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丁香精油诱导杜氏利什曼原虫前鞭毛体发生类似于细胞凋亡的死亡。

Apoptosis-like death in Leishmania donovani promastigotes induced by eugenol-rich oil of Syzygium aromaticum.

机构信息

Parasite Immunology Laboratory, Department of Biotechnology, Jamia Hamdard (Hamdard University), New Delhi 110 062, India.

International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi 110 067, India.

出版信息

J Med Microbiol. 2014 Jan;63(Pt 1):74-85. doi: 10.1099/jmm.0.064709-0. Epub 2013 Oct 25.

DOI:10.1099/jmm.0.064709-0
PMID:24161990
Abstract

Leishmaniasis consists of a complex spectrum of infectious diseases with worldwide distribution of which visceral leishmaniasis or kala-azar caused by Leishmania donovani is the most devastating. In the absence of vaccines, chemotherapy remains the mainstay for the control of leishmaniasis. The drugs of choice are expensive and associated with multiple adverse side effects. Because of these limitations, the development of new antileishmanial compounds is imperative and plants offer prospects in this regard. The present work was conducted to study the antileishmanial potential of oil from Syzygium aromaticum flower buds (clove). The S. aromaticum oil was characterized by gas chromatography and GC-MS and eugenol as well as eugenyl acetate were found to be the most abundant compounds, composing 59.75 % and 29.24 %, respectively of the oil. Our findings have shown that eugenol-rich essential oil from S. aromaticum (EROSA) possesses significant activity against L. donovani, with 50 % inhibitory concentration of 21 ± 0.16 µg ml(-1) and 15.24 ± 0.14 µg ml(-1), respectively, against promastigotes and intracellular amastigotes. Alterations in cellular morphology and growth reversibility assay substantiated the leishmanicidal activity of EROSA. The leishmanicidal effect was mediated via apoptosis as confirmed by externalization of phosphatidylserine, DNA nicking by TdT-mediated dUTP nick-end labelling (TUNEL) assay, dyskinetoplastidy, cell cycle arrest at sub-G0-G1 phase, loss of mitochondrial membrane potential and reactive oxygen species generation. EROSA presented no adverse cytotoxic effects against murine macrophages even at 200 µg ml(-1). Our studies authenticate the promising antileishmanial activity of EROSA, which is mediated by programmed cell death, and, accordingly, EROSA may be a source of novel agents for the treatment of leishmaniasis.

摘要

利什曼病是一组具有全球分布的传染病,其中内脏利什曼病或黑热病是由杜氏利什曼原虫引起的最具破坏性的疾病。在没有疫苗的情况下,化疗仍然是控制利什曼病的主要方法。首选药物昂贵,且伴有多种不良反应。由于这些限制,开发新的抗利什曼化合物势在必行,而植物在这方面提供了前景。本研究旨在研究丁香花蕾油(丁香)的抗利什曼原虫活性。通过气相色谱和 GC-MS 对丁香油进行了表征,发现丁香酚和乙酸丁香酚是最丰富的化合物,分别占油的 59.75%和 29.24%。我们的研究结果表明,富含丁香酚的丁香精油(EROSA)对杜氏利什曼原虫具有显著的活性,对前鞭毛体和细胞内无鞭毛体的 50%抑制浓度分别为 21±0.16μg/ml 和 15.24±0.14μg/ml。细胞形态改变和生长可逆性试验证实了 EROSA 的杀利什曼原虫活性。通过磷脂酰丝氨酸外翻、TdT 介导的 dUTP 缺口末端标记(TUNEL)试验证实的 DNA 切口、动力变形、细胞周期停滞在亚 G0-G1 期、线粒体膜电位丧失和活性氧生成,证明了 EROSA 的杀利什曼原虫作用是通过细胞凋亡介导的。即使在 200μg/ml 的浓度下,EROSA 对鼠巨噬细胞也没有不良的细胞毒性作用。我们的研究证实了 EROSA 具有有前途的抗利什曼原虫活性,这种活性是通过程序性细胞死亡介导的,因此,EROSA 可能是治疗利什曼病的新型药物的来源。

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