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丙烯醛吸入会急性影响大鼠肺中线粒体代谢的调节。

Acrolein inhalation acutely affects the regulation of mitochondrial metabolism in rat lung.

机构信息

School of Nutrition and Translational Research in Metabolism (NUTRIM), Department of Pharmacology and Toxicology, Maastricht University Medical Center+, Maastricht, the Netherlands.

Public Health and Integrated Toxicology Division, Center for Public Health and Environmental Assessment, US Environmental Protection Agency, Durham, NC, United States; ICF, Durham, NC, United States.

出版信息

Toxicology. 2022 Mar 15;469:153129. doi: 10.1016/j.tox.2022.153129. Epub 2022 Feb 10.

Abstract

Exposure of the airways to cigarette smoke (CS) is the primary risk factor for developing several lung diseases such as Chronic Obstructive Pulmonary Disease (COPD). CS consists of a complex mixture of over 6000 chemicals including the highly reactive α,β-unsaturated aldehyde acrolein. Acrolein is thought to be responsible for a large proportion of the non-cancer disease risk associated with smoking. Emerging evidence suggest a key role for CS-induced abnormalities in mitochondrial morphology and function in airway epithelial cells in COPD pathogenesis. Although in vitro studies suggest acrolein-induced mitochondrial dysfunction in airway epithelial cells, it is unknown if in vivo inhalation of acrolein affects mitochondrial content or the pathways controlling this. In this study, rats were acutely exposed to acrolein by inhalation (nose-only; 0-4 ppm), 4 h/day for 1 or 2 consecutive days (n = 6/group). Subsequently, the activity and abundance of key constituents of mitochondrial metabolic pathways as well as expression of critical proteins and genes controlling mitochondrial biogenesis and mitophagy were investigated in lung homogenates. A transient decreasing response in protein and transcript abundance of subunits of the electron transport chain complexes was observed following acrolein inhalation. Moreover, acrolein inhalation caused a decreased abundance of key regulators associated with mitochondrial biogenesis, respectively a differential response on day 1 versus day 2. Abundance of components of the mitophagy machinery was in general unaltered in response to acrolein exposure in rat lung. Collectively, this study demonstrates that acrolein inhalation acutely and dose-dependently disrupts the molecular regulation of mitochondrial metabolism in rat lung. Hence, understanding the effect of acrolein on mitochondrial function will provide a scientifically supported reasoning to shortlist aldehydes regulation in tobacco smoke.

摘要

气道暴露于香烟烟雾(CS)是导致多种肺部疾病的主要危险因素,如慢性阻塞性肺疾病(COPD)。CS 由超过 6000 种化学物质组成,其中包括高度反应性的α,β-不饱和醛丙烯醛。丙烯醛被认为是与吸烟相关的非癌症疾病风险的主要原因。新出现的证据表明,CS 诱导的气道上皮细胞中线粒体形态和功能异常在 COPD 发病机制中起关键作用。尽管体外研究表明丙烯醛诱导气道上皮细胞中线粒体功能障碍,但尚不清楚体内吸入丙烯醛是否会影响线粒体含量或控制这一过程的途径。在这项研究中,大鼠通过吸入(仅鼻腔;0-4ppm)急性暴露于丙烯醛,每天 4 小时,连续 1 或 2 天(每组 6 只)。随后,研究了肺匀浆中线粒体代谢途径的关键成分的活性和丰度,以及控制线粒体生物发生和线粒体自噬的关键蛋白质和基因的表达。丙烯醛吸入后,电子传递链复合物亚基的蛋白和转录物丰度出现短暂下降。此外,丙烯醛吸入导致与线粒体生物发生相关的关键调节剂的丰度降低,分别在第 1 天和第 2 天表现出不同的反应。线粒体自噬机制的组成部分的丰度一般不受丙烯醛暴露的影响。总之,这项研究表明,丙烯醛吸入急性和剂量依赖性地破坏了大鼠肺中线粒体代谢的分子调节。因此,了解丙烯醛对线粒体功能的影响将为筛选烟草烟雾中醛类调节提供科学依据。

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