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组蛋白:具有治疗潜力的抗菌肽。

Histatins: antimicrobial peptides with therapeutic potential.

作者信息

Kavanagh Kevin, Dowd Susan

机构信息

Medical Mycology Unit, Department of Biology, National Institute for Cellular Biotechnology, NUI Maynooth, Co. Kildare, Ireland.

出版信息

J Pharm Pharmacol. 2004 Mar;56(3):285-9. doi: 10.1211/0022357022971.

Abstract

Histatins are a group of antimicrobial peptides, found in the saliva of man and some higher primates, which possess antifungal properties. Histatins bind to a receptor on the fungal cell membrane and enter the cytoplasm where they target the mitochondrion. They induce the non-lytic loss of ATP from actively respiring cells, which can induce cell death. In addition, they have been shown to disrupt the cell cycle and lead to the generation of reactive oxygen species. Their mode of action is distinct from those exhibited by the conventional azole and polyene drugs, hence histatins may have applications in controlling drug-resistant fungal infections. The possibility of utilising histatins for the control of fungal infections of the oral cavity is being actively pursued with the antifungal properties of topical histatin preparations and histatin-impregnated denture acrylic being evaluated. Initial clinical studies are encouraging, having demonstrated the safety and efficacy of histatin preparations in blocking the adherence of the yeast Candida albicans to denture acrylic, retarding plaque formation and reducing the severity of gingivitis. Histatins may represent a new generation of antimicrobial compounds for the treatment of oral fungal infections and have the advantage, compared with conventional antifungal agents, of being a normal component of human saliva with no apparent adverse effects on host tissues and having a mode of action distinct to azole and polyene antifungals.

摘要

组蛋白是一类抗菌肽,存在于人类和一些高等灵长类动物的唾液中,具有抗真菌特性。组蛋白与真菌细胞膜上的受体结合并进入细胞质,在细胞质中它们以线粒体为靶点。它们会导致活跃呼吸的细胞非溶解性地丧失ATP,从而诱导细胞死亡。此外,它们还被证明会扰乱细胞周期并导致活性氧的产生。它们的作用方式与传统的唑类和多烯类药物不同,因此组蛋白可能在控制耐药真菌感染方面有应用价值。利用组蛋白控制口腔真菌感染的可能性正在积极探索中,局部用组蛋白制剂和含组蛋白的义齿丙烯酸树脂的抗真菌特性正在接受评估。初步临床研究令人鼓舞,已证明组蛋白制剂在阻止白色念珠菌酵母粘附于义齿丙烯酸树脂、延缓菌斑形成和减轻牙龈炎严重程度方面的安全性和有效性。与传统抗真菌剂相比,组蛋白可能代表了新一代用于治疗口腔真菌感染的抗菌化合物,具有作为人类唾液正常成分、对宿主组织无明显不良影响且作用方式不同于唑类和多烯类抗真菌剂的优势。

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