没药提取物和没药银纳米粒子对旋毛虫感染小鼠的治疗效果:寄生虫学、组织病理学和免疫学(IFN-γ、IL-10 和 MMP-9)研究。

IF 2.6 2区 农林科学 Q1 VETERINARY SCIENCES Frontiers in Veterinary Science Pub Date : 2024-10-03 eCollection Date: 2024-01-01 DOI:10.3389/fvets.2024.1433964
Salwa Mahmoud Abd-ELrahman, Ahmed Kamal Dyab, Abeer El-Sayed Mahmoud, Shaymaa M Mohamed, Alamira Marzouk Fouad, Ahmed Gareh, Jamal Asseri, Naief Dahran, Hind Alzaylaee, Hayat M Albisihi, Ahmed Mahmoud Abd Elrahman, Fahd M Alsharif, Heba Mostafa, Nashwa Hamad, Ehab Kotb Elmahallawy, Nahed Ahmed Elossily
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引用次数: 0

摘要

导言:由螺旋毛癣菌(T. spiralis)引起的毛癣菌病仍然是一种流行的寄生性人畜共患病。开发新的靶向药物并了解针对该感染的免疫反应势在必行。以往的研究对没药提取物和没药银纳米粒子(AgNPs)对旋毛虫病的疗效及其对组织病理学和免疫学因素的影响探讨不足:本研究评估了用没药、没药粗提取物和阿苯达唑生物合成的银纳米粒子对旋毛虫肠道阶段的影响。研究还考察了相关的组织病理学变化和主要免疫学标志物的变化,包括γ干扰素(IFN-γ)、白细胞介素-10(IL-10)和基质金属蛋白酶-9(MMP-9)。五组 12 只小鼠分配如下:第 1 组:未感染、未处理(阴性对照);第 2 组:感染、未处理(阳性对照);第 3 组:感染并用生物合成的纳米银颗粒(40 μg/mL)处理;第 4 组:感染并用没药粗提取物(800 mg/kg)处理;第 5 组:感染并用阿苯达唑(50 mg/kg)处理。从感染后第二天开始口服治疗,连续三天。各组小鼠在感染后第 6 天安乐死,各组小鼠肠道分离,进行寄生虫学、组织病理学和 MMP-9 免疫组化评估,并通过实时 PCR 技术评估细胞因子水平(IFN-γ 和 IL-10 基因表达):结果:本研究显示,治疗组的成虫数量显著减少。纳米银颗粒处理组的成虫死亡率为 88.64%,没药提取物处理组为 85.17%,阿苯达唑处理组为 94.07%。组织病理学检查显示,未接受治疗的受感染小鼠的肠道出现了明显的病变,而经过治疗后,这些病变得到了明显的恢复。免疫组化检查显示,与未受感染的小鼠相比,AgNPs 治疗组小鼠的 MMP-9 表达明显减少,这反映了 AgNPs 在减轻受感染小鼠肠道炎症反应方面的作用:总之,本研究证明了没药生物合成的银纳米粒子对感染小鼠螺旋体的新型抗寄生虫潜力。治疗与 IFN-γ 基因表达和 IL-10 表达的适度升高有关,凸显了其对螺旋体的疗效。
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Therapeutic effects of myrrh extract and myrrh-based silver nanoparticles on Trichinella spiralis-infected mice: parasitological, histopathological, and immunological (IFN-γ, IL-10, and MMP-9) investigations.

Introduction: Trichinellosis, caused by Trichinella spiralis (T. spiralis), remains a prevalent parasitic zoonosis. Developing new drugs targeting and understanding the immune response against the infection is imperative. Previous research has inadequately explored the efficacy of crude myrrh extract and myrrh-based silver nanoparticles (AgNPs) against trichinellosis, as well as their impact on histopathological, and immunological factors.

Methods: This study evaluated the effects of silver nanoparticles biosynthesized using myrrh, crude myrrh extracts, and albendazole on the intestinal phase of T. spiralis. It also examined the associated histopathological changes and alterations in key immunological markers, including Interferon-gamma (IFN-γ), Interleukin-10 (IL-10), and Matrix Metalloproteinase-9 (MMP-9). Five groups of 12 mice were allocated as follows: group 1: non-infected, non-treated (negative control), group 2: infected, non-treated (positive control), group 3: infected and treated with biosynthesized silver nanoparticles (40 μg/mL), group 4: infected and treated with myrrh crude extract (800 mg/kg), and group 5: infected and treated with albendazole (50 mg/kg). Treatment was orally administered starting on the 2nd day post-infection and continued for three successive days. Mice of all groups were euthanized on the 6th day post-infection, and the intestine of each was isolated for parasitological, histopathological, and immunohistochemistry evaluation of MMP-9, as well as assessment of cytokines level (IFN-γ and IL-10 gene expressions) via Real-time PCR technique.

Results: The present study showed a considerable reduction in adult worm count among the treated groups. The mortality rates of adult worms were 88.64% in the silver nanoparticles treated group, 85.17% in the myrrh crude extract group, and 94.07% in the albendazole-treated group. Histopathological examination revealed prominent alterations in the intestine of the infected non-treated mice, which were markedly restored by treatment. Immunohistochemical examination accompanied by significant reduction in MMP-9 expression in the infected mice treated with AgNPs compared to the infected non-treated group, reflecting the role of AgNPs in downgrading the inflammatory reaction in the intestine of infected mice.

Conclusion: Collectively, this study demonstrates the novel antiparasitic potential of silver nanoparticles biosynthesized with myrrh against T. spiralis in infected mice. The treatment was associated with moderate rise in IFN-γ gene expression and IL-10 expression, highlighting its therapeutic efficacy against T. spiralis.

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来源期刊
Frontiers in Veterinary Science
Frontiers in Veterinary Science Veterinary-General Veterinary
CiteScore
4.80
自引率
9.40%
发文量
1870
审稿时长
14 weeks
期刊介绍: Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy. Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field. Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.
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