BHBA Treatment Improves Cognitive Function by Targeting Pleiotropic Mechanisms in a Transgenic Mouse Model of Alzheimer's Disease

Abstract

Background: Accumulation of amyloid β (Aβ) peptide, inflammation, and oxidative stress contribute to Alzheimer's disease (AD) and trigger complex pathogenesis. The ketone body β-hydroxybutyrate (BHBA) is an endogenous metabolic intermediate that protects against stroke and neurodegenerative diseases, but the underlying mechanisms are unclear. The present study aims to elucidate the protective effects of BHBA in the early stage of AD model and investigate the underlying molecular mechanisms. Methods: 3.5-month old double-transgenic mice (5XFAD) overexpressing β-amyloid precursor protein (APP) and presenilin-1 (PS1) were used as the AD model. The 5XFAD mice received 1.5 mmol/kg/d BHBA subcutaneously for 28 days. Morris water maze test, nest construction, and passive avoidance experiments were performed to assess the therapeutic effects on AD prevention in vivo, and brain pathology of 5XFAD mice including amyloid plaque deposition and microglia activation were assessed. Gene expression profiles in the cortexes of 5XFAD and BHBA-treated 5XFAD mice were performed with high-throughput sequencing and bioinformatic analysis. Mouse HT22 cells were treated with 2 mM BHBA to explore its in vitro protective effects of BHBA on hippocampal neurons against Aβ oligomer toxicity, ATP production, ROS generation, and mitochondrial aerobic respiratory function. APP, BACE1, and neprilysin (NEP) expression levels were evaluated in HT22 cells following treatment with BHBA by measuring the presence or absence of G protein-coupled receptor 109A(GPR109A). Findings: BHBA improved cognitive function of 5XFAD mice in Morris water maze test, nesting construction, and passive avoidance experiments, and attenuated Aβ accumulation and microglia overactivation in the brain. BHBA also enhanced mitochondrial respiratory function and histone butyrylation of hippocampal neurons and protected them from Aβ toxicity. The enzymes, APP and NEP were regulated by BHBA via G protein-coupled receptor 109A (GPR109A). Furthermore, RNA sequencing revealed that BHBA regulated genes mainly annotated in aging, immune system, nervous system, and neurodegenerative diseases. Interpretation: Our data suggested that BHBA confers protection against the AD-like pathological events in the AD mouse model by targeting multiple aspects of AD and it may become a promising candidate for the prevention and treatment of AD. Funding Statement: This work was funded by the National Nature Science Foundation of China (31572479, 31872442) and Program for JLU Science and Technology Innovative Research Team (2017TD-30). Declaration of Interests: The authors declare that they have no competing interests. Ethics Approval Statement: All animal experiments in this study have been approved by the Jilin University Institutional Animal Care and Use Committee (Permit number: 201704005).