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Bergdahl, A.

Publications and source records attributed to Bergdahl, A..

2 recordsLinked to original sources

A Preventive Effect of Exercise in a Mouse Model of Essential Tremor

The effects of exercise have not been widely studied for potential benefits in essential tremor (ET), while this has been growing for other neurodegenerative disorders. This study examines the effects of two types of exercise [high-intensity interval training (HIIT) and resistance training (RT)] on mice that were subjected to harmaline injections to trigger tremor. We employed a repeated-measures design with three groups: a HIIT group, a RT group, and a sedentary (SED) control group. Each group received an injection before and after the intervention. Tremor kinetics (power within the 8-14 and 14-29 Hz bands) were assessed using accelerometry. Tremor kinematics were also assessed using high-speed video analysis, for validation. As potential signalling molecules from exercise, we also tested for blood lactate and BDNF in each group. Compared to pre-intervention measurements, we found a significant decrease in power within the 8-14 Hz band combined with an increase in the 14-29 Hz band, for the HIIT group, but not in the RT or SED groups. We also found a change in BDNF concentration for the HIIT group. These results suggest that the HIIT protocol may have helped the animal to shift tremor frequency to higher bands, thereby offering functional resistance to harmaline-induced tremor. This study supports high intensity aerobic physical exercise as a potential therapeutic/preventive intervention for ET, with translational implications for human studies.

neuroscience↗

Integrated Metabolic Complex Genetic Interaction 1 Network of Chromosome 4p Loss in Basal Breast Cancer

Basal breast cancer subtype is enriched for triple-negative breast cancer (TNBC) and exhibits a recurrent large chromosomal deletion in chromosome 4p (chr4p). Chr4p loss is associated with poor survival, evolves early in tumorigenesis and confers on cells a proliferative state. Here, we map the integrated metabolic complex genetic interaction network of chr4p in basal breast cancer to identify targetable vulnerabilities. Differential gene expression analysis of patient derived xenografts and cancer cell models revealed that chr4p loss is associated with changes in cellular energetics and reduction/oxidation balance. Analysis of DepMap pooled genome-wide CRISPR-Cas9 screens identified complex genetic interactions specific to chr4p deletion in basal breast cancer cell models. Functional assays revealed that chr4p loss is associated with disrupted mitochondrial respiratory function and reduced glycolytic capacity, suggesting metabolic rewiring. Increased reactive oxygen species and lipid peroxidation compromised antioxidant defense mechanisms. Ultimately, this study sheds light on targeted therapies for basal breast cancer harboring large chromosomal deletions.

genomics↗