在动脉粥样硬化的诱导性小鼠模型中,暴露于电子烟会导致早期促动脉粥样硬化变化。

IF 3.6 Q2 TOXICOLOGY
Frontiers in toxicology Pub Date : 2023-12-18 eCollection Date: 2023-01-01 DOI:10.3389/ftox.2023.1244596
Bayan Alakhtar, Cynthia Guilbert, Nivetha Subramaniam, Vincenza Caruana, Kiran Makhani, Carolyn J Baglole, Koren K Mann
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引用次数: 0

摘要

导言:有证据表明,使用电子烟(吸食电子烟)会增加心血管疾病的风险,但吸食电子烟的人还需要数十年才会出现病变。因此,动脉粥样硬化的小鼠模型可用作了解疾病易感性、风险和发病机制的工具。此外,人们对动脉粥样硬化的危险因素(即高脂血症、高脂饮食)如何与吸食电子烟交织在一起以促进疾病风险还缺乏了解。在此,我们评估了一只诱导性高脂血症小鼠暴露于来自商用豆荚式装置和电子液体的气溶胶中是否有动脉粥样硬化的早期证据。研究方法给小鼠注射含有人蛋白枯草酶/kexin 9 型(PCSK9)变体的腺相关病毒,以促进高脂血症。给这些小鼠喂食高脂肪饮食,并将其暴露于室内空气或由含有聚乙二醇/植物甘油(PG/VG)或5%尼古丁与芒果香精的JUUL豆荚产生的气溶胶中4周;利用这个时间点来评估动脉粥样硬化斑块形成前可能出现的动脉粥样硬化标志物。结果这些数据表明,体重、循环脂蛋白/葡萄糖水平和脾脏免疫细胞等各种参数受到接触 PG/VG 和/或含尼古丁气溶胶的显著影响。讨论:这种小鼠模型不仅可用于慢性吸烟研究以评估血管病理学,而且这些数据还支持吸烟并非无风险,可能会增加日后心血管疾病的发病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
E-cigarette exposure causes early pro-atherogenic changes in an inducible murine model of atherosclerosis.

Introduction: Evidence suggests that e-cigarette use (vaping) increases cardiovascular disease risk, but decades are needed before people who vape would develop pathology. Thus, murine models of atherosclerosis can be utilized as tools to understand disease susceptibility, risk and pathogenesis. Moreover, there is a poor understanding of how risk factors for atherosclerosis (i.e., hyperlipidemia, high-fat diet) intersect with vaping to promote disease risk. Herein, we evaluated whether there was early evidence of atherosclerosis in an inducible hyperlipidemic mouse exposed to aerosol from commercial pod-style devices and e-liquid. Methods: Mice were injected with adeno-associated virus containing the human protein convertase subtilisin/kexin type 9 (PCSK9) variant to promote hyperlipidemia. These mice were fed a high-fat diet and exposed to room air or aerosol derived from JUUL pods containing polyethylene glycol/vegetable glycerin (PG/VG) or 5% nicotine with mango flavoring for 4 weeks; this timepoint was utilized to assess markers of atherosclerosis that may occur prior to the development of atherosclerotic plaques. Results: These data show that various parameters including weight, circulating lipoprotein/glucose levels, and splenic immune cells were significantly affected by exposure to PG/VG and/or nicotine-containing aerosols. Discussion: Not only can this mouse model be utilized for chronic vaping studies to assess the vascular pathology but these data support that vaping is not risk-free and may increase CVD outcomes later in life.

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来源期刊
CiteScore
3.80
自引率
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