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仓鼠颊囊作为微循环研究的模型。

The hamster cheek pouch as a model in microcirculation research.

作者信息

Svensjö E

机构信息

Dept of Exploratory Pharmacology, Draco, Lund, Sweden.

出版信息

Eur Respir J Suppl. 1990 Dec;12:595s-600s; discussion 600s-601s.

PMID:2076153
Abstract

Hamster cheek pouches are bilateral invaginations of the oral mucosa and can easily be everted with their blood flow intact and are, therefore, well suited for intravital microscopy. The preparation has been used extensively for studies of inflammation, tumour growth, vascular smooth muscle function, blood flow regulation, and cellular behaviour at the microcirculatory level. The introduction and use of fluorescein-labelled dextrans (FITC-dextran) as tracers of macromolecular permeability changes have provided evidence that macromolecular permeability is subject to physiological and pharmacological regulation by gap formation between endothelial cells in the postcapillary venules. Studies with clinically used asthma drugs like isoprenaline, terbutaline, budesonide, theophylline and cromoglycate have shown that they all counteract histamine-induced permeability increase in postcapillary venules and, furthermore, that budesonide and terbutaline inhibit increased permeability caused by bradykinin, LTB4 and phorbol-dibutyrate, tertiary butylhydroperoxide and ischaemia. Pharmacological studies on the inhibition of mediator-induced leakage and migration of neutrophils in the cheek pouch could be of value not only for a better understanding of the inflammatory process in general but also for the characterization of asthma drugs having an anti-inflammatory action on the airways.

摘要

仓鼠颊囊是口腔黏膜的双侧内陷结构,能够轻易外翻且血流保持完整,因此非常适合用于活体显微镜观察。该制备方法已广泛应用于炎症、肿瘤生长、血管平滑肌功能、血流调节以及微循环水平细胞行为的研究。荧光素标记葡聚糖(FITC-葡聚糖)作为大分子通透性变化示踪剂的引入和应用,提供了证据表明大分子通透性受毛细血管后微静脉内皮细胞间缝隙形成的生理和药理调节。对临床使用的哮喘药物如异丙肾上腺素、特布他林、布地奈德、茶碱和色甘酸的研究表明,它们均能对抗组胺诱导的毛细血管后微静脉通透性增加,此外,布地奈德和特布他林还能抑制缓激肽、白三烯B4、佛波醇二丁酸酯、叔丁基过氧化氢和缺血引起的通透性增加。对颊囊中介质诱导的中性粒细胞渗漏和迁移抑制的药理学研究不仅有助于更好地理解炎症过程,也有助于对气道具有抗炎作用的哮喘药物进行特性描述。

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