狼皮提取物合成的铜纳米颗粒绿色的抗菌、抗炎、血管生成和伤口愈合活性。

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Iranian Journal of Pharmaceutical Research Pub Date : 2025-03-26 eCollection Date: 2025-01-01 DOI:10.5812/ijpr-147434
Nizar H Saeedi, Abdullah D Alanazi, Rawaf Alenazy, Abdullah F Shater
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引用次数: 0

摘要

背景:伤口愈合和病原菌的抗生素耐药性已成为全球性问题,严重影响着传染病的治疗。目的:研究狼皮提取物合成的铜纳米颗粒的抗菌、抗炎、血管生成和伤口愈合性能。方法:采用沉淀法进行绿色合成。研究了CuNPs对甲氧西林敏感和耐甲氧西林金黄色葡萄球菌(MRSA)的抑菌活性。我们评估了CuNPs对MRSA蛋白渗漏的影响、生物膜相关基因(如细胞内粘附A (icaA)、细胞内粘附D (icaD)和弹性蛋白结合蛋白(EbpS)基因)的表达水平,以及其对伤口愈合、血管生成和抗炎作用的影响。结果:孔蛋白呈球形,尺寸在10 ~ 85 nm之间。单独使用CuNPs和联合使用庆大霉素(GNT)均可抑制MRSA生物膜的形成,MRSA的最小生物膜抑制浓度(MBIC50)分别为6.6µg/mL和0.50µg/mL。CuNPs显著下调MRSA中icaA、icaD和EbpS的表达水平(P < 0.05),特别是在最低抑制浓度(MIC)和最低抑制浓度(MIC)的一半时。此外,CuNPs显著(P < 0.001)增加了MRSA的蛋白渗漏。CuNPs在体外伤口愈合中表现出强大的作用,以剂量依赖的方式促进成纤维细胞增殖和伤口愈合。我们的研究结果显示,暴露于CuNPs的细胞中HLA-G5和VEGF-A基因的表达显著(P < 0.05)增加。此外,CuNPs降低了脂多糖(LPS)刺激的RAW 264.7细胞中炎症基因的表达水平(P < 0.05)。结论:本实验结果表明,CuNPs,特别是与GNT结合使用,对MRSA具有良好的抗菌作用,而不会对正常细胞产生细胞毒性。该研究还表明,绿色合成的CuNPs通过其抗菌活性、抑制生物膜形成、诱导血管生成和减少炎症,具有显著的伤口愈合特性。然而,需要进一步的实验来阐明CuNPs的确切作用机制和潜在毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antimicrobial, Anti-inflammatory, Angiogenesis, and Wound Healing Activities of Copper Nanoparticles Green Synthesized by <i>Lupinus arcticus</i> Extract.

Antimicrobial, Anti-inflammatory, Angiogenesis, and Wound Healing Activities of Copper Nanoparticles Green Synthesized by <i>Lupinus arcticus</i> Extract.

Antimicrobial, Anti-inflammatory, Angiogenesis, and Wound Healing Activities of Copper Nanoparticles Green Synthesized by <i>Lupinus arcticus</i> Extract.

Antimicrobial, Anti-inflammatory, Angiogenesis, and Wound Healing Activities of Copper Nanoparticles Green Synthesized by Lupinus arcticus Extract.

Background: Wound healing and antibiotic resistance of pathogenic microbes have become global issues with serious consequences for the treatment of infectious diseases.

Objectives: The present study aimed to evaluate the antibacterial, anti-inflammatory, angiogenic, and wound healing properties of copper nanoparticles (CuNPs) synthesized using Lupinus arcticus extract.

Methods: The green synthesis was conducted using the precipitation method. The antibacterial activity of CuNPs against both methicillin-sensitive and methicillin-resistant Staphylococcus aureus (MRSA) strains was evaluated. The effects of CuNPs on protein leakage, the expression levels of biofilm-related genes [e.g., intracellular adhesion A (icaA), intracellular adhesion D (icaD), and elastin-binding protein (EbpS) genes] in MRSA, as well as its impact on wound healing, angiogenesis, and anti-inflammatory effects, were assessed.

Results: The CuNPs exhibited a spherical shape with dimensions ranging from 10 to 85 nm. Both CuNPs alone and in combination with gentamicin (GNT) inhibited biofilm formation in MRSA, with minimum biofilm inhibitory concentration (MBIC50) values of 6.6 µg/mL and 0.50 µg/mL for MRSA, respectively. The CuNPs significantly (P < 0.05) downregulated the expression levels of icaA, icaD, and EbpS in MRSA, particularly at half the minimum inhibitory concentration (1/2 MIC) and the minimum inhibitory concentration (MIC). Additionally, CuNPs markedly (P < 0.001) increased protein leakage in MRSA. The CuNPs demonstrated potent in vitro wound healing effects, promoting fibroblast cell proliferation and wound closure in a dose-dependent manner. Our results indicated a significant (P < 0.05) increase in the expression of HLA-G5 and VEGF-A genes in cells exposed to CuNPs. Furthermore, CuNPs reduced the expression levels of inflammatory genes in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells (P < 0.05).

Conclusions: The findings of this experimental test indicate that CuNPs, particularly in conjunction with GNT, exhibits promising antibacterial effects against MRSA without causing cytotoxicity to normal cells. This study also demonstrated that green-synthesized CuNPs possesses significant wound-healing properties through its antibacterial activity, inhibition of biofilm formation, induction of angiogenesis, and reduction of inflammation. However, further experiments are necessary to elucidate the precise mechanisms of action and potential toxicity of CuNPs.

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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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