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Echinacea alkylamides modulate TNF-α gene expression via cannabinoid receptor CB2 and multiple signal transduction pathways

Echinacea plant preparations are widely used in the prevention and treatment of common cold. However, so far no molecular mechanism of action has been proposed. We analyzed the standardized tincture Echinaforce TM and found that it induced de novo synthesis of tumor necrosis factor α (TNF-α) mRNA in...

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Published in:FEBS letters 2004-11, Vol.577 (3), p.563-569
Main Authors: Gertsch, Juerg, Schoop, Roland, Kuenzle, Urs, Suter, Andy
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Kuenzle, Urs
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description Echinacea plant preparations are widely used in the prevention and treatment of common cold. However, so far no molecular mechanism of action has been proposed. We analyzed the standardized tincture Echinaforce TM and found that it induced de novo synthesis of tumor necrosis factor α (TNF-α) mRNA in primary human monocytes/macrophages, but not TNF-α protein. Moreover, LPS-stimulated TNF-α protein was potently inhibited in the early phase but prolonged in the late phase. A study of the main constituents of the extract showed that the alkylamides dodeca-2 E,4 E,8 Z,10 E/ Z-tetraenoic acid isobutylamides (1/2), trienoic (3) and dienoic acid (4) derivatives are responsible for this effect. The upregulation of TNF-α mRNA was found to be mediated by CB2 receptors, increased cAMP, p38/MAPK and JNK signaling, as well as NF-κB and ATF-2/CREB-1 activation. This study is the first to report a possible molecular mechanism of action of Echinacea, highlighting the role of alkylamides as potent immunomodulators and potential ligands for CB2 receptors.
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However, so far no molecular mechanism of action has been proposed. We analyzed the standardized tincture Echinaforce TM and found that it induced de novo synthesis of tumor necrosis factor α (TNF-α) mRNA in primary human monocytes/macrophages, but not TNF-α protein. Moreover, LPS-stimulated TNF-α protein was potently inhibited in the early phase but prolonged in the late phase. A study of the main constituents of the extract showed that the alkylamides dodeca-2 E,4 E,8 Z,10 E/ Z-tetraenoic acid isobutylamides (1/2), trienoic (3) and dienoic acid (4) derivatives are responsible for this effect. The upregulation of TNF-α mRNA was found to be mediated by CB2 receptors, increased cAMP, p38/MAPK and JNK signaling, as well as NF-κB and ATF-2/CREB-1 activation. This study is the first to report a possible molecular mechanism of action of Echinacea, highlighting the role of alkylamides as potent immunomodulators and potential ligands for CB2 receptors.</description><subject>Alkylamide</subject><subject>ATF-2, activating transcription factor-2</subject><subject>cAMP, cyclic adenosine monophosphate</subject><subject>Cannabinoid receptor CB2</subject><subject>CB2, cannabinoid receptor 2</subject><subject>Cells, Cultured</subject><subject>CREB-1, cAMP responsive element binding protein-1</subject><subject>Cyclic AMP - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Echinacea</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Flow Cytometry</subject><subject>Gene Expression Regulation - drug effects</subject><subject>GM-CSF, granulocyte colony stimulating factor</subject><subject>Humans</subject><subject>Immunomodulation</subject><subject>JNK Mitogen-Activated Protein Kinases - metabolism</subject><subject>JNK, Jun N-terminal kinase</subject><subject>Kinetics</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>LPS, lipopolysaccharide</subject><subject>Macrophages - drug effects</subject><subject>MAPK, mitogen-activated protein kinase</subject><subject>Molecular Structure</subject><subject>Mφs, macrophages</subject><subject>NF-AT, nuclear factor of activated T-cells</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB, nuclear factor κB</subject><subject>NK-cells, natural killer cells</subject><subject>p38 Mitogen-Activated Protein Kinases - metabolism</subject><subject>PBMCs, peripheral blood mononuclear cells</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>RANTES, regulated upon activation, normal T-cell expressed and secreted</subject><subject>Receptor, Cannabinoid, CB2 - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction</subject><subject>STAT-4, signal transducer and activator of transcription-4</subject><subject>TNF-α, tumor necrosis factor α</subject><subject>Tumor necrosis factor α</subject><subject>Tumor Necrosis Factor-alpha - antagonists &amp; 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Schoop, Roland ; Kuenzle, Urs ; Suter, Andy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4573-4a882efe9e1a51a2f17b0975b04997823c4f5ef6da92bb94871a2977a6261aed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Alkylamide</topic><topic>ATF-2, activating transcription factor-2</topic><topic>cAMP, cyclic adenosine monophosphate</topic><topic>Cannabinoid receptor CB2</topic><topic>CB2, cannabinoid receptor 2</topic><topic>Cells, Cultured</topic><topic>CREB-1, cAMP responsive element binding protein-1</topic><topic>Cyclic AMP - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Echinacea</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Flow Cytometry</topic><topic>Gene Expression Regulation - drug effects</topic><topic>GM-CSF, granulocyte colony stimulating factor</topic><topic>Humans</topic><topic>Immunomodulation</topic><topic>JNK Mitogen-Activated Protein Kinases - metabolism</topic><topic>JNK, Jun N-terminal kinase</topic><topic>Kinetics</topic><topic>Leukocytes, Mononuclear - drug effects</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>LPS, lipopolysaccharide</topic><topic>Macrophages - drug effects</topic><topic>MAPK, mitogen-activated protein kinase</topic><topic>Molecular Structure</topic><topic>Mφs, macrophages</topic><topic>NF-AT, nuclear factor of activated T-cells</topic><topic>NF-kappa B - metabolism</topic><topic>NF-κB, nuclear factor κB</topic><topic>NK-cells, natural killer cells</topic><topic>p38 Mitogen-Activated Protein Kinases - metabolism</topic><topic>PBMCs, peripheral blood mononuclear cells</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>RANTES, regulated upon activation, normal T-cell expressed and secreted</topic><topic>Receptor, Cannabinoid, CB2 - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction</topic><topic>STAT-4, signal transducer and activator of transcription-4</topic><topic>TNF-α, tumor necrosis factor α</topic><topic>Tumor necrosis factor α</topic><topic>Tumor Necrosis Factor-alpha - antagonists &amp; inhibitors</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gertsch, Juerg</creatorcontrib><creatorcontrib>Schoop, Roland</creatorcontrib><creatorcontrib>Kuenzle, Urs</creatorcontrib><creatorcontrib>Suter, Andy</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gertsch, Juerg</au><au>Schoop, Roland</au><au>Kuenzle, Urs</au><au>Suter, Andy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Echinacea alkylamides modulate TNF-α gene expression via cannabinoid receptor CB2 and multiple signal transduction pathways</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>2004-11-19</date><risdate>2004</risdate><volume>577</volume><issue>3</issue><spage>563</spage><epage>569</epage><pages>563-569</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><abstract>Echinacea plant preparations are widely used in the prevention and treatment of common cold. However, so far no molecular mechanism of action has been proposed. We analyzed the standardized tincture Echinaforce TM and found that it induced de novo synthesis of tumor necrosis factor α (TNF-α) mRNA in primary human monocytes/macrophages, but not TNF-α protein. Moreover, LPS-stimulated TNF-α protein was potently inhibited in the early phase but prolonged in the late phase. A study of the main constituents of the extract showed that the alkylamides dodeca-2 E,4 E,8 Z,10 E/ Z-tetraenoic acid isobutylamides (1/2), trienoic (3) and dienoic acid (4) derivatives are responsible for this effect. The upregulation of TNF-α mRNA was found to be mediated by CB2 receptors, increased cAMP, p38/MAPK and JNK signaling, as well as NF-κB and ATF-2/CREB-1 activation. This study is the first to report a possible molecular mechanism of action of Echinacea, highlighting the role of alkylamides as potent immunomodulators and potential ligands for CB2 receptors.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>15556647</pmid><doi>10.1016/j.febslet.2004.10.064</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source ScienceDirect Journals; Wiley-Blackwell Read & Publish Collection
subjects Alkylamide
ATF-2, activating transcription factor-2
cAMP, cyclic adenosine monophosphate
Cannabinoid receptor CB2
CB2, cannabinoid receptor 2
Cells, Cultured
CREB-1, cAMP responsive element binding protein-1
Cyclic AMP - metabolism
Dose-Response Relationship, Drug
Echinacea
Enzyme-Linked Immunosorbent Assay
Flow Cytometry
Gene Expression Regulation - drug effects
GM-CSF, granulocyte colony stimulating factor
Humans
Immunomodulation
JNK Mitogen-Activated Protein Kinases - metabolism
JNK, Jun N-terminal kinase
Kinetics
Leukocytes, Mononuclear - drug effects
Lipopolysaccharides - pharmacology
LPS, lipopolysaccharide
Macrophages - drug effects
MAPK, mitogen-activated protein kinase
Molecular Structure
Mφs, macrophages
NF-AT, nuclear factor of activated T-cells
NF-kappa B - metabolism
NF-κB, nuclear factor κB
NK-cells, natural killer cells
p38 Mitogen-Activated Protein Kinases - metabolism
PBMCs, peripheral blood mononuclear cells
Plant Extracts - chemistry
Plant Extracts - pharmacology
RANTES, regulated upon activation, normal T-cell expressed and secreted
Receptor, Cannabinoid, CB2 - metabolism
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - analysis
RNA, Messenger - metabolism
Signal Transduction
STAT-4, signal transducer and activator of transcription-4
TNF-α, tumor necrosis factor α
Tumor necrosis factor α
Tumor Necrosis Factor-alpha - antagonists & inhibitors
Tumor Necrosis Factor-alpha - metabolism
Up-Regulation
title Echinacea alkylamides modulate TNF-α gene expression via cannabinoid receptor CB2 and multiple signal transduction pathways
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