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大鼠被动性腹膜过敏反应期间血管通透性增加。色甘酸二钠和一种硝基茚二酮的作用。

Increased vascular permeability during passive peritoneal anaphylaxis in the rat. The effects of disodium cromoglycate and a nitroindanedione.

作者信息

Ross J W, Smith H, Spicer B A

出版信息

Int Arch Allergy Appl Immunol. 1976;51(2):226-37. doi: 10.1159/000231595.

Abstract

Following intraperitoneal sensitisation of rats with rat serum containing reaginic antibody, intravenous injection of blue dye and intraperitoneal challenge with antigen caused a release of histamine, slow-reacting substance of anaphylaxis (SRS-A) and dye into their peritoneal fluids. The times taken to reach peak concentrations after challenge were less than 2 min for histamine and between 5 and 10 min for SRS-A, whilst concentrations of dye were still increasing after 2 1/2 h. The amounts of histamine released by antigen were sufficient to account for about 60% of this extravasation of dye. Disodium cromoglycate (DSCG) and a nitroindanedione (BRL 10833) inhibited extravasation by inhibition of mediator release. BRL 10833, unlike DSCG, was active after oral administration, and for a given inhibition of histamine release it produced a greater effect on extravasation when given orally than when injected intraperitoneally.

摘要

用含有反应素抗体的大鼠血清对大鼠进行腹腔致敏后,静脉注射蓝色染料并腹腔注射抗原,会导致组胺、过敏反应慢反应物质(SRS - A)和染料释放到它们的腹腔液中。激发后达到峰值浓度的时间,组胺少于2分钟,SRS - A为5至10分钟,而2个半小时后染料浓度仍在增加。抗原释放的组胺量足以解释约60%的染料渗出。色甘酸钠(DSCG)和一种硝基茚二酮(BRL 10833)通过抑制介质释放来抑制渗出。与DSCG不同,BRL 10833口服后有活性,对于给定的组胺释放抑制作用,口服给药时对渗出的影响比腹腔注射时更大。

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