Macrophage activity regulation by high dilution of aspirin and its possible mechanism

Adalberto von Ancken, F. Eizayaga, L. Bonamin
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Abstract

Background: Under LPS-stimulus, platelets can activate macrophages by a cell-to-cell contact or through cytokine degranulation. Rebound effects of anti-thrombotic agents, such as prostanoids and COX inhibitors can lead to thrombosis, infarct, and stroke. Aspirin has been prescribed for decades due to its powerful antiplatelet action, but it is also related to paradoxical effects such as withdrawal syndrome peaks, resistance, and thrombogenesis. Ultra-diluted aspirin can also produce the same effect in one hour, regardless of Cox-2, by still unknown pathways. Antithrombotic effects of aspirin are also reversed by its high dilutions. Aims: This study aims to characterize the effects of aspirin 15cH on macrophages challenged with LPS, a Cox-2 activator. Methodology: RAW 264.7 macrophages were sown in 24 wells plates using R10 medium, boosted with 1μg/ml LPS, and treated with aspirin 15 cH and controls. The activity was evaluated after 24 hours. Supernatants were evaluated for cytokines, nitric oxide, and dielectric oscillations, through solvatochromic dyes (Cartwright’s method). Results and discussion: macrophage spreading was increased by aspirin 15 cH, an LPS-like effect. Paradoxically, a significant reduction of this effect was noted when both, LPS and aspirin 15 cH, were added. Succussed water reversed the effect of LPS, leading to TNF (p<0.05) production close to baseline levels. Also, the single treatment with succussed water inhibited IL-10 production (p<0.05), but aspirin 200 µg/mL (positive control) highly increased it (p<0.0001), showing the validity of the model. Nitric oxide production was strengthened by LPS presence (p<0.0001), as expected, but partially downregulated after treatment with aspirin 200 µg/mL, water and succussed water. A pilot study with solvatochromic dyes showed no significant difference among treatments. Conclusion: The main data suggest that aspirin 15 cH increases macrophage activity but presents a paradoxal effect when mixed with LPS. On the other hand, succussed water itself has modulatory effects on macrophages.
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高稀释阿司匹林对巨噬细胞活性的调节及其可能机制
背景:在lps刺激下,血小板可以通过细胞间接触或细胞因子脱颗粒激活巨噬细胞。抗血栓药物的反跳效应,如前列腺素和COX抑制剂可导致血栓形成、梗死和中风。由于其强大的抗血小板作用,阿司匹林已经被开了几十年,但它也与诸如戒断综合征高峰、耐药性和血栓形成等矛盾效应有关。超稀释阿司匹林也可以在一小时内产生同样的效果,而不考虑Cox-2,其途径尚不清楚。阿司匹林的抗血栓作用也因其高度稀释而被逆转。目的:本研究旨在描述阿司匹林15cH对LPS(一种Cox-2激活剂)刺激的巨噬细胞的影响。方法:采用R10培养基将RAW 264.7巨噬细胞播撒于24孔板中,用1μg/ml LPS增强,并用阿司匹林15ch和对照组处理。24小时后评估活性。通过溶剂致变色染料(Cartwright的方法)评估上清液的细胞因子、一氧化氮和介电振荡。结果与讨论:阿司匹林15ch可增加巨噬细胞的扩散,具有类似lps的作用。矛盾的是,当LPS和阿司匹林15ch同时加入时,这种效果显著降低。琥珀水逆转了LPS的作用,使TNF的生成接近基线水平(p<0.05)。单水处理抑制IL-10生成(p<0.05),阳性对照阿司匹林200µg/mL显著提高IL-10生成(p<0.0001),表明模型的有效性。正如预期的那样,LPS的存在增强了一氧化氮的产生(p<0.0001),但在阿司匹林200µg/mL、水和琥珀水处理后,一氧化氮的产生部分下调。溶剂化变色染料的初步研究表明,处理之间没有显着差异。结论:主要数据表明,阿司匹林15ch可增加巨噬细胞活性,但与LPS混合后出现矛盾效应。另一方面,琥珀水本身对巨噬细胞具有调节作用。
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