Unveiling the antimicrobial, antivirulence, and wound-healing accelerating potentials of resveratrol against carbapenem-resistant Pseudomonas aeruginosa (CRPA)-septic wound in a murine model.

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Rana Elshimy, Riham A El-Shiekh, Mona M Okba, Rehab M S Ashour, Marwa A Ibrahim, Eman I Hassanen, Hassan Aboul-Ella, Merhan E Ali
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引用次数: 0

Abstract

Pseudomonas aeruginosa is a repertoire of several virulence factors that create a frightening high pathogenicity level as well as high antimicrobial resistance toward commercially used antibiotics. Therefore, finding a new alternative to traditional antimicrobials is a must. Resveratrol is a very famous phytochemical that harbors many beneficial health properties by possessing antibacterial, anti-inflammatory, and antioxidant properties. The current study aimed to explore the antimicrobial efficacy of resveratrol against P. aeruginosa and explore its ability to accelerate wound healing in a murine model. The obtained results revealed the potent antimicrobial, antivirulence, and wound-healing accelerating potentials of resveratrol against carbapenem-resistant P. aeruginosa (CRPA)-septic wounds. It significantly lowered the transcript levels of P. aeruginosa virulent genes toxA, pelA, and lasB. Additionally, resveratrol significantly accelerated skin wound healing by shortening the inflammatory phase and promoting re-vascularization, cell proliferation, re-epithelialization, and collagen deposition. Furthermore, it increased the immunoexpression of αSMA along with a reduction of the mRNA levels of VEGF, IL-1β, and TNF-α genes. Resveratrol has high therapeutic potential for the treatment of P. aeruginosa wound infection and is a prospective and promising candidate for this problem.

在小鼠模型中揭示白藜芦醇对耐碳青霉烯类铜绿假单胞菌(CRPA)败血症伤口的抗菌、抗病毒和加速伤口愈合潜力。
铜绿假单胞菌(Pseudomonas aeruginosa)具有多种致病因子,不仅致病性高得吓人,而且对市售抗生素具有很强的抗药性。因此,寻找传统抗菌剂的新替代品势在必行。白藜芦醇是一种非常著名的植物化学物质,具有抗菌、消炎和抗氧化等多种有益健康的特性。本研究旨在探讨白藜芦醇对铜绿假单胞菌的抗菌功效,并探索其在小鼠模型中加速伤口愈合的能力。研究结果表明,白藜芦醇对耐碳青霉烯类的铜绿假单胞菌(CRPA)败血症伤口具有强效的抗菌、抗病毒和加速伤口愈合的潜力。它能明显降低铜绿假单胞菌毒力基因 toxA、pelA 和 lasB 的转录水平。此外,白藜芦醇还能缩短炎症期,促进血管再通、细胞增殖、再上皮化和胶原沉积,从而明显加快皮肤伤口的愈合。此外,白藜芦醇还能提高 αSMA 的免疫表达,降低血管内皮生长因子、IL-1β 和 TNF-α 基因的 mRNA 水平。白藜芦醇在治疗铜绿假单胞菌伤口感染方面具有很高的治疗潜力,是解决这一问题的前景广阔的候选药物。
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来源期刊
Inflammopharmacology
Inflammopharmacology IMMUNOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
8.00
自引率
3.40%
发文量
200
期刊介绍: Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas: -Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states -Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs -Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents -Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain -Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs -Muscle-immune interactions during inflammation [...]
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