Suppr超能文献

烟雾吸入合并烧伤绵羊肺组织中一氧化氮合酶同工型的表达

Pulmonary expression of nitric oxide synthase isoforms in sheep with smoke inhalation and burn injury.

作者信息

Cox Robert A, Jacob Sam, Oliveras Gloria, Murakami Kazunori, Enkhbaatar Perenlei, Traber Lillian, Schmalstieg Frank C, Herndon David N, Traber Daniel L, Hawkins Hal K

机构信息

Department of Pathology, University of Texas Medical Branch and Shriners Hospitals for Children, Galveston, Texas 77550, USA.

出版信息

Exp Lung Res. 2009 Mar;35(2):104-18. doi: 10.1080/01902140802446832.

Abstract

Previous studies have indicated increased plasma levels of inducible nitric oxide synthase in lung. This study further examines the pulmonary expression of nitric oxide synthase (NOS) isoforms in an ovine model of acute lung injury induced by smoke inhalation and burn injury (S+B injury). Female range bred sheep (4 per group) were sacrificed at 4, 8, 12, 24, and 48 hours after injury and immunohistochemistry was performed in tissues for various NOS isoforms. The study indicates that in uninjured sheep lung, endothelial (eNOS) is constitutively expressed in the endothelial cells associated with the airways and parenchyma, and in macrophages. Similarly, neuronal (nNOS) is constitutively present in the mucous cells of the epithelium and in neurons of airway ganglia. In uninjured lung, inducible (iNOS) was present in bronchial secretory cells and macrophages. In tissue after S+B injury, new expression of iNOS was evident in bronchial ciliated cells, basal cells, and mucus gland cells. In the parenchyma, a slight increase in iNOS immunostaining was seen in type I cells at 12 and 24 hours after injury only. Virtually no change in eNOS or nNOS was seen after injury.

摘要

先前的研究表明,肺中诱导型一氧化氮合酶的血浆水平升高。本研究进一步检测了烟雾吸入和烧伤(S+B损伤)诱导的急性肺损伤绵羊模型中一氧化氮合酶(NOS)亚型的肺表达。将雌性草原绵羊(每组4只)在损伤后4、8、12、24和48小时处死,并对组织进行各种NOS亚型的免疫组织化学检测。研究表明,在未受伤的绵羊肺中,内皮型(eNOS)在与气道和实质相关的内皮细胞以及巨噬细胞中组成性表达。同样,神经元型(nNOS)在支气管上皮的黏液细胞和气道神经节的神经元中组成性存在。在未受伤的肺中,诱导型(iNOS)存在于支气管分泌细胞和巨噬细胞中。在S+B损伤后的组织中,iNOS在支气管纤毛细胞、基底细胞和黏液腺细胞中有明显的新表达。在实质中,仅在损伤后12和24小时,I型细胞中iNOS免疫染色略有增加。损伤后eNOS或nNOS几乎没有变化。

相似文献

1
Pulmonary expression of nitric oxide synthase isoforms in sheep with smoke inhalation and burn injury.
Exp Lung Res. 2009 Mar;35(2):104-18. doi: 10.1080/01902140802446832.
2
The inducible nitric oxide synthase inhibitor BBS-2 prevents acute lung injury in sheep after burn and smoke inhalation injury.
Am J Respir Crit Care Med. 2003 Apr 1;167(7):1021-6. doi: 10.1164/rccm.200209-1031PP.
3
Nitric oxide synthase isoform expression in the developing lung epithelium.
Am J Physiol. 1999 Feb;276(2):L383-90. doi: 10.1152/ajplung.1999.276.2.L383.
4
Regulation of murine airway responsiveness by endothelial nitric oxide synthase.
Am J Physiol Lung Cell Mol Physiol. 2001 Jul;281(1):L258-67. doi: 10.1152/ajplung.2001.281.1.L258.
7
Expression of nitric oxide synthase isoforms is reduced in late-gestation ovine fetal brainstem.
Am J Physiol Regul Integr Comp Physiol. 2005 Aug;289(2):R613-R619. doi: 10.1152/ajpregu.00722.2004.
9
Inhibition of neuronal nitric oxide synthase in ovine model of acute lung injury.
Crit Care Med. 2009 Jan;37(1):208-14. doi: 10.1097/CCM.0b013e318193226a.
10
Mechanistic aspects of inducible nitric oxide synthase-induced lung injury in burn trauma.
Burns. 2011 Jun;37(4):638-45. doi: 10.1016/j.burns.2010.12.011. Epub 2011 Feb 18.

引用本文的文献

1
Effects of simvastatin on iNOS and caspase‑3 levels and oxidative stress following smoke inhalation injury.
Mol Med Rep. 2020 Oct;22(4):3405-3417. doi: 10.3892/mmr.2020.11413. Epub 2020 Aug 4.
2
Emerging therapies for smoke inhalation injury: a review.
J Transl Med. 2020 Mar 30;18(1):141. doi: 10.1186/s12967-020-02300-4.
3
OXIDATIVE STRESS IN A RAT MODEL OF COTTON SMOKE INHALATION-INDUCED PULMONARY INJURY.
Afr J Tradit Complement Altern Med. 2016 Aug 12;13(5):132-138. doi: 10.21010/ajtcam.v13i5.17. eCollection 2016.
5
Ozone-induced injury and oxidative stress in bronchiolar epithelium are associated with altered pulmonary mechanics.
Toxicol Sci. 2013 Jun;133(2):309-19. doi: 10.1093/toxsci/kft071. Epub 2013 Mar 14.
6
Understanding cellular mechanisms underlying airway epithelial repair: selecting the most appropriate animal models.
ScientificWorldJournal. 2012;2012:961684. doi: 10.1100/2012/961684. Epub 2012 Sep 23.

本文引用的文献

1
Pulmonary changes in a mouse model of combined burn and smoke inhalation-induced injury.
J Appl Physiol (1985). 2008 Aug;105(2):678-84. doi: 10.1152/japplphysiol.00232.2007. Epub 2008 Apr 24.
2
Production of pro-inflammatory polypeptides by airway mucous glands and its potential significance.
Pulm Pharmacol Ther. 2007;20(2):172-7. doi: 10.1016/j.pupt.2006.03.013. Epub 2006 May 13.
3
Acute bronchial obstruction in sheep: histopathology and gland cytokine expression.
Exp Lung Res. 2005 Nov-Dec;31(9-10):819-37. doi: 10.1080/01902140600574967.
5
Airway obstruction in sheep with burn and smoke inhalation injuries.
Am J Respir Cell Mol Biol. 2003 Sep;29(3 Pt 1):295-302. doi: 10.1165/rcmb.4860.
6
Inhibition of neuronal nitric oxide synthase by 7-nitroindazole attenuates acute lung injury in an ovine model.
Am J Physiol Regul Integr Comp Physiol. 2003 Aug;285(2):R366-72. doi: 10.1152/ajpregu.00148.2003. Epub 2003 May 22.
7
The inducible nitric oxide synthase inhibitor BBS-2 prevents acute lung injury in sheep after burn and smoke inhalation injury.
Am J Respir Crit Care Med. 2003 Apr 1;167(7):1021-6. doi: 10.1164/rccm.200209-1031PP.
9
Expression of endothelial nitric oxide synthase in ciliated epithelia of rats.
J Histochem Cytochem. 2003 Jan;51(1):81-7. doi: 10.1177/002215540305100110.
10
Analysis of nitric oxide synthase and nitrotyrosine expression in human pulmonary tuberculosis.
Am J Respir Crit Care Med. 2002 Jul 15;166(2):178-86. doi: 10.1164/rccm.2201023.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验