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Michael Lardelli

Publications and source records attributed to Michael Lardelli.

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Computational identification of ketone metabolism as a key regulator of sleep stability and circadian dynamics via real-time metabolic profiling

Metabolism plays a crucial role in sleep regulation, yet its effects are challenging to track in real time. This study introduces a machine learning-based framework to analyze sleep patterns and identify how metabolic changes influence sleep at specific time points. We first established that sleep periods in Drosophila melanogaster function independently, with no causal relationship between different sleep episodes. Using gradient boosting models and explainable artificial intelligence techniques, we quantified the influence of time-dependent sleep features. Causal inference and autocorrelation analyses further confirmed that sleep states at different times are statistically independent, providing a robust foundation for exploring metabolic effects on sleep. Applying this framework to flies with altered monocarboxylate transporter 2 expression, we found that changes in ketone transport modified sleep stability and disrupted transitions between day and night sleep. In an Alzheimers disease model, metabolic interventions such as beta hydroxybutyrate supplementation and intermittent fasting selectively influenced the timing of day to night transitions rather than uniformly altering sleep duration. Autoencoder based similarity scoring and wavelet analysis reinforced that metabolic effects on sleep were highly time dependent. This study presents a novel approach to studying sleep-metabolism interactions, revealing that metabolic states exert their strongest influence at distinct time points, shaping sleep stability and circadian transitions.

q-bio.QM

beta Hydroxybutyrate remodels the C99 interactome and coincides with restored organelle homeostasis in a Drosophila Alzheimers model

Early endolysosomal and autophagic defects are among the earliest cellular alterations observed in Alzheimers disease (AD), yet the molecular drivers linking amyloid precursor protein (APP) metabolism to vesicle trafficking dysfunction remain incompletely understood. The APP-derived fragment C99 has emerged as a potential upstream mediator of intracellular toxicity, but its impact on organelle homeostasis and its modulation by metabolic interventions remain unclear. Here, we show that neuronal expression of human C99 in Drosophila induces profound vesicular abnormalities, impaired autophagic turnover, and disrupted mitochondrial quality control. Ultrastructural analysis revealed extensive accumulation of enlarged vesicular compartments, accompanied by reduced mitochondrial turnover and accumulation of aged mitochondria. Treatment with the ketone body beta-hydroxybutyrate (BHB) restored autophagic cargo clearance, improved mitochondrial turnover, and normalized vesicular ultrastructure. These protective effects required neuronal ketone transport, indicating a neuron-intrinsic metabolic mechanism. Proteomic mapping of the C99-associated interactome revealed that ketone treatment remodels networks enriched for vesicle trafficking and proteostasis pathways. Network prioritization identified the retromer component VPS35 as a candidate regulatory hub. Functional analyses demonstrated that depletion of VPS35 abolished the BHB-dependent restoration of autophagy, mitochondrial turnover, and vesicle morphology. Together, these findings suggest that ketone treatment restores mitochondrial quality control through a VPS35-dependent mechanism in C99 induced neurodegeneration, providing mechanistic insight into how metabolic interventions may restore intracellular homeostasis in Alzheimers disease.

q-bio.NC