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大鼠中过敏反应诱导的空肠环形平滑肌收缩的介导作用。

Mediation of anaphylaxis-induced jejunal circular smooth muscle contraction in rats.

作者信息

Scott R B, Maric M

机构信息

GI Research Group, University of Calgary, Alberta, Canada.

出版信息

Dig Dis Sci. 1993 Mar;38(3):396-402. doi: 10.1007/BF01316490.

Abstract

Altered intestinal motility and diarrhea are features of food protein-induced intestinal anaphylaxis in the conscious rat. These experiments were performed to determine the mediator(s) responsible for jejunal circular smooth muscle contraction during this response. Hooded-Lister rats were sensitized by intraperitoneal injection of 10-micrograms egg albumin, and controls were sham-sensitized with saline. Fourteen days later the contractility of the circular muscle in jejunal segments (mucosa intact) was examined in standard tissue baths in response to antigen (Ag) or other agents. While control and sensitized tissues contracted in similar fashion in response to stretch, bethanechol, histamine, or 5-hydroxytryptamine (5HT), Ag contracted only the segments of sensitized animals. The contractile response was: (1) specific to the sensitizing Ag, as bovine serum albumin did not induce contraction and (2) could be passively transferred with serum containing specific immunoglobulin E antibody (IgE-Ab). Concanavalin A, which degranulates both mucosal and connective tissue-type mast cells, and compound 48/80, which degranulates only connective tissue-type mast cells produced contractile responses. Ag-induced contraction was significantly inhibited by the mucosal and connective tissue-type mast cell stabilizer doxantrazole, but not the connective tissue mast cell stabilizer disodium cromoglycate. Diphenhydramine and cimetidine together significantly inhibited histamine-induced contraction, but failed to effect the Ag-induced contraction in sensitized tissues. While the contractile response to 5HT was reduced in the presence of methysergide (5HT1-receptor antagonist), cinanserin (5HT2-receptor antagonist), and ICS 205-930 (5HT3-receptor antagonist), only cinanserin significantly inhibited the contractile response to Ag. Indomethacin significantly inhibited Ag-induced contraction. Ag-induced contraction was resistant to atropine and tetrodotoxin.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

肠道运动改变和腹泻是清醒大鼠食物蛋白诱导的肠道过敏反应的特征。进行这些实验以确定在该反应过程中负责空肠环形平滑肌收缩的介质。通过腹腔注射10微克卵清蛋白使Hooded-Lister大鼠致敏,对照组用生理盐水进行假致敏。14天后,在标准组织浴中检查空肠段(黏膜完整)环形肌对抗原(Ag)或其他试剂的收缩性。虽然对照组织和致敏组织对拉伸、氨甲酰甲胆碱、组胺或5-羟色胺(5HT)的收缩方式相似,但Ag仅使致敏动物的肠段收缩。收缩反应为:(1)对致敏Ag具有特异性,因为牛血清白蛋白不会诱导收缩;(2)可被含有特异性免疫球蛋白E抗体(IgE-Ab)的血清被动转移。能使黏膜型和结缔组织型肥大细胞脱颗粒的刀豆球蛋白A以及仅使结缔组织型肥大细胞脱颗粒的化合物48/80产生了收缩反应。Ag诱导的收缩被黏膜型和结缔组织型肥大细胞稳定剂多沙唑嗪显著抑制,但未被结缔组织肥大细胞稳定剂色甘酸钠抑制。苯海拉明和西咪替丁共同显著抑制组胺诱导的收缩,但未能影响致敏组织中Ag诱导的收缩。虽然在存在麦角新碱(5HT1受体拮抗剂)、辛那色林(5HT2受体拮抗剂)和ICS 205-930(5HT3受体拮抗剂)的情况下对5HT的收缩反应减弱,但只有辛那色林显著抑制对Ag的收缩反应。吲哚美辛显著抑制Ag诱导的收缩。Ag诱导的收缩对阿托品和河豚毒素具有抗性。(摘要截取自250字)

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