Literature DB >> 12542980

Oxidative stress, chromatin remodeling and gene transcription in inflammation and chronic lung diseases.

Irfan Rahman1.   

Abstract

Inflammatory lung diseases are characterized by chronic inflammation and oxidant/antioxidant imbalance. The sources of the increased oxidative stress in patients with chronic inflammatory lung diseases such as asthma and chronic obstructive pulmonary disease (COPD) derive from the increased burden of inhaled oxidants, and from the increased amounts of reactive oxygen species (ROS) generated by several inflammatory, immune and various structural cells of the airways. Increased levels of ROS produced in the airways is reflected by increased markers of oxidative stress in the airspaces, sputum, breath, lungs and blood in patients with lung diseases. ROS, either directly or via the formation of lipid peroxidation products such as 4-hydroxy-2-nonenal may play a role in enhancing the inflammation through the activation of stress kinases (JNK, MAPK, p38) and redox sensitive transcription factors such as NF-capital KJE, MacedonianB and AP-1. Recent evidences have indicated that oxidative stress and pro-inflammatory mediators can alter nuclear histone acetylation/deacetylation allowing access for transcription factor DNA binding leading to enhanced pro-inflammatory gene expression in various lung cells. Understanding of the mechanisms of redox signaling, NF-kappaB/AP-1 regulation, the balance between histone acetylation and deacetylation and the release and expression of pro- and antiinflammatory mediators may lead to the development of novel therapies based on the pharmacological manipulation of antioxidants in lung inflammation and injury. Antioxidants that have effective wide spectrum activity and good bioavailability, thiols or molecules which have dual antioxidant and anti-inflammatory activity, may be potential therapeutic agents which not only protect against the direct injurious effects of oxidants, but may fundamentally alter the underlying inflammatory processes which play an important role in the pathogenesis of chronic inflammatory lung diseases.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12542980     DOI: 10.5483/bmbrep.2003.36.1.095

Source DB:  PubMed          Journal:  J Biochem Mol Biol        ISSN: 1225-8687


  72 in total

Review 1.  Degradable Controlled-Release Polymers and Polymeric Nanoparticles: Mechanisms of Controlling Drug Release.

Authors:  Nazila Kamaly; Basit Yameen; Jun Wu; Omid C Farokhzad
Journal:  Chem Rev       Date:  2016-02-08       Impact factor: 60.622

2.  Association of CAT polymorphisms with catalase activity and exposure to environmental oxidative stimuli.

Authors:  Rachel Nadif; Margaret Mintz; Anne Jedlicka; Jean-Pierre Bertrand; Steven R Kleeberger; Francine Kauffmann
Journal:  Free Radic Res       Date:  2005-12

3.  Age alters cerebrovascular inflammation and effects of estrogen.

Authors:  Lorraine Sunday; Christa Osuna; Diana N Krause; Sue P Duckles
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-01-05       Impact factor: 4.733

Review 4.  Environmental epigenetics and asthma: current concepts and call for studies.

Authors:  Rachel L Miller; Shuk-Mei Ho
Journal:  Am J Respir Crit Care Med       Date:  2008-01-10       Impact factor: 21.405

Review 5.  Dietary polyphenols mediated regulation of oxidative stress and chromatin remodeling in inflammation.

Authors:  Irfan Rahman
Journal:  Nutr Rev       Date:  2008-08       Impact factor: 7.110

6.  Comparison between exhaled and sputum oxidative stress biomarkers in chronic airway inflammation.

Authors:  M Corradi; P Pignatti; P Manini; R Andreoli; M Goldoni; M Poppa; G Moscato; B Balbi; A Mutti
Journal:  Eur Respir J       Date:  2004-12       Impact factor: 16.671

Review 7.  Nanoplatforms for Targeted Stimuli-Responsive Drug Delivery: A Review of Platform Materials and Stimuli-Responsive Release and Targeting Mechanisms.

Authors:  Yuzhe Sun; Edward Davis
Journal:  Nanomaterials (Basel)       Date:  2021-03-16       Impact factor: 5.076

8.  The Effects of Portulaca oleracea on Hypoxia-Induced Pulmonary Edema in Mice.

Authors:  Tan Yue; Wen Xiaosa; Qi Ruirui; Shi Wencai; Xin Hailiang; Li Min
Journal:  High Alt Med Biol       Date:  2015-03-11       Impact factor: 1.981

9.  Neither neutrophils nor reactive oxygen species contribute to tissue damage during Pneumocystis pneumonia in mice.

Authors:  Steve D Swain; Terry W Wright; Peter M Degel; Francis Gigliotti; Allen G Harmsen
Journal:  Infect Immun       Date:  2004-10       Impact factor: 3.441

10.  DNA damage in peripheral blood lymphocytes from patients with OSAHS.

Authors:  Jing Xie; Jianzhong Jiang; Keyun Shi; Tingting Zhang; Taofeng Zhu; Hong Chen; Ruhua Chen; Liming Qi; Weiliang Ding; Qiyi Yi; Tieliang Ma
Journal:  Sleep Breath       Date:  2014-01-29       Impact factor: 2.816

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.