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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of ethnopharmacology 2022-01, Vol.283, p.114738-114738, Article 114738
Hauptverfasser: Jose, Svenia P., M, Ratheesh, S, Sheethal, Rajan, Sony, Saji, Sangeeth, Narayanan, Vimal, S, Sandya
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