母亲使用电子烟及其对后代的影响:双击模型

IF 3.3 3区 医学 Q1 PHYSIOLOGY Journal of applied physiology Pub Date : 2024-09-01 Epub Date: 2024-08-01 DOI:10.1152/japplphysiol.00345.2024
Amber Mills, Murugesan Velayutham, Debbie Corbin, Lindsey Suter, Madison Robinson, Valery V Khramtsov, Lainey Shouldis, Mary Cook, Duaa Dakhallah, Paul D Chantler, I Mark Olfert
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引用次数: 0

摘要

内皮功能障碍是心血管疾病的预兆。临床前数据表明,围产期接触电子烟(Ecig)的后代会出现长期的心血管和脑血管功能障碍。此外,直接使用电子烟会增加活性氧并损害脑血管功能,但直接使用电子烟对有围产期接触史(即双重打击条件)的后代的综合影响尚不清楚。我们对以下假设进行了测试:与仅在子宫内接触相比,后代如果接触双击电子烟,将导致更严重的脑血管和神经认知功能障碍。雄性和雌性后代来自暴露于空气(5 只母鼠)或暴露于电子烟(5 只母鼠)的经时间交配的 Sprague Dawley 雌性大鼠,并在出生后 3 个月或 6 个月进行研究。双击后代的电子烟暴露从时间点前 1 个月开始,持续 4 周(5 天/周,90 分钟/天)。我们发现,与母体(Ecig:Air)或直接(Air:Ecig)暴露的后代相比,双重暴露的后代(Ecig:Ecig=暴露水坝:后代)的MCA反应性进一步减弱,神经元损伤的严重程度增加,星形胶质细胞和内皮细胞的相互作用增加。与对照组(Air:Air)相比,所有暴露于生态毒气的组别中循环细胞外囊泡(EVs)都有所增加,而 SIRT1 则有所减少,其中生态毒气暴露组的变化最大。电子顺磁共振波谱显示,Ecig:Ecig 组血浆中的氧化应激最高(p
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Maternal use of electronic cigarettes and impact on offspring: a double-hit model.

Endothelial dysfunction is a predictor for cardiovascular disease. Preclinical data suggest longstanding cardiovascular and cerebrovascular dysfunction occurs in offspring with perinatal electronic cigarette (Ecig) exposure. Furthermore, direct use of Ecigs increases reactive oxygen species and impairs cerebrovascular function, but the combined effect of direct use in offspring with a history of perinatal exposure (i.e. double-hit condition) is not known. We tested the hypothesis that offspring with double-hit Ecig exposure will lead to greater cerebrovascular and neurocognitive dysfunction compared with in utero exposure only. Male and female offspring were obtained from time-mated Sprague Dawley female rats exposed to air (n = 5 dams) or Ecig exposed (n = 5 dams) and studied at either 3 or 6 mo after birth. Ecig exposure for double-hit offspring began at 1-mo before the timepoints and lasted 4 wk (5 days/wk with 90-min exposure/day). We found double-hit offspring (Ecig:Ecig = exposure dam:offspring) sustained further blunted middle cerebral artery (MCA) reactivity, increased severity of neuronal damage, and increased interactions of astrocytes and endothelial cells compared with offspring with maternal (Ecig:Air) or direct (Air:Ecig) exposure only. Circulating extracellular vesicles (EVs) were increased, whereas sirtuin 1 (SIRT1) was decreased, in all Ecig-exposed groups compared with controls (Air:Air), with Ecig:Ecig group showing the greatest respective change for each. Electron paramagnetic resonance (EPR) spectroscopy revealed oxidative stress was the highest in the plasma of Ecig:Ecig group (P < 0.05) than the other groups. These data show that a double-hit exposure in adolescent or adult offspring results in a greater decline in cerebrovascular function, biomarkers of neuronal dysfunction, and increased circulation of EVs compared with a single-hit exposure.NEW & NOTEWORTHY These data add to the growing body of literature demonstrating that electronic cigarette (Ecig) use during pregnancy (even without nicotine) is not safe, and primes offspring to have worse cardiovascular health outcomes in early and adult life. A key finding from this work is that a second insult from direct vaping in offspring with prior in utero exposure induces greater vascular dysfunction, increased oxidative stress, and shows evidence of neuronal dysfunction compared with either direct- or maternal-only exposure.

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来源期刊
CiteScore
6.00
自引率
9.10%
发文量
296
审稿时长
2-4 weeks
期刊介绍: The Journal of Applied Physiology publishes the highest quality original research and reviews that examine novel adaptive and integrative physiological mechanisms in humans and animals that advance the field. The journal encourages the submission of manuscripts that examine the acute and adaptive responses of various organs, tissues, cells and/or molecular pathways to environmental, physiological and/or pathophysiological stressors. As an applied physiology journal, topics of interest are not limited to a particular organ system. The journal, therefore, considers a wide array of integrative and translational research topics examining the mechanisms involved in disease processes and mitigation strategies, as well as the promotion of health and well-being throughout the lifespan. Priority is given to manuscripts that provide mechanistic insight deemed to exert an impact on the field.
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