Hals Ik, Ma Z, Kylling M, Bjørkvik A, Zhao A, Catrina S-B, Zhang X, Björklund A, Grill V
Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Department of Research, Nord-Trøndelag Hospital Trust, Levanger, Norway.
Islets. 2025 Dec;17(1):2503515. doi: 10.1080/19382014.2025.2503515. Epub 2025 May 19.
Chronic hyperglycemia impairs mitochondrial function of beta cells. Changes in mitochondrial function preceding a negative glucose effect have not been fully characterized, nor interactions with ketones. To compare effects on beta cell mitochondrial function by short and longer exposures to elevated glucose and interactions with ketones oxygen consumption rate (OCR) was measured in intact clonal beta cells by an OROBOROS and in rat islets by a Seahorse instrument. Proteins (subunits) of mitochondrial complexes (C) were measured by immunoblotting. ATP and ROS were measured in islets. In INS-1 832/13 cells, overnight exposure to 27 vs. 11 mm glucose increased OCR and uncoupled mitochondrial respiration. These effects vanished when prolonging the exposure time of elevated glucose. C1 was decreased after two days of culture with high glucose. Interactions with racemic 5 and 20 mm beta-hydroxybutyrate (BHB) were not detected. In islets, culture overnight at 27 vs.11 mm glucose enhanced basal OCR. No decrease in glucose-induced OCR was seen after prolonging 27 mm glucose for two days. Interactions with 5 mm BHB were not detected. Prolonged exposure to 27 mm glucose enhanced basal ECAR (extracellular acidification rate) and an ECAR response to acute elevation of glucose. C1 and 3 and 4 were decreased after two days of 27 vs. 11 mm glucose. ATP levels were decreased at this time-point and extracellular ROS increased. High glucose time-dependently affects mitochondrial function in clonal beta cells and islets. C1 was uniformly decreased. Interactions with BHB were not detected.
慢性高血糖会损害β细胞的线粒体功能。在负性葡萄糖效应之前线粒体功能的变化尚未完全明确,与酮体的相互作用也未明确。为了比较短期和长期暴露于高葡萄糖对β细胞线粒体功能的影响以及与酮体的相互作用,通过OROBOROS在完整的克隆β细胞中以及通过海马仪器在大鼠胰岛中测量了氧消耗率(OCR)。通过免疫印迹法测量线粒体复合物(C)的蛋白质(亚基)。在胰岛中测量了ATP和活性氧(ROS)。在INS-1 832/13细胞中,过夜暴露于27 mM与11 mM葡萄糖会增加OCR并使线粒体呼吸解偶联。当延长高葡萄糖暴露时间时,这些效应消失。在高葡萄糖培养两天后,C1减少。未检测到与外消旋5 mM和20 mM β-羟基丁酸(BHB)的相互作用。在胰岛中,在27 mM与11 mM葡萄糖下过夜培养可增强基础OCR。将27 mM葡萄糖延长两天后,未观察到葡萄糖诱导的OCR降低。未检测到与5 mM BHB的相互作用。长时间暴露于27 mM葡萄糖会增强基础细胞外酸化率(ECAR)以及对葡萄糖急性升高的ECAR反应。在27 mM与11 mM葡萄糖培养两天后,C1以及C3和C4减少。此时ATP水平降低,细胞外ROS增加。高葡萄糖对克隆β细胞和胰岛的线粒体功能具有时间依赖性影响。C1均一性降低。未检测到与BHB的相互作用。