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Article: Protection of lethal toxicity of endotoxin by Salvia miltiorrhiza BUNGE is via reduction in tumor necrosis factor alpha release and liver injury
Title | Protection of lethal toxicity of endotoxin by Salvia miltiorrhiza BUNGE is via reduction in tumor necrosis factor alpha release and liver injury |
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Authors | |
Keywords | Danshen LPS Salvia miltiorrhiza TNF |
Issue Date | 2006 |
Publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/intimp |
Citation | International Immunopharmacology, 2006, v. 6 n. 5, p. 750-758 How to Cite? |
Abstract | Lipopolysaccharide (LPS) has been implicated as one of the major cause of Gram-negative bacteria-induced sepsis that are life-threatening syndromes occurring in intensive care unit patients. Many natural products derived from medicinal plants may contain therapeutic values on protecting endotoxemia-induced sepsis by virtue their ability to modulate multiple pro-inflammatory cytokines. In the present study, we show that Salvia miltiorrhiza (SM) BUNGE or Danshen, used in treatment of various systemic and surgical infections in the hospitals of China, was able to block the lethal toxicity of LPS in mice via suppression of TNF-α release and protection on liver injury. The ability of SM to suppress LPS-induced TNF-α release is further confirmed by in vitro experiments conducted on human peripheral blood leukocytes (PBL) and the RAW 264.7 macrophage cell line. Immunophenotyping by flow cytometry shows improved T-helper cell (CD4) and T-suppressor cells (CD8) ratio in SM-treated PBL and splenocytes of LPS-challenged mice. The drop in plasma glutamate-pyruvate transaminase (GPT) induced by LPS provides evidence that SM can protect hepatic damage. The present study explains some known biological activities of SM, and supports the clinical application of SM in the prevention of inflammatory diseases induced by Gram-negative bacteria. © 2005 Elsevier B.V. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/48685 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 1.167 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Wan, JMF | en_HK |
dc.contributor.author | Sit, WH | en_HK |
dc.contributor.author | Lee, CL | en_HK |
dc.contributor.author | Fu, KHM | en_HK |
dc.contributor.author | Chan, DKO | en_HK |
dc.date.accessioned | 2008-05-22T04:21:20Z | - |
dc.date.available | 2008-05-22T04:21:20Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | International Immunopharmacology, 2006, v. 6 n. 5, p. 750-758 | en_HK |
dc.identifier.issn | 1567-5769 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/48685 | - |
dc.description.abstract | Lipopolysaccharide (LPS) has been implicated as one of the major cause of Gram-negative bacteria-induced sepsis that are life-threatening syndromes occurring in intensive care unit patients. Many natural products derived from medicinal plants may contain therapeutic values on protecting endotoxemia-induced sepsis by virtue their ability to modulate multiple pro-inflammatory cytokines. In the present study, we show that Salvia miltiorrhiza (SM) BUNGE or Danshen, used in treatment of various systemic and surgical infections in the hospitals of China, was able to block the lethal toxicity of LPS in mice via suppression of TNF-α release and protection on liver injury. The ability of SM to suppress LPS-induced TNF-α release is further confirmed by in vitro experiments conducted on human peripheral blood leukocytes (PBL) and the RAW 264.7 macrophage cell line. Immunophenotyping by flow cytometry shows improved T-helper cell (CD4) and T-suppressor cells (CD8) ratio in SM-treated PBL and splenocytes of LPS-challenged mice. The drop in plasma glutamate-pyruvate transaminase (GPT) induced by LPS provides evidence that SM can protect hepatic damage. The present study explains some known biological activities of SM, and supports the clinical application of SM in the prevention of inflammatory diseases induced by Gram-negative bacteria. © 2005 Elsevier B.V. All rights reserved. | en_HK |
dc.format.extent | 264776 bytes | - |
dc.format.extent | 581 bytes | - |
dc.format.mimetype | application/pdf | - |
dc.format.mimetype | text/plain | - |
dc.language | eng | en_HK |
dc.publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/intimp | en_HK |
dc.relation.ispartof | International Immunopharmacology | en_HK |
dc.rights | International Immunopharmacology. Copyright © Elsevier Ltd. | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Danshen | en_HK |
dc.subject | LPS | en_HK |
dc.subject | Salvia miltiorrhiza | en_HK |
dc.subject | TNF | en_HK |
dc.title | Protection of lethal toxicity of endotoxin by Salvia miltiorrhiza BUNGE is via reduction in tumor necrosis factor alpha release and liver injury | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1567-5769&volume=6&issue=5&spage=750&epage=758&date=2006&atitle=Protection+of+lethal+toxicity+of+endotoxin+by+Salvia+miltiorrhiza+BUNGE+is+via+reduction+in+tumor+necrosis+factor+alpha+release+and+liver+injury | en_HK |
dc.identifier.email | Wan, JMF: jmfwan@hku.hk | en_HK |
dc.identifier.email | Chan, DKO: chand@hku.hk | en_HK |
dc.identifier.authority | Wan, JMF=rp00798 | en_HK |
dc.identifier.authority | Chan, DKO=rp00540 | en_HK |
dc.description.nature | postprint | en_HK |
dc.identifier.doi | 10.1016/j.intimp.2005.11.008 | en_HK |
dc.identifier.pmid | 16546705 | - |
dc.identifier.scopus | eid_2-s2.0-33645035494 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33645035494&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 6 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 750 | en_HK |
dc.identifier.epage | 758 | en_HK |
dc.identifier.isi | WOS:000236555700005 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Wan, JMF=8930305000 | en_HK |
dc.identifier.scopusauthorid | Sit, WH=8528923000 | en_HK |
dc.identifier.scopusauthorid | Lee, CL=9277221100 | en_HK |
dc.identifier.scopusauthorid | Fu, KHM=36902086200 | en_HK |
dc.identifier.scopusauthorid | Chan, DKO=7402216545 | en_HK |
dc.identifier.issnl | 1567-5769 | - |