异常大麻素衍生物的抗真菌特性:破坏念珠菌的生物膜形成和基因表达。

IF 9.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Prince Ofori , Natalia Zemliana , Ilan Zaffran , Tatiana Etzion , Ronit Vogt Sionov , Doron Steinberg , Raphael Mechoulam , Natalya M. Kogan , Francesca Levi-Schaffer
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引用次数: 0

摘要

异常大麻素(包括化合物 3)是一类合成脂质化合物,具有非精神活性特性和雷公藤异构体结构,但与传统大麻素不同,因为它们不与已有的 CB1 和 CB2 受体相互作用。以前的研究表明,comp 3 具有保护心脏和抗炎的潜力,最近的研究还表明了它对耐甲氧西林金黄色葡萄球菌(MRSA)的抗菌作用。鉴于念珠菌感染带来的挑战不断升级以及抗真菌药物耐药性的增加,探索新的治疗途径至关重要。本研究旨在评估新合成的 AbnCBD 衍生物的抗念珠菌特性。AbnCBD 衍生物由酸催化偶联合成,并进一步衍生化。我们评估了 AbnCBD 衍生物抑制各种念珠菌生长阶段的潜力。通过体外比色实验和体内小鼠实验,我们发现 AbnCBD 衍生物对念珠菌的生长有不同程度的抑制作用。与对照组(FLC 和 0.5% DMSO)相比,AbnCBD 衍生物,尤其是化合物 3、化合物 10 和化合物 9 能显著降低白色念珠菌(包括 FLC 耐药菌株)、热带念珠菌和副丝状念珠菌的生长,但不能降低白色念珠菌的生长。化合物 3 还能破坏白僵菌生物膜的形成并根除成熟的生物膜。值得注意的是,AbnCBD 的其他衍生物会破坏白僵菌生物膜的形成和成熟,但不会影响酵母的生长。在小鼠 VVC 模型中,与药物和 FLC 对照组相比,化合物 3 能显著清除真菌并减少白僵菌的负担。这些发现凸显了 AbnCBD 作为抗念珠菌感染的抗真菌药物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antifungal properties of abnormal cannabinoid derivatives: Disruption of biofilm formation and gene expression in Candida species
Abnormal cannabinoids (including comp 3) are a class of synthetic lipid compounds with non-psychoactive properties and regioisomer configurations, but distinct from traditional cannabinoids since they do not interact with the established CB1 and CB2 receptors. Previous research showed the cardioprotective and anti-inflammatory potentials of comp 3 and more recently its antimicrobial effect on methicillin-resistant Staphylococcus aureus (MRSA). Given the escalating challenges posed by Candida infections and the rise of antifungal drug resistance, the exploration of novel therapeutic avenues is crucial. This study aimed to assess the anti-Candida properties of newly synthesized AbnCBD derivatives. AbnCBD derivatives were synthesized by acid catalysis-induced coupling and further derivatized. We evaluated the potential of the AbnCBD derivatives to inhibit the growth stages of various Candida species. By in vitro colorimetric assays and in vivo mice experiments, we have shown that AbnCBD derivatives induce differential inhibition of Candida growth. The AbnCBD derivatives, especially comp 3, comp 10, and comp 9 significantly reduced the growth of C. albicans, including FLC-resistant strains, and of C. tropicalis and C. parapsilosis but not of C auris compared to their controls (FLC and 0.5 % DMSO). Comp 3 also disrupted C. albicans biofilm formation and eradicated mature biofilms. Notably, other derivatives of AbnCBD disrupted the biofilm formation and maturation of C. albicans but did not affect yeast growth. In a murine model of VVC, comp 3 demonstrated significant fungal clearance and reduced C. albicans burden compared to vehicle and FLC controls. These findings highlight the potential of AbnCBDs as promising antifungal agents against Candida infections.
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来源期刊
Pharmacological research
Pharmacological research 医学-药学
CiteScore
18.70
自引率
3.20%
发文量
491
审稿时长
8 days
期刊介绍: Pharmacological Research publishes cutting-edge articles in biomedical sciences to cover a broad range of topics that move the pharmacological field forward. Pharmacological research publishes articles on molecular, biochemical, translational, and clinical research (including clinical trials); it is proud of its rapid publication of accepted papers that comprises a dedicated, fast acceptance and publication track for high profile articles.
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