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柑橘属茎皮中的吖啶酮生物碱对乳腺癌、肝癌、肺癌和前列腺癌人类癌细胞具有选择性细胞毒性。

Acridone alkaloids from the stem bark of Citrus aurantium display selective cytotoxicity against breast, liver, lung and prostate human carcinoma cells.

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria; Medicinal Chemistry and Natural Products Research Group, School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, United Kingdom; Department of Pharmacognosy, Faculty of Pharmacy, Olabisi Onabanjo University, Sagamu Campus, Nigeria.

Medicinal Chemistry and Natural Products Research Group, School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, United Kingdom.

出版信息

J Ethnopharmacol. 2018 Dec 5;227:131-138. doi: 10.1016/j.jep.2018.08.039. Epub 2018 Sep 3.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Citrus aurantium L. (Rutaceae) is used, either singly or as a part of a polyherbal preparation, in Nigerian traditional medicine for the management of cancer and inflammatory diseases. Currently, there is a dearth of knowledge demonstrating its anticancer potential.

AIM OF THE STUDY

This study was carried out to determine the in vitro cytotoxicity of the crude extract of the stem bark of C. aurantium, identify and isolate the bioactive constituents and to establish the cytotoxicity of such constituents.

MATERIALS AND METHODS

The powdered bark of C. aurantium was extracted by MeOH at room temperature (25-34 °C) and the crude extract was partitioned successively, with n-hexane, dichloromethane and methanol. Amongst the fractions, the DCM fraction was the most active and compounds were isolated from this fraction using a combination of chromatographic techniques. The structures of the isolated compounds were elucidated by spectroscopic means (MS, 1D and 2D NMR). The cytotoxicity of the extract, and the isolated compounds were evaluated by the MTT assay against four human cancer cell lines: A549 (lung), HepG2 (liver), MCF7 (breast) and PC3 (prostate). The selectivity of the isolated compounds was assessed using the normal human prostate epithelium cells (PNT2).

RESULTS AND DISCUSSION

Of the three plant fractions, the DCM fraction showed significant cytotoxicity, with its highest activity against A549 cells (IC = 3.88 µg/mL) and the least activity on HepG2 cells (IC = 5.73 µg/mL). Six acridone alkaloids, citrusinine-I (1), citracridone-I (2), 5-hydroxynoracronycine (3), natsucitrine-I (4), glycofolinine (5) and citracridone-III (6), were isolated from the DCM fraction of C. aurantium. The isolated compounds demonstrated potent to moderate cytotoxicity (IC = 12.65-50.74 µM) against the cancer cells under investigation. It is noteworthy that the compounds exerted cytotoxicity at least four times more selective towards the carcinoma cells than the PNT2 cells.

CONCLUSION

The results obtained from this study have provided some evidence for the ethnomedicinal use of C. aurantium against cancer and the acridone alkaloids present in its stem bark, have appeared to be responsible for the anticancer effects.

摘要

民族药理学相关性

芸香科柑橘(Rutaceae),无论是单独使用还是作为复方草药制剂的一部分,在尼日利亚传统医学中都被用于癌症和炎症性疾病的治疗。目前,几乎没有知识表明其具有抗癌潜力。

研究目的

本研究旨在确定柑橘茎皮的粗提取物的体外细胞毒性,鉴定和分离生物活性成分,并确定这些成分的细胞毒性。

材料和方法

将柑橘的粉末状树皮用甲醇在室温(25-34°C)下提取,然后将粗提取物依次用正己烷、二氯甲烷和甲醇进行分配。在这些馏分中,二氯甲烷馏分最为活跃,并用色谱技术组合从该馏分中分离出化合物。通过光谱手段(MS、1D 和 2D NMR)阐明分离化合物的结构。通过 MTT 测定法评估提取物和分离化合物对四种人类癌细胞系的细胞毒性:A549(肺)、HepG2(肝)、MCF7(乳腺)和 PC3(前列腺)。使用正常的人前列腺上皮细胞(PNT2)评估分离化合物的选择性。

结果与讨论

在三种植物馏分中,二氯甲烷馏分显示出显著的细胞毒性,对 A549 细胞的活性最高(IC = 3.88µg/mL),对 HepG2 细胞的活性最低(IC = 5.73µg/mL)。从柑橘的二氯甲烷馏分中分离出六种吖啶酮生物碱,即柑橘宁-I(1)、柠檬酸-I(2)、5-羟基去甲野百合碱(3)、纳曲西丁-I(4)、甘草啉(5)和柠檬酸-III(6)。分离得到的化合物对所研究的癌细胞表现出较强的至中等的细胞毒性(IC = 12.65-50.74µM)。值得注意的是,这些化合物对癌细胞的细胞毒性至少比 PNT2 细胞高四倍。

结论

本研究结果为柑橘治疗癌症的民间医学用途提供了一些证据,其茎皮中的吖啶酮生物碱似乎是其抗癌作用的原因。

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