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豚鼠肺死后支气管收缩期间速激肽的恢复情况。

Tachykinin recovery during postmortem bronchoconstriction in guinea pig lungs.

作者信息

Martins M A, Shore S A, Drazen J M

机构信息

Departments of Medicine, Beth Israel Hospital, Brigham and Women's Hospital, Boston, Massachusetts.

出版信息

J Appl Physiol (1985). 1991 Mar;70(3):1215-9. doi: 10.1152/jappl.1991.70.3.1215.

Abstract

We examined the role of substance P (SP) and neurokinin A (NKA) in the postmortem bronchoconstriction in guinea pig lungs using isolated lungs superfused via the trachea. Airway opening pressure (Pao) during superfusion was monitored and the superfusate collected for analysis of SP- and NKA-like immunoreactivities (SP-LI and NKA-LI, respectively). Peak Pao (39.0 +/- 3.9 cmH2O) was reached 10 min after starting superfusion; Pao decreased slowly thereafter, reaching only 9.9 +/- 2.2% of the peak value 2 h after starting superfusion (P less than 0.005); 12.6 +/- 2.6 and 34.0 +/- 9.7 fmol of SP-LI and NKA-LI, respectively, were found in the fraction corresponding to 10-20 min of superfusion. Recovered immunoreactivities decreased to 5.2 +/- 0.3 and 9.3 +/- 1.8 fmol of SP-LI and NKA-LI, respectively, in the fraction corresponding to 110-120 min of superfusion (P less than 0.05). Inhibition of neutral endopeptidase with thiorphan resulted in significantly greater increases in Pao (P less than 0.005) and augmentation of the recovery of SP-LI and NKA-LI (P less than 0.05 and P less than 0.001, respectively). Capsaicin treatment of animals 7-10 days before the removal of their lungs abolished the increase in Pao during superfusion and resulted in a significant decrease in the amount of SP-LI and NKA-LI recovered. Our data confirm that tachykinin release occurs during postmortem bronchoconstriction in guinea pig lungs and, furthermore, that tachykinin degradation by NEP modulates the intensity of this response.

摘要

我们使用经气管灌注的离体豚鼠肺,研究了P物质(SP)和神经激肽A(NKA)在豚鼠肺死后支气管收缩中的作用。灌注期间监测气道开口压力(Pao),并收集灌注液分析SP样免疫反应性(SP-LI)和NKA样免疫反应性(分别为NKA-LI)。开始灌注后10分钟达到Pao峰值(39.0±3.9 cmH₂O);此后Pao缓慢下降,开始灌注2小时后仅达到峰值的9.9±2.2%(P<0.005);在对应于灌注10-20分钟的部分中,分别发现12.6±2.6和34.0±9.7 fmol的SP-LI和NKA-LI。在对应于灌注110-120分钟的部分中,回收的免疫反应性分别降至5.2±0.3和9.3±1.8 fmol的SP-LI和NKA-LI(P<0.05)。用硫磷酰胺抑制中性内肽酶导致Pao显著增加(P<0.005),并增强SP-LI和NKA-LI的回收率(分别为P<0.05和P<0.001)。在摘除肺前7-10天用辣椒素处理动物,消除了灌注期间Pao的增加,并导致回收的SP-LI和NKA-LI量显著减少。我们的数据证实,速激肽在豚鼠肺死后支气管收缩期间释放,此外,NEP对速激肽的降解调节了这种反应的强度。

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