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伊文思蓝在大鼠肠黏膜中的渗透情况。

Evans blue permeation of intestinal mucosa in the rat.

作者信息

Lange S, Delbro D S, Jennische E

机构信息

Dept. of Clinical Bacteriology, University of Göteborg, Sweden.

出版信息

Scand J Gastroenterol. 1994 Jan;29(1):38-46. doi: 10.3109/00365529409090435.

Abstract

The azo dye Evans blue (EB; molecular weight, 960.83) is widely used as an indicator of increased capillary permeability. In the present study, however, rat gut absorption of EB was investigated after dye instillation in either the small or large intestine. During a brief period of ether anaesthesia, EB was injected either into jejunal loops with a challenge period of 30 or 60 min or into a proximal and a distal colon loop with a challenge period of 30, 60, or 120 min. After the rats had been killed the intestinal specimens were washed with 6 mM acetylcysteine dissolved in phosphate-buffered saline, which efficiently cleared the tissues of mucus, and thus of EB trapped in mucus. Only EB absorbed by the gut wall remained to be estimated, and this absorption was found to be both dose- and time-dependent in the jejunum and the colon. After instillation in the colon, but not in jejunum, EB could be detected in the blood. EB absorption from the jejunum remained unaffected by the addition of either ouabain (1 mM) or lidocaine (0.38 mM). Either of these compounds inhibited EB uptake in the proximal part of the colon, while enhancing it in the distal part. Fluorescence microscopy showed penetration into the intestinal wall to be a prerequisite for EB to become fluorescent, and EB fluorescence increased with time. It is proposed that EB is transported over the mucosa by the paracellular route and that the amount of absorbed EB reflects epithelial permeability differently in different parts of the gastrointestinal tract.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

偶氮染料伊文思蓝(EB;分子量960.83)被广泛用作毛细血管通透性增加的指标。然而,在本研究中,在大鼠小肠或大肠滴注染料后,对EB的肠道吸收情况进行了研究。在短暂的乙醚麻醉期间,将EB注入空肠肠袢,激发期为30或60分钟,或注入近端和远端结肠肠袢,激发期为30、60或120分钟。大鼠处死之后,用溶解于磷酸盐缓冲盐水中的6 mM乙酰半胱氨酸冲洗肠道标本,该溶液能有效清除组织中的黏液,从而清除被困在黏液中的EB。仅估算肠壁吸收的EB,发现这种吸收在空肠和结肠中均呈剂量和时间依赖性。在结肠而非空肠滴注后,可在血液中检测到EB。空肠中EB的吸收不受哇巴因(1 mM)或利多卡因(0.38 mM)添加的影响。这两种化合物中的任何一种均可抑制结肠近端部分对EB的摄取,同时增强结肠远端部分对EB的摄取。荧光显微镜检查显示,EB渗透到肠壁是其产生荧光的前提条件,且EB荧光随时间增加。有人提出,EB通过细胞旁途径在黏膜上转运,且吸收的EB量在胃肠道不同部位对上皮通透性的反映有所不同。(摘要截于250词)

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