脂多糖刺激的人外周血单个核细胞中ORSL®免疫+的抗炎、吞噬和抗氧化潜能的评价

Q3 Medicine
Sanjay Kalra, Trupti Gilada, Ashwin Dabhi, Vijay Chamle, Deepanshi Dhar, Tarique Meer, Michael Southall, Ashok Godavarthi, Amol Patil, Harshad Malve, Ashley Barlow
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引用次数: 0

摘要

背景:维持最佳的水合和电解质平衡对免疫功能至关重要,因为它支持细胞稳态和免疫防御机制。以电解质为基础的微量营养素饮料有助于补充必需营养素,包括锌、硒和维生素E,它们在调节免疫反应、减轻氧化应激和调节炎症方面起着关键作用。脂多糖(LPS)诱导的炎症和氧化应激是免疫功能障碍的主要原因,需要增强免疫恢复力的干预措施。目的:评价ORSL®Immunity+在LPS刺激下外周血单核细胞(peripheral blood mononuclear cells, PBMCs)中减轻炎症、增强吞噬活性和提供抗氧化保护的免疫调节潜力。材料和方法:从人血液中分离外周血单核细胞,LPS刺激其诱导炎症反应。采用3-(4,5-二甲基噻唑-2-酰基)-2,5-二苯基溴化四唑(MTT)测定细胞毒性、酶联免疫吸附法(ELISA)测定炎症标志物[肿瘤坏死因子α (TNF-α)、白细胞介素-1β (IL-1β)、白细胞介素6 (IL-6)、干扰素γ (IFN-γ)、一氧化氮(NO)]、抗氧化能力氧自由基吸收能力(ORAC)测定抗氧化能力和吞噬能力测定]评估ORSL®Immunity+对处理细胞免疫功能的影响。结果:ORSL®Immunity+对PBMCs无细胞毒性作用。治疗显著降低了炎症标志物的水平,表明有抗炎作用。此外,ORSL®Immunity+对大肠杆菌的吞噬活性呈剂量依赖性增强,表明免疫应答得到改善。抗氧化能力也显著提高,正如ORAC试验所证明的那样,突出了其减轻氧化应激的潜力。结论:ORSL®Immunity+在lps刺激的PBMCs中表现出良好的免疫调节特性,可减轻炎症、增强吞噬和提高抗氧化能力。这些发现支持免疫健康的潜在作用以及改善水合状态,需要进一步的临床评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Anti-inflammatory, Phagocytic, and Antioxidant Potential of ORSL® Immunity+ in Lipopolysaccharide-stimulated Human Peripheral Blood Mononuclear Cells.

Background: Maintaining optimal hydration and electrolyte balance is essential for immune function, as it supports cellular homeostasis and immune defense mechanisms. Electrolyte-based micronutrient drinks helps replenish essential nutrients, including zinc, selenium, and vitamin E, which play key roles in modulating immune responses, mitigating oxidative stress, and regulating inflammation. Lipopolysaccharide (LPS)-induced inflammation and oxidative stress are major contributors to immune dysfunction, necessitating interventions that enhance immune resilience.

Objective: To evaluate the immunomodulatory potential of ORSL® Immunity+ in mitigating inflammation, enhancing phagocytic activity, and providing antioxidant protection in LPS-stimulated peripheral blood mononuclear cells (PBMCs) Materials and methods: PBMCs were isolated from human blood and stimulated with LPS to induce an inflammatory response. The effects of ORSL® Immunity+ on the immune function of treated cells were assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay for cytotoxicity, enzyme-linked immunosorbent assay (ELISA) for inflammatory markers [tumor necrosis factor alpha (TNF-α), interleukin-1 beta (IL-1β), interleukin 6 (IL-6), interferon gamma (IFN-γ), nitric oxide (NO)], oxygen radical absorbance capacity (ORAC) assay for antioxidant capacity, and phagocytosis assay.

Results: ORSL® Immunity+ demonstrated no cytotoxic effects on PBMCs. The treatment significantly reduced the levels of inflammatory markers, indicating an anti-inflammatory effect. Additionally, ORSL® Immunity+ enhanced phagocytic activity in a dose-dependent manner against Escherichia coli, suggesting improved immune response. Antioxidant capacity was also significantly increased, as evidenced by the ORAC assay, highlighting its potential in mitigating oxidative stress.

Conclusion: ORSL® Immunity+ exhibits promising immunomodulatory properties by reducing inflammation, enhancing phagocytosis, and improving antioxidant potential in LPS-stimulated PBMCs. These findings support a potential role in immune health alongside improving hydration status, warranting further clinical evaluation.

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