• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

大鼠模型中呼吸道合胞病毒相关性哮喘的神经内分泌机制

Neural-endocrine mechanisms of respiratory syncytial virus-associated asthma in a rat model.

作者信息

Li Q G, Wu X R, Li X Z, Yu J, Xia Y, Wang A P, Wang J

机构信息

Second Department of Respiratory Disease, Jiangxi Provincial People's Hospital, Nanchang, P.R. China.

出版信息

Genet Mol Res. 2012 Aug 24;11(3):2780-9. doi: 10.4238/2012.August.24.3.

DOI:10.4238/2012.August.24.3
PMID:23007973
Abstract

We examined the underlying neural-endocrine mechanisms of asthma associated with respiratory syncytial virus infection. Thirty Sprague-Dawley rats were randomly divided into control group, respiratory syncytial virus (RSV) group, and anti-nerve growth factor (NGF) IgG group. An RSV infection model was established by nasal drip once a week. In the anti-NGF antibody intervention group, each rat was given an intraperitoneal injection of anti-NGF IgG 3 h before RSV infection. Optical microscopy and transmission electron microscopy were used to observe the structural changes in adrenal medulla cells. Changes in adrenaline and norepinephrine in serum were detected by ELISA. NGF expression was assayed by immunohistochemistry. Expression differences in synaptophysin mRNA were detected by RT-PCR. Transmission electron microscopy displayed widened adrenal medulla intercellular spaces, reduced chromaffin particle concentration, and increased mitochondria in the RSV infection group. At the same time, NGF expression was increased in the RSV infection group significantly. In addition, the adrenaline concentration was significantly decreased compared with the control and anti-NGF antibody groups. Synaptophysin mRNA expression was significantly increased in the RSV infection and anti-NGF antibody groups. However, compared with the RSV infection group, synaptophysin mRNA expression was significantly decreased in the anti-NGF antibody group. We conclude that RSV infection could induce adrenal medulla cell differentiation to nerve cells by over-expression of NGF, resulting in the decreased endocrine function found in asthma progression.

摘要

我们研究了与呼吸道合胞病毒感染相关的哮喘潜在神经内分泌机制。将30只Sprague-Dawley大鼠随机分为对照组、呼吸道合胞病毒(RSV)组和抗神经生长因子(NGF)IgG组。通过每周滴鼻一次建立RSV感染模型。在抗NGF抗体干预组中,每只大鼠在RSV感染前3小时腹腔注射抗NGF IgG。采用光学显微镜和透射电子显微镜观察肾上腺髓质细胞的结构变化。用ELISA检测血清中肾上腺素和去甲肾上腺素的变化。用免疫组织化学法检测NGF表达。用RT-PCR检测突触素mRNA的表达差异。透射电子显微镜显示RSV感染组肾上腺髓质细胞间隙增宽、嗜铬颗粒浓度降低、线粒体增多。同时,RSV感染组NGF表达显著增加。此外,与对照组和抗NGF抗体组相比,肾上腺素浓度显著降低。RSV感染组和抗NGF抗体组突触素mRNA表达显著增加。然而,与RSV感染组相比,抗NGF抗体组突触素mRNA表达显著降低。我们得出结论,RSV感染可通过NGF的过度表达诱导肾上腺髓质细胞向神经细胞分化,导致哮喘进展过程中内分泌功能下降。

相似文献

1
Neural-endocrine mechanisms of respiratory syncytial virus-associated asthma in a rat model.大鼠模型中呼吸道合胞病毒相关性哮喘的神经内分泌机制
Genet Mol Res. 2012 Aug 24;11(3):2780-9. doi: 10.4238/2012.August.24.3.
2
[Dysfunction of releasing adrenaline in asthmatic adrenaline medullary chromaffin cells due to functional redundancy primed by nerve growth factor].[由于神经生长因子引发的功能冗余导致哮喘患者肾上腺髓质嗜铬细胞中肾上腺素释放功能障碍]
Zhonghua Jie He He Hu Xi Za Zhi. 2006 Dec;29(12):812-5.
3
Contribution of neuroimmune mechanisms to airway inflammation and remodeling during and after respiratory syncytial virus infection.神经免疫机制在呼吸道合胞病毒感染期间及之后对气道炎症和重塑的作用。
Pediatr Infect Dis J. 2003 Feb;22(2 Suppl):S66-74; discussion S74-5. doi: 10.1097/01.inf.0000053888.67311.1d.
4
Neural plasticity occurs in the adrenal medulla of asthmatic rats.哮喘大鼠肾上腺髓质中存在神经可塑性。
Chin Med J (Engl). 2010 May 20;123(10):1333-7.
5
[Changes of nerve growth factor and its receptors in the lung tissues in asthmatic rats and their effects on the airway inflammation].[哮喘大鼠肺组织中神经生长因子及其受体的变化及其对气道炎症的影响]
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2005 Dec;30(6):660-5.
6
[Toll-like receptor 4 expression and function of respiratory syncytial virus-infected airway epithelial cells].[呼吸道合胞病毒感染的气道上皮细胞中Toll样受体4的表达及功能]
Zhonghua Jie He He Hu Xi Za Zhi. 2008 Mar;31(3):213-7.
7
Neutralization of nerve growth factor (NGF) inhibits the Th2 response and protects against the respiratory syncytial virus (RSV) infection.神经生长因子(NGF)的中和作用可抑制Th2反应,并预防呼吸道合胞病毒(RSV)感染。
Immunol Res. 2017 Jun;65(3):721-728. doi: 10.1007/s12026-017-8909-z.
8
[A guinea pig model of respiratory syncytial virus infection for cough and its neurogenic inflammatory mechanism].[呼吸道合胞病毒感染致豚鼠咳嗽及其神经源性炎症机制的模型]
Zhonghua Yi Xue Za Zhi. 2011 Jun 28;91(24):1708-12.
9
Effects of primary and secondary low-grade respiratory syncytial virus infections in a murine model of asthma.原发性和继发性轻度呼吸道合胞病毒感染在哮喘小鼠模型中的作用。
Clin Exp Allergy. 2004 Aug;34(8):1307-13. doi: 10.1111/j.1365-2222.2004.02033.x.
10
Respiratory syncytial virus induces leukotriene C4 synthase expression in bronchial epithelial cells.呼吸道合胞病毒诱导支气管上皮细胞白三烯 C4 合酶的表达。
Respirology. 2013 Nov;18 Suppl 3:40-6. doi: 10.1111/resp.12188.

引用本文的文献

1
Nerve growth factor causes epinephrine release dysfunction by regulating phenotype alterations and the function of adrenal medullary chromaffin cells in mice with allergic rhinitis.神经生长因子通过调节变应性鼻炎小鼠肾上腺髓质嗜铬细胞的表型改变和功能导致肾上腺素释放功能障碍。
Mol Med Rep. 2023 Feb;27(2). doi: 10.3892/mmr.2023.12926. Epub 2023 Jan 5.
2
An overview on the RSV-mediated mechanisms in the onset of non-allergic asthma.呼吸道合胞病毒介导的非过敏性哮喘发病机制概述。
Front Pediatr. 2022 Sep 20;10:998296. doi: 10.3389/fped.2022.998296. eCollection 2022.
3
Neutralization of nerve growth factor (NGF) inhibits the Th2 response and protects against the respiratory syncytial virus (RSV) infection.
神经生长因子(NGF)的中和作用可抑制Th2反应,并预防呼吸道合胞病毒(RSV)感染。
Immunol Res. 2017 Jun;65(3):721-728. doi: 10.1007/s12026-017-8909-z.
4
Lung dendritic cells undergo maturation and polarization towards a T helper type 2-stimulating phenotype in a mouse model of asthma: Role of nerve growth factor.在哮喘小鼠模型中,肺树突状细胞向促2型辅助性T细胞表型发生成熟和极化:神经生长因子的作用
Exp Ther Med. 2014 Nov;8(5):1402-1408. doi: 10.3892/etm.2014.1967. Epub 2014 Sep 15.