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变应原激发致敏的棕色挪威大鼠气道对腺苷高反应性的机制

Mechanism of airway hyperresponsiveness to adenosine induced by allergen challenge in actively sensitized Brown Norway rats.

作者信息

Hannon J P, Tigani B, Williams I, Mazzoni L, Fozard J R

机构信息

Research Department, Novartis Pharma AG, CH-4002 Basel, Switzerland.

出版信息

Br J Pharmacol. 2001 Apr;132(7):1509-23. doi: 10.1038/sj.bjp.0703961.

Abstract
  1. We have explored the role of allergen sensitization and challenge in defining the response of the airways of the Brown Norway (BN) rat to adenosine. 2. In naïve animals or in rats sensitized to ovalbumin (OA) adenosine induced only weak bronchoconstrictor responses. Challenge of sensitized animals with OA induced a marked airway hyperresponsiveness to adenosine which was not seen with methacholine or bradykinin. 3. The augmented bronchoconstrictor response to adenosine was not affected by acute bivagotomy or atropine nor mimicked by an i.v. injection of capsaicin. It was, however, blocked selectively by disodium cromoglycate methysergide or ketanserin and reduced in animals treated sub-chronically with compound 48/80. 4. The augmented response to adenosine was associated with increases in the plasma concentrations of both histamine and 5-hydroxytryptamine (5-HT), which were attenuated by pretreatment with disodium cromoglycate, and degranulation of mast cells in the lung. 5. Parenchymal strips from lungs removed from sensitized rats challenged with OA gave augmented bronchoconstrictor responses to adenosine relative to strips from sensitized animals challenged with saline. Responses were inhibited by methysergide and disodium cromoglycate. 6. These data demonstrate a marked augmentation of the bronchoconstrictor response to adenosine in actively sensitized BN rats challenged with OA. The augmented response is primarily a consequence of mast cell activation, leading to the release of 5-HT, which in turn induces bronchoconstriction. Our data further suggest the involvement of a discrete lung-based population of mast cells containing and releasing mainly 5-HT and brought into play by prior exposure to allergen.
摘要
  1. 我们探讨了变应原致敏和激发在确定棕色挪威(BN)大鼠气道对腺苷反应中的作用。2. 在未致敏动物或对卵清蛋白(OA)致敏的大鼠中,腺苷仅诱导微弱的支气管收缩反应。用OA激发致敏动物会诱导对腺苷的明显气道高反应性,而用乙酰甲胆碱或缓激肽激发则未观察到这种反应。3. 对腺苷增强的支气管收缩反应不受急性双侧迷走神经切断术或阿托品的影响,静脉注射辣椒素也不能模拟这种反应。然而,它被色甘酸钠、麦角新碱或酮色林选择性阻断,并且在亚慢性给予化合物48/80处理的动物中反应减弱。4. 对腺苷的增强反应与组胺和5-羟色胺(5-HT)血浆浓度的增加有关,色甘酸钠预处理可减弱这种增加,并且与肺中肥大细胞的脱颗粒有关。5. 相对于用盐水激发的致敏动物的肺组织条,用OA激发的致敏大鼠切除的肺组织条对腺苷的支气管收缩反应增强。麦角新碱和色甘酸钠可抑制反应。6. 这些数据表明,在用OA激发的主动致敏BN大鼠中,对腺苷的支气管收缩反应明显增强。增强的反应主要是肥大细胞活化的结果,导致5-HT释放,进而诱导支气管收缩。我们的数据进一步表明,存在一群基于肺的离散肥大细胞,主要含有和释放5-HT,并因先前接触变应原而被激活。

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本文引用的文献

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