to be established. The aim of the current study was to systematically assess the metabolic alterations in response to diarrhea-predominant IBS (IBS-D) and therapeutic effect of HPM. Proton nuclear magnetic resonance spectroscopy (1H NMR)-based metabolomics approach was used to investigate fecal and serum metabolome of rat model of IBS-D with and without HPM treatment. The current results showed that IBS-induced metabolic alterations in fecal and serum sample include higher level of threonine and UDP-glucose together with lower levels of aspartate, ornithine, leucine, isoleucine, proline, 2-hydroxy butyrate, valine, lactate, ethanol, arginine, 2-oxoisovalerate and bile acids. These altered metabolites potentially involve in impaired gut secretory immune system and intestinal inflammation, malabsorption of nutrients, and disordered metabolism of bile acids. Notably, the HPM treatment was found able to normalize the Bristol stool forms scale scores, fecal water content, plasma endotoxin level, and a number of IBS-induced metabolic changes. These findings may provide useful insight into the molecular basis of IBS and mechanism of the HPM intervention.
机译:肠易激综合症(IBS)是一种常见的功能性胃肠道疾病,通常用止泻药,解痉药,血清素能药物或通便药治疗。这些疗法可缓解IBS症状,但也可能导致不良副作用。以前,草药分隔的艾灸(HPM)治疗已被证明可有效缓解IBS症状。但是,这种有益治疗的潜在机制尚未建立。本研究的目的是系统评估因腹泻为主的IBS(IBS-D)和HPM的治疗作用引起的代谢改变。基于质子核磁共振波谱(1H NMR)的代谢组学方法研究了有或没有HPM治疗的IBS-D大鼠模型的粪便和血清代谢组。目前的结果表明,IBS诱导的粪便和血清样品代谢变化包括较高水平的苏氨酸和UDP-葡萄糖,以及较低水平的天冬氨酸,鸟氨酸,亮氨酸,异亮氨酸,脯氨酸,2-羟基丁酸酯,缬氨酸,乳酸,乙醇,精氨酸,2-氧代异戊酸和胆汁酸。这些改变的代谢物可能涉及肠道分泌免疫系统受损和肠道炎症,营养吸收不良以及胆汁酸代谢紊乱。值得注意的是,发现HPM治疗能够使布里斯托尔的粪便形式量表评分,粪便水含量,血浆内毒素水平和许多IBS诱导的代谢变化正常化。这些发现可能为IBS的分子基础和HPM干预的机制提供有用的见解。

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