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本文引用的文献

1
Clinical significance of translocation.易位的临床意义。
Gut. 1994 Jan;35(1 Suppl):S28-34. doi: 10.1136/gut.35.1_suppl.s28.
2
Bacterial translocation: the influence of dietary variables.细菌易位:饮食变量的影响
Gut. 1994 Jan;35(1 Suppl):S23-7. doi: 10.1136/gut.35.1_suppl.s23.
3
Uptake and translocation of microparticles in small intestine. Morphology and quantification of particle distribution.微粒在小肠中的摄取与转运。微粒分布的形态学及定量分析。
Dig Dis Sci. 1995 May;40(5):967-75. doi: 10.1007/BF02064184.
4
Hyperplasia of the mesenterial windows precedes that of the small gut in the streptozotocin-diabetic rat.在链脲佐菌素诱导的糖尿病大鼠中,肠系膜窗的增生先于小肠的增生。
APMIS. 1988 May;96(5):407-14. doi: 10.1111/j.1699-0463.1988.tb05323.x.
5
Modified smooth muscle responses of jejunum in streptozotocin-diabetic rats.链脲佐菌素诱导的糖尿病大鼠空肠平滑肌反应的改变
J Pharmacol Exp Ther. 1988 Mar;244(3):1045-50.
6
Effects of streptozotocin-diabetes on rat intestinal mucin and goblet cells.链脲佐菌素诱导的糖尿病对大鼠肠道黏蛋白和杯状细胞的影响。
Gastroenterology. 1989 Jul;97(1):68-75. doi: 10.1016/0016-5085(89)91417-0.
7
The uptake and translocation of latex nanospheres and microspheres after oral administration to rats.
J Pharm Pharmacol. 1989 Dec;41(12):809-12. doi: 10.1111/j.2042-7158.1989.tb06377.x.
8
Adaptation of small intestinal membrane transport processes during diabetes mellitus in rats.大鼠糖尿病期间小肠膜转运过程的适应性变化
Can J Physiol Pharmacol. 1990 May;68(5):630-5. doi: 10.1139/y90-092.
9
Nanoparticle uptake by the rat gastrointestinal mucosa: quantitation and particle size dependency.大鼠胃肠道黏膜对纳米颗粒的摄取:定量分析及粒径依赖性
J Pharm Pharmacol. 1990 Dec;42(12):821-6. doi: 10.1111/j.2042-7158.1990.tb07033.x.
10
Proliferation rate and transit time of mucosal cells in small intestine of the diabetic rat.糖尿病大鼠小肠黏膜细胞的增殖率和转运时间
Gastroenterology. 1977 Dec;73(6):1326-32.

链脲佐菌素诱导糖尿病大鼠体内微粒的胃肠道摄取与转运

Gastrointestinal uptake and translocation of microparticles in the streptozotocin-diabetic rat.

作者信息

McMinn L H, Hodges G M, Carr K E

机构信息

School of Biomedical Science/Anatomy, Queen's University of Belfast, Northern Ireland, UK.

出版信息

J Anat. 1996 Dec;189 ( Pt 3)(Pt 3):553-9.

PMID:8982830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1167697/
Abstract

Uptake and translocation of particulates across the mucosal barrier of the gastrointestinal (GI) tract is now generally recognised but the effect of pathophysiologically induced changes on this process is less well established. This study evaluated the effect of diabetes mellitus on GI absorption of particles, comparing particle localisation and particle loading in different microanatomical sites of the primary organ (small intestine) and possible particle translocation pathways to selected secondary organs (mesenteric lymph nodes, liver, spleen) in normal and streptozotocin-induced diabetic animals. Fluorescent polystyrene latex particles (approximately 2 microns diameter) were fed orally to young adult Sprague-Dawley rats and quantitative bulk tissue and morphological techniques used to chart particle transit across the small intestine to secondary organs 0.5 h postadministration. In the normal animal, epifluorescence and confocal laser scanning microscopy provided confirmatory evidence for particle absorption within the primary organ and transport to other sites in the body. By contrast, in the diabetic animal, particle translocation and peripheral distribution were reduced with approximately 30% decrease in particle loading in the epithelial/nonepithelial tissue compartments. This could be a consequence of gastric retention and altered intestinal motility and permeability which are known to be associated with diabetes.

摘要

颗粒物质穿过胃肠道(GI)粘膜屏障的摄取和转运现已得到普遍认可,但病理生理诱导的变化对这一过程的影响尚不明确。本研究评估了糖尿病对颗粒物质胃肠道吸收的影响,比较了正常动物和链脲佐菌素诱导的糖尿病动物中,颗粒在主要器官(小肠)不同微观解剖部位的定位和负载情况,以及颗粒向选定二级器官(肠系膜淋巴结、肝脏、脾脏)的可能转运途径。将荧光聚苯乙烯乳胶颗粒(直径约2微米)经口投喂给年轻成年Sprague-Dawley大鼠,并使用定量整体组织和形态学技术绘制给药后0.5小时颗粒从小肠到二级器官的转运情况。在正常动物中,落射荧光和共聚焦激光扫描显微镜为颗粒在主要器官内的吸收以及向身体其他部位的转运提供了确凿证据。相比之下,在糖尿病动物中,颗粒转运和外周分布减少,上皮/非上皮组织隔室中的颗粒负载量减少了约30%。这可能是胃潴留以及肠道运动和通透性改变的结果,已知这些都与糖尿病有关。