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在感染副流感病毒的豚鼠中,咳嗽反射敏感性增加。

Cough reflex sensitivity is increased in guinea pigs with parainfluenza virus infection.

作者信息

Ye X M, Zhong N S, Liu C L, Chen R C

机构信息

Department of Respiration, Nanjing Children's Hospital, Nanjing Medical University, Nanjing, China.

出版信息

Exp Lung Res. 2011 Apr;37(3):186-94. doi: 10.3109/01902148.2010.540768. Epub 2011 Feb 11.

Abstract

The purpose of this study was to investigate for the change in cough reflex sensitivity (CRS) caused by parainfluenza virus type 3 (PIV3) infection. Guinea pigs were randomized into a vehicle control, an asthma control, or 1 of 4 PIV3-inoculated groups (referred to as postinfection day [PID] 6, 12, 28, and 42 groups). Evidence of viral protein and nucleic acid within the lung confirmed successful PIV3 infection. Plethysmography was used to assess CRS and airway reaction and airway inflammation was assessed via bronchoalveolar lavage fluid cytology and lung histopathology. Compared with the vehicle control group, CRS was significantly increased in all PID groups (P <.05) in concert with an obvious airway hyperresponsiveness in the PID 6 group. Though a small increase in CRS in the asthma control group was noted, it was not significant compared to the vehicle control group. Total cell counts from the bronchoalveolar lavage fluid of all PIV3-inoculated groups increased markedly and the number of lymphocytes was significantly increased in the PID 6 and PID 12 groups. The lung pathology of PIV3-inoculated animals showed airway inflammation without pneumonia in the acute infectious phase. The temporal and spatial variation of CRS may be the essential mechanism of cough caused by PIV3.

摘要

本研究的目的是调查3型副流感病毒(PIV3)感染引起的咳嗽反射敏感性(CRS)变化。将豚鼠随机分为溶剂对照组、哮喘对照组或4个PIV3接种组之一(分别称为感染后第6天、12天、28天和42天组)。肺内病毒蛋白和核酸的证据证实PIV3感染成功。使用体积描记法评估CRS和气道反应,并通过支气管肺泡灌洗液体细胞学和肺组织病理学评估气道炎症。与溶剂对照组相比,所有PID组的CRS均显著增加(P <.05),同时PID 6组出现明显的气道高反应性。虽然哮喘对照组的CRS有小幅增加,但与溶剂对照组相比并不显著。所有PIV3接种组的支气管肺泡灌洗液体细胞总数均显著增加,PID 6组和PID 12组的淋巴细胞数量显著增加。PIV3接种动物的肺部病理学显示,在急性感染期气道有炎症但无肺炎。CRS的时空变化可能是PIV3引起咳嗽的基本机制。

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