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16,16 - 二甲基前列腺素E2或硫代硫酸钠对大鼠胃黏膜免受高渗氯化钠损伤的保护作用:损伤因子黏膜渗透减少的证据

Protection of gastric mucosa against hypertonic sodium chloride by 16,16-dimethyl prostaglandin E2 or sodium thiosulfate in the rat: evidence for decreased mucosal penetration of damaging agent.

作者信息

Pihan G, Szabo S

机构信息

Department of Pathology, Brigham & Women's Hospital, Boston, Massachusetts 02115.

出版信息

Dig Dis Sci. 1989 Dec;34(12):1865-72. doi: 10.1007/BF01536704.

Abstract

Protection of the gastric mucosa may be the result of either increased cellular resistance to injury (cytoprotection) or, alternatively, decreased exposure of mucosal cells to the damaging agent. To determine whether decreased exposure of mucosal cells to damaging agents plays a role in mucosal protection by 16,16-dm PGE2 or sodium thiosulfate, we estimated the intramucosal concentration of 22NaCl and measured its absorption from the gastric lumen into the systemic circulation 1 and 5 min after intragastric administration of hypertonic (25% w/v) 22NaCl. In an attempt to explain the differences observed, we also measured the net transmucosal water flux in control animals and rats pretreated with the protective agents. Administration of hypertonic NaCl rapidly (within 1 min) induced extensive hemorrhagic mucosal lesions that were significantly reduced by pretreatment with 16,16-dm PGE2 or sodium thiosulfate. Ultra-low temperature autoradiography indicated that luminal hypertonic 22NaCl penetrates the upper layers of the mucosa in relatively high concentrations (12.5% w/v) within 1 min but its concentration decreases rapidly and reached low levels (3.12% w/v) by 5 min. Absorption of NaCl from the gastric lumen into the systemic circulation 1 and 5 min after hypertonic NaCl was lower in both pretreatment groups than in the control. Net gastric transmucosal water flux (from serosa to mucosa) increased (P less than 0.05) from 100 +/- 2 in controls, to 1470 +/- 8 and 715 +/- 9 microliters in rats pretreated with 16,16-dm PGE2 and sodium thiosulfate, respectively. We conclude that 16,16-dm PGE2 and sodium thiosulfate protect the gastric mucosa against hypertonic NaCl, diminish mucosal penetration of NaCl, decrease mucosal absorption of NaCl, and significantly increase serosal to mucosal transmucosal water flux.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

胃黏膜的保护作用可能是细胞对损伤的抵抗力增强(细胞保护作用)的结果,或者是黏膜细胞与损伤因子接触减少的结果。为了确定黏膜细胞与损伤因子接触减少是否在16,16 - 二甲基前列腺素E2(16,16 - dm PGE2)或硫代硫酸钠对黏膜的保护作用中发挥作用,我们估计了胃黏膜内22氯化钠(22NaCl)的浓度,并在胃内给予高渗(25% w/v)22NaCl后1分钟和5分钟测量其从胃腔吸收进入体循环的情况。为了解释观察到的差异,我们还测量了对照动物和用保护剂预处理的大鼠的净跨黏膜水通量。给予高渗氯化钠后迅速(1分钟内)诱发广泛的出血性黏膜损伤,而用16,16 - dm PGE2或硫代硫酸钠预处理可显著减轻这种损伤。超低温放射自显影显示,腔内高渗22NaCl在1分钟内以相对较高的浓度(12.5% w/v)穿透黏膜上层,但在5分钟时其浓度迅速下降并达到低水平(3.12% w/v)。在两个预处理组中,高渗氯化钠后1分钟和5分钟时,从胃腔到体循环的氯化钠吸收均低于对照组。胃净跨黏膜水通量(从浆膜到黏膜)从对照组的100±2微升增加(P<0.05)到用16,16 - dm PGE2和硫代硫酸钠预处理的大鼠分别为1470±8微升和715±9微升。我们得出结论,16,16 - dm PGE2和硫代硫酸钠可保护胃黏膜免受高渗氯化钠的损伤,减少氯化钠对黏膜的穿透,降低黏膜对氯化钠的吸收,并显著增加从浆膜到黏膜的跨黏膜水通量。(摘要截短为250字)

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