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早期哮喘反应后变应原诱导的气道对收缩性激动剂高反应性中一氧化氮缺乏:一项体外研究

Deficiency of nitric oxide in allergen-induced airway hyperreactivity to contractile agonists after the early asthmatic reaction: an ex vivo study.

作者信息

de Boer J, Meurs H, Coers W, Koopal M, Bottone A E, Visser A C, Timens W, Zaagsma J

机构信息

Department of Medicinal Chemistry and Molecular Pharmacology, University Centre for Pharmacy, Groningen, The Netherlands.

出版信息

Br J Pharmacol. 1996 Nov;119(6):1109-16. doi: 10.1111/j.1476-5381.1996.tb16011.x.

Abstract
  1. Using a guinea-pig model of allergic asthma, we investigated the role of nitric oxide (NO) in allergen-induced airway hyperreactivity after the early asthmatic reaction, by examining the effects of the NO-synthase inhibitor N omega-nitro-L-arginine methyl ester (L-NAME) on the responsiveness to methacholine and histamine of isolated perfused tracheae from unchallenged (control) animals and from animals 6 h after ovalbumin challenge. 2. All animals developed airway hyperreactivity to inhaled histamine at 6 h after ovalbumin challenge, with a mean 3.11 +/- 0.45 fold increase in sensitivity to the agonist (P < 0.001). 3. In perfused tracheal preparations from the ovalbumin-challenged guinea-pigs, the maximal responses (Emax) to methacholine and histamine were significantly enhanced compared to controls, both after intraluminal (IL) and extraluminal (EL) administration of the contractile agonists. In addition, a small but significant increase in the pD2 (-log10 EC50) for IL and EL methacholine and for IL histamine was observed. As a consequence, the delta pD2 (EL-IL) for histamine was slightly decreased from 1.67 +/- 0.13 to 1.23 +/- 0.14 (P < 0.05). However, the delta pD2 for methacholine was unchanged (1.85 +/- 0.11 and 1.77 +/- 0.12, respectively; NS). 4. Incubation of control tracheae with 100 microM L-NAME (IL) significantly enhanced the Emax for both IL and EL methacholine and histamine to approximately the same degree as observed after ovalbumin challenge, with no effect on the pD2 and delta pD2 for both agonists. On the contrary, L-NAME had no effect on Emax and pD2 values of tracheal preparations from ovalbumin-challenged guinea-pigs. 5. L-NAME (10 microM-1 mM) had no effect on methacholine-induced contraction of isolated tracheal strip preparations obtained from control animals, indicating that L-NAME has no antimuscarinic effect on tracheal smooth muscle. 6. Histological examination of the intact tracheal preparations indicated epithelial and subepithelial infiltration of eosinophils after ovalbumin challenge. However, no apparent damage of the airway epithelium was observed in these preparations. 7. The results indicate that a deficiency of NO contributes to allergen-induced airway hyperreactivity after the early asthmatic reaction and that this deficiency appears not to be due to epithelial shedding.
摘要
  1. 我们使用变应性哮喘豚鼠模型,通过检测一氧化氮合酶抑制剂Nω-硝基-L-精氨酸甲酯(L-NAME)对未激发(对照)动物以及卵清蛋白激发后6小时动物的离体灌注气管对乙酰甲胆碱和组胺反应性的影响,研究了一氧化氮(NO)在早期哮喘反应后变应原诱导的气道高反应性中的作用。2. 所有动物在卵清蛋白激发后6小时对吸入组胺出现气道高反应性,对激动剂的敏感性平均增加3.11±0.45倍(P<0.001)。3. 在来自卵清蛋白激发的豚鼠的灌注气管制备物中,与对照相比,在腔内(IL)和腔外(EL)给予收缩性激动剂后,对乙酰甲胆碱和组胺的最大反应(Emax)均显著增强。此外,观察到IL和EL乙酰甲胆碱以及IL组胺的pD2(-log10 EC50)有小幅但显著的增加。因此,组胺的δpD2(EL-IL)从1.67±0.13略微降低至1.23±0.14(P<0.05)。然而,乙酰甲胆碱的δpD2未改变(分别为1.85±0.11和1.77±0.12;无显著性差异)。4. 用100μM L-NAME(IL)孵育对照气管,显著增强了IL和EL乙酰甲胆碱以及组胺的Emax,达到与卵清蛋白激发后观察到的大致相同程度,对两种激动剂的pD2和δpD2无影响。相反,L-NAME对卵清蛋白激发的豚鼠的气管制备物的Emax和pD2值无影响。5. L-NAME(10μM - 1mM)对从对照动物获得的离体气管条制备物的乙酰甲胆碱诱导的收缩无影响,表明L-NAME对气管平滑肌无抗毒蕈碱作用。6. 对完整气管制备物的组织学检查表明,卵清蛋白激发后嗜酸性粒细胞在上皮和上皮下浸润。然而,在这些制备物中未观察到气道上皮有明显损伤。7. 结果表明,NO缺乏促成了早期哮喘反应后变应原诱导的气道高反应性,且这种缺乏似乎不是由于上皮脱落所致。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573e/1915910/3b0800d5ebf5/brjpharm00075-0038-a.jpg

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