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Oral absorption mechanism of the polysaccharides from Gastrodia elata Blume base on fluorescence labeling

机译:来自荧光标记胃窦碱基碱的多糖的口腔吸收机制

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摘要

The mechanisms of action of polysaccharides in vivo have been widely elucidated. However, the systematic research of its absorption and transport mechanisms remains unclear. Herein, we extracted a polysaccharide fraction (GEP) from Gastrodia elata by water extraction and alcohol precipitation and aimed to reveal its oral absorption processes through animal models and Caco-2 cells monolayer models. Our research data showed that GEP-Cy5.5 could be absorbed through the small intestine and the main absorption intestinal segment was the ileum (the absorption rate constant [Ka]: (3.64 +/- 0.70) x 10-4 cm/s; the effective apparent permeability [Papp value]: (4.88 +/- 1.02) x 10-5 cm/s). The ligated intestinal loops also revealed that GEP-Cy5.5 could pass through the villi of the small intestine and the mucosal barrier into the submucosa. Furthermore, GEP-Cy5.5 was readily absorbed into the blood through the gastrointestinal tract, then distributed in the liver and the kidney. The Papp value of in vitro transport study was (1.29 +/- 0.08) x 10-6 cm/s, which was a time-dependent process. Notably, GEP-Cy5.5 was transported through the endocytosis process mediated by clathrin and macropinocytosis. The underlying absorptive mechanisms of GEP in vivo and in vitro were clarified, which provided the guidance for clinical medicine administration and could deepen the biological understanding of oral polysaccharides.
机译:体内多糖的作用机制已被广泛阐明。然而,对其吸收和运输机制的系统研究仍不清楚。在此,我们通过水萃取和醇沉淀从胃脂菌的多糖馏分(GEP)提取,并旨在通过动物模型和Caco-2细胞单层模型揭示其口腔吸收过程。我们的研究数据显示GEP-Cy5.5可以通过小肠吸收,主要吸收肠道片段是回肠(吸收率常数[Ka]:(3.64 +/- 0.70)×10-4cm / s;有效的表观渗透率[PAPP值] :( 4.88 +/- 1.02)×10-5cm / s)。连接的肠环还透露,Gep-Cy5.5可以通过小肠的绒毛和粘膜屏障进入粘膜下。此外,GEP-CY5.5通过胃肠道容易地吸收到血液中,然后分布在肝脏和肾脏中。体外运输研究的PAPP值是(1.29 +/- 0.08)×10-6cm / s,这是一个时间依赖的过程。值得注意的是,GEP-CY5.5通过克拉仑和大磷肾病症介导的内吞作用。澄清了GEP和体外GEP的潜在吸收机制,为临床医学给药提供了指导,可以加深对口服多糖的生物学理解。

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