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豚鼠离体气管条上皮对免疫和非免疫诱导的组胺释放及收缩影响的药理学调节

Pharmacologic modulation of the influence of the epithelium on immunologic- and nonimmunologic-induced histamine release and contraction in guinea pig superfused tracheal strips.

作者信息

Buckner C K, Fishleder R I, Conklin R, Will J A, Doran O, Graziano F M

机构信息

ICI Pharmaceuticals Group, ICI Americas Inc., Wilmington, Delaware.

出版信息

J Pharmacol Exp Ther. 1993 Feb;264(2):717-25.

PMID:7679735
Abstract

The influence of the epithelium on contractions and histamine release evoked by ovalbumin and d-tubocurarine has been examined in guinea pig superfused tracheal strips under several experimental conditions. Without drug pretreatment, removal of the epithelium resulted in larger (P < .05) total histamine released by ovalbumin, 10(-4) to 10(-1) mg/ml, and by d-tubocurarine, 3 x 10(-3) M. In the presence of indomethacin, 5 x 10(-6) M, epithelium removal resulted in elevated histamine release only at smaller ovalbumin concentrations, 10(-4) and 10(-3) mg/ml. Indomethacin did not change the influence of the epithelium on histamine release by d-tubocurarine. Indomethacin treatment abolished the influence of the epithelium on ovalbumin-induced tracheal contraction. With indomethacin, larger (P < .05) histamine release was seen with ovalbumin, 10(-1) and 1 mg/ml, when the epithelium was intact. The larger histamine release in response to ovalbumin, 10(-1) mg/ml, in the presence of the epithelium was unaltered by pyrilamine, 10(-6) M, cimetidine, 10(-4) M, and thioperamide, 10(-6) M, to block histamine H1, H2 and H3 receptors, respectively. Therefore, histamine released by ovalbumin does not stimulate histamine release through an action on these receptors when the epithelium is intact. In the presence, but not in the absence, of the epithelium, A64077, 10(-5) M, and ICI198615, 10(-8) and 10(-6) M, inhibitors of 5-lipoxygenase and LTD4/E4 receptors, respectively, inhibited histamine release by ovalbumin, 10(-1) mg/ml. Histamine release by ovalbumin, 10(-4) mg/ml, and d-tubocurarine, 3 x 10(-3) M, studied with or without epithelium was not altered by A64077 or ICI198615.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在几种实验条件下,研究了豚鼠离体气管条中上皮对卵清蛋白和d - 筒箭毒碱诱发的收缩及组胺释放的影响。在未进行药物预处理时,去除上皮会使卵清蛋白(浓度为10⁻⁴至10⁻¹mg/ml)和d - 筒箭毒碱(3×10⁻³M)释放的总组胺量增加(P <.05)。在存在5×10⁻⁶M吲哚美辛的情况下,去除上皮仅在较小的卵清蛋白浓度(10⁻⁴和10⁻³mg/ml)时导致组胺释放增加。吲哚美辛并未改变上皮对d - 筒箭毒碱组胺释放的影响。吲哚美辛处理消除了上皮对卵清蛋白诱导的气管收缩的影响。使用吲哚美辛时,当上皮完整时,卵清蛋白浓度为10⁻¹和1mg/ml时可见更大(P <.05)的组胺释放。上皮存在时,针对卵清蛋白(10⁻¹mg/ml)更大的组胺释放不受10⁻⁶M吡咯胺、10⁻⁴M西咪替丁和10⁻⁶M硫代哌酰胺的影响,它们分别用于阻断组胺H1、H2和H3受体。因此,当上皮完整时,卵清蛋白释放的组胺不会通过作用于这些受体来刺激组胺释放。在上皮存在但非不存在时,10⁻⁵M的5 - 脂氧合酶抑制剂A64077和10⁻⁸及10⁻⁶M的LTD4/E4受体抑制剂ICI198615可抑制卵清蛋白(10⁻¹mg/ml)诱导的组胺释放。无论有无上皮,研究发现10⁻⁴mg/ml的卵清蛋白和3×10⁻³M的d - 筒箭毒碱诱发的组胺释放不受A64077或ICI198615的影响。(摘要截断于250字)

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