A major ingredient of green tea rescues mice from lethal sepsis partly by inhibiting HMGB1.
The pathogenesis of sepsis is mediated in part by bacterial endotoxin, which stimulates macrophages/monocytes to sequentially release early (e.g., TNF, IL-1, and IFN-gamma) and late (e.g., HMGB1) pro-inflammatory cytokines. Our recent discovery of HMGB1 as a late mediator of lethal sepsis has prompt...
Main Authors: | Wei Li, Mala Ashok, Jianhua Li, Huan Yang, Andrew E Sama, Haichao Wang |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2007-11-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC2048740?pdf=render |
Similar Items
-
A small molecule binding HMGB1 inhibits caspase-11-mediated lethality in sepsis
by: Xiangyu Wang, et al.
Published: (2021-04-01) -
CBP Bromodomain Inhibition Rescues Mice From Lethal Sepsis Through Blocking HMGB1-Mediated Inflammatory Responses
by: Xiaowen Bi, et al.
Published: (2021-02-01) -
Suppression of HMGB1 release by stearoyl lysophosphatidylcholine:an additional mechanism for its therapeutic effects in experimental sepsis
by: Guoqian Chen, et al.
Published: (2005-04-01) -
Endogenous Regulation and Pharmacological Modulation of Sepsis-Induced HMGB1 Release and Action: An Updated Review
by: Cassie Shu Zhu, et al.
Published: (2021-08-01) -
Carbenoxolone Blocks Endotoxin-Induced Protein Kinase R (PKR) Activation and High Mobility Group Box 1 (HMGB1) Release
by: Wei Li, et al.
Published: (2013-07-01)