Labaj, P. | Search bioRxiv

bioRxiv2024

Integrative Metagenomic and Blood Biomarker Analysis Reveals Distinct Metabolic Responses to Aerobic and Anaerobic Interventions in Athletic and Non-Athletic Individuals

BackgroundThe gut microbiome influences physiological responses to exercise through interactions with inflammatory markers and metabolite production. Athletes often exhibit a more diverse gut microbiome that is associated with improved performance, but the mechanisms, particularly in relation to different training modalities, are not fully understood. This study aims to integrate blood serum markers with metagenomic data to explore the interplay between exercise type, gut microbiome, and biochemical responses in athletic and non-athletic individuals. MethodsFifty-two male participants (endurance athletes, strength athletes, and controls) underwent two maximal exercise tests: the anaerobic Wingate test and the aerobic Bruce treadmill test. Blood and stool samples were collected at multiple time points for biochemical analysis and metagenomic sequencing. Blood markers were correlated with shifts in microbiome composition and function. ResultsWhile most biochemical parameters showed similar trends across all groups post-exercise, SPARC and adiponectin levels showed distinct responses depending on the exercise modality. The strength group showed unique microbiome associations with blood markers after the Wingate test. Baseline enrichment of specific bacteria (Clostridium phoceensis and Catenibacterium spp.) was associated with an inhibited response to the Bruce test in strength athletes. ConclusionsThe integration of metagenomic and blood serum analyses reveals that exercise modality and training background elicit complex physiological and biochemical responses mediated by the gut microbiome. These findings suggest that specific microbial species may play significant roles in recovery and adaptation processes following acute exercise. Further research with larger cohorts is needed to validate these findings and explore microbiome-targeted interventions to improve performance and recovery.

microbiology↗

bioRxiv2023

Mitochondrial fitness influences neuronal excitability of dopaminergic neurons from patients with idiopathic form of Parkinson's disease

Parkinson disease is the second most common neurodegenerative disease defined by presence of Lewy bodies and the loss of dopaminergic neurons in the substantia nigra pars compacta (SNc). There are three types of PD - familial, early-onset and idiopathic. Idiopathic PD (IPD) accounts for approximately 90% of all PD cases. Mitochondrial dysfunction accompanies the pathogenesis of Parkinsons disease. Loss of mitochondrial function increases oxidative stress and calcium buffering, which in turn hinders the production of ATP and disrupts the functioning of dopaminergic neurons. The main barrier in PD research was the lack of proper human models to study the mechanisms of PD development and progression. Using induced pluripotent stem (iPS) cells we generated patient-specific dopaminergic neurons. We observed differences in the mitochondria fitness but not differences in mitochondria mass, morphology or membrane potential. Expression of OXPHOS mitochondrial complexes were lower in PD patients in comparison to control group what resulted in changes in mitochondria respiratory status. We observed also lower expression levels of Na+/K+-ATPase subunits and ATP-sensitive K+ (K-ATP) channel subunits. The lower oxygen consumption rate and extracellular acidification rate values were observed in dopaminergic progenitors and iPSC from PD patients compared to the control group. Importantly, observed decrease in the availability of ATP and in the energy consumption, as well as changes in acidification, may constitute contributing factors to the observed reduced neuronal excitability of PD patients dopaminergic neurons.

neuroscience↗