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IZP-94005(角鲨烯甾醇)对卵清蛋白致敏豚鼠抗原诱导的支气管反应性的影响。

Effects of IZP-94005 (contignasterol) on antigen-induced bronchial responsiveness in ovalbumin-sensitized guinea-pigs.

作者信息

Bramley A M, Langlands J M, Jones A K, Burgoyne D L, Li Y, Andersen R J, Salari H

机构信息

Inflazyme Pharmaceuticals Ltd, Vancouver, Canada.

出版信息

Br J Pharmacol. 1995 Aug;115(8):1433-8. doi: 10.1111/j.1476-5381.1995.tb16634.x.

Abstract
  1. We have investigated the novel naturally occurring marine compound, IZP-94005 (contignasterol), as a potential anti-asthma agent, using both in vivo and in vitro models of allergen-induced bronchoconstriction and airway smooth muscle contraction. 2. Tracheal rings from ovalbumin (OA)-sensitized guinea-pigs were treated with various concentrations of IZP-94005 for 20 min prior to challenge with ovalbumin. IZP-94005 (3-30 microM) inhibited responses of sensitized tracheal rings stimulated with OA in a concentration-dependent manner, with an IC50 of 10 microM. 3. IZP-94005 (10 microM) had no effect on carbachol-induced contractions of sensitized guinea-pig tracheal rings, although it did inhibit histamine-induced responses of OA sensitized guinea-pig tracheal rings. 4. The effects of IZP-94005 in vivo were examined using OA-sensitized guinea-pigs which were tracheotomized under anaesthesia and placed in a body plethysmograph. Measurements of lung resistance and compliance were performed by isovolumetric analysis of volume and trans-pulmonary pressure. 5. IZP-94005 (50 and 200 micrograms kg-1), by inhalation 20 min prior to OA challenge caused significant inhibition of the increase in lung resistance induced by OA in sensitized guinea-pigs, compared to vehicle-treated animals. Nedocromil sodium (20 mg kg-1), with a similar protocol, also inhibited OA-induced responses in this model. 6. We therefore suggest that IZP-94005 is a good candidate for further investigation as a possible antiasthma agent.
摘要
  1. 我们使用变应原诱导的支气管收缩和气道平滑肌收缩的体内和体外模型,研究了新型天然存在的海洋化合物IZP-94005(邻萜甾醇)作为一种潜在的抗哮喘药物。2. 用不同浓度的IZP-94005处理卵清蛋白(OA)致敏豚鼠的气管环20分钟,然后用卵清蛋白进行激发。IZP-94005(3 - 30微摩尔)以浓度依赖的方式抑制OA刺激的致敏气管环的反应,IC50为10微摩尔。3. IZP-94005(10微摩尔)对卡巴胆碱诱导的致敏豚鼠气管环收缩没有影响,尽管它确实抑制了OA致敏豚鼠气管环对组胺的反应。4. 使用在麻醉下进行气管切开并置于体容积描记器中的OA致敏豚鼠,研究IZP-94005的体内作用。通过对容积和跨肺压进行等容分析来测量肺阻力和顺应性。5. 与载体处理的动物相比,在OA激发前20分钟吸入IZP-94005(50和200微克/千克)可显著抑制致敏豚鼠中OA诱导的肺阻力增加。按照类似方案,奈多罗米钠(20毫克/千克)也抑制该模型中OA诱导的反应。6. 因此,我们认为IZP-94005作为一种可能的抗哮喘药物,是进一步研究的良好候选物。

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