Mourad F H, O'Donnell L J, Ogutu E, Dias J A, Farthing M J
Department of Gastroenterology, St Bartholomew's Hospital, London.
Gut. 1995 Apr;36(4):553-7. doi: 10.1136/gut.36.4.553.
Exposure of sensitised intestine to specific allergen is known to produce appreciable reduction in water and electrolyte absorption. The mediators participating in this process have not been fully characterised. The effects of the 5-hydroxytryptamine2 (5-HT2) and 5-HT3 receptor antagonists, ketanserin and granisetron, respectively, on water movement during intestinal anaphylaxis were studied. Hooded Lister rats (120-150 g) were sensitised to ovalbumen and 14 days later, intestinal water and electrolyte movement was assessed at 10 minute intervals by in situ jejunal perfusion with a plasma electrolyte solution (PES) or PES containing 20 mg/l ovalbumen. Within 20 minutes of exposure to PES+ovalbumen, net water secretion that could be completely prevented by the mast cell stabilising agent doxantrazole occurred compared with absorption with PES alone (median -20 microliters/min/g (interquartile range -43 to -5), n = 11), v (107 (86 to 113), n = 10; p < 0.01). Pre-treatment with subcutaneous ketanserin 200 micrograms/kg (n = 7) or granisetron 300 micrograms/kg (n = 8) partially inhibited the secretory response to PES+ovalbumen (18 (11 to 48) and 13 (6 to 32) respectively; both p < 0.01 compared with PES+ovalbumen control). After 40 minutes perfusion with PES+ovalbumen, the changes in water movement were less pronounced 24 (-3 to 43) and neither ketanserin or granisetron had any effect (ketanserin: 48 (28 to 87), granisetron: 41 (32 to 83); NS). In all experiments, sodium and chloride movement paralleled that of water. Thus, the profound water secretion that occurs in the early stages of intestinal anaphylaxis is partly 5-HT dependent because it can be reversed by 5-HT2 and 5-HT3 receptor antagonists. Other mediators must also be involved, especially in the late phase of anaphylaxis.
已知致敏肠道暴露于特定变应原会导致水和电解质吸收明显减少。参与这一过程的介质尚未完全明确。分别研究了5-羟色胺2(5-HT2)受体拮抗剂酮色林和5-HT3受体拮抗剂格拉司琼对肠道过敏反应期间水分移动的影响。将体重120 - 150克的带帽利斯特大鼠对卵清蛋白进行致敏,14天后,通过用血浆电解质溶液(PES)或含20毫克/升卵清蛋白的PES原位空肠灌注,每隔10分钟评估肠道水和电解质的移动情况。与单独用PES时的吸收情况相比(中位数为107微升/分钟/克(四分位间距为86至113),n = 10),在暴露于PES +卵清蛋白后20分钟内,出现了可被肥大细胞稳定剂多沙唑抑制的净水分分泌(中位数为 - 20微升/分钟/克(四分位间距为 - 43至 - 5),n = 11),差异有统计学意义(p < 0.01)。皮下注射200微克/千克酮色林(n = 7)或300微克/千克格拉司琼(n = 8)预处理可部分抑制对PES +卵清蛋白的分泌反应(分别为18微升/分钟/克(11至48)和13微升/分钟/克(6至32);与PES +卵清蛋白对照组相比,两者p均 < 0.01)。在用PES +卵清蛋白灌注40分钟后,水分移动的变化不太明显(24微升/分钟/克( - 3至43)),酮色林和格拉司琼均无任何作用(酮色林:48微升/分钟/克(28至87),格拉司琼:41微升/分钟/克(32至83);无统计学差异)。在所有实验中,钠和氯的移动与水的移动情况平行。因此,肠道过敏反应早期出现的大量水分分泌部分依赖于5-羟色胺,因为它可被5-HT2和5-HT3受体拮抗剂逆转。其他介质也必定参与其中,尤其是在过敏反应的后期阶段。