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富含类黄酮的白毛银莲花氯仿提取物具有体内抗炎和镇痛活性。

The flavonol-enriched Cistus albidus chloroform extract possesses in vivo anti-inflammatory and anti-nociceptive activity.

机构信息

Laboratoire de Biochimie Appliquée, Faculté des Sciences de la Nature et de la Vie, Université de Bejaia, 06000, Algeria.

Laboratoire de Biochimie Appliquée, Faculté des Sciences de la Nature et de la Vie, Université de Bejaia, 06000, Algeria.

出版信息

J Ethnopharmacol. 2017 Sep 14;209:210-218. doi: 10.1016/j.jep.2017.07.012. Epub 2017 Jul 8.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Cistus albidus L. (Cistaceae) has been traditionally used to treat various inflammatory diseases, but no systematic studies on the anti-inflammatory and anti-nociceptive actions of C. albidus and its putative mechanism have been reported. We aimed to explore the anti-inflammatory and anti-nociceptive effects of this plant and to characterize its polyphenolic composition by liquid chromatography coupled to mass spectrometry (MS).

MATERIALS AND METHODS

A chloroform extract derived from C. albidus leaves was obtained by solid-liquid and liquid-liquid extraction. The tail immersion test and acetic-acid-induced writhing test were used to evaluate the anti-nociceptive action, while the experimental λ-carrageenan-induced paw edema model was used to test the anti-inflammatory action. Changes in cyclooxygenase (COX)-2 and inducible nitric oxide synthase (iNOS) expression, as well as the role of mitogen-activated protein kinases (MAPKs) and the nuclear transcription factor kappa B (NF-kB) signaling pathways on lipopolysaccharide (LPS)-stimulated murine peritoneal macrophages were analyzed by western blotting. HPLC with diode array detection coupled to tandem mass spectrometry detection with electrospray ionization (HPLC-DAD-ESI-MS/MS) was performed to determine the phytochemical profile of the extract.

RESULTS

Significant anti-nociceptive activity was observed both in the tail immersion (59.63% reduction at 120min) and in the acetic acid (65.94% inhibition) tests at 100mg/kg. The extract (50mg/kg) exhibited a substantial reduction in paw edema (51.6%) and significantly inhibited nitrite generation (72.62%) without affecting cell viability of LPS-stimulated murine peritoneal macrophages. These results were concomitant with a down-regulation of the pro-inflammatory enzymes COX-2 and iNOS in extract-treated macrophages and a decrease in p38 MAPK phosphorylation. HPLC-DAD-ESI-MS/MS analysis revealed that flavonols such as kaempferol and quercetin derivatives were potentially responsible for such effects.

CONCLUSION

These results support the widespread use of C. albidus in popular medicine and indicate that this plant has therapeutic potential with analgesic and anti-inflammatory properties based on the presence of flavonol derivatives.

摘要

民族药理学相关性

乳香黄连木(乳香科)传统上用于治疗各种炎症性疾病,但尚未有关于乳香黄连木及其潜在机制的抗炎和抗伤害作用的系统研究。我们旨在探索该植物的抗炎和抗伤害作用,并通过液相色谱-质谱联用(LC-MS)对其多酚成分进行表征。

材料与方法

通过固液萃取和液液萃取从乳香黄连木叶中提取氯仿提取物。采用尾部浸入试验和醋酸诱导扭体试验评价其镇痛作用,采用实验性角叉菜胶诱导的足肿胀模型评价其抗炎作用。通过Western blot 分析环氧化酶(COX)-2和诱导型一氧化氮合酶(iNOS)表达的变化,以及丝裂原激活蛋白激酶(MAPK)和核转录因子κB(NF-κB)信号通路在脂多糖(LPS)刺激的小鼠腹腔巨噬细胞中的作用。采用二极管阵列检测与电喷雾串联质谱检测相结合的高效液相色谱法(HPLC-DAD-ESI-MS/MS)测定提取物的植物化学成分谱。

结果

在 100mg/kg 时,尾部浸入试验(120 分钟时减少 59.63%)和醋酸试验(抑制 65.94%)均观察到显著的镇痛活性。该提取物(50mg/kg)显著减少足肿胀(51.6%),显著抑制亚硝酸盐生成(72.62%),而不影响 LPS 刺激的小鼠腹腔巨噬细胞的细胞活力。这些结果与在提取物处理的巨噬细胞中下调促炎酶 COX-2 和 iNOS 以及降低 p38 MAPK 磷酸化相一致。HPLC-DAD-ESI-MS/MS 分析表明,类黄酮如槲皮素和山奈酚衍生物可能是产生这种作用的原因。

结论

这些结果支持乳香黄连木在民间医学中的广泛应用,并表明该植物具有基于类黄酮衍生物的镇痛和抗炎特性的治疗潜力。

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