Galactomannan of Delonix regia seeds reduces nociception and morphological damage in the rat model of osteoarthritis induced by sodium monoiodoacetate
This study investigated the effects of the protein-free galactomannan obtained from Delonix regia seeds (GM-DR) in an experimental osteoarthritis (OA) model. GM-DR was obtained from water-homogenized endosperms by collection of the supernatant and precipitation with ethanol. The remaining proteins i...
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creator | da Silva Nascimento, Francisco Glerison de Souza Ferreira Bringel, Pedro Henrique Maia, Francisco Wildson Silva Lima, Carlos Pinheiro Chagas Alves, Rômulo Couto Feitosa, Judith Pessoa Andrade Mota, Mário Rogério Lima Assreuy, Ana Maria Sampaio Castro, Rondinelle Ribeiro |
description | This study investigated the effects of the protein-free galactomannan obtained from
Delonix regia
seeds (GM-DR) in an experimental osteoarthritis (OA) model. GM-DR was obtained from water-homogenized endosperms by collection of the supernatant and precipitation with ethanol. The remaining proteins in the galactomannan were removed by alkaline hydrolysis. Weight average molar mass (
M
w
) of the galactomannan was estimated in 5.8 × 10
5
g mol
−1
, presenting mannose:galactose ratio of 2.39:1. Rats received sodium monoiodoacetate (OA groups, 1 mg/25 μL) or saline (sham group) in the right tibio-tarsal joint. GM-DR (30–300 μg) was administered by intra-articular route at days 14 and 21 after OA induction. Hypernociception was evaluated daily by the measurement of the mechanical threshold required to cause joint flexion and paw withdrawal reflex. The 56-day animal groups were euthanized for joint histopahological analysis using the OARSI score system. Lower doses of GM-DR (30 and 100 μg) promoted antinociception from day 15 until the endpoint at day 56. Joint damage was reduced by GM-DR administration (100 μg) in OA-subjected animals, compared to the vehicle-treated OA group (5.9 ± 1.8 vs 19.0 ± 1.8, respectively,
p
< 0.05). Conclusion: Both antinociception and damage reduction suggest that
Delonix regia
galactomannan is a promising approach for osteoarthritis therapy. |
doi_str_mv | 10.1007/s00210-020-01996-x |
format | Article |
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Delonix regia
seeds (GM-DR) in an experimental osteoarthritis (OA) model. GM-DR was obtained from water-homogenized endosperms by collection of the supernatant and precipitation with ethanol. The remaining proteins in the galactomannan were removed by alkaline hydrolysis. Weight average molar mass (
M
w
) of the galactomannan was estimated in 5.8 × 10
5
g mol
−1
, presenting mannose:galactose ratio of 2.39:1. Rats received sodium monoiodoacetate (OA groups, 1 mg/25 μL) or saline (sham group) in the right tibio-tarsal joint. GM-DR (30–300 μg) was administered by intra-articular route at days 14 and 21 after OA induction. Hypernociception was evaluated daily by the measurement of the mechanical threshold required to cause joint flexion and paw withdrawal reflex. The 56-day animal groups were euthanized for joint histopahological analysis using the OARSI score system. Lower doses of GM-DR (30 and 100 μg) promoted antinociception from day 15 until the endpoint at day 56. Joint damage was reduced by GM-DR administration (100 μg) in OA-subjected animals, compared to the vehicle-treated OA group (5.9 ± 1.8 vs 19.0 ± 1.8, respectively,
p
< 0.05). Conclusion: Both antinociception and damage reduction suggest that
Delonix regia
galactomannan is a promising approach for osteoarthritis therapy.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/s00210-020-01996-x</identifier><identifier>PMID: 33057779</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analgesics - therapeutic use ; Animals ; Arthritis ; Biomedical and Life Sciences ; Biomedicine ; Delonix regia ; Disease Models, Animal ; Ethanol ; Fabaceae ; Foot Joints - drug effects ; Foot Joints - pathology ; Galactose ; Galactose - analogs & derivatives ; Iodoacetic Acid ; Male ; Mannans - therapeutic use ; Mannose ; Neurosciences ; Nociception - drug effects ; Original Article ; Osteoarthritis ; Osteoarthritis - chemically induced ; Osteoarthritis - drug therapy ; Osteoarthritis - pathology ; Pain - chemically induced ; Pain - drug therapy ; Pain - pathology ; Pain perception ; Pharmacology/Toxicology ; Rats ; Rats, Wistar ; Seeds</subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 2021-03, Vol.394 (3), p.491-501</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-fe1f3a134e6bdde795fc4f87454c658efc5660474617cbce2ec01bf02f5123e83</citedby><cites>FETCH-LOGICAL-c375t-fe1f3a134e6bdde795fc4f87454c658efc5660474617cbce2ec01bf02f5123e83</cites><orcidid>0000-0003-2481-5733 ; 0000-0003-3778-0584 ; 0000-0001-7336-6773 ; 0000-0002-2323-5385 ; 0000-0002-9399-4109 ; 0000-0003-4680-5317 ; 0000-0002-4466-0452 ; 0000-0001-6278-2755 ; 0000-0001-9539-9840</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/s00210-020-01996-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00210-020-01996-x$$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/33057779$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>da Silva Nascimento, Francisco Glerison</creatorcontrib><creatorcontrib>de Souza Ferreira Bringel, Pedro Henrique</creatorcontrib><creatorcontrib>Maia, Francisco Wildson Silva</creatorcontrib><creatorcontrib>Lima, Carlos Pinheiro Chagas</creatorcontrib><creatorcontrib>Alves, Rômulo Couto</creatorcontrib><creatorcontrib>Feitosa, Judith Pessoa Andrade</creatorcontrib><creatorcontrib>Mota, Mário Rogério Lima</creatorcontrib><creatorcontrib>Assreuy, Ana Maria Sampaio</creatorcontrib><creatorcontrib>Castro, Rondinelle Ribeiro</creatorcontrib><title>Galactomannan of Delonix regia seeds reduces nociception and morphological damage in the rat model of osteoarthritis induced by sodium monoiodoacetate</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn-Schmiedeberg's Arch Pharmacol</addtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>This study investigated the effects of the protein-free galactomannan obtained from
Delonix regia
seeds (GM-DR) in an experimental osteoarthritis (OA) model. GM-DR was obtained from water-homogenized endosperms by collection of the supernatant and precipitation with ethanol. The remaining proteins in the galactomannan were removed by alkaline hydrolysis. Weight average molar mass (
M
w
) of the galactomannan was estimated in 5.8 × 10
5
g mol
−1
, presenting mannose:galactose ratio of 2.39:1. Rats received sodium monoiodoacetate (OA groups, 1 mg/25 μL) or saline (sham group) in the right tibio-tarsal joint. GM-DR (30–300 μg) was administered by intra-articular route at days 14 and 21 after OA induction. Hypernociception was evaluated daily by the measurement of the mechanical threshold required to cause joint flexion and paw withdrawal reflex. The 56-day animal groups were euthanized for joint histopahological analysis using the OARSI score system. Lower doses of GM-DR (30 and 100 μg) promoted antinociception from day 15 until the endpoint at day 56. Joint damage was reduced by GM-DR administration (100 μg) in OA-subjected animals, compared to the vehicle-treated OA group (5.9 ± 1.8 vs 19.0 ± 1.8, respectively,
p
< 0.05). Conclusion: Both antinociception and damage reduction suggest that
Delonix regia
galactomannan is a promising approach for osteoarthritis therapy.</description><subject>Analgesics - therapeutic use</subject><subject>Animals</subject><subject>Arthritis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Delonix regia</subject><subject>Disease Models, Animal</subject><subject>Ethanol</subject><subject>Fabaceae</subject><subject>Foot Joints - drug effects</subject><subject>Foot Joints - pathology</subject><subject>Galactose</subject><subject>Galactose - analogs & derivatives</subject><subject>Iodoacetic Acid</subject><subject>Male</subject><subject>Mannans - therapeutic use</subject><subject>Mannose</subject><subject>Neurosciences</subject><subject>Nociception - drug effects</subject><subject>Original Article</subject><subject>Osteoarthritis</subject><subject>Osteoarthritis - chemically induced</subject><subject>Osteoarthritis - drug therapy</subject><subject>Osteoarthritis - pathology</subject><subject>Pain - chemically induced</subject><subject>Pain - drug therapy</subject><subject>Pain - pathology</subject><subject>Pain perception</subject><subject>Pharmacology/Toxicology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Seeds</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kU9rFDEYh4NY7Fr9Ah4k4MXL2PydzByl1SoUvLTnkEne7KbMJGuSge0X8fOadauCBw8hgd_zPm_gh9AbSj5QQtRlIYRR0hHWDh3Hvjs8QxsqOOvoSNlztGn50FE2DufoZSkPhJCeSvkCnXNOpFJq3KAfN2Y2tqbFxGgiTh5fw5xiOOAM22BwAXClvd1qoeCYbLCwryFFbKLDS8r7XZrTNlgzY2cWswUcIq47wNnUljuYj9JUKiST6y6HGkpDjj6Hp0dckgvr0siYQnLJWKimwit05s1c4PXTfYHuP3-6u_rS3X67-Xr18bazXMnaeaCeG8oF9JNzoEbprfCDElLYXg7grex7IpToqbKTBQaW0MkT5iVlHAZ-gd6fvPucvq9Qql5CsTDPJkJai2ZC0kEKKceGvvsHfUhrju13jRrJMMiRqUaxE2VzKiWD1_scFpMfNSX62Jo-taZba_pXa_rQht4-qddpAfdn5HdNDeAnoLQobiH_3f0f7U8O_6ZM</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>da Silva Nascimento, Francisco Glerison</creator><creator>de Souza Ferreira Bringel, Pedro Henrique</creator><creator>Maia, Francisco Wildson Silva</creator><creator>Lima, Carlos Pinheiro Chagas</creator><creator>Alves, Rômulo Couto</creator><creator>Feitosa, Judith Pessoa Andrade</creator><creator>Mota, Mário Rogério Lima</creator><creator>Assreuy, Ana Maria Sampaio</creator><creator>Castro, Rondinelle Ribeiro</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature 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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2481-5733</orcidid><orcidid>https://orcid.org/0000-0003-3778-0584</orcidid><orcidid>https://orcid.org/0000-0001-7336-6773</orcidid><orcidid>https://orcid.org/0000-0002-2323-5385</orcidid><orcidid>https://orcid.org/0000-0002-9399-4109</orcidid><orcidid>https://orcid.org/0000-0003-4680-5317</orcidid><orcidid>https://orcid.org/0000-0002-4466-0452</orcidid><orcidid>https://orcid.org/0000-0001-6278-2755</orcidid><orcidid>https://orcid.org/0000-0001-9539-9840</orcidid></search><sort><creationdate>20210301</creationdate><title>Galactomannan of Delonix regia seeds reduces nociception and morphological damage in the rat model of osteoarthritis induced by sodium monoiodoacetate</title><author>da Silva Nascimento, Francisco Glerison ; de Souza Ferreira Bringel, Pedro Henrique ; Maia, Francisco Wildson Silva ; Lima, Carlos Pinheiro Chagas ; Alves, Rômulo Couto ; Feitosa, Judith Pessoa Andrade ; Mota, Mário Rogério Lima ; Assreuy, Ana Maria Sampaio ; Castro, Rondinelle Ribeiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-fe1f3a134e6bdde795fc4f87454c658efc5660474617cbce2ec01bf02f5123e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Analgesics - therapeutic use</topic><topic>Animals</topic><topic>Arthritis</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Delonix regia</topic><topic>Disease Models, Animal</topic><topic>Ethanol</topic><topic>Fabaceae</topic><topic>Foot Joints - drug effects</topic><topic>Foot Joints - pathology</topic><topic>Galactose</topic><topic>Galactose - analogs & derivatives</topic><topic>Iodoacetic Acid</topic><topic>Male</topic><topic>Mannans - therapeutic use</topic><topic>Mannose</topic><topic>Neurosciences</topic><topic>Nociception - drug effects</topic><topic>Original Article</topic><topic>Osteoarthritis</topic><topic>Osteoarthritis - chemically induced</topic><topic>Osteoarthritis - drug therapy</topic><topic>Osteoarthritis - pathology</topic><topic>Pain - chemically induced</topic><topic>Pain - drug therapy</topic><topic>Pain - pathology</topic><topic>Pain perception</topic><topic>Pharmacology/Toxicology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Seeds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>da Silva Nascimento, Francisco Glerison</creatorcontrib><creatorcontrib>de Souza Ferreira Bringel, Pedro Henrique</creatorcontrib><creatorcontrib>Maia, Francisco Wildson Silva</creatorcontrib><creatorcontrib>Lima, Carlos Pinheiro Chagas</creatorcontrib><creatorcontrib>Alves, Rômulo Couto</creatorcontrib><creatorcontrib>Feitosa, Judith Pessoa Andrade</creatorcontrib><creatorcontrib>Mota, Mário Rogério Lima</creatorcontrib><creatorcontrib>Assreuy, Ana Maria Sampaio</creatorcontrib><creatorcontrib>Castro, Rondinelle Ribeiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>da Silva Nascimento, Francisco Glerison</au><au>de Souza Ferreira Bringel, Pedro Henrique</au><au>Maia, Francisco Wildson Silva</au><au>Lima, Carlos Pinheiro Chagas</au><au>Alves, Rômulo Couto</au><au>Feitosa, Judith Pessoa Andrade</au><au>Mota, Mário Rogério Lima</au><au>Assreuy, Ana Maria Sampaio</au><au>Castro, Rondinelle Ribeiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Galactomannan of Delonix regia seeds reduces nociception and morphological damage in the rat model of osteoarthritis induced by sodium monoiodoacetate</atitle><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle><stitle>Naunyn-Schmiedeberg's Arch Pharmacol</stitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>394</volume><issue>3</issue><spage>491</spage><epage>501</epage><pages>491-501</pages><issn>0028-1298</issn><eissn>1432-1912</eissn><abstract>This study investigated the effects of the protein-free galactomannan obtained from
Delonix regia
seeds (GM-DR) in an experimental osteoarthritis (OA) model. GM-DR was obtained from water-homogenized endosperms by collection of the supernatant and precipitation with ethanol. The remaining proteins in the galactomannan were removed by alkaline hydrolysis. Weight average molar mass (
M
w
) of the galactomannan was estimated in 5.8 × 10
5
g mol
−1
, presenting mannose:galactose ratio of 2.39:1. Rats received sodium monoiodoacetate (OA groups, 1 mg/25 μL) or saline (sham group) in the right tibio-tarsal joint. GM-DR (30–300 μg) was administered by intra-articular route at days 14 and 21 after OA induction. Hypernociception was evaluated daily by the measurement of the mechanical threshold required to cause joint flexion and paw withdrawal reflex. The 56-day animal groups were euthanized for joint histopahological analysis using the OARSI score system. Lower doses of GM-DR (30 and 100 μg) promoted antinociception from day 15 until the endpoint at day 56. Joint damage was reduced by GM-DR administration (100 μg) in OA-subjected animals, compared to the vehicle-treated OA group (5.9 ± 1.8 vs 19.0 ± 1.8, respectively,
p
< 0.05). Conclusion: Both antinociception and damage reduction suggest that
Delonix regia
galactomannan is a promising approach for osteoarthritis therapy.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33057779</pmid><doi>10.1007/s00210-020-01996-x</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2481-5733</orcidid><orcidid>https://orcid.org/0000-0003-3778-0584</orcidid><orcidid>https://orcid.org/0000-0001-7336-6773</orcidid><orcidid>https://orcid.org/0000-0002-2323-5385</orcidid><orcidid>https://orcid.org/0000-0002-9399-4109</orcidid><orcidid>https://orcid.org/0000-0003-4680-5317</orcidid><orcidid>https://orcid.org/0000-0002-4466-0452</orcidid><orcidid>https://orcid.org/0000-0001-6278-2755</orcidid><orcidid>https://orcid.org/0000-0001-9539-9840</orcidid></addata></record> |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Analgesics - therapeutic use Animals Arthritis Biomedical and Life Sciences Biomedicine Delonix regia Disease Models, Animal Ethanol Fabaceae Foot Joints - drug effects Foot Joints - pathology Galactose Galactose - analogs & derivatives Iodoacetic Acid Male Mannans - therapeutic use Mannose Neurosciences Nociception - drug effects Original Article Osteoarthritis Osteoarthritis - chemically induced Osteoarthritis - drug therapy Osteoarthritis - pathology Pain - chemically induced Pain - drug therapy Pain - pathology Pain perception Pharmacology/Toxicology Rats Rats, Wistar Seeds |
title | Galactomannan of Delonix regia seeds reduces nociception and morphological damage in the rat model of osteoarthritis induced by sodium monoiodoacetate |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T21%3A03%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Galactomannan%20of%20Delonix%20regia%20seeds%20reduces%20nociception%20and%20morphological%20damage%20in%20the%20rat%20model%20of%20osteoarthritis%20induced%20by%20sodium%20monoiodoacetate&rft.jtitle=Naunyn-Schmiedeberg's%20archives%20of%20pharmacology&rft.au=da%20Silva%20Nascimento,%20Francisco%20Glerison&rft.date=2021-03-01&rft.volume=394&rft.issue=3&rft.spage=491&rft.epage=501&rft.pages=491-501&rft.issn=0028-1298&rft.eissn=1432-1912&rft_id=info:doi/10.1007/s00210-020-01996-x&rft_dat=%3Cproquest_cross%3E2490885927%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2490885927&rft_id=info:pmid/33057779&rfr_iscdi=true |