探索乙醇在口腔黏膜下的毒性:C57BL/6小鼠的慢性暴露与戒断。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Devaraj Ezhilarasan, Karthik Shree Harini, Karthick Munusamy
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引用次数: 0

摘要

1. 饮酒是口腔癌前病变发展的公认危险因素。本研究探讨慢性乙醇暴露对小鼠炎症和纤维化的影响。将18只C57BL/6小鼠分为3组:1组仅饮水,2组和3组无限制灌胃25%乙醇,灌胃14周。第2组小鼠在第14周末处死,第3组小鼠在处死前禁欲4周。我们分析了与炎症和纤维化相关的基因表达,以及粘膜下组织的组织病理学变化。慢性乙醇暴露显著上调粘膜下组织中的MAPK信号标记物以及炎症和纤维化标记物。在III组中,炎症标志物如NF-κB、p65、NLRP3和caspase-1在禁欲后部分恢复到正常水平,而纤维化标志物,特别是MMP-9,仍然升高。组织病理学分析显示,乙醇暴露小鼠上皮细胞萎缩,细胞外基质积累。这些结果表明,14周的乙醇暴露可诱导口腔粘膜下层持续上皮损伤、炎症和纤维化,禁欲4周后不完全逆转。这强调了酒精对口腔组织的持久影响,即使在戒烟后也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring ethanol's toxicity in the oral submucosa: chronic exposure versus abstinence in C57BL/6 mice.

Alcohol consumption is a recognised risk factor for the development of precancerous lesions in the oral cavity. This study investigates the effects of chronic ethanol exposure on inflammation and fibrosis in mice.Eighteen C57BL/6 mice were divided into three groups: Group I received only drinking water, while Groups II and III were exposed to 25% ethanol ad libitum for 14 weeks. Group II mice were sacrificed at the end of the 14th week, whereas Group III underwent a 4-week abstinence period before sacrifice. Gene expression related to inflammation and fibrosis, along with histopathological changes in submucosal tissue, was analysed.Chronic ethanol exposure significantly upregulated MAPK signalling markers, as well as inflammatory and fibrotic markers, in submucosal tissue. In Group III, inflammatory markers such as NF-κB, p65, NLRP3, and caspase-1 partially returned to normal levels after abstinence, whereas fibrotic markers, particularly MMP-9, remained elevated. Histopathological analysis of oral submucosa revealed epithelial atrophy and extracellular matrix accumulation in ethanol-exposed mice.These findings suggest that 14 weeks of ethanol exposure induces persistent epithelial damage, inflammation, and fibrosis in the oral submucosa, with incomplete reversal after 4 weeks of abstinence. This underscores the lasting impact of alcohol on oral tissue, even after cessation.

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来源期刊
Xenobiotica
Xenobiotica 医学-毒理学
CiteScore
3.80
自引率
5.60%
发文量
96
审稿时长
2 months
期刊介绍: Xenobiotica covers seven main areas, including:General Xenobiochemistry, including in vitro studies concerned with the metabolism, disposition and excretion of drugs, and other xenobiotics, as well as the structure, function and regulation of associated enzymesClinical Pharmacokinetics and Metabolism, covering the pharmacokinetics and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in manAnimal Pharmacokinetics and Metabolism, covering the pharmacokinetics, and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in animalsPharmacogenetics, defined as the identification and functional characterisation of polymorphic genes that encode xenobiotic metabolising enzymes and transporters that may result in altered enzymatic, cellular and clinical responses to xenobioticsMolecular Toxicology, concerning the mechanisms of toxicity and the study of toxicology of xenobiotics at the molecular levelXenobiotic Transporters, concerned with all aspects of the carrier proteins involved in the movement of xenobiotics into and out of cells, and their impact on pharmacokinetic behaviour in animals and manTopics in Xenobiochemistry, in the form of reviews and commentaries are primarily intended to be a critical analysis of the issue, wherein the author offers opinions on the relevance of data or of a particular experimental approach or methodology
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