Lung Damage Induced by Plasmodium berghei ANKA in Murine Model of Malarial Infection is Mitigated by Dietary Supplementation with DHA-Rich Omega-3.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-10-11 Epub Date: 2024-09-20 DOI:10.1021/acsinfecdis.4c00482
Carolina David-Vieira, Barbara Albuquerque Carpinter, Jéssica Correia Bezerra-Bellei, Letícia Ferreira Machado, Felipe Oliveira Raimundo, Cinthia Magalhães Rodolphi, Daniela Chaves Renhe, Isabella Rodrigues Nogueira Guedes, Fernanda Mikaela Moreira Gonçalves, Ludmila Ponce Monken Custódio Pereira, Marcos Vinicius Rangel Ferreira, Haroldo Lobo Dos Santos Nascimento, Adolfo Firmino Neto, Flávia Lima Ribeiro Gomes, Vinicius Novaes Rocha, Juciane Maria de Andrade Castro, Kézia Katiani Gorza Scopel
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Abstract

Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are severe complications that can occur in infections caused by any Plasmodium species. Due to the high lethality rate and the lack of specific treatment for ALI/ARDS, studies aimed at understanding and searching for treatment strategies for such complications have been fundamental. Here, we investigated the protective role of dietary supplementation with DHA-rich fish oil against lung damage induced by Plasmodium berghei ANKA in a murine model. Our results demonstrated that alveolar vascular damage, lung edema, and histopathological alterations were significantly reduced in mice that received dietary supplementation compared to those that did not receive the supplementation. Furthermore, a significant reduction in the number of CD8+ T lymphocytes, in addition to reduced infiltration of inflammatory cells in the bronchoalveolar lavage fluid was also observed. High levels of IL-10, but not of TNF-α and IFN-γ, were also observed in infected mice that received the supplementation, along with a reduction in local oxidative stress. Together, the data suggest that dietary supplementation with DHA-rich fish oil in malarial endemic areas may help reduce lung damage resulting from the infection, thus preventing worsening of the condition.

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膳食中补充富含 DHA 的 Omega-3 可减轻疟原虫 ANKA 在小鼠疟疾感染模型中引起的肺损伤。
急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是疟原虫感染时可能出现的严重并发症。由于急性肺损伤和急性呼吸窘迫综合征的致死率很高,而且缺乏特效治疗方法,因此,旨在了解和寻找治疗此类并发症的策略的研究非常重要。在这里,我们研究了在小鼠模型中通过膳食补充富含 DHA 的鱼油对伯格氏疟原虫 ANKA 诱导的肺损伤的保护作用。结果表明,与未补充 DHA 的小鼠相比,补充 DHA 的小鼠肺泡血管损伤、肺水肿和组织病理学改变明显减少。此外,除了支气管肺泡灌洗液中的炎症细胞浸润减少外,还观察到 CD8+ T 淋巴细胞数量明显减少。在接受补充剂的感染小鼠体内还观察到了高水平的 IL-10,但 TNF-α 和 IFN-γ 的水平并不高,同时局部氧化应激也有所降低。这些数据表明,在疟原虫流行地区补充富含 DHA 的鱼油可能有助于减少感染造成的肺损伤,从而防止病情恶化。
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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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