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Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions

BACKGROUND: Postoperative pain remains a major clinical problem as there are limited analgesic strategies that have been proven to be effective in preventing and relieving this type of pain. Natural products, including flavonoids, have distinct pharmacological properties and play an important role i...

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Autor principal: Alghamdi, Saad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7183786/
https://www.ncbi.nlm.nih.gov/pubmed/32368133
http://dx.doi.org/10.2147/JPR.S250391
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author Alghamdi, Saad
author_facet Alghamdi, Saad
author_sort Alghamdi, Saad
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description BACKGROUND: Postoperative pain remains a major clinical problem as there are limited analgesic strategies that have been proven to be effective in preventing and relieving this type of pain. Natural products, including flavonoids, have distinct pharmacological properties and play an important role in the discovery of analgesic drugs. MATERIALS AND METHODS: In this study, the flavonoid eriocitrin (eriodictyol 7-O-rutinoside), which is the main flavonoid in lemon fruit (Citrus limon), was mechanistically investigated for its prospective antinociceptive effect in a mouse model of postoperative pain. The antinociceptive property was evaluated by utilizing both tonic (acetic acid-induced writhing behavior) and phasic (hot-plate) nociception modalities. The hindpaw incisional surgery was performed and hyperalgesia was assessed using von Frey filaments. RESULTS: The tested doses of eriocitrin significantly attenuated (P<0.01, P<0.001) the chemically-induced tonic visceral nociception (5, 10, 15, and 30 mg/kg) and acute phasic thermal nociception (10, 15, and 30 mg/kg). A significant dose-dependent reduction in the incisional nociceptive hyperalgesia was exhibited by eriocitrin, with a marked antinociception observed at doses of 15 mg/kg (P<0.05 during 30–60 minutes) and 30 mg/kg (P<0.05, P<0.01 during 30–120 minutes). CONCLUSION: The antinociceptive effect of eriocitrin (30 mg/kg) was strongly blocked by the antagonists of the opioid receptor, naltrexone, and GABA(A) receptor, bicuculline, thereby suggesting the involvement of opioidergic and GABAergic mechanisms in the nociception, reducing proclivity of eriocitrin during transmission of incisional nociception. These results concluded that eriocitrin has a potent antinociceptive effect in postoperative pain conditions, probably mediated through opioid and GABA(A) receptors.
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spelling pubmed-71837862020-05-04 Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions Alghamdi, Saad J Pain Res Original Research BACKGROUND: Postoperative pain remains a major clinical problem as there are limited analgesic strategies that have been proven to be effective in preventing and relieving this type of pain. Natural products, including flavonoids, have distinct pharmacological properties and play an important role in the discovery of analgesic drugs. MATERIALS AND METHODS: In this study, the flavonoid eriocitrin (eriodictyol 7-O-rutinoside), which is the main flavonoid in lemon fruit (Citrus limon), was mechanistically investigated for its prospective antinociceptive effect in a mouse model of postoperative pain. The antinociceptive property was evaluated by utilizing both tonic (acetic acid-induced writhing behavior) and phasic (hot-plate) nociception modalities. The hindpaw incisional surgery was performed and hyperalgesia was assessed using von Frey filaments. RESULTS: The tested doses of eriocitrin significantly attenuated (P<0.01, P<0.001) the chemically-induced tonic visceral nociception (5, 10, 15, and 30 mg/kg) and acute phasic thermal nociception (10, 15, and 30 mg/kg). A significant dose-dependent reduction in the incisional nociceptive hyperalgesia was exhibited by eriocitrin, with a marked antinociception observed at doses of 15 mg/kg (P<0.05 during 30–60 minutes) and 30 mg/kg (P<0.05, P<0.01 during 30–120 minutes). CONCLUSION: The antinociceptive effect of eriocitrin (30 mg/kg) was strongly blocked by the antagonists of the opioid receptor, naltrexone, and GABA(A) receptor, bicuculline, thereby suggesting the involvement of opioidergic and GABAergic mechanisms in the nociception, reducing proclivity of eriocitrin during transmission of incisional nociception. These results concluded that eriocitrin has a potent antinociceptive effect in postoperative pain conditions, probably mediated through opioid and GABA(A) receptors. Dove 2020-04-22 /pmc/articles/PMC7183786/ /pubmed/32368133 http://dx.doi.org/10.2147/JPR.S250391 Text en © 2020 Alghamdi. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Alghamdi, Saad
Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions
title Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions
title_full Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions
title_fullStr Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions
title_full_unstemmed Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions
title_short Antinociceptive Effect of the Citrus Flavonoid Eriocitrinon Postoperative Pain Conditions
title_sort antinociceptive effect of the citrus flavonoid eriocitrinon postoperative pain conditions
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7183786/
https://www.ncbi.nlm.nih.gov/pubmed/32368133
http://dx.doi.org/10.2147/JPR.S250391
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