Medium-Chain Chlorinated Paraffins Trigger Thyroid Hormone Synthesis and Interfere with Mitochondrial Function in the Thyroid Gland.
Lin ChengShuangshuang ChenYun LuoYuan GaoYan RenHaijun ZhangJiping ChenNingbo GengPublished in: Environmental science & technology (2024)
Medium-chain chlorinated paraffins (MCCPs, C 14 -C 17 ) are frequently detected in diverse environmental media. It has been proposed to be listed in Annex A of the Convention on Persistent Organic Pollutants in 2023. Although MCCPs are a crucial health concern, their toxicity remains unclear. This study investigated the toxic effects of MCCPs (0.1-50 mg/kg body weight/day) on the thyroid gland of female Sprague-Dawley rats and characterized the potential toxic pathways via transcriptomics and metabolomics approaches. MCCPs exposure caused histopathological changes to the endoplasmic reticula and mitochondria in thyroid follicular cells at a dose of 50 mg/kg bw/d and increased serum thyrotropin-releasing hormone, thyroid-stimulating hormones, and thyroxine when exposed to a higher dose of MCCPs. Transcriptomic analysis indicated the excessive expression of key genes related to thyroid hormone synthesis induced by MCCPs. Integrating the dual-omics analysis revealed mitochondrial dysfunction of the thyroid by mediating fatty acid oxidation, Kreb's cycle, and oxidative phosphorylation. Significant metabolic toxicity on the thyroid might be linked to the characteristics of the chlorine content of MCCPs. This study revealed the toxicity of MCCPs to the thyroid gland via triggering thyroid hormone synthesis and interfering with mitochondrial function, which can provide new insights into the modes of action and mechanism-based risk assessment of MCCPs.
Keyphrases
- risk assessment
- body weight
- single cell
- fatty acid
- healthcare
- mass spectrometry
- public health
- poor prognosis
- mental health
- gene expression
- cell death
- signaling pathway
- hydrogen peroxide
- cell cycle arrest
- reactive oxygen species
- climate change
- weight loss
- single molecule
- high resolution
- genome wide identification
- atomic force microscopy
- oxide nanoparticles
- pi k akt
- high speed