Anti-inflammatory effect of Kaba Sura Kudineer (AYUSH approved COVID-19 drug)-A Siddha poly-herbal formulation against lipopolysaccharide induced inflammatory response in RAW-264.7 macrophages cells
Medicinal importance and potential activity of Siddha herbal formulations have proved over several centuries against a wide range of causative agents as Influenza, Dengue, Chikungunya, and Tuberculosis. The traditional medicine system of Siddha is a valuable therapeutic approach for treating viral r...
Gespeichert in:
Veröffentlicht in: | Journal of ethnopharmacology 2022-01, Vol.283, p.114738-114738, Article 114738 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 114738 |
---|---|
container_issue | |
container_start_page | 114738 |
container_title | Journal of ethnopharmacology |
container_volume | 283 |
creator | Jose, Svenia P. M, Ratheesh S, Sheethal Rajan, Sony Saji, Sangeeth Narayanan, Vimal S, Sandya |
description | Medicinal importance and potential activity of Siddha herbal formulations have proved over several centuries against a wide range of causative agents as Influenza, Dengue, Chikungunya, and Tuberculosis. The traditional medicine system of Siddha is a valuable therapeutic approach for treating viral respiratory infections like Coronavirus disease 2019 (COVID-19) and can be effectively employed to target the host response and preventive care to boost the immune system. Kaba Sura Kudineer (KSK), an official polyherbal formulation has been used in Siddha traditional medicine for centuries. However, the role of KSK in regulating inflammation and the underlying molecular mechanisms has remained elusive.
The goal of this study was to evaluate the anti-inflammatory effect of KSK using lipopolysaccharide (LPS) stimulated RAW 264.7 murine macrophage cells.
Raw 264.7 murine macrophage cells were used for this study. The Inflammatory mediators and cytokines were measured by enzyme-linked immunosorbent assay (ELISA). The NF-κB nulcear translocation and protein expression of iNOS, COX-2 was analyzed with westernblot.
KSK supplementation decreased LPS mediated TLR-4 production and secretion of pro-inflammatory mediators and cytokines including IL-6, TNF-α, COX-2 and PGE-2. Moreover, it inhibited the production of nitric oxide (NO) and thereby inhibited the expression of iNOS in the cell. The Western blot analysis further confirmed that KSK strongly prevented the LPS-induced degradation of IκB which is normally required for the activation of NF-κB and hereby suppressed nuclear translocation of NF-κB. The protein expression of iNOS, COX-2 was significantly decreased with the presence of KSK treatment. Results suggested that KSK manipulates its anti-inflammatory effects mainly through blocking the TLR mediated NF-κB signal transduction pathways.
Together, this study has proven that KSK could be a potential therapeutic drug for alleviating excessive inflammation in many inflammation-associated diseases like COVID-19.
[Display omitted] |
doi_str_mv | 10.1016/j.jep.2021.114738 |
format | Article |
fullrecord | <record><control><sourceid>elsevier_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8507575</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0378874121009673</els_id><sourcerecordid>S0378874121009673</sourcerecordid><originalsourceid>FETCH-LOGICAL-c451t-24c62ab8cb70fdc07e5ef04f792dde0d4ab425ae4058079a7359e1bbbeaafd403</originalsourceid><addsrcrecordid>eNp9kcFu1DAURSMEokPhA9ggL-kiwU6ccUZISNFAadVKlRgKYmW92M8Tj5I4spOR5gf5rno0UNENKy_evcd-PknyltGMUbb8sMt2OGY5zVnGGBdF9SxZsErkqShF8TxZ0EJUaSU4O0tehbCjlArG6cvkrODLsihztkh-18NkUzuYDvoeJucPBI1BNRFnyA00QDazB3IzazsgevK-_nW_uSIwjt7tUZP13Y_rzylbEe3n7UVak43VugUyuu6Qtugb6Ihxvp87mKwbCGzBDmEinR3dMRNAqRa81UjsoGcVkU8e4zGMbgjHKflW_0zzJc8E6UF5N7awxUAUdl14nbww0AV88-c8T-4vv3xfX6W3d1-v1_VtqnjJpjTnaplDU6lGUKMVFViiodyIVa41Us2h4XkJyGlZUbECUZQrZE3TIIDRnBbnyacTd5ybHrXCYfLQydHbHvxBOrDy6WSwrdy6vaxKGqWUEcBOgLhACB7NY5dReZQqdzJKlUep8iQ1dt79e-lj46_FGPh4CmBcfW_Ry6AsDvEzrY8qpXb2P_gHEgy3Sw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Anti-inflammatory effect of Kaba Sura Kudineer (AYUSH approved COVID-19 drug)-A Siddha poly-herbal formulation against lipopolysaccharide induced inflammatory response in RAW-264.7 macrophages cells</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Jose, Svenia P. ; M, Ratheesh ; S, Sheethal ; Rajan, Sony ; Saji, Sangeeth ; Narayanan, Vimal ; S, Sandya</creator><creatorcontrib>Jose, Svenia P. ; M, Ratheesh ; S, Sheethal ; Rajan, Sony ; Saji, Sangeeth ; Narayanan, Vimal ; S, Sandya</creatorcontrib><description>Medicinal importance and potential activity of Siddha herbal formulations have proved over several centuries against a wide range of causative agents as Influenza, Dengue, Chikungunya, and Tuberculosis. The traditional medicine system of Siddha is a valuable therapeutic approach for treating viral respiratory infections like Coronavirus disease 2019 (COVID-19) and can be effectively employed to target the host response and preventive care to boost the immune system. Kaba Sura Kudineer (KSK), an official polyherbal formulation has been used in Siddha traditional medicine for centuries. However, the role of KSK in regulating inflammation and the underlying molecular mechanisms has remained elusive.
The goal of this study was to evaluate the anti-inflammatory effect of KSK using lipopolysaccharide (LPS) stimulated RAW 264.7 murine macrophage cells.
Raw 264.7 murine macrophage cells were used for this study. The Inflammatory mediators and cytokines were measured by enzyme-linked immunosorbent assay (ELISA). The NF-κB nulcear translocation and protein expression of iNOS, COX-2 was analyzed with westernblot.
KSK supplementation decreased LPS mediated TLR-4 production and secretion of pro-inflammatory mediators and cytokines including IL-6, TNF-α, COX-2 and PGE-2. Moreover, it inhibited the production of nitric oxide (NO) and thereby inhibited the expression of iNOS in the cell. The Western blot analysis further confirmed that KSK strongly prevented the LPS-induced degradation of IκB which is normally required for the activation of NF-κB and hereby suppressed nuclear translocation of NF-κB. The protein expression of iNOS, COX-2 was significantly decreased with the presence of KSK treatment. Results suggested that KSK manipulates its anti-inflammatory effects mainly through blocking the TLR mediated NF-κB signal transduction pathways.
Together, this study has proven that KSK could be a potential therapeutic drug for alleviating excessive inflammation in many inflammation-associated diseases like COVID-19.
[Display omitted]</description><identifier>ISSN: 0378-8741</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2021.114738</identifier><identifier>PMID: 34653521</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Animals ; Anti-Inflammatory Agents - pharmacology ; COVID-19 Drug Treatment ; Cycloxygenase-2 ; Dietary Supplements ; Inflammation ; Inflammation - drug therapy ; Interleukins-6 ; Kaba sura kudineer ; Lipopolysaccharides - toxicity ; Macrophages - drug effects ; Medicine, Ayurvedic ; Mice ; NF-ӄB ; Nitric oxide ; Pharmaceutical Preparations ; Phytotherapy ; Plant Preparations - pharmacology ; Plant Preparations - therapeutic use ; RAW 264.7 Cells ; SARS-CoV-2</subject><ispartof>Journal of ethnopharmacology, 2022-01, Vol.283, p.114738-114738, Article 114738</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><rights>2021 Elsevier B.V. All rights reserved. 2021 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-24c62ab8cb70fdc07e5ef04f792dde0d4ab425ae4058079a7359e1bbbeaafd403</citedby><cites>FETCH-LOGICAL-c451t-24c62ab8cb70fdc07e5ef04f792dde0d4ab425ae4058079a7359e1bbbeaafd403</cites><orcidid>0000-0001-7339-6390</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378874121009673$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34653521$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jose, Svenia P.</creatorcontrib><creatorcontrib>M, Ratheesh</creatorcontrib><creatorcontrib>S, Sheethal</creatorcontrib><creatorcontrib>Rajan, Sony</creatorcontrib><creatorcontrib>Saji, Sangeeth</creatorcontrib><creatorcontrib>Narayanan, Vimal</creatorcontrib><creatorcontrib>S, Sandya</creatorcontrib><title>Anti-inflammatory effect of Kaba Sura Kudineer (AYUSH approved COVID-19 drug)-A Siddha poly-herbal formulation against lipopolysaccharide induced inflammatory response in RAW-264.7 macrophages cells</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>Medicinal importance and potential activity of Siddha herbal formulations have proved over several centuries against a wide range of causative agents as Influenza, Dengue, Chikungunya, and Tuberculosis. The traditional medicine system of Siddha is a valuable therapeutic approach for treating viral respiratory infections like Coronavirus disease 2019 (COVID-19) and can be effectively employed to target the host response and preventive care to boost the immune system. Kaba Sura Kudineer (KSK), an official polyherbal formulation has been used in Siddha traditional medicine for centuries. However, the role of KSK in regulating inflammation and the underlying molecular mechanisms has remained elusive.
The goal of this study was to evaluate the anti-inflammatory effect of KSK using lipopolysaccharide (LPS) stimulated RAW 264.7 murine macrophage cells.
Raw 264.7 murine macrophage cells were used for this study. The Inflammatory mediators and cytokines were measured by enzyme-linked immunosorbent assay (ELISA). The NF-κB nulcear translocation and protein expression of iNOS, COX-2 was analyzed with westernblot.
KSK supplementation decreased LPS mediated TLR-4 production and secretion of pro-inflammatory mediators and cytokines including IL-6, TNF-α, COX-2 and PGE-2. Moreover, it inhibited the production of nitric oxide (NO) and thereby inhibited the expression of iNOS in the cell. The Western blot analysis further confirmed that KSK strongly prevented the LPS-induced degradation of IκB which is normally required for the activation of NF-κB and hereby suppressed nuclear translocation of NF-κB. The protein expression of iNOS, COX-2 was significantly decreased with the presence of KSK treatment. Results suggested that KSK manipulates its anti-inflammatory effects mainly through blocking the TLR mediated NF-κB signal transduction pathways.
Together, this study has proven that KSK could be a potential therapeutic drug for alleviating excessive inflammation in many inflammation-associated diseases like COVID-19.
[Display omitted]</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>COVID-19 Drug Treatment</subject><subject>Cycloxygenase-2</subject><subject>Dietary Supplements</subject><subject>Inflammation</subject><subject>Inflammation - drug therapy</subject><subject>Interleukins-6</subject><subject>Kaba sura kudineer</subject><subject>Lipopolysaccharides - toxicity</subject><subject>Macrophages - drug effects</subject><subject>Medicine, Ayurvedic</subject><subject>Mice</subject><subject>NF-ӄB</subject><subject>Nitric oxide</subject><subject>Pharmaceutical Preparations</subject><subject>Phytotherapy</subject><subject>Plant Preparations - pharmacology</subject><subject>Plant Preparations - therapeutic use</subject><subject>RAW 264.7 Cells</subject><subject>SARS-CoV-2</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu1DAURSMEokPhA9ggL-kiwU6ccUZISNFAadVKlRgKYmW92M8Tj5I4spOR5gf5rno0UNENKy_evcd-PknyltGMUbb8sMt2OGY5zVnGGBdF9SxZsErkqShF8TxZ0EJUaSU4O0tehbCjlArG6cvkrODLsihztkh-18NkUzuYDvoeJucPBI1BNRFnyA00QDazB3IzazsgevK-_nW_uSIwjt7tUZP13Y_rzylbEe3n7UVak43VugUyuu6Qtugb6Ihxvp87mKwbCGzBDmEinR3dMRNAqRa81UjsoGcVkU8e4zGMbgjHKflW_0zzJc8E6UF5N7awxUAUdl14nbww0AV88-c8T-4vv3xfX6W3d1-v1_VtqnjJpjTnaplDU6lGUKMVFViiodyIVa41Us2h4XkJyGlZUbECUZQrZE3TIIDRnBbnyacTd5ybHrXCYfLQydHbHvxBOrDy6WSwrdy6vaxKGqWUEcBOgLhACB7NY5dReZQqdzJKlUep8iQ1dt79e-lj46_FGPh4CmBcfW_Ry6AsDvEzrY8qpXb2P_gHEgy3Sw</recordid><startdate>20220130</startdate><enddate>20220130</enddate><creator>Jose, Svenia P.</creator><creator>M, Ratheesh</creator><creator>S, Sheethal</creator><creator>Rajan, Sony</creator><creator>Saji, Sangeeth</creator><creator>Narayanan, Vimal</creator><creator>S, Sandya</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7339-6390</orcidid></search><sort><creationdate>20220130</creationdate><title>Anti-inflammatory effect of Kaba Sura Kudineer (AYUSH approved COVID-19 drug)-A Siddha poly-herbal formulation against lipopolysaccharide induced inflammatory response in RAW-264.7 macrophages cells</title><author>Jose, Svenia P. ; M, Ratheesh ; S, Sheethal ; Rajan, Sony ; Saji, Sangeeth ; Narayanan, Vimal ; S, Sandya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-24c62ab8cb70fdc07e5ef04f792dde0d4ab425ae4058079a7359e1bbbeaafd403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>COVID-19 Drug Treatment</topic><topic>Cycloxygenase-2</topic><topic>Dietary Supplements</topic><topic>Inflammation</topic><topic>Inflammation - drug therapy</topic><topic>Interleukins-6</topic><topic>Kaba sura kudineer</topic><topic>Lipopolysaccharides - toxicity</topic><topic>Macrophages - drug effects</topic><topic>Medicine, Ayurvedic</topic><topic>Mice</topic><topic>NF-ӄB</topic><topic>Nitric oxide</topic><topic>Pharmaceutical Preparations</topic><topic>Phytotherapy</topic><topic>Plant Preparations - pharmacology</topic><topic>Plant Preparations - therapeutic use</topic><topic>RAW 264.7 Cells</topic><topic>SARS-CoV-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jose, Svenia P.</creatorcontrib><creatorcontrib>M, Ratheesh</creatorcontrib><creatorcontrib>S, Sheethal</creatorcontrib><creatorcontrib>Rajan, Sony</creatorcontrib><creatorcontrib>Saji, Sangeeth</creatorcontrib><creatorcontrib>Narayanan, Vimal</creatorcontrib><creatorcontrib>S, Sandya</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of ethnopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jose, Svenia P.</au><au>M, Ratheesh</au><au>S, Sheethal</au><au>Rajan, Sony</au><au>Saji, Sangeeth</au><au>Narayanan, Vimal</au><au>S, Sandya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-inflammatory effect of Kaba Sura Kudineer (AYUSH approved COVID-19 drug)-A Siddha poly-herbal formulation against lipopolysaccharide induced inflammatory response in RAW-264.7 macrophages cells</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2022-01-30</date><risdate>2022</risdate><volume>283</volume><spage>114738</spage><epage>114738</epage><pages>114738-114738</pages><artnum>114738</artnum><issn>0378-8741</issn><eissn>1872-7573</eissn><abstract>Medicinal importance and potential activity of Siddha herbal formulations have proved over several centuries against a wide range of causative agents as Influenza, Dengue, Chikungunya, and Tuberculosis. The traditional medicine system of Siddha is a valuable therapeutic approach for treating viral respiratory infections like Coronavirus disease 2019 (COVID-19) and can be effectively employed to target the host response and preventive care to boost the immune system. Kaba Sura Kudineer (KSK), an official polyherbal formulation has been used in Siddha traditional medicine for centuries. However, the role of KSK in regulating inflammation and the underlying molecular mechanisms has remained elusive.
The goal of this study was to evaluate the anti-inflammatory effect of KSK using lipopolysaccharide (LPS) stimulated RAW 264.7 murine macrophage cells.
Raw 264.7 murine macrophage cells were used for this study. The Inflammatory mediators and cytokines were measured by enzyme-linked immunosorbent assay (ELISA). The NF-κB nulcear translocation and protein expression of iNOS, COX-2 was analyzed with westernblot.
KSK supplementation decreased LPS mediated TLR-4 production and secretion of pro-inflammatory mediators and cytokines including IL-6, TNF-α, COX-2 and PGE-2. Moreover, it inhibited the production of nitric oxide (NO) and thereby inhibited the expression of iNOS in the cell. The Western blot analysis further confirmed that KSK strongly prevented the LPS-induced degradation of IκB which is normally required for the activation of NF-κB and hereby suppressed nuclear translocation of NF-κB. The protein expression of iNOS, COX-2 was significantly decreased with the presence of KSK treatment. Results suggested that KSK manipulates its anti-inflammatory effects mainly through blocking the TLR mediated NF-κB signal transduction pathways.
Together, this study has proven that KSK could be a potential therapeutic drug for alleviating excessive inflammation in many inflammation-associated diseases like COVID-19.
[Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>34653521</pmid><doi>10.1016/j.jep.2021.114738</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-7339-6390</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0378-8741 |
ispartof | Journal of ethnopharmacology, 2022-01, Vol.283, p.114738-114738, Article 114738 |
issn | 0378-8741 1872-7573 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8507575 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Animals Anti-Inflammatory Agents - pharmacology COVID-19 Drug Treatment Cycloxygenase-2 Dietary Supplements Inflammation Inflammation - drug therapy Interleukins-6 Kaba sura kudineer Lipopolysaccharides - toxicity Macrophages - drug effects Medicine, Ayurvedic Mice NF-ӄB Nitric oxide Pharmaceutical Preparations Phytotherapy Plant Preparations - pharmacology Plant Preparations - therapeutic use RAW 264.7 Cells SARS-CoV-2 |
title | Anti-inflammatory effect of Kaba Sura Kudineer (AYUSH approved COVID-19 drug)-A Siddha poly-herbal formulation against lipopolysaccharide induced inflammatory response in RAW-264.7 macrophages cells |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T14%3A01%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Anti-inflammatory%20effect%20of%20Kaba%20Sura%20Kudineer%20(AYUSH%20approved%20COVID-19%20drug)-A%20Siddha%20poly-herbal%20formulation%20against%20lipopolysaccharide%20induced%20inflammatory%20response%20in%20RAW-264.7%20macrophages%20cells&rft.jtitle=Journal%20of%20ethnopharmacology&rft.au=Jose,%20Svenia%20P.&rft.date=2022-01-30&rft.volume=283&rft.spage=114738&rft.epage=114738&rft.pages=114738-114738&rft.artnum=114738&rft.issn=0378-8741&rft.eissn=1872-7573&rft_id=info:doi/10.1016/j.jep.2021.114738&rft_dat=%3Celsevier_pubme%3ES0378874121009673%3C/elsevier_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/34653521&rft_els_id=S0378874121009673&rfr_iscdi=true |