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从青蒿中分离得到的青蒿素和去氧青蒿素在动物模型中表现出不同的抗伤害感受和抗炎作用。

Artemisinin and deoxyartemisinin isolated from Artemisia annua L. promote distinct antinociceptive and anti-inflammatory effects in an animal model.

机构信息

School of Pharmaceutical Sciences (FCF), Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.

School of Pharmaceutical Sciences (FCF), Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil; Sao Leopoldo Mandic Institute, Campinas, SP, Brazil.

出版信息

Biomed Pharmacother. 2024 Sep;178:117299. doi: 10.1016/j.biopha.2024.117299. Epub 2024 Aug 13.

Abstract

Artemisia annua L., known for antimalarial activity, has demonstrated evidence of anti-inflammatory potential. Previously our research group reported the anti-inflammatory and antinociceptive effect of a sesquiterpene lactone-enriched fraction (Lac-FR) obtained from plant, containing artemisinin and deoxyartemisinin. Both the isolated compounds and Lac-FR evaluated on experimental animal models, in the formalin test showed that deoxyartemisinin reduced both neurogenic pain (56.55 %) and inflammatory pain (45.43 %). These findings were superior to the effect of artemisinin (reduction of 28.66 % and 33.35 %, respectively). In the tail flick test, the antinociceptive effect reported as a percentage of the maximum possible effect (%MPE), deoxyartemisinin showed a lower antinociceptive effect (41.57 %) compared to morphine (75.94 %) in 0.5 h. After 1.5 h, the MPE of deoxyartemisinin (87.99 %) exceeded the effect of morphine (47.55 %), without reversal with naloxone. The MPE of artemisinin (23.3 %) observed after 2 h was lower than deoxiartemisinin, without reversal with the opioid antagonist. Lac-FR and artemisinin demonstrated reductions in ear edema of 43.37 % and 48.19 %, respectively, higher than the effect of deoxyartemisinin (33.64 %). Artemisinin reduced tumor necrosis factor alpha (TNF-α) (76.96 %) more selectively when compared to interleukin-1beta (IL-1β) (48.23 %) and interleukin-6 (IL-6) (44.49 %). Lac-FR showed greater selectivity in IL-6 reduction (56.49 %) in relationship to TNF-α (46.71 %) and IL-1β (45.12 %), whereas deoxyartemisinin selectively reduced TNF-α (37.37 %). The results of our study indicate that the lactones isolated did not have relationship with the opioid system. Deoxyartemisinin showed a higher antinociceptive potential than artemisinin. Whereas, artemisinin showed a higher reduction of inflammation and mediators, with a better anti-inflammatory activity outcome.

摘要

黄花蒿 L.,以抗疟活性而闻名,具有抗炎潜力的证据。此前,我们的研究小组报道了从植物中获得的一种富含倍半萜内酯的馏分(Lac-FR)的抗炎和镇痛作用,其中含有青蒿素和脱氧青蒿素。在福尔马林试验中,无论是单独的化合物还是 Lac-FR 评估的实验动物模型,脱氧青蒿素都能减少神经源性疼痛(56.55%)和炎症性疼痛(45.43%)。这些发现优于青蒿素的效果(分别减少 28.66%和 33.35%)。在尾巴闪烁试验中,作为最大可能效应的百分比(%MPE)报告的镇痛作用,脱氧青蒿素在 0.5 小时时显示出比吗啡(75.94%)更低的镇痛作用(41.57%)。在 1.5 小时后,脱氧青蒿素的 MPE(87.99%)超过了吗啡(47.55%)的效果,而纳洛酮不能逆转。2 小时后观察到的青蒿素(23.3%)的 MPE 低于脱氧青蒿素,且没有阿片类拮抗剂逆转。Lac-FR 和青蒿素分别显示出 43.37%和 48.19%的耳部水肿减少,高于脱氧青蒿素的作用(33.64%)。与白细胞介素-1β(IL-1β)(48.23%)和白细胞介素-6(IL-6)(44.49%)相比,青蒿素对肿瘤坏死因子-α(TNF-α)(76.96%)的选择性降低更为明显。Lac-FR 在降低白细胞介素-6(56.49%)方面的选择性更高,与 TNF-α(46.71%)和 IL-1β(45.12%)相比,而脱氧青蒿素则选择性地降低 TNF-α(37.37%)。我们的研究结果表明,分离出的内酯与阿片样物质系统无关。脱氧青蒿素的镇痛潜力高于青蒿素。然而,青蒿素表现出更高的炎症和介质减少,具有更好的抗炎活性结果。

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