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首页> 外文期刊>Journal of Pharmacy and Pharmacology >Transepithelial transport of large particles in rat: a new model for the quantitative study of particle uptake.
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Transepithelial transport of large particles in rat: a new model for the quantitative study of particle uptake.

机译:大鼠大颗粒经上皮运输:定量研究颗粒吸收的新模型。

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The transport of large particles across the intestinal mucosa and the mechanisms of transfer of the particles into the body are still little understood. Fluorescent polystyrene latex particles (2 microm diam.) were administered orally to young male Sprague-Dawley rats in doses of 2.33 x 10(3), 2.33 x 10(6) and 2.33 x 10(9) particles. After 60 min, Peyer's patches and Peyer's patch-free tissues were collected from the small intestine and colon. A novel technique was used to exclude non-translocated particles adherent to the mucosal surface; the intestinal epithelium was stripped from the intestine by immersion in Hanks' balanced salt solution containing 1.5 mM EDTA. Particles in solubilized samples of intact and epithelium-stripped Peyer's patches and Peyer's patch-free intestinal tissue and colon were quantified by fluorescence microscopy. The location of particles within the intact and epithelium-stripped gut samples was revealed by confocal microscopy. Particles were shown to have been taken up along the entire length of the small and large intestines via both Peyer's patches and the normal intestinal epithelium. The number of particles detected in the distal region was greater than in the proximal part of the small intestine, although the difference was not statistically significant. This study has revealed that large numbers of non-translocated particles adhered to the mucosal surface resulting in a high background count. The assay system was considerably improved by the epithelium-stripping technique. The process of transepithelial uptake is a potentially important route of uptake of toxic, immunologically active and radioactive substances. These particles are much larger than the conventionally accepted upper limit for absorbed materials.
机译:大颗粒跨肠粘膜的运输以及颗粒向体内的转移机制仍然鲜为人知。将荧光聚苯乙烯乳胶颗粒(直径为2微米)以2.33 x 10(3),2.33 x 10(6)和2.33 x 10(9)的剂量口服给予年轻的雄性Sprague-Dawley大鼠。 60分钟后,从小肠和结肠收集派伊尔氏淋巴结和没有派伊尔氏淋巴结的组织。一种新颖的技术被用来排除粘附在粘膜表面的非易位颗粒。通过浸入含1.5 mM EDTA的汉克斯平衡盐溶液中,将肠上皮从肠中剥离。通过荧光显微镜对完整和上皮剥离的Peyer's贴片和无Peyer's贴片的肠组织和结肠的溶解样品中的颗粒进行定量。共聚焦显微镜显示完整和上皮剥离的肠道样品中颗粒的位置。已显示颗粒已通过Peyer斑块和正常肠上皮细胞沿小肠和大肠的整个长度吸收。尽管在差异上无统计学意义,但在小肠远端区域检测到的颗粒数量大于小肠近端区域。这项研究表明,大量未移位的颗粒附着在粘膜表面,导致本底计数很高。通过上皮剥离技术大大改善了测定系统。经上皮摄取的过程是摄取有毒,免疫活性和放射性物质的潜在重要途径。这些颗粒比吸收材料的常规接受上限大得多。

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