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α-蒎烯和β-蒎烯对映异构体的生物活性。

Biological activities of α-pinene and β-pinene enantiomers.

机构信息

Institute of Microbiology Paulo de Góes, Federal University of Rio de Janeiro-IMPG-UFRJ, CCS, Ilha do Fundão, Rio de Janeiro, RJ 21941-590, Brazil.

出版信息

Molecules. 2012 May 25;17(6):6305-16. doi: 10.3390/molecules17066305.

Abstract

The antimicrobial activities of the isomers and enantiomers of pinene were evaluated against bacterial and fungal cells. The agar diffusion test showed that only the positive enantiomers of the α- and β-isomers of pinene were active. The minimal inhibitory concentration (MIC) and minimal microbicidal concentration (MMC) of these monoterpenes were also determined, confirming that the positive enantiomers exhibited microbicidal activity against all fungi and bacteria tested with MICs ranging from 117 to 4,150 μg/mL. However, no antimicrobial activity was detected with the negative enantiomers up to 20 mg/mL. Time-kill curves showed that (+)-α-pinene and (+)-β-pinene were highly toxic to Candida albicans, killing 100% of inoculum within 60 min. By contrast, the bactericidal effect occurred after 6 h in methicillin-resistant Staphylococcus aureus (MRSA). In combination with commercial antimicrobials, ciprofloxacin plus (+)-α-pinene or (+)-β-pinene presented synergistic activity against MRSA whereas an indifferent effect against all fungi was detected when amphotericin B was combined with the positive enantiomers of pinene. The potential of (+)-α-pinene and (+)-β-pinene to inhibit phospholipase and esterase activities was also evaluated, and the best inhibition results were obtained with Cryptococcus neoformans. C. albicans biofilm formation was prevented with the MIC concentration of (+)-α-pinene and twice the MIC value of (+)-β-pinene. Finally, the cytotoxicity of the positive enantiomers of pinene to murine macrophages was evaluated, and 250 μg/mL of (+)-α-pinene and (+)-β-pinene reduced the cell viability to 66.8% and 57.7%, respectively.

摘要

对蒎烯的对映异构体和非对映异构体的抗菌活性进行了评估,以测试其对细菌和真菌细胞的作用。琼脂扩散试验表明,只有蒎烯的 α-和 β-异构体的正对映异构体具有活性。还确定了这些单萜的最小抑菌浓度(MIC)和最小杀菌浓度(MMC),证实正对映异构体对所有测试的真菌和细菌均具有杀菌活性,MIC 范围为 117 至 4,150 μg/mL。但是,在高达 20 mg/mL 的浓度下,未检测到负对映异构体的抗菌活性。时间杀伤曲线表明,(+)-α-蒎烯和(+)-β-蒎烯对白色念珠菌具有高毒性,在 60 分钟内可杀死 100%的接种物。相比之下,耐甲氧西林金黄色葡萄球菌(MRSA)的杀菌作用在 6 小时后发生。与商业抗菌药物联合使用时,环丙沙星与(+)-α-蒎烯或(+)-β-蒎烯联合使用对 MRSA 表现出协同作用,而当两性霉素 B 与蒎烯的正对映异构体联合使用时,对所有真菌均检测到无差异作用。还评估了(+)-α-蒎烯和(+)-β-蒎烯抑制磷脂酶和酯酶活性的潜力,并且在新型隐球菌中获得了最佳的抑制效果。(+)-α-蒎烯的 MIC 浓度和(+)-β-蒎烯的 MIC 值的两倍均可防止白色念珠菌生物膜的形成。最后,评估了正对映异构体对小鼠巨噬细胞的细胞毒性,250μg/mL 的(+)-α-蒎烯和(+)-β-蒎烯将细胞活力分别降低至 66.8%和 57.7%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ab1/6268778/70a170a0a423/molecules-17-06305-g001.jpg

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