Literature DB >> 19079688

Caging a Beast in the Inflammation Arena: Use of Chinese Medicinal Herbs to Inhibit a Late Mediator of Lethal Sepsis, HMGB1.

Shu Zhu, Wei Li, Jianhua Li, Andrew E Sama, Haichao Wang.   

Abstract

Sepsis refers to a systemic inflammatory response syndrome resulting from a microbial infection, which kills > 225,000 people annually in the U.S. alone. The high mortality of sepsis is partly mediated by bacterial endotoxin, which stimulates macrophages/monocytes to sequentially release early (e.g., TNF) and late (e.g., HMGB1) pro-inflammatory cytokines. Although early proinflammatory cytokines may be protective against infection, excessive accumulation of late-acting proinflammatory mediators (such as HMGB1) may sustain a potentially injurious inflammatory response. Agents capable of inhibiting HMGB1 activities (e.g., neutralizing antibodies) or release [e.g., Chinese herbs, Danggui (Angelica sinensis), Danshen (Salvia miltiorrhiza) and Green tea (Camellia sinensis)] rescue mice from lethal sepsis even when given 24 hours after onset of the disease. Here we review emerging evidence that support a critical role for extracellular HMGB1 as a late mediator of lethal sepsis, and several commonly used Chinese herbs (Danggui, Danshen and Green tea) as potential HMGB1- targeting therapeutic agents in experimental sepsis.

Entities:  

Keywords:  Chinese herbs; Inate immune cells; catechin; cytokines; sepsis; tanshinone

Year:  2008        PMID: 19079688      PMCID: PMC2596337     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN: 1940-5901


  73 in total

1.  Protection from septic shock by neutralization of macrophage migration inhibitory factor.

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Journal:  Nat Med       Date:  2000-02       Impact factor: 53.440

2.  Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion.

Authors:  Tiziana Bonaldi; Fabio Talamo; Paola Scaffidi; Denise Ferrera; Annalisa Porto; Angela Bachi; Anna Rubartelli; Alessandra Agresti; Marco E Bianchi
Journal:  EMBO J       Date:  2003-10-15       Impact factor: 11.598

Review 3.  Myocardial dysfunction in meningococcal septic shock.

Authors:  N Makwana; P B Baines
Journal:  Curr Opin Crit Care       Date:  2005-10       Impact factor: 3.687

4.  Alpha-chemokine receptor blockade reduces high mobility group box 1 protein-induced lung inflammation and injury and improves survival in sepsis.

Authors:  Xinchun Lin; Huan Yang; Tohru Sakuragi; Maowen Hu; Lin L Mantell; Shinichiro Hayashi; Yousef Al-Abed; Kevin J Tracey; Luis Ulloa; Edmund J Miller
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2005-06-03       Impact factor: 5.464

5.  IFN-gamma induces high mobility group box 1 protein release partly through a TNF-dependent mechanism.

Authors:  Beatriz Rendon-Mitchell; Mahendar Ochani; Jianhua Li; Jialian Han; Hong Wang; Huan Yang; Seenu Susarla; Christopher Czura; Robert A Mitchell; Guoqian Chen; Andrew E Sama; Kevin J Tracey; Haichao Wang
Journal:  J Immunol       Date:  2003-04-01       Impact factor: 5.422

6.  High mobility group 1 B-box mediates activation of human endothelium.

Authors:  C J Treutiger; G E Mullins; A-S M Johansson; A Rouhiainen; H M E Rauvala; H Erlandsson-Harris; U Andersson; H Yang; K J Tracey; J Andersson; J E W Palmblad
Journal:  J Intern Med       Date:  2003-10       Impact factor: 8.989

Review 7.  Antioxidant activity of tea polyphenols in vivo: evidence from animal studies.

Authors:  Balz Frei; Jane V Higdon
Journal:  J Nutr       Date:  2003-10       Impact factor: 4.798

8.  Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene.

Authors:  A Poltorak; X He; I Smirnova; M Y Liu; C Van Huffel; X Du; D Birdwell; E Alejos; M Silva; C Galanos; M Freudenberg; P Ricciardi-Castagnoli; B Layton; B Beutler
Journal:  Science       Date:  1998-12-11       Impact factor: 47.728

9.  High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes.

Authors:  U Andersson; H Wang; K Palmblad; A C Aveberger; O Bloom; H Erlandsson-Harris; A Janson; R Kokkola; M Zhang; H Yang; K J Tracey
Journal:  J Exp Med       Date:  2000-08-21       Impact factor: 14.307

10.  Extracellular HMGB1, a signal of tissue damage, induces mesoangioblast migration and proliferation.

Authors:  Roberta Palumbo; Maurilio Sampaolesi; Francesco De Marchis; Rossana Tonlorenzi; Sara Colombetti; Anna Mondino; Giulio Cossu; Marco E Bianchi
Journal:  J Cell Biol       Date:  2004-01-26       Impact factor: 10.539

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  5 in total

1.  Sirt1 restrains lung inflammasome activation in a murine model of sepsis.

Authors:  Rong Gao; Zhongsen Ma; Yuxin Hu; Jiao Chen; Sreerama Shetty; Jian Fu
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2015-02-06       Impact factor: 5.464

Review 2.  High mobility group box 1 protein as a potential drug target for infection- and injury-elicited inflammation.

Authors:  Shu Zhu; Wei Li; Mary F Ward; Andrew E Sama; Haichao Wang
Journal:  Inflamm Allergy Drug Targets       Date:  2010-03

Review 3.  Novel HMGB1-inhibiting therapeutic agents for experimental sepsis.

Authors:  Haichao Wang; Mary F Ward; Andrew E Sama
Journal:  Shock       Date:  2009-10       Impact factor: 3.454

Review 4.  Therapeutic potential of HMGB1-targeting agents in sepsis.

Authors:  Haichao Wang; Shu Zhu; Rongrong Zhou; Wei Li; Andrew E Sama
Journal:  Expert Rev Mol Med       Date:  2008-11-04       Impact factor: 5.600

5.  Immunomodulatory Effects of Danshen (Salvia miltiorrhiza) in BALB/c Mice.

Authors:  Donghong Gao; Alvaro Mendoza; Shijun Lu; David A Lawrence
Journal:  ISRN Inflamm       Date:  2012-10-16
  5 in total

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