LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 1 of total 1

Search options

Article ; Online: Ability of recombinant human catalase to suppress inflammation of the murine lung induced by influenza A.

Shi, Xunlong / Shi, Zhihui / Huang, Hai / Zhu, Hongguang / Zhou, Pei / Zhu, Haiyan / Ju, Dianwen

Inflammation

2014  Volume 37, Issue 3, Page(s) 809–817

Abstract: ... We have previously investigated the therapeutic efficacy of recombinant human catalase (rhCAT) against ... intranasally with high pathogenicity (H1N1) influenza A virus followed by treatment with recombinant human ... generic pharmacological strategies that reduce both viral replication and inflammation of the lung ...

Abstract Influenza A virus pandemics and emerging antiviral resistance highlight the urgent need for novel generic pharmacological strategies that reduce both viral replication and inflammation of the lung. We have previously investigated the therapeutic efficacy of recombinant human catalase (rhCAT) against viral pneumonia in mice, but the protection mechanisms involved were not explored. In the present study, we have performed a more in-depth analysis covering survival, lung inflammation, immune cell responses, production of cytokines, and inflammation signaling pathways in mice. Male imprinting control region mice were infected intranasally with high pathogenicity (H1N1) influenza A virus followed by treatment with recombinant human catalase. The administration of rhCAT resulted in a significant reduction in inflammatory cell infiltration (e.g., macrophages and neutrophils), inflammatory cytokine levels (e.g., IL-2, IL-6, TNF-α, IFN-γ), the level of the intercellular adhesion molecule 1 chemokine and the mRNA levels of toll-like receptors TLR-4, TLR-7, and NF-κB, as well as partially maintaining the activity of the antioxidant enzymes system. These findings indicated that rhCAT might play a key protective role in viral pneumonia of mice via suppression of inflammatory immune responses.
MeSH term(s) Animals ; Catalase/genetics ; Catalase/pharmacology ; Cytokines/biosynthesis ; Cytokines/blood ; Cytokines/genetics ; Humans ; Inflammation/drug therapy ; Influenza A Virus, H1N1 Subtype/pathogenicity ; Lung/pathology ; Macrophage Activation/drug effects ; Macrophages/immunology ; Male ; Malondialdehyde/metabolism ; Mice ; Mice, Inbred ICR ; Neutrophil Infiltration/drug effects ; Neutrophils/immunology ; Orthomyxoviridae Infections/drug therapy ; Oxidative Stress/immunology ; Pneumonia, Viral/drug therapy ; RNA, Messenger/genetics ; Random Allocation ; Reactive Oxygen Species/metabolism ; Recombinant Proteins/genetics ; Recombinant Proteins/pharmacology ; Signal Transduction/immunology
Chemical Substances Cytokines ; RNA, Messenger ; Reactive Oxygen Species ; Recombinant Proteins ; Malondialdehyde (4Y8F71G49Q) ; Catalase (EC 1.11.1.6)
Keywords covid19
Language English
Publishing date 2014-01-03
Publishing country United States
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 434408-x
ISSN 1573-2576 ; 0360-3997
ISSN (online) 1573-2576
ISSN 0360-3997
DOI 10.1007/s10753-013-9800-2
Shelf mark
Zs.A 1401: Show issues Location:
Je nach Verfügbarkeit (siehe Angabe bei Bestand)
bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
Jg. 1995 - 2021: Lesesall (1.OG)
ab Jg. 2022: Lesesaal (EG)
Database MEDical Literature Analysis and Retrieval System OnLINE

More links

Kategorien

To top