Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene Therapy

Abstract.: In recent years, extensive basic science research has led to a clear understanding of the molecular mechanisms contributing to the pathophysiology of sepsis. Sepsis is now defined as a systemic inflammatory response syndrome (SIRS) in which there is an identifiable focus of infection. SIR...

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Main Authors: Matsuda Naoyuki, Hattori Yuichi
Format: Article
Language:English
Published: Elsevier 2006-01-01
Series:Journal of Pharmacological Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1347861319344445
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spelling doaj-d0fd73e896324de29a43721ff2ff3e7e2020-11-24T21:49:56ZengElsevierJournal of Pharmacological Sciences1347-86132006-01-011013189198Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene TherapyMatsuda Naoyuki0Hattori Yuichi1Department of Pharmacology, School of Medicine, University of Toyama, Toyama 930-0194, JapanDepartment of Pharmacology, School of Medicine, University of Toyama, Toyama 930-0194, Japan; Corresponding author. yhattori@med.u-toyama.ac.jpAbstract.: In recent years, extensive basic science research has led to a clear understanding of the molecular mechanisms contributing to the pathophysiology of sepsis. Sepsis is now defined as a systemic inflammatory response syndrome (SIRS) in which there is an identifiable focus of infection. SIRS can be also precipitated by non-infective events such as trauma, pancreatitis, and surgery. As a consequence of an overactive SIRS response, the function of various organ systems may be compromised, resulting in multiple organ dysfunction syndrome (MODS) and death. Production and activation of multiple proinflammatory genes are likely to play a key role in the pathogenesis of MODS development. This review article focuses on the molecular mechanisms and components involved in the pathogenesis of severe sepsis. This includes cellular targets of sepsis-inducing bacterial products and their signaling pathways with a major emphasis on transcription factors and new therapeutic approaches to severe sepsis. Keywords:: systemic inflammatory response syndrome (SIRS), sepsis, Toll-like receptor, nuclear factor-κB, activating protein-1http://www.sciencedirect.com/science/article/pii/S1347861319344445
collection DOAJ
language English
format Article
sources DOAJ
author Matsuda Naoyuki
Hattori Yuichi
spellingShingle Matsuda Naoyuki
Hattori Yuichi
Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene Therapy
Journal of Pharmacological Sciences
author_facet Matsuda Naoyuki
Hattori Yuichi
author_sort Matsuda Naoyuki
title Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene Therapy
title_short Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene Therapy
title_full Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene Therapy
title_fullStr Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene Therapy
title_full_unstemmed Systemic Inflammatory Response Syndrome (SIRS): Molecular Pathophysiology and Gene Therapy
title_sort systemic inflammatory response syndrome (sirs): molecular pathophysiology and gene therapy
publisher Elsevier
series Journal of Pharmacological Sciences
issn 1347-8613
publishDate 2006-01-01
description Abstract.: In recent years, extensive basic science research has led to a clear understanding of the molecular mechanisms contributing to the pathophysiology of sepsis. Sepsis is now defined as a systemic inflammatory response syndrome (SIRS) in which there is an identifiable focus of infection. SIRS can be also precipitated by non-infective events such as trauma, pancreatitis, and surgery. As a consequence of an overactive SIRS response, the function of various organ systems may be compromised, resulting in multiple organ dysfunction syndrome (MODS) and death. Production and activation of multiple proinflammatory genes are likely to play a key role in the pathogenesis of MODS development. This review article focuses on the molecular mechanisms and components involved in the pathogenesis of severe sepsis. This includes cellular targets of sepsis-inducing bacterial products and their signaling pathways with a major emphasis on transcription factors and new therapeutic approaches to severe sepsis. Keywords:: systemic inflammatory response syndrome (SIRS), sepsis, Toll-like receptor, nuclear factor-κB, activating protein-1
url http://www.sciencedirect.com/science/article/pii/S1347861319344445
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