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来自小花盖加拉的具有前列腺素E2抑制活性的化合物可能解释了其用于缓解疼痛的传统用途。

Compounds from Geijera parviflora with prostaglandin E2 inhibitory activity may explain its traditional use for pain relief.

作者信息

Banbury Linda K, Shou Qingyao, Renshaw Dane E, Lambley Eleanore H, Griesser Hans J, Mon Htwe, Wohlmuth Hans

机构信息

Southern Cross Plant Science, Southern Cross University, PO Box 157, Lismore, NSW 2480, Australia.

Mawson Institute, University of South Australia, Mawson Lakes SA 5095, Australia.

出版信息

J Ethnopharmacol. 2015 Apr 2;163:251-5. doi: 10.1016/j.jep.2015.01.033. Epub 2015 Feb 2.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Australian Aboriginal people used crushed leaves of Geijera parviflora Lindl. both internally and externally for pain relief, including for toothache (Cribb and Cribb, 1981). This study tested the hypothesis that this traditional use might be at least in part explained by the presence of compounds with anti-inflammatory activity.

MATERIALS AND METHODS

A crude extract (95% EtOH) was prepared from powdered dried leaves. From the CH3Cl fraction of this extract compounds were isolated by bioassay-guided fractionation and tested for: (1) cytotoxicity in RAW 264.7 murine leukemic monocyte-macrophages, (2) prostaglandin E2 (PGE2) inhibitory activity in 3T3 Swiss albino mouse embryonic fibroblast cells, as well as (3) nitric oxide (NO) and (4) tumour necrosis factor alpha (TNFα) inhibitory activity in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Isolated compounds were also tested for (5) antibacterial activity against a panel of Gram-positive (Staphylococcus aureus ATCC 29213 and ATCC 25923, Staphylococcus epidermidis ATCC 35984, biofilm-forming) and Gram-negative (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853) strains by broth microdilution.

RESULTS

Eleven compounds were isolated, including one new flavone and one new natural product, with a further four compounds reported from this species for the first time. Some of the compounds showed good anti-inflammatory activity in vitro. In particular, flindersine (1) and N-(acetoxymethyl) flindersine (3) inhibited PGE2 release with IC50 values of 5.0μM and 4.9μM, respectively, without any significant cytotoxicity. Several other compounds showed moderate inhibition of NO (5, 6, 7) and TNF-α (6), with IC50 in the low micromolar range; however much of this apparent activity could be accounted for by the cytotoxicity of these compounds. None of the compounds showed anti-bacterial activity.

CONCLUSIONS

The inhibition of PGE2, an important mediator of inflammation and pain, by flindersine and a derivative thereof, along with the moderate anti-inflammatory activity shown by several other compounds isolated from Geijera parviflora leaf extract, support the traditional use of this plant for pain relief by Australian Aboriginal people.

摘要

民族药理学关联

澳大利亚原住民将小花吉氏木(Geijera parviflora Lindl.)的粉碎叶片用于内服和外用以缓解疼痛,包括牙痛(克里布和克里布,1981年)。本研究检验了这样一个假设,即这种传统用途可能至少部分是由于存在具有抗炎活性的化合物。

材料与方法

从干燥的粉末状叶片中制备粗提物(95%乙醇)。从该提取物的氯仿馏分中通过生物测定导向的分级分离法分离化合物,并对其进行以下测试:(1)对RAW 264.7小鼠白血病单核巨噬细胞的细胞毒性,(2)对3T3瑞士白化小鼠胚胎成纤维细胞中前列腺素E2(PGE2)的抑制活性,以及(3)对脂多糖(LPS)刺激的RAW 264.7细胞中一氧化氮(NO)和(4)肿瘤坏死因子α(TNFα)的抑制活性。还对分离出的化合物进行了(5)通过肉汤微量稀释法对一组革兰氏阳性菌(金黄色葡萄球菌ATCC 29213和ATCC 25923、表皮葡萄球菌ATCC 35984、形成生物膜的菌株)和革兰氏阴性菌(大肠杆菌ATCC 25922、铜绿假单胞菌ATCC 27853)的抗菌活性测试。

结果

分离出11种化合物,包括一种新黄酮和一种新天然产物,另有4种化合物首次从该物种中报道。其中一些化合物在体外显示出良好的抗炎活性。特别是,弗林德辛(1)和N -(乙酰氧基甲基)弗林德辛(3)抑制PGE2释放,IC50值分别为5.0μM和4.9μM,且无任何明显的细胞毒性。其他几种化合物对NO(5、6、7)和TNF -α(6)有中度抑制作用,IC50在低微摩尔范围内;然而,这种明显的活性大部分可归因于这些化合物的细胞毒性。所有化合物均未显示抗菌活性。

结论

弗林德辛及其衍生物对炎症和疼痛的重要介质PGE2的抑制作用,以及从小花吉氏木叶提取物中分离出的其他几种化合物所显示的中度抗炎活性,支持了澳大利亚原住民将这种植物用于缓解疼痛的传统用途。

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