Literature DB >> 23054707

Role of high mobility group box 1 in inflammatory disease: focus on sepsis.

Jong-Sup Bae1.   

Abstract

High mobility group box 1 (HMGB1) is a highly conserved, ubiquitous protein present in the nuclei and cytoplasm of nearly all cell types. In response to infection or injury, HMGB1 is actively secreted by innate immune cells and/or released passively by injured or damaged cells. Thus, serum and tissue levels of HMGB1 are elevated during infection, and especially during sepsis. Sepsis is a systemic inflammatory response to disease and the most severe complication of infections, and HMGB1 acts as a potent proinflammatory cytokine and is involved in delayed endotoxin lethality and sepsis. Furthermore, the targeting of HMGB1 with antibodies or specific antagonists has been found to have protective effects in established preclinical inflammatory disease models, including models of lethal endotoxemia and sepsis. In the present study, emerging evidence supporting the notion that extracellular HMGB1 acts as a proinflammatory danger signal is reviewed, and the potential therapeutic effects of a wide array of HMGB1 inhibitors agents in sepsis and ischemic injury are discussed.

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Year:  2012        PMID: 23054707     DOI: 10.1007/s12272-012-0901-5

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN: 0253-6269            Impact factor:   4.946


  58 in total

1.  Emodin-6-O-β-D--glucoside inhibits high-glucose-induced vascular inflammation.

Authors:  Wonhwa Lee; Sae-Kwang Ku; Doohyun Lee; Taeho Lee; Jong-Sup Bae
Journal:  Inflammation       Date:  2014-04       Impact factor: 4.092

2.  Orientin inhibits high glucose-induced vascular inflammation in vitro and in vivo.

Authors:  Sae-Kwang Ku; Soyoung Kwak; Jong-Sup Bae
Journal:  Inflammation       Date:  2014-12       Impact factor: 4.092

3.  Paeonol Inhibits Lipopolysaccharide-Induced HMGB1 Translocation from the Nucleus to the Cytoplasm in RAW264.7 Cells.

Authors:  Hang Lei; Quan Wen; Hui Li; Shaohui Du; Jing-Jing Wu; Jing Chen; Haiyuan Huang; Dongfeng Chen; Yiwei Li; Saixia Zhang; Jianhong Zhou; Rudong Deng; Qinglin Yang
Journal:  Inflammation       Date:  2016-06       Impact factor: 4.092

4.  Continuous hemodiafiltration therapy reduces damage of multi-organs by ameliorating of HMGB1/TLR4/NFκB in a dog sepsis model.

Authors:  Jing Sun; Shaolan Shi; Qun Wang; Kezhou Yu; Rong Wang
Journal:  Int J Clin Exp Pathol       Date:  2015-02-01

5.  Anti-inflammatory effects of vicenin-2 and scolymoside in vitro and in vivo.

Authors:  Hyejin Kang; Sae-Kwang Ku; Byeongjin Jung; Jong-Sup Bae
Journal:  Inflamm Res       Date:  2015-12       Impact factor: 4.575

6.  Anti-inflammatory effects of hyperoside in human endothelial cells and in mice.

Authors:  Sae-Kwang Ku; Wei Zhou; Wonhwa Lee; Min-Su Han; MinKyun Na; Jong-Sup Bae
Journal:  Inflammation       Date:  2015-04       Impact factor: 4.092

7.  Orientin inhibits HMGB1-induced inflammatory responses in HUVECs and in murine polymicrobial sepsis.

Authors:  Hayoung Yoo; Sae-Kwang Ku; Taeho Lee; Jong-Sup Bae
Journal:  Inflammation       Date:  2014-10       Impact factor: 4.092

8.  Vascular barrier protective effects of piperlonguminine in vitro and in vivo.

Authors:  Sae-Kwang Ku; Jeong Ah Kim; Jong-Sup Bae
Journal:  Inflamm Res       Date:  2014-01-29       Impact factor: 4.575

9.  Anti-inflammatory effects of rutin on HMGB1-induced inflammatory responses in vitro and in vivo.

Authors:  Hayoung Yoo; Sae-Kwang Ku; Young-Doo Baek; Jong-Sup Bae
Journal:  Inflamm Res       Date:  2013-12-01       Impact factor: 4.575

10.  The first cyclomegastigmane rhododendroside A from Rhododendron brachycarpum alleviates HMGB1-induced sepsis.

Authors:  Wei Zhou; Joonseok Oh; Lee Wonhwa; Soyoung Kwak; Wei Li; Amar G Chittiboyina; Daneel Ferreira; Mark T Hamann; Seung Ho Lee; Jong-Sup Bae; MinKyun Na
Journal:  Biochim Biophys Acta       Date:  2014-02-24
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