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Antinociceptive activity of methanolic extract of Clinacanthus nutans leaves: possible mechanisms of action involved


Citation

Zakaria, Zainul Amiruddin and Abdul Rahim, Mohammad Hafiz and Roosli, Rushduddin Al Jufri and Mohd Sani, Mohd Hijaz and Omar, Maizatul Hasyima and Mohd Tohid, Siti Farah and Othman, Fezah and Siew, Mooi Ching and Abdul Kadir, Arifah (2018) Antinociceptive activity of methanolic extract of Clinacanthus nutans leaves: possible mechanisms of action involved. Pain Research & Management, 2018. art. no. 9536406. pp. 1-15. ISSN 1203-6765; ESSN: 1918-1523

Abstract

Methanolic extract of Clinacanthus nutans Lindau leaves (MECN) has been proven to possess antinociceptive activity that works via the opioid and NO-dependent/cGMP-independent pathways. In the present study, we aimed to further determine the possible mechanisms of antinociception of MECN using various nociceptive assays. +e antinociceptive activity of MECN was (i) tested against capsaicin-, glutamate-, phorbol 12-myristate 13-acetate-, bradykinin-induced nociception model; (ii) prechallenged against selective antagonist of opioid receptor subtypes (β-funaltrexamine, naltrindole, and nor-binaltorphimine); (iii) prechallenged against antagonist of nonopioid systems, namely, α2-noradrenergic (yohimbine), β-adrenergic (pindolol), adenosinergic (caffeine), dopaminergic (haloperidol), and cholinergic (atropine) receptors; (iv) prechallenged with inhibitors of various potassium channels (glibenclamide, apamin, charybdotoxin, and tetraethylammonium chloride). +e results demonstrated that the orally administered MECN (100, 250, and 500 mg/kg) significantly (p < 0.05) reversed the nociceptive effect of all models in a dose-dependent manner. Moreover, the antinociceptive activity of 500 mg/kg MECN was significantly (p < 0.05) inhibited by (i) antagonists of μ-, δ-, and κ-opioid receptors; (ii) antagonists of α2-noradrenergic, β-adrenergic, adenosinergic, dopaminergic, and cholinergic receptors; and (iii) blockers of different K+ channels (voltage-activated-, Ca2+-activated, and ATP-sensitive-K+ channels, resp.). In conclusion, MECN-induced antinociception involves modulation of protein kinase C-, bradykinin-, TRVP1 receptors-, and glutamatergic signaling pathways; opioidergic, α2-noradrenergic, β-adrenergic, adenosinergic, dopaminergic, and cholinergic receptors; and nonopioidergic receptors as well as the opening of various K+ channels. +e antinociceptive activity could be associated with the presence of several flavonoid-based bioactive compounds and their synergistic action with nonvolatile bioactive compounds.


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Additional Metadata

Item Type: Article
Divisions: Faculty of Medicine and Health Science
Faculty of Veterinary Medicine
DOI Number: https://doi.org/10.1155/2018/9536406
Publisher: Hindawi
Keywords: Clinacanthus nutans; Antinociception; Pain; Antiinflammatory drugs
Depositing User: Ms. Nuraida Ibrahim
Date Deposited: 07 May 2021 00:24
Last Modified: 07 May 2021 00:24
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.1155/2018/9536406
URI: http://psasir.upm.edu.my/id/eprint/73162
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