504 电子香烟燃烧物二羟基丙酮通过新陈代谢和线粒体失衡促进心脏特异性损伤

IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Arlet Hernandez, M Gwin, LA Wiggins, H Bryant, M Vasilyev, VL Dal Zotto, ML Bates, M Schuler, NR Gassman
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引用次数: 0

摘要

目的/目标:电子香烟越来越受欢迎,在使用过程中会产生各种燃烧产物。二羟基丙酮(DHA)是加热过程中产生的一种碳水化合物。每天接触的 DHA 剂量可能从高微摩尔到低毫摩尔不等,目前还没有研究了解 DHA 对心脏的影响。方法/研究人群:在此,我们将使用大鼠心肌细胞、H9c2 细胞和大鼠心脏组织来研究 DHA 是否会对代谢和线粒体效应产生影响。利用这些细胞,我们将使用海马研究代谢和线粒体途径、营养传感途径中的蛋白质表达变化,并了解 DHA 在心脏中的剂量依赖性效应。还将对代谢物池进行评估,以了解 DHA 促进的变化。还将测量之前在其他细胞模型中观察到的氧化应激。心脏细胞中的主要发现将在暴露于 DHA 的心脏组织中进行研究。结果/预期结果:我们以前曾在各种细胞系模型中发现 DHA 会诱导氧化应激、新陈代谢变化和线粒体功能障碍。有趣的是,这些影响高度依赖于细胞类型。众所周知,电子烟具有毒性心脏效应,包括动脉僵化、内皮功能障碍、血管损伤和氧化应激。在 H9c2 细胞中发现了糖酵解、脂肪酸合成、柠檬酸循环酶和代谢物的变化。我们还观察到线粒体 ROS 的增加以及 DHA 暴露导致的燃料变化。在暴露于 DHA 的心脏组织中,我们观察到氧化应激和线粒体裂变与融合动力学发生了改变。讨论/意义:这些数据表明,有必要对生理相关剂量进行进一步研究,以了解吸入的 DHA 如何影响吸食者的长期健康。以及对电子烟中 DHA 的监管,因为 DHA 被认为对局部应用是安全的,但警告不要吸入。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
504 Dihydroxyacetone, a combustion of electronic cigarettes, promotes cardiac-specific injury through metabolic and mitochondrial imbalances
OBJECTIVES/GOALS: Electronic cigarettes have become increasingly popular, with various combustion products generated in the process. Dihydroxyacetone (DHA), a carbohydrate made during the heating process. Exposures may reach high micromolar to low millimolar doses of DHA per day and no studies have been done to understand the effects of DHA in the heart. METHODS/STUDY POPULATION: Here, we examine if DHA contributes to these using rat cardiomyocytes, H9c2 cells, and rat cardiac tissues to DHA evaluating metabolic and mitochondrial effects. Using the cells, we will investigate metabolic and mitochondrial pathways using Seahorse, protein expression changes in nutrient sensing pathways, and understand dose-dependent effects of DHA in the heart. Metabolite pools will also be evaluated to understand the changes promoted by DHA. Oxidative stress as previously observed in other cell models will also be measured. Key findings in the cardiac cells will be investigated in the cardiac tissues exposed to DHA. RESULTS/ANTICIPATED RESULTS: We have previously shown DHA induces oxidative stress, metabolic changes, and mitochondrial dysfunction in various cell line models. Interestingly, these effects are highly cell-type dependent. E-cigarettes are known to have toxic cardiac effects, including arterial stiffness, endothelial dysfunction, vascular injury, and oxidative stress. Changes in glycolytic, fatty acid synthesis, and the citric acid cycle enzymes and metabolites were found in the H9c2 cells. We also observed increased mitochondrial ROS and fuel changes due to DHA exposure. In DHA exposed cardiac tissues, we observed oxidative stress and mitochondrial fission and fusion dynamics altered. DISCUSSION/SIGNIFICANCE: These data suggest further study at physiologically relevant doses is warranted to understand how DHA inhaled impacts the long-term health of vapers. As well as the regulation of DHA in e-cigarettes as it has been deemed as safe for topical applications and warned against inhalation.
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来源期刊
Journal of Clinical and Translational Science
Journal of Clinical and Translational Science MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
2.80
自引率
26.90%
发文量
437
审稿时长
18 weeks
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