达尼奥
斑马鱼
化学
对接(动物)
药理学
生物物理学
生物化学
生物
基因
医学
护理部
作者
Hortência Ribeiro Liberato,Jéssica Bezerra Maciel,Antônio Wlisses da Silva,Maria Eduarda Uchoa Bezerra,Luana San de O. Brito,Jacilene Silva,Maria Kuerislene Amâncio Ferreira,Márcia Machado Marinho,Gabrielle Silva Marinho,Otília Deusdênia Loiola Pessoa,Maria Izabel Florindo Guedes,Paulo Goberlânio de Barros Silva,Andreia Ferreira de Castro Gomes,Jane Eire Silva Alencar de Menezes,Hélcio Silva dos Santos
标识
DOI:10.1002/cbdv.202400063
摘要
Abstract The xanthone lichenxanthone did not show toxic effects (LC 50 >1.0 mg/mL). lichenxanthone prevented nociceptive behavior induced by acidic saline, and its analgesic effect was blocked by amiloride, highlighting the involvement of neuromodulation of acid‐sensitive ion channels (ASICs). In the analysis of anti‐inflammatory activity, concentrations of 0.1 and 0.5 mg/mL of lichenxanthone reduced the edema induced by k‐carrageenan 3.5 %, observed from the fourth hour of analysis. This effect was similar to that observed with ibuprofen (positive control). No leukocyte infiltrates were observed in lichenxanthone, suggesting that the compound acts in the acute inflammatory response. The results of the molecular docking study revealed that lichenxanthone exhibited better affinity energy when compared to the ibuprofen control against the two targets evaluated.
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