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柠檬醛抗白色念珠菌的有效性及其作用机制的研究。

Anti-Candida albicans effectiveness of citral and investigation of mode of action.

机构信息

Programa de Pós-Graduação em Produtos Naturais e Sintéticos Bioativos, Centro de Ciências da Saúde-CCS, Universidade Federal da Paraíba-UFPB, João Pessoa, Paraíba, Brasil.

出版信息

Pharm Biol. 2012 Dec;50(12):1536-41. doi: 10.3109/13880209.2012.694893. Epub 2012 Nov 2.

Abstract

CONTEXT

Candidiasis is a mycosis caused by Candida species, which is of clinical importance due to the increase in resistant yeasts. Candida infection has been a serious health problem due to the inappropriate use of antibiotics. Therefore, it is necessary to study molecules with an antifungal action. Citral is a monoterpene with known pharmacological properties, including antimicrobial action.

OBJECTIVE

The aim of this work was to determine the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of citral and the probable mode of action.

MATERIALS AND METHODS

The MIC of citral was determined by the broth microdilution method using Sabouraud dextrose medium. Additionally, the interference of citral in cell wall (sorbitol assay) and the binding of citral to ergosterol and cholesterol were studied, carried out by broth microdilution method.

RESULTS

The MIC and MFC of citral were 512 and 1024 µg/mL, respectively. The MIC of amphotericin B was 1 µg/mL. The mechanism of action did not involve either the cell wall or ergosterol. However, the presence of cholesterol increased the MIC of citral to 1024 µg/mL, indicating there is some interaction between citral and cholesterol. Amphotericin B was used as the positive control, and it showed a high MIC in the presence of ergosterol (32 µg/mL), while in the presence of cholesterol MIC increased to 4 µg/mL.

CONCLUSION

Citral inhibits the growth of C. albicans. The probable mechanism of action did not involve the cell wall or ergosterol. Citral is able to interact with cholesterol. More studies are necessary to describe their effects completely.

摘要

背景

念珠菌病是由念珠菌属引起的真菌感染,由于耐药酵母的增加,其具有重要的临床意义。由于抗生素的不适当使用,念珠菌感染已成为一个严重的健康问题。因此,有必要研究具有抗真菌作用的分子。柠檬醛是一种具有已知药理作用的单萜烯,包括抗菌作用。

目的

本工作旨在测定柠檬醛的最小抑菌浓度(MIC)和最小杀菌浓度(MFC),并探讨其可能的作用机制。

材料和方法

采用肉汤微量稀释法,用沙氏葡萄糖琼脂培养基测定柠檬醛的 MIC。此外,通过肉汤微量稀释法研究了柠檬醛对细胞壁(山梨醇试验)的干扰作用以及与麦角固醇和胆固醇的结合作用。

结果

柠檬醛的 MIC 和 MFC 分别为 512 和 1024 µg/mL,两性霉素 B 的 MIC 为 1 µg/mL。作用机制不涉及细胞壁或麦角固醇。然而,胆固醇的存在使柠檬醛的 MIC 增加到 1024 µg/mL,表明柠檬醛与胆固醇之间存在一定的相互作用。两性霉素 B 作为阳性对照,在麦角固醇存在时 MIC 较高(32 µg/mL),而在胆固醇存在时 MIC 增加到 4 µg/mL。

结论

柠檬醛抑制白色念珠菌的生长。可能的作用机制不涉及细胞壁或麦角固醇。柠檬醛能够与胆固醇相互作用。还需要进一步的研究来完全描述它们的作用。

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