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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Veröffentlicht in:Naunyn-Schmiedeberg's archives of pharmacology 2021-03, Vol.394 (3), p.491-501
Hauptverfasser: 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
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container_title Naunyn-Schmiedeberg's archives of pharmacology
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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
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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 &lt; 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 &amp; 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 &lt; 0.05). 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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 &amp; 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 &amp; 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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. 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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
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