Prince Ofori , Natalia Zemliana , Ilan Zaffran , Tatiana Etzion , Ronit Vogt Sionov , Doron Steinberg , Raphael Mechoulam , Natalya M. Kogan , Francesca Levi-Schaffer
{"title":"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。","authors":"Prince Ofori , Natalia Zemliana , Ilan Zaffran , Tatiana Etzion , Ronit Vogt Sionov , Doron Steinberg , Raphael Mechoulam , Natalya M. Kogan , Francesca Levi-Schaffer","doi":"10.1016/j.phrs.2024.107441","DOIUrl":null,"url":null,"abstract":"<div><div>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 <em>Staphylococcus aureus</em> (MRSA). Given the escalating challenges posed by <em>Candida</em> infections and the rise of antifungal drug resistance, the exploration of novel therapeutic avenues is crucial. This study aimed to assess the anti-<em>Candida</em> 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 <em>Candida</em> species. By <em>in vitro</em> colorimetric assays and <em>in vivo</em> mice experiments, we have shown that AbnCBD derivatives induce differential inhibition of <em>Candida</em> growth. The AbnCBD derivatives, especially comp 3, comp 10, and comp 9 significantly reduced the growth of <em>C. albicans</em>, including FLC-resistant strains, and of <em>C. tropicalis</em> and <em>C. parapsilosis</em> but not of <em>C auris</em> compared to their controls (FLC and 0.5 % DMSO). Comp 3 also disrupted <em>C. albicans</em> biofilm formation and eradicated mature biofilms. Notably, other derivatives of AbnCBD disrupted the biofilm formation and maturation of <em>C. albicans</em> but did not affect yeast growth. In a murine model of VVC, comp 3 demonstrated significant fungal clearance and reduced <em>C. albicans</em> burden compared to vehicle and FLC controls. These findings highlight the potential of AbnCBDs as promising antifungal agents against <em>Candida</em> infections.</div></div>","PeriodicalId":19918,"journal":{"name":"Pharmacological research","volume":"209 ","pages":"Article 107441"},"PeriodicalIF":9.1000,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antifungal properties of abnormal cannabinoid derivatives: Disruption of biofilm formation and gene expression in Candida species\",\"authors\":\"Prince Ofori , Natalia Zemliana , Ilan Zaffran , Tatiana Etzion , Ronit Vogt Sionov , Doron Steinberg , Raphael Mechoulam , Natalya M. Kogan , Francesca Levi-Schaffer\",\"doi\":\"10.1016/j.phrs.2024.107441\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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 <em>Staphylococcus aureus</em> (MRSA). Given the escalating challenges posed by <em>Candida</em> infections and the rise of antifungal drug resistance, the exploration of novel therapeutic avenues is crucial. This study aimed to assess the anti-<em>Candida</em> 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 <em>Candida</em> species. By <em>in vitro</em> colorimetric assays and <em>in vivo</em> mice experiments, we have shown that AbnCBD derivatives induce differential inhibition of <em>Candida</em> growth. The AbnCBD derivatives, especially comp 3, comp 10, and comp 9 significantly reduced the growth of <em>C. albicans</em>, including FLC-resistant strains, and of <em>C. tropicalis</em> and <em>C. parapsilosis</em> but not of <em>C auris</em> compared to their controls (FLC and 0.5 % DMSO). Comp 3 also disrupted <em>C. albicans</em> biofilm formation and eradicated mature biofilms. Notably, other derivatives of AbnCBD disrupted the biofilm formation and maturation of <em>C. albicans</em> but did not affect yeast growth. In a murine model of VVC, comp 3 demonstrated significant fungal clearance and reduced <em>C. albicans</em> burden compared to vehicle and FLC controls. These findings highlight the potential of AbnCBDs as promising antifungal agents against <em>Candida</em> infections.</div></div>\",\"PeriodicalId\":19918,\"journal\":{\"name\":\"Pharmacological research\",\"volume\":\"209 \",\"pages\":\"Article 107441\"},\"PeriodicalIF\":9.1000,\"publicationDate\":\"2024-10-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmacological research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1043661824003864\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacological research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1043661824003864","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
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.
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.