2012
DOI: 10.7324/japs.2012.2811
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Anti-inflammatory Effect of Apigenin-7-neohesperidoside (Rhoifolin) in Carrageenin-Induced Rat Oedema Model

Abstract: Flavonoids are normal constituents of the human diet and are known for a variety of biological activities. They have been reported to bring benefits in lowering inflammation and oxidative stress. The present investigation was performed first, to evaluate the anti-inflammatory activity of rhoifolin and second, to search for the possible contributing mechanisms for this hypothesized effect. Rhoifolin caused a time and reverse dose dependent reduction of carrageenin-induced rat paw oedema. Following 4 hr of treat… Show more

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Cited by 20 publications
(23 citation statements)
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“…The test for oral acute toxicity revealed no mortality or toxicity signs for apigenin at doses up to 5000 mg/kg either in mice or rats. Based on these results, and according to, 24,26 the doses of 25 and 50 mg/kg were selected for further evaluation of antinociceptive and antiinflammatory activities. 30 Analgesic activities.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The test for oral acute toxicity revealed no mortality or toxicity signs for apigenin at doses up to 5000 mg/kg either in mice or rats. Based on these results, and according to, 24,26 the doses of 25 and 50 mg/kg were selected for further evaluation of antinociceptive and antiinflammatory activities. 30 Analgesic activities.…”
Section: Resultsmentioning
confidence: 99%
“…The rat doses of apigenin (25 and 50 mg/kg bw) were selected in accordance with those reported previously. 26 The fourth group was given diclofenac sodium (100 mg/kg) and kept as a standard group.…”
Section: Methodsmentioning
confidence: 99%
“…It was proven that, flavonoids isolated from some medicinal plants have an antinociceptive and/or antiinflammatory effect (Eldahshan and Azab 2012). Flavonoids inhibit the biosynthesis of prostaglandins, which are involved in various immunologic responses and are the end products of the cyclooxygenase and lipoxygenase pathways (Moroney et al 1988;Di Rosa and Willoughby 1971).…”
Section: Discussionmentioning
confidence: 99%
“…Increasing doses of Rho significantly reduced the tumor necrosis factor-α (TNF-α) release. It also elevated the total antioxidant capacity in a reverse dose order, with the highest ability obtained with the lowest dose tested [ 11 ]. The in vitro study showed that Rho could actively suppress the receptor activators of nuclear factor-kappa B (NF-kB) ligand-stimulated osteoclastogenesis, F-actin formation, hydroxyapatite resorption, and the gene expression of osteoclast-related genes [ 12 ].…”
Section: Introductionmentioning
confidence: 99%