Department of Chemistry and Biology "A. Zambelli", University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, Italy.
Department of Biology, University of Naples Federico II, Complesso Monte Sant'Angelo Via Cinthia 26, 80126 Napoli, Italy.
Nutrients. 2024 Aug 8;16(16):2616. doi: 10.3390/nu16162616.
Brown adipose tissue (BAT) participates in thermogenesis and energy homeostasis. Studies on factors capable of influencing BAT function, such as a high-fat diet (HFD) or exposure to environmental pollutants, could be useful for finding metabolic targets for maintaining energy homeostasis. We evaluated the effect of chronic exposure to dichlorodiphenyldichloroethylene (DDE), the major metabolite of dichlorodiphenyltrichloroethane (DDT), and/or a HFD on BAT morphology, mitochondrial mass, dynamics, and oxidative stress in rats. To this end, male Wistar rats were treated for 4 weeks with a standard diet, or a HFD alone, or together with DDE. An increase in paucilocular adipocytes and the lipid droplet size were observed in HFD-treated rats, which was associated with a reduction in mitochondrial mass and in mitochondrial fragmentation, as well as with increased oxidative stress and upregulation of the superoxide dismutase-2. DDE administration mimics most of the effects induced by a HFD on BAT, and it aggravates the increase in the lipid droplet size when administered together with a HFD. Considering the known role of oxidative stress in altering BAT functionality, it could underlie the ability of both DDE and a HFD to induce similar metabolic adaptations in BAT, leading to reduced tissue thermogenesis, which can result in a predisposition to the onset of energy homeostasis disorders.
棕色脂肪组织 (BAT) 参与产热和能量稳态调节。研究能够影响 BAT 功能的因素,如高脂肪饮食 (HFD) 或暴露于环境污染物,可能有助于寻找维持能量稳态的代谢靶点。我们评估了慢性接触二氯二苯二氯乙烯 (DDE),即滴滴涕 (DDT) 的主要代谢物,以及/或 HFD 对大鼠 BAT 形态、线粒体质量、动力学和氧化应激的影响。为此,雄性 Wistar 大鼠用标准饮食或 HFD 单独处理或与 DDE 一起处理 4 周。在 HFD 处理的大鼠中观察到少脂细胞脂肪细胞和脂滴大小增加,这与线粒体质量和线粒体碎片化减少以及氧化应激增加和超氧化物歧化酶-2 上调有关。DDE 给药模拟了 HFD 对 BAT 引起的大多数影响,并且当与 HFD 一起给药时加剧了脂滴大小的增加。考虑到氧化应激在改变 BAT 功能中的已知作用,它可能是 DDE 和 HFD 诱导 BAT 发生类似代谢适应的基础,导致组织产热减少,从而导致能量稳态紊乱的易感性增加。