Werner Siemens Imaging Center, Department of Preclinical Imaging and Radiopharmacy, Eberhard Karls University Tübingen, Tübingen, Germany.
Department of Pathology and Neuropathology, University Hospital Tübingen, Eberhard Karls University, Tübingen, Germany.
J Neuroinflammation. 2024 May 14;21(1):129. doi: 10.1186/s12974-024-03080-0.
Diet-induced increase in body weight is a growing health concern worldwide. Often accompanied by a low-grade metabolic inflammation that changes systemic functions, diet-induced alterations may contribute to neurodegenerative disorder progression as well. This study aims to non-invasively investigate diet-induced metabolic and inflammatory effects in the brain of an APPPS1 mouse model of Alzheimer's disease. [F]FDG, [F]FTHA, and [F]GE-180 were used for in vivo PET imaging in wild-type and APPPS1 mice. Ex vivo flow cytometry and histology in brains complemented the in vivo findings. H- magnetic resonance spectroscopy in the liver, plasma metabolomics and flow cytometry of the white adipose tissue were used to confirm metaflammatory condition in the periphery. We found disrupted glucose and fatty acid metabolism after Western diet consumption, with only small regional changes in glial-dependent neuroinflammation in the brains of APPPS1 mice. Further ex vivo investigations revealed cytotoxic T cell involvement in the brains of Western diet-fed mice and a disrupted plasma metabolome. H-magentic resonance spectroscopy and immunological results revealed diet-dependent inflammatory-like misbalance in livers and fatty tissue. Our multimodal imaging study highlights the role of the brain-liver-fat axis and the adaptive immune system in the disruption of brain homeostasis in amyloid models of Alzheimer's disease.
饮食诱导的体重增加是全球日益严重的健康问题。通常伴随着低度代谢性炎症,改变全身功能,饮食引起的改变也可能导致神经退行性疾病的进展。本研究旨在非侵入性地研究阿尔茨海默病 APPPS1 小鼠模型中饮食诱导的代谢和炎症对大脑的影响。[F]FDG、[F]FTHA 和[F]GE-180 用于野生型和 APPPS1 小鼠的体内 PET 成像。大脑的离体流式细胞术和组织学补充了体内发现。肝脏的 H-磁共振波谱、血浆代谢组学和白色脂肪组织的流式细胞术用于证实外周的代谢性炎症状态。我们发现,在摄入西方饮食后,葡萄糖和脂肪酸代谢受到干扰,而 APPPS1 小鼠大脑中的神经胶质依赖性神经炎症只有小的区域性变化。进一步的离体研究显示,在西方饮食喂养的小鼠大脑中存在细胞毒性 T 细胞的参与以及血浆代谢组的破坏。H-磁共振波谱和免疫学结果显示,肝脏和脂肪组织中存在依赖饮食的炎症样失衡。我们的多模态成像研究强调了脑-肝-脂肪轴和适应性免疫系统在阿尔茨海默病淀粉样模型中破坏大脑内稳态中的作用。