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色甘酸钠抑制豚鼠离体气道平滑肌抗原诱导收缩的双重作用模式。

Dual modes of action for disodium cromoglycate in inhibition of antigen-induced contractions of guinea-pig isolated airways smooth muscle.

作者信息

Stewart A G, Fennessy M R

出版信息

Clin Exp Pharmacol Physiol. 1983 Sep-Oct;10(5):595-603. doi: 10.1111/j.1440-1681.1983.tb00228.x.

Abstract

Disodium cromoglycate (DSCG; 10 mumol/l-1 mmol/l) relaxed the tone induced in the guinea-pig isolated trachea by histamine (5 mumol/l). Both isoprenaline and fenoterol were approximately 1000 times more potent than DSCG in relaxing tracheal smooth muscle. Ovalbumin (1 microgram/ml) contracted isolated tracheal and parenchymal strips from sensitized guinea-pigs. The sensitization procedure used was selective for eliciting IgG antibody production. In concentrations equieffective for relaxation of the isolated trachea, fenoterol (20 nmol/l), isoprenaline (60 nmol/l) and DSCG (100 mumol/l) inhibited ovalbumin-induced contractions of both tracheal and parenchymal strip preparations. DSCG produced a significantly greater (P less than 0.05) inhibition of ovalbumin-induced contractions of isolated trachea than did isoprenaline, suggesting that at 100 mumol/l DSCG produced a greater inhibition of mediator release than that produced by isoprenaline. Compound 48/80 (200 micrograms/ml) contracted the isolated trachea whereas this concentration had no contractile effect on the parenchymal strip. The failure of DSCG to inhibit compound 48/80 induced contractions of the isolated trachea together with the lack of contractile effect of compound 48/80 on the parenchymal strip suggest that compound 48/80 is inferior to antigenic stimulation as a reliable analogue of immunological activation of mast cells and consequent mediator release.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

色甘酸钠(DSCG;10微摩尔/升 - 1毫摩尔/升)可舒张组胺(5微摩尔/升)诱导的豚鼠离体气管的张力。在舒张气管平滑肌方面,异丙肾上腺素和非诺特罗的效力比DSCG约强1000倍。卵清蛋白(1微克/毫升)可使致敏豚鼠的离体气管和实质条收缩。所采用的致敏程序对引发IgG抗体产生具有选择性。在对离体气管舒张等效的浓度下,非诺特罗(20纳摩尔/升)、异丙肾上腺素(60纳摩尔/升)和DSCG(100微摩尔/升)均抑制卵清蛋白诱导的气管和实质条制剂的收缩。与异丙肾上腺素相比,DSCG对卵清蛋白诱导的离体气管收缩的抑制作用显著更强(P小于0.05),这表明在100微摩尔/升时,DSCG对介质释放的抑制作用比异丙肾上腺素更强。化合物48/80(200微克/毫升)可使离体气管收缩,而该浓度对实质条无收缩作用。DSCG未能抑制化合物48/80诱导的离体气管收缩,以及化合物48/80对实质条无收缩作用,这表明化合物48/80作为肥大细胞免疫激活及随后介质释放的可靠类似物,不如抗原刺激有效。(摘要截短于250字)

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