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褪黑素对被动吸烟大鼠肺部的治疗作用。

Therapeutic effects of melatonin on the lungs of rats exposed to passive smoking.

机构信息

College of Animal Science and Food Engineering, Jinling Institute of Technology, Qixia, Nanjing, 210046, China.

出版信息

Respir Res. 2024 Nov 19;25(1):411. doi: 10.1186/s12931-024-03042-3.


DOI:10.1186/s12931-024-03042-3
PMID:39563345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11577718/
Abstract

BACKGROUND: Passive smoke has a significant impact on lung function and constitutes a critical public health issue, as smoking generates free radicals that damage the lungs and other tissues. Currently, limited research exists on whether the antioxidant melatonin can mitigate lung damage caused by smoking. This study aims to investigate the mechanisms through which melatonin alleviates acute lung disease induced by passive smoking. METHODS: Rats were divided into five groups (n = 6): a control group and three groups exposed to low, medium, and high concentrations of smoke, and a melatonin treatment group. RESULTS: Data indicated that in the high concentration passive smoking group, the alveolar structure of the lung tissue was destroyed, and the total antioxidant capacity in lung tissue diminished as the concentration of smoke increased. The expressions of TNF-α, IL-6, and IL-1β exhibited similar results. The anti-apoptotic factors Bcl-2 and Bcl-xL mRNA level significantly decreased in the high concentration smoking group, while no significant changes were observed in the medium and low concentration groups. Conversely, the high concentration passive smoking increased the pro-apoptotic factors Bax and Caspase-3 mRNA levels. Additionally, endogenous melatonin levels in lung tissue gradually decreased following exposure to smoke, whereas the exogenous melatonin alleviated the changes in inflammatory factors and apoptosis-related factors in lung tissue. Furthermore, at high smoking concentrations, the mRNA levels of lung cancer-related genes vascular endothelial growth factor (VEGF), cytochromeP450 1A1 (CYP1A1), and cytochrome P450 1B1 (CYP1B1) were significantly increased, while exogenous melatonin reduced the expression of these genes in lung tissue. CONCLUSIONS: These findings suggest that melatonin can diminish lung tissue damage, apoptosis, and inflammatory responses induced by passive smoking, as well as decrease the expression of lung cancer-related genes. Further experimental investigations involving exogenous melatonin treatments will be needed.

摘要

背景:被动吸烟对肺功能有重大影响,是一个关键的公共卫生问题,因为吸烟会产生自由基,损害肺部和其他组织。目前,关于抗氧化剂褪黑素是否能减轻吸烟引起的肺损伤的研究有限。本研究旨在探讨褪黑素缓解被动吸烟引起的急性肺损伤的机制。

方法:将大鼠分为五组(n=6):对照组和三组分别暴露于低、中、高浓度烟雾中,以及褪黑素治疗组。

结果:数据表明,在高浓度被动吸烟组中,肺组织的肺泡结构被破坏,随着烟雾浓度的增加,肺组织中的总抗氧化能力下降。TNF-α、IL-6 和 IL-1β的表达结果相似。高浓度吸烟组中抗凋亡因子 Bcl-2 和 Bcl-xL mRNA 水平显著降低,而中、低浓度组无明显变化。相反,高浓度被动吸烟增加了促凋亡因子 Bax 和 Caspase-3 mRNA 水平。此外,肺组织中内源性褪黑素水平随着烟雾暴露逐渐降低,而外源性褪黑素缓解了肺组织中炎症因子和凋亡相关因子的变化。此外,在高吸烟浓度下,肺癌相关基因血管内皮生长因子(VEGF)、细胞色素 P450 1A1(CYP1A1)和细胞色素 P450 1B1(CYP1B1)的 mRNA 水平显著升高,而外源性褪黑素降低了这些基因在肺组织中的表达。

结论:这些发现表明,褪黑素可以减轻被动吸烟引起的肺组织损伤、细胞凋亡和炎症反应,并降低肺癌相关基因的表达。需要进一步进行涉及外源性褪黑素治疗的实验研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/25f823a54254/12931_2024_3042_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/62a5f9e5adb6/12931_2024_3042_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/5310c1d8d655/12931_2024_3042_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/53394e1ce7e2/12931_2024_3042_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/aca409e1d913/12931_2024_3042_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/25f823a54254/12931_2024_3042_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/62a5f9e5adb6/12931_2024_3042_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/5310c1d8d655/12931_2024_3042_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/53394e1ce7e2/12931_2024_3042_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/aca409e1d913/12931_2024_3042_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a59/11577718/25f823a54254/12931_2024_3042_Fig5_HTML.jpg

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Synergistic effect of secondhand smoke and apical periodontitis on lung tissue damage in rats.

Sci Rep. 2025-4-16

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Smoking-Related Interstitial Lung Disease and Emphysema.

Clin Chest Med. 2024-6

[2]
Melatonin improves influenza virus infection-induced acute exacerbation of COPD by suppressing macrophage M1 polarization and apoptosis.

Respir Res. 2024-4-27

[3]
The association of cigarette smoking with DNA methylation and gene expression in human tissue samples.

Am J Hum Genet. 2024-4-4

[4]
Mechanisms Contributing to the Comorbidity of COPD and Lung Cancer.

Int J Mol Sci. 2023-2-2

[5]
Cigarette smoke alters inflammatory genes and the extracellular matrix - investigations on viable sections of peripheral human lungs.

Cell Tissue Res. 2022-2

[6]
The Involvement of PDE4 in the Protective Effects of Melatonin on Cigarette-Smoke-Induced Chronic Obstructive Pulmonary Disease.

Molecules. 2021-10-30

[7]
Therapeutic potential and mechanism of Dendrobium officinale polysaccharides on cigarette smoke-induced airway inflammation in rat.

Biomed Pharmacother. 2021-11

[8]
Cigarette smoke exposure and alveolar macrophages: mechanisms for lung disease.

Thorax. 2022-1

[9]
Melatonin attenuates smoking-induced atherosclerosis by activating the Nrf2 pathway via NLRP3 inflammasomes in endothelial cells.

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[10]
Effects of melatonin on protecting against lung injury (Review).

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