首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Herbal Formula Fo Shou San Attenuates Alzheimers Disease-Related Pathologies via the Gut-Liver-Brain Axis in APP/PS1 Mouse Model of Alzheimers Disease
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Herbal Formula Fo Shou San Attenuates Alzheimers Disease-Related Pathologies via the Gut-Liver-Brain Axis in APP/PS1 Mouse Model of Alzheimers Disease

机译:佛手散中草药配方通过肠-肝-脑轴在阿尔茨海默氏病APP / PS1小鼠模型中减轻与阿尔茨海默氏病相关的病理

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摘要

Fo Shou San (FSS) is an ancient paired-herb decoction, used in China to treat blood deficiency, blood stasis, stroke, and ischemic cerebral vascular disease for about one thousand years. The mechanisms associated with these properties, however, are not completely understood. Gut bacteria, gut bacterial lipopolysaccharides (LPS), alkaline phosphatase (AP), and lipid peroxidation are common biochemical signaling that takes place on gut-liver-brain axis. Growing evidences have revealed that gut bacterial lipopolysaccharides (LPS) enter the systemic circulation via the portal vein, and finally entering the brain tissue is an important cause of inflammatory degeneration of Alzheimer's disease (AD). Alkaline phosphatase (AP) dephosphorylates LPS forming a nontoxic LPS and reduces systemic inflammation via gut-liver-brain axis. In this study, to identify the differentially gut-liver-brain axis among APP/PS1 mice, FSS-treated APP/PS1 mice, and control mice, behavioral tests were performed to assess the cognitive ability and hematoxylin-eosin staining was used to assess neuronal damage in the hippocampus; immunohistochemistry, western blotting, a quantitative chromogenic end-point Tachypleus amebocyte lysate (TAL) assay kit, Malondialdehyde (MDA) assay kit, AP Assay Kit, and real-time quantitative PCR (qPCR) were used to assess the level of LPS, MDA, AP, and gut bacteria. We found that FSS regulates gut-liver-brain axis to regulate AP and gut bacteria and attenuate the LPS-related systemic inflammation, oxidative stress (MDA), and thereby AD-related pathology in APP/PS1 mice. This is the first study to provide a reference for FSS-treated AD mice to aid in understanding the underlying mechanisms of FSS. FSS may also improve gastrointestinal tract barrier and blood-brain barrier and thus ameliorates the symptoms of AD; this is subject to our further study.
机译:佛手散(FSS)是一种古老的成对汤剂,在中国用于治疗血虚,血瘀,中风和局部缺血性脑血管疾病约一千年。但是,与这些属性相关的机制尚未完全理解。肠细菌,肠细菌脂多糖(LPS),碱性磷酸酶(AP)和脂质过氧化是在肠肝脑轴上发生的常见生化信号。越来越多的证据表明,肠道细菌脂多糖(LPS)通过门静脉进入全身循环,最后进入脑组织是阿尔茨海默氏病(AD)炎症性变性的重要原因。碱性磷酸酶(AP)使LPS脱磷酸化,形成无毒LPS,并通过肠肝脑轴减少全身性炎症。在这项研究中,为了识别APP / PS1小鼠,FSS处理的APP / PS1小鼠和对照小鼠之间的肠肝肝轴差异,进行了行为测试以评估认知能力,并使用苏木精-伊红染色来评估海马神经元损伤;免疫组化,免疫印迹,定量生色终点速殖壶菌溶胞产物(TAL)检测试剂盒,丙二醛(MDA)检测试剂盒,AP检测试剂盒和实时定量PCR(qPCR)用于评估LPS,MDA的水平,AP和肠道细菌。我们发现FSS调节肠肝脑轴,以调节AP和肠细菌,并减轻APP / PS1小鼠的LPS相关的全身性炎症,氧化应激(MDA),从而减轻AD相关的病理。这是第一项为FSS治疗的AD小鼠提供参考,以帮助了解FSS潜在机制的研究。 FSS还可以改善胃肠道屏障和血脑屏障,从而改善AD的症状。这有待我们进一步研究。

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