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本文引用的文献

1
Acute experimental distal colitis alters colonic transit in rats.急性实验性远端结肠炎会改变大鼠的结肠运输。
J Surg Res. 1997 Apr;69(1):107-12. doi: 10.1006/jsre.1997.5042.
2
The immunomodulation of enteric neuromuscular function: implications for motility and inflammatory disorders.肠道神经肌肉功能的免疫调节:对运动和炎症性疾病的影响
Gastroenterology. 1996 Dec;111(6):1683-99. doi: 10.1016/s0016-5085(96)70034-3.
3
Comparison between the lactulose/mannitol and 51Cr-ethylenediaminetetraacetic acid/14C-mannitol methods for intestinal permeability. Frequency distribution pattern and variability of markers and marker ratios in healthy subjects.乳果糖/甘露醇法与51铬-乙二胺四乙酸/14C-甘露醇法检测肠道通透性的比较。健康受试者中标志物及其比值的频率分布模式和变异性。
Scand J Gastroenterol. 1993 Mar;28(3):274-80. doi: 10.3109/00365529309096085.
4
Mechanisms and sites of mannitol permeability of small and large intestine in the rat.大鼠小肠和大肠中甘露醇通透性的机制及部位
Dig Dis Sci. 1994 Apr;39(4):796-801. doi: 10.1007/BF02087426.
5
Test conditions greatly influence permeation of water soluble molecules through the intestinal mucosa: need for standardisation.试验条件对水溶性分子透过肠黏膜的渗透作用有很大影响:需要标准化。
Gut. 1994 Oct;35(10):1404-8. doi: 10.1136/gut.35.10.1404.
6
Dextran sulfate sodium-induced colitis occurs in severe combined immunodeficient mice.硫酸葡聚糖钠诱导的结肠炎发生在严重联合免疫缺陷小鼠中。
Gastroenterology. 1994 Dec;107(6):1643-52. doi: 10.1016/0016-5085(94)90803-6.
7
Differential in vivo and in vitro intestinal permeability to lactulose and mannitol in animals and humans: a hypothesis.动物和人类体内及体外对乳果糖和甘露醇的肠道通透性差异:一种假说。
Gastroenterology. 1995 Mar;108(3):687-96. doi: 10.1016/0016-5085(95)90440-9.
8
Intestinal permeability: an overview.肠道通透性:综述
Gastroenterology. 1995 May;108(5):1566-81. doi: 10.1016/0016-5085(95)90708-4.
9
Absorption of 51chromium-labeled ethylenediaminetetraacetate in inflammatory bowel disease.51铬标记的乙二胺四乙酸在炎症性肠病中的吸收情况
Gastroenterology. 1983 Aug;85(2):318-22.
10
Small bowel and colonic permeability to 51Cr-EDTA in patients with active inflammatory bowel disease.活动性炎症性肠病患者小肠和结肠对51铬-乙二胺四乙酸的通透性
Clin Invest Med. 1988 Apr;11(2):151-5.

小鼠结肠炎中的肠道通透性和收缩性

Intestinal permeability and contractility in murine colitis.

作者信息

van Meeteren M E, van Bergeijk J D, van Dijk A P, Tak C J, Meijssen M A, Zijlstra F J

机构信息

Department of Pharmacology, Erasmus University Rotterdam, The Netherlands.

出版信息

Mediators Inflamm. 1998;7(3):163-8. doi: 10.1080/09629359891090.

DOI:10.1080/09629359891090
PMID:9705603
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1781840/
Abstract

We developed an in vitro organ bath method to measure permeability and contractility simultaneously in murine intestinal segments. To investigate whether permeability and contractility are correlated and influenced by mucosal damage owing to inflammation, BALB/c mice were exposed to a 10% dextran sulphate sodium (DSS) solution for 8 days to induce colitis. The effect of pharmacologically induced smooth muscle relaxation and contraction on permeability was tested in vitro. Regional permeability differences were observed in both control and 10% DSS-treated mice. Distal colon segments were less permeable to 3H-mannitol and 14C-PEG 400 molecules compared with proximal colon and ileum. Intestinal permeability in control vs. 10% DSS mice was not altered, although histologic inflammation score and IFN-gamma pro-inflammatory cytokine levels were significantly increased in proximal and distal colon. IL-1beta levels were enhanced in these proximal and distal segments, but not significantly different from controls. Any effect of pharmacologically induced contractility on intestinal permeability could not be observed. In conclusion, intestinal permeability and contractility are not correlated in this model of experimentally induced colitis in mice. Although simultaneous measurement in a physiological set-up is possible, this method has to be further validated.

摘要

我们开发了一种体外器官浴方法,用于同时测量小鼠肠段的通透性和收缩性。为了研究通透性和收缩性是否相关,以及是否受炎症引起的粘膜损伤影响,将BALB/c小鼠暴露于10%硫酸葡聚糖钠(DSS)溶液中8天以诱导结肠炎。在体外测试了药理学诱导的平滑肌舒张和收缩对通透性的影响。在对照小鼠和10% DSS处理的小鼠中均观察到区域通透性差异。与近端结肠和回肠相比,远端结肠段对3H-甘露醇和14C-聚乙二醇400分子的通透性较低。尽管近端和远端结肠的组织学炎症评分和IFN-γ促炎细胞因子水平显著升高,但对照小鼠与10% DSS小鼠的肠道通透性没有改变。这些近端和远端节段中IL-1β水平升高,但与对照无显著差异。未观察到药理学诱导的收缩性对肠道通透性的任何影响。总之,在这种实验性诱导的小鼠结肠炎模型中,肠道通透性和收缩性不相关。虽然在生理环境中进行同步测量是可能的,但这种方法必须进一步验证。