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吸入色甘酸通过拮抗速激肽来减轻气道神经源性炎症。

Inhaled cromoglycate reduces airway neurogenic inflammation via tachykinin antagonism.

作者信息

Yamawaki I, Tamaoki J, Takeda Y, Nagai A

机构信息

First Department of Medicine, Tokyo Women's Medical College, Japan.

出版信息

Res Commun Mol Pathol Pharmacol. 1997 Dec;98(3):265-72.

PMID:9485521
Abstract

To determine whether sodium cromoglycate (SCG) inhibits airway neurogenic inflammation and, if so, to elucidate the mechanism of its action, we studied plasma extravasation evoked by hypertonic saline in the rat trachea by measuring the amount of extravasated Evans blue dye. Inhalation of hypertonic saline (5-15% NaCl) produced microvascular leakage, an effect that was reduced by pretreatment with SCG in a dose-dependent manner. Inhaled SCG (10 mg/ml) for 2 min did not affect the basal vascular permeability, but significantly inhibited the 10% NaCl-induced plasma extravasation by 34%. SCG likewise inhibited the responses of microvascular leakage to substance P aerosols, whereas it was without effect on those to platelet activating factor aerosols. These results suggest that SCG inhibits airway neurogenic inflammation presumably via functional antagonism of tachykinins, and that this novel effect may be involved in the therapeutic efficacy of SCG in the treatment of airway inflammatory diseases including asthma.

摘要

为了确定色甘酸钠(SCG)是否能抑制气道神经源性炎症,如果能抑制,还要阐明其作用机制,我们通过测量渗出的伊文思蓝染料量,研究了高渗盐水诱发的大鼠气管血浆外渗情况。吸入高渗盐水(5%-15% NaCl)会导致微血管渗漏,而预先使用SCG可使其剂量依赖性降低。吸入SCG(10 mg/ml)2分钟对基础血管通透性无影响,但能显著抑制10% NaCl诱导的血浆外渗达34%。SCG同样能抑制微血管对P物质气雾剂渗漏的反应,而对血小板活化因子气雾剂渗漏的反应则无影响。这些结果表明,SCG可能通过对速激肽的功能拮抗作用来抑制气道神经源性炎症,并且这种新作用可能与SCG治疗包括哮喘在内的气道炎症性疾病的疗效有关。

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