Flavonoid as Anti-Candida Agents

S. Susilawati, C. Anwar, Irsan Saleh, Salni Salni
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引用次数: 1

Abstract

Vulvovaginal candidiasis is the second most common cause of vaginitis after bacterial vaginosis with at least 75 – 80% of women have had one episode of VVC in their lifetime. Their prevalent resistance to most commonly used antifungal agents makes their treatment a challenge to physicians. Flavonoids have been shown to possess potent anti-Candida properties which can inhibit the growth and proliferation of Candida species through various mechanisms, including inhibition of fungal cell wall synthesis, disruption of fungal cell membrane integrity, and interference with fungal cell signaling pathways. Their potency makes them potential candidates for the development of antifungal agents for the treatment of candidiasis, alone or in combination with existing antifungal drugs. The review aims to explore the mechanisms by which flavonoids inhibit the growth and proliferation of Candida species, including the inhibition of fungal cell wall synthesis, disruption of fungal cell membrane integrity, and interference with fungal cell signaling pathways.
作为抗念珠菌药物的黄酮类化合物
外阴阴道念珠菌病是继细菌性阴道病之后阴道炎的第二大常见原因,至少75 - 80%的女性一生中有过一次VVC发作。他们对大多数常用抗真菌药物的普遍耐药性使他们的治疗成为医生的挑战。黄酮类化合物已被证明具有有效的抗念珠菌特性,可以通过抑制真菌细胞壁合成、破坏真菌细胞膜完整性和干扰真菌细胞信号通路等多种机制抑制念珠菌的生长和增殖。它们的效力使它们成为开发用于治疗念珠菌病的抗真菌药物的潜在候选者,可以单独使用或与现有的抗真菌药物联合使用。本文旨在探讨黄酮类化合物抑制念珠菌生长和增殖的机制,包括抑制真菌细胞壁合成、破坏真菌细胞膜完整性和干扰真菌细胞信号通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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