2010
DOI: 10.1016/j.jep.2010.06.003
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Analgesic compounds from Scorzonera latifolia (Fisch. and Mey.) DC.

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Cited by 30 publications
(28 citation statements)
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“…Mouse ear edema induced with topically-applied TPA is also an excellent acute inflammation animal model, closely Scorzonera species were in focus of our previous research touching testing of analgesic, anti-inflammatory, and wound healing activities. Aerial part extracts of Scorzonera showed significant inhibitory effects in carrageenan and PGE 2 induced hind paw edema model in vivo [21][22][23]. The concentrations of extracts showing the activity was 100 mg/kg of body weight of mice, and the effect was comparable with indomethacine used as the standard at the some concentration.…”
Section: Resultsmentioning
confidence: 86%
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“…Mouse ear edema induced with topically-applied TPA is also an excellent acute inflammation animal model, closely Scorzonera species were in focus of our previous research touching testing of analgesic, anti-inflammatory, and wound healing activities. Aerial part extracts of Scorzonera showed significant inhibitory effects in carrageenan and PGE 2 induced hind paw edema model in vivo [21][22][23]. The concentrations of extracts showing the activity was 100 mg/kg of body weight of mice, and the effect was comparable with indomethacine used as the standard at the some concentration.…”
Section: Resultsmentioning
confidence: 86%
“…From the above mentioned, we suggested that chlorogenic acid (8), derivatives of dicaffeoyl-quinic acid (6 and 7), and flavonoids, especially quercetin-3-O-β-D-glucoside (1) and hyperoside (2) could be responsible for the anti-inflammatory activity of tested extracts. Therefore, further experiments were carried out with phenolic compounds previously obtained from Scorzonera species (1)(2)(3)(4)(5)(6)(7)(8), to assay the inhibition of TNF-α and IL-1β production in THP-1 cells, and later also with triterpenes 9-16, because taraxasterol acetate (9) isolated from S. latifolia showed previously analgesic activity in vivo in writhing and tail-flick tests [21] and also other triterpenoid substances like lupeol derivatives (10 and 11), β-sitosterol (12) and other triterpenes (13)(14)(15)(16) could potentially demonstrate anti-phlogistic effect [38,39]. Unfortunately, only weak activity of compounds tested was observed, and no statistically significant activity has been observed in comparison with standard used (prednisone, Supplementary Materials, Figure S1).…”
Section: Resultsmentioning
confidence: 99%
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“…szowitsii, S. suberosa ssp. suberosa were proven scientifically by previous studies and triterpenoids were isolated as responsible compounds [3][4][5] . Antiinflammatory, antioxidant, and wound healing activities have also been reported [6][7][8][9] .…”
Section: Research Papermentioning
confidence: 99%