罗勒和圣木的抗念珠菌作用:揭示体外和体内对全身念珠菌病的疗效。

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Saurabh Gupta, Lokesh Nagar, Madhav Singla, Smriti -, Sachin Singh, Gaurav Gupta, Suresh Bhojraj, Rahamat Unissa Syed, Aliaa D Alshammari, Maali D Alshammari, Njoud Nahi Omer Alshammari, Atheer Nahi Omer Alshammari, Entsar Mohammed Alhaidan
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引用次数: 0

摘要

背景:本研究探讨了两种草药提取物:basilicum (HEOB)和Ocimum sanctum (HEOS)的抑菌、抗真菌和体内抗药活性。此外,本研究还分析了这些提取物的植物化学成分。目的:研究HEOB和HEOS提取物的抗菌、抗真菌和抗念珠菌活性,并分析其体内植物化学成分、抗氧化潜力和免疫调节特性。方法:采用冷浸渍法,以1:1乙醇-水水溶液提取罗勒和圣露的干花和干叶。植物化学分析遵循既定的方案,并采用比色法测定总酚和类黄酮含量。采用高效液相色谱法测定了迷迭香酸、芦丁、丁香酚、槲皮素等特定化合物的浓度。用杯盘法测定其体外抗氧化活性,特别是清除一氧化氮(NO)和抗菌性能。研究人员对患有全身性念珠菌病的免疫功能低下小鼠进行了体内研究,分别用200和400 mg/kg的植物提取物或酮康唑作为对照。评估生存率、组织组织学和白细胞计数,并使用方差分析进行统计分析。结果:HEOB和HEOS提取物具有较强的抗菌和抗氧化活性,主要是由于芦丁、槲皮素、迷迭香酸和丁香酚等类黄酮。体内实验表明,这两种提取物都能有效降低真菌负荷,提高生存率,减轻全身念珠菌病小鼠的免疫抑制。提取物还表现出显著的免疫调节特性,通过促进细胞介导的免疫反应。在较高浓度下,HEOB和HEOS的抑菌效果与酮康唑相似。结论:HEOB和HEOS具有较强的抗菌、抗真菌和抗念珠菌作用,对治疗全身性念珠菌病疗效显著。它们的免疫调节作用和增强细胞介导免疫的能力使这些提取物成为解决系统性念珠菌病的有希望的选择,特别是在免疫系统较弱的个体中。这项研究提供了有价值的见解,并为未来调查口腔和阴道念珠菌病的治疗奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticandidal Effects of Ocimum basilicum and Ocimum sanctum: Unveiling in vitro and in vivo Efficacy against Systemic Candidiasis.

Background: This research explored the antimicrobial, antifungal, and in vivo anticandidal activities of two herbal extracts: Ocimum basilicum (HEOB) and Ocimum sanctum (HEOS). Additionally, the study analyzed the phytochemical components of these extracts.

Aim: To examine the efficacy of HEOB and HEOS extracts in terms of their antimicrobial, antifungal, and anti-candidal activities and analyze their phytochemical composition, antioxidant potential, and immunomodulatory properties in vivo.

Methods: Dried flowers and leaves from Ocimum basilicum and Ocimum sanctum were extracted using a cold maceration process with a 1:1 ethanol-water solution. Phytochemical analysis followed established protocols, and the total phenolic and flavonoid contents were measured using colourimetric methods. HPLC was used to determine the concentrations of specific compounds, including rosmarinic acid, rutin, eugenol, and quercetin. Antioxidant activity, specifically nitric oxide (NO) scavenging and antimicrobial properties, was assessed in vitro using the cup plate method. In vivo studies were conducted on immunocompromised mice with systemic candidiasis, treated with plant extracts at 200 and 400 mg/kg or with ketoconazole as a control. Survival rates, tissue histology, and leukocyte counts were evaluated, and statistical analysis was performed using ANOVA.

Results: HEOB and HEOS extracts possess strong antimicrobial and antioxidant activities, largely due to flavonoids such as rutin, quercetin, rosmarinic acid and eugenol. In vivo experiments revealed that both extracts effectively reduced fungal load, increased survival rates, and alleviated immunosuppression in mice with systemic candidiasis. The extracts also exhibited significant immunomodulatory properties by boosting cellmediated immune responses. At higher concentrations, the antifungal performance of HEOB and HEOS was similar to that of ketoconazole.

Conclusion: HEOB and HEOS exhibited strong antibacterial, antifungal, and anticandidal properties, showing significant effectiveness in treating systemic candidiasis. Their immunomodulatory effects and ability to boost cell-mediated immunity make these extracts promising options for addressing systemic candidiasis, particularly in individuals with weakened immune systems. This research offers valuable insights and sets the stage for future investigations into the treatment of oral and vaginal candidiasis.

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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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