Natural Product Usnic Acid as an Antibacterial Therapeutic Agent: Current Achievements and Further Prospects.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
Tian Li, Zhanhui Wang, Xiuying Zhang, Zhihui Hao, Yong Guo, Jianzhong Shen, Tony Velkov, Chongshan Dai
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引用次数: 0

Abstract

Antimicrobial resistance (AMR) poses a significant global public health threat, endangering both human and animal health. In clinical environments, AMR often undermines the effectiveness of antibacterial treatments, underscoring the urgent need to discover and develop new antibacterial agents or alternatives to antibiotics. Usnic acid, a secondary metabolite derived from lichens, has emerged as a promising candidate owing to its diverse pharmacological properties, which include antibacterial, immune-regulating, antiaging, and anti-inflammatory activities. Extensive research has shown that usnic acid exhibits strong direct antibacterial effects against Gram-positive bacteria and acts as an antimicrobial adjuvant to enhance the therapeutic efficacy of antibiotic drugs against Gram-negative pathogens. Its mechanisms of action are multifaceted, encompassing the inhibition of RNA, DNA, and protein synthesis; suppression of bacterial efflux pump protein expression and membrane-localized drug-resistant enzyme activity; disruption of cell membrane integrity and metabolic homeostasis; and reduction of virulence factor production and biofilm formation. Despite its potential, the clinical application of usnic acid as an antibacterial agent faces significant challenges including poor aqueous solubility, low bioavailability, and dose-dependent toxicity. To overcome these limitations, nanodelivery systems such as liposomes and polymeric nanoparticles have been developed to enhance solubility, improve targeted delivery, and reduce toxicity, thereby expanding its therapeutic potential. Structural modification can also enhance the antibacterial activity and address solubility issues. This review systematically consolidates current knowledge on usnic acid's antibacterial properties, molecular mechanisms, and combinatorial therapies. It critically evaluates advancements in nanoformulation strategies, assesses safety and toxicity profiles, and identifies obstacles to its development as a clinically viable antibacterial agent. By addressing these aspects, this review aims to provide actionable insights, foster interdisciplinary dialogue, and catalyze further innovation in leveraging this natural product to combat AMR.

天然产物枸杞酸作为抗菌治疗剂的研究进展及展望。
抗菌素耐药性(AMR)对全球公共卫生构成重大威胁,危及人类和动物健康。在临床环境中,抗生素耐药性往往会破坏抗菌治疗的有效性,这凸显了发现和开发新的抗菌药物或抗生素替代品的迫切需要。Usnic酸是地衣的次生代谢物,由于其多种药理特性,包括抗菌、免疫调节、抗衰老和抗炎活性,已成为一种有希望的候选药物。大量研究表明,枸杞酸对革兰氏阳性菌具有较强的直接抗菌作用,并可作为抗菌佐剂增强抗生素药物对革兰氏阴性病原菌的治疗效果。其作用机制是多方面的,包括抑制RNA、DNA和蛋白质的合成;细菌外排泵蛋白表达及膜域耐药酶活性的抑制破坏细胞膜完整性和代谢稳态;减少毒力因子的产生和生物膜的形成。尽管具有潜力,但作为抗菌药物的临床应用面临着水溶性差、生物利用度低和剂量依赖性毒性等重大挑战。为了克服这些限制,人们开发了纳米递送系统,如脂质体和聚合物纳米颗粒,以提高溶解度,改善靶向递送,降低毒性,从而扩大其治疗潜力。结构修饰也可以提高抗菌活性和解决溶解度问题。这篇综述系统地整合了目前关于枸杞酸的抗菌特性、分子机制和联合治疗的知识。它批判性地评估纳米制剂策略的进展,评估安全性和毒性概况,并确定其发展为临床可行的抗菌剂的障碍。通过解决这些问题,本综述旨在提供可操作的见解,促进跨学科对话,并促进利用这种天然产物对抗抗生素耐药性的进一步创新。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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