从大麻植物中提取的独特生物活性分子抗菌效果的最新进展。

Mathis Werner, Stefan Bereswill, Markus M Heimesaat
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摘要

在全球范围内,人类感染耐多药(MDR)细菌的数量不断增加,对人类健康构成了严重威胁。鉴于新型抗生素化合物的缺乏使这一窘境进一步恶化,应用天然化合物替代抗生素治疗和预防传染病的策略显得非常重要。鉴于众所周知的大麻有益健康和缓解疾病的特性,我们进行了一次文献检索,总结了目前有关大麻植物不同部位提取物和确定的大麻衍生分子的抗菌效果及其潜在作用模式的知识。这些研究表明,大麻的各种提取物和精油以及主要的大麻素对广谱革兰氏阳性菌和一些革兰氏阴性菌(包括耐药菌株)具有很强的抗菌活性。特别是一些大麻素对细菌细胞质膜的破坏导致了对革兰氏阳性细菌(包括耐甲氧西林金黄色葡萄球菌)的强效抗菌作用。此外,确定的大麻素还能抑制和消除现有的细菌生物膜。总之,鉴于其独特的抗菌特性,大麻衍生分子扩大了抗生素依赖性治疗选择的范围,可用于抗击细菌感染性疾病,这应在未来的研究(包括临床试验)中进一步探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A recent update on the antibacterial effects of distinct bioactive molecules derived from the Cannabis plant.

The number of human infections with multidrug-resistant (MDR) bacteria is increasing worldwide and constitutes a serious threat to human health. Given the lack of novel antibiotic compounds worsening this dilemma, alternative antibiotic-independent treatment and prevention strategies of infectious diseases applying natural compounds appear highly appreciable. Given the long-known health-beneficial and disease-alleviating properties of Cannabis, we performed a literature search summarizing current knowledge regarding the antibacterial effects of extracts from different parts of the Cannabis sativa plant and of defined Cannabis-derived molecules and their potential mode of action. The included studies revealed that various extracts and essential oils of C. sativa as well as major cannabinoids exerted potent activities against a broad spectrum of Gram-positive bacteria and against some Gram-negative bacterial species including MDR strains. Particularly the disruption of the bacterial cytoplasmic membrane by some cannabinoids resulted in potent antibacterial effects against Gram-positive bacteria including methicillin-resistant Staphylococcus aureus. Furthermore, defined cannabinoids inhibited the formation of and eradicated existing bacterial biofilms. In conclusion, given their antibacterial properties distinct Cannabis-derived molecules expand the repertoire of antibiotics-independent treatment options in the combat of bacterial infectious diseases which should be further addressed in future studies including clinical trials.

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