Java Tea (Orthosiphon stamineus) protected against osteoarthritis by mitigating inflammation and cartilage degradation: a preclinical study
The effect of Orthosiphon stamineus aqueous (OSA) extract against osteoarthritis (OA) was investigated in explant cartilage culture and in postmenopausal OA rat model. Female rats were bilaterally ovariectomized (OVX). Osteoarthritis was induced after surgical recovery, by intra-articular injection...
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Veröffentlicht in: | Inflammopharmacology 2018-08, Vol.26 (4), p.939-949 |
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creator | Bokhari, Rubiatul Adawiyah Tantowi, Nur Adeelah Che Ahmad Lau, Seng Fong Mohamed, Suhaila |
description | The effect of
Orthosiphon stamineus
aqueous (OSA) extract against osteoarthritis (OA) was investigated in explant cartilage culture and in postmenopausal OA rat model. Female rats were bilaterally ovariectomized (OVX). Osteoarthritis was induced after surgical recovery, by intra-articular injection of monosodium iodoacetate (MIA) into the right knee. Rats were grouped (
n
= 8) into: healthy sham control; non-treated OA; OA + diclofenac (positive control 5 mg/kg); and two doses OSA (150–300 mg/kg). After 4 weeks’ treatment, rats were evaluated for OA-related parameters and biomarkers. The OSA reduced proteoglycan and ROS release from the cartilage explants under inflammatory (IL-1b) conditions. In the OA-induced rats’ cartilages, the OSA downregulated the mRNA expressions for IL-1β, IL-6, IL-10, TNF-α, NF-κβ, NOS2, PTGS2, PTGER2, ACAN, COL2A1, MMP1, MMP13, ADAMTS4, ADAMTS5 and TIMP1, mostly dose-dependently. The OSA reduced the OA rats’ serum levels for PGE
2
, CTX-II, TNF-α, MMP1, MMP13, PIINP, OPG, RANKL, OC and BALP, but not dose-dependently. The OSA contained polyphenols and flavonoids (tetramethoxyflavone). The OSA alleviated articular cartilage degradation, inflammation, collagenase/aggrecanase activities, to improve joint and subchondral bone structure.
O. stamineus
mitigated osteoarthritis by downregulating inflammation, peptidases and aggrecanases, at a dose equivalent to about 30 mg/kg for humans. |
doi_str_mv | 10.1007/s10787-017-0432-2 |
format | Article |
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Orthosiphon stamineus
aqueous (OSA) extract against osteoarthritis (OA) was investigated in explant cartilage culture and in postmenopausal OA rat model. Female rats were bilaterally ovariectomized (OVX). Osteoarthritis was induced after surgical recovery, by intra-articular injection of monosodium iodoacetate (MIA) into the right knee. Rats were grouped (
n
= 8) into: healthy sham control; non-treated OA; OA + diclofenac (positive control 5 mg/kg); and two doses OSA (150–300 mg/kg). After 4 weeks’ treatment, rats were evaluated for OA-related parameters and biomarkers. The OSA reduced proteoglycan and ROS release from the cartilage explants under inflammatory (IL-1b) conditions. In the OA-induced rats’ cartilages, the OSA downregulated the mRNA expressions for IL-1β, IL-6, IL-10, TNF-α, NF-κβ, NOS2, PTGS2, PTGER2, ACAN, COL2A1, MMP1, MMP13, ADAMTS4, ADAMTS5 and TIMP1, mostly dose-dependently. The OSA reduced the OA rats’ serum levels for PGE
2
, CTX-II, TNF-α, MMP1, MMP13, PIINP, OPG, RANKL, OC and BALP, but not dose-dependently. The OSA contained polyphenols and flavonoids (tetramethoxyflavone). The OSA alleviated articular cartilage degradation, inflammation, collagenase/aggrecanase activities, to improve joint and subchondral bone structure.
O. stamineus
mitigated osteoarthritis by downregulating inflammation, peptidases and aggrecanases, at a dose equivalent to about 30 mg/kg for humans.</description><identifier>ISSN: 0925-4692</identifier><identifier>EISSN: 1568-5608</identifier><identifier>DOI: 10.1007/s10787-017-0432-2</identifier><identifier>PMID: 29380171</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Allergology ; Biomedical and Life Sciences ; Biomedicine ; Dermatology ; Gastroenterology ; Immunology ; Original Article ; Pharmacology/Toxicology ; Rheumatology</subject><ispartof>Inflammopharmacology, 2018-08, Vol.26 (4), p.939-949</ispartof><rights>Springer International Publishing AG, part of Springer Nature 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-1a5edc7398642ff542ce81b55ab30683681376afb2344ee263bc7819b9f603ce3</citedby><cites>FETCH-LOGICAL-c344t-1a5edc7398642ff542ce81b55ab30683681376afb2344ee263bc7819b9f603ce3</cites><orcidid>0000-0002-2954-3821</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10787-017-0432-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10787-017-0432-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29380171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bokhari, Rubiatul Adawiyah</creatorcontrib><creatorcontrib>Tantowi, Nur Adeelah Che Ahmad</creatorcontrib><creatorcontrib>Lau, Seng Fong</creatorcontrib><creatorcontrib>Mohamed, Suhaila</creatorcontrib><title>Java Tea (Orthosiphon stamineus) protected against osteoarthritis by mitigating inflammation and cartilage degradation: a preclinical study</title><title>Inflammopharmacology</title><addtitle>Inflammopharmacol</addtitle><addtitle>Inflammopharmacology</addtitle><description>The effect of
Orthosiphon stamineus
aqueous (OSA) extract against osteoarthritis (OA) was investigated in explant cartilage culture and in postmenopausal OA rat model. Female rats were bilaterally ovariectomized (OVX). Osteoarthritis was induced after surgical recovery, by intra-articular injection of monosodium iodoacetate (MIA) into the right knee. Rats were grouped (
n
= 8) into: healthy sham control; non-treated OA; OA + diclofenac (positive control 5 mg/kg); and two doses OSA (150–300 mg/kg). After 4 weeks’ treatment, rats were evaluated for OA-related parameters and biomarkers. The OSA reduced proteoglycan and ROS release from the cartilage explants under inflammatory (IL-1b) conditions. In the OA-induced rats’ cartilages, the OSA downregulated the mRNA expressions for IL-1β, IL-6, IL-10, TNF-α, NF-κβ, NOS2, PTGS2, PTGER2, ACAN, COL2A1, MMP1, MMP13, ADAMTS4, ADAMTS5 and TIMP1, mostly dose-dependently. The OSA reduced the OA rats’ serum levels for PGE
2
, CTX-II, TNF-α, MMP1, MMP13, PIINP, OPG, RANKL, OC and BALP, but not dose-dependently. The OSA contained polyphenols and flavonoids (tetramethoxyflavone). The OSA alleviated articular cartilage degradation, inflammation, collagenase/aggrecanase activities, to improve joint and subchondral bone structure.
O. stamineus
mitigated osteoarthritis by downregulating inflammation, peptidases and aggrecanases, at a dose equivalent to about 30 mg/kg for humans.</description><subject>Allergology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Dermatology</subject><subject>Gastroenterology</subject><subject>Immunology</subject><subject>Original Article</subject><subject>Pharmacology/Toxicology</subject><subject>Rheumatology</subject><issn>0925-4692</issn><issn>1568-5608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1TAQhS1ERS8tD8AGeVkWof5JnJgdqvhVpW7atTVxJqmrxLnYTqX7DLw0U25hycKyrfnmjOYcxt5K8UEK0V5mKdqurYSkU2tVqRdsJxvTVY0R3Uu2E1Y1VW2sOmWvc34QQpjW2FfsVFndUZfcsV8_4BH4LQK_uEnlfs1hf79GngssIeKW3_N9Wgv6ggOHCULMha-54ApEp1BC5v2BL_SYoIQ48RDHGZaFPiQDceCeyDDDhHzAKcHwp_KRAwmjn0MMHmaatw2Hc3YywpzxzfN9xu6-fL69-lZd33z9fvXpuvK6rkslocHBt9p2plbj2NTKYyf7poFeC9Np00ndGhh7RTiiMrr3bSdtb0cjtEd9xi6OurTazw1zcUvIHucZIq5bdtJaTVZZYwiVR9SnNeeEo9unsEA6OCncUwbumIEjN91TBk5Rz7tn-a1fcPjX8dd0AtQRyFSKEyb3sG4p0sr_Uf0NDNmUlw</recordid><startdate>20180801</startdate><enddate>20180801</enddate><creator>Bokhari, Rubiatul Adawiyah</creator><creator>Tantowi, Nur Adeelah Che Ahmad</creator><creator>Lau, Seng Fong</creator><creator>Mohamed, Suhaila</creator><general>Springer International Publishing</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2954-3821</orcidid></search><sort><creationdate>20180801</creationdate><title>Java Tea (Orthosiphon stamineus) protected against osteoarthritis by mitigating inflammation and cartilage degradation: a preclinical study</title><author>Bokhari, Rubiatul Adawiyah ; Tantowi, Nur Adeelah Che Ahmad ; Lau, Seng Fong ; Mohamed, Suhaila</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-1a5edc7398642ff542ce81b55ab30683681376afb2344ee263bc7819b9f603ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Allergology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Dermatology</topic><topic>Gastroenterology</topic><topic>Immunology</topic><topic>Original Article</topic><topic>Pharmacology/Toxicology</topic><topic>Rheumatology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bokhari, Rubiatul Adawiyah</creatorcontrib><creatorcontrib>Tantowi, Nur Adeelah Che Ahmad</creatorcontrib><creatorcontrib>Lau, Seng Fong</creatorcontrib><creatorcontrib>Mohamed, Suhaila</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inflammopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bokhari, Rubiatul Adawiyah</au><au>Tantowi, Nur Adeelah Che Ahmad</au><au>Lau, Seng Fong</au><au>Mohamed, Suhaila</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Java Tea (Orthosiphon stamineus) protected against osteoarthritis by mitigating inflammation and cartilage degradation: a preclinical study</atitle><jtitle>Inflammopharmacology</jtitle><stitle>Inflammopharmacol</stitle><addtitle>Inflammopharmacology</addtitle><date>2018-08-01</date><risdate>2018</risdate><volume>26</volume><issue>4</issue><spage>939</spage><epage>949</epage><pages>939-949</pages><issn>0925-4692</issn><eissn>1568-5608</eissn><abstract>The effect of
Orthosiphon stamineus
aqueous (OSA) extract against osteoarthritis (OA) was investigated in explant cartilage culture and in postmenopausal OA rat model. Female rats were bilaterally ovariectomized (OVX). Osteoarthritis was induced after surgical recovery, by intra-articular injection of monosodium iodoacetate (MIA) into the right knee. Rats were grouped (
n
= 8) into: healthy sham control; non-treated OA; OA + diclofenac (positive control 5 mg/kg); and two doses OSA (150–300 mg/kg). After 4 weeks’ treatment, rats were evaluated for OA-related parameters and biomarkers. The OSA reduced proteoglycan and ROS release from the cartilage explants under inflammatory (IL-1b) conditions. In the OA-induced rats’ cartilages, the OSA downregulated the mRNA expressions for IL-1β, IL-6, IL-10, TNF-α, NF-κβ, NOS2, PTGS2, PTGER2, ACAN, COL2A1, MMP1, MMP13, ADAMTS4, ADAMTS5 and TIMP1, mostly dose-dependently. The OSA reduced the OA rats’ serum levels for PGE
2
, CTX-II, TNF-α, MMP1, MMP13, PIINP, OPG, RANKL, OC and BALP, but not dose-dependently. The OSA contained polyphenols and flavonoids (tetramethoxyflavone). The OSA alleviated articular cartilage degradation, inflammation, collagenase/aggrecanase activities, to improve joint and subchondral bone structure.
O. stamineus
mitigated osteoarthritis by downregulating inflammation, peptidases and aggrecanases, at a dose equivalent to about 30 mg/kg for humans.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>29380171</pmid><doi>10.1007/s10787-017-0432-2</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2954-3821</orcidid></addata></record> |
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subjects | Allergology Biomedical and Life Sciences Biomedicine Dermatology Gastroenterology Immunology Original Article Pharmacology/Toxicology Rheumatology |
title | Java Tea (Orthosiphon stamineus) protected against osteoarthritis by mitigating inflammation and cartilage degradation: a preclinical study |
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