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Walker, W. J.

Publications and source records attributed to Walker, W. J..

2 recordsLinked to original sources

Brief high-fat diet exposure temporally reshapes affective behavior and prefrontal cortex function

High-fat diet consumption is linked to a higher risk of obesity, diabetes, cardiometabolic diseases, psychiatric disorders, and cognitive dysfunction. Energy homeostasis and mood fluctuate throughout the 24-hour day, and perturbations in these rhythms have consequences for brain, body, and behavior. Our recent work demonstrates that layer 2/3 pyramidal neurons in the prelimbic prefrontal cortex (plPFC), a key region in affective behavior and cognitive function, undergo daily rhythms in their physiological function. In this study, we investigate how a one-week acute high-fat diet (aHFD) alters affective behavior and plPFC function. Further, we used time-of-day as a tool to determine how initiation of a HFD impacts the physiological properties of layer 2/3 plPFC pyramidal neurons in male and female mice. To explore these phenomena, we implemented the open-field test (OFT) and DeepLabCut to gain dynamic whole-body spatiotemporal resolution in our behavioral analysis. Next, we employed patch-clamp electrophysiology to determine how aHFD alters the intrinsic membrane properties and action potential dynamics of these neurons. Here we show that aHFD produces time-of-day dependent changes in exploratory behavior and physiology of plPFC pyramidal neurons, including altered intrinsic properties, firing profiles, and voltage-dependent membrane conductance in both sexes. These results lay the groundwork to explore the physiological mechanisms by which aHFD impacts plPFC function, affective behavior, and cognition. Overall, this study highlights the importance of understanding how diet impacts neural function before the onset of obesity.

neuroscience↗

Optimizing spinal cord injury in zebrafish larvae: effects of age on the injury response

Zebrafish are an increasingly popular model to study regeneration after spinal cord injury (SCI). The transparency of larval zebrafish makes them ideal to study cellular processes in real time. Standardized approaches, including age at the time of injury, are not readily available making comparisons of the results with other models challenging. In this study, we systematically examined the response to spinal cord transection of larval zebrafish at three different larval ages (3-, 5-, or 7-days post fertilization (dpf)) to determine whether the developmental complexity of the larvae affects the overall response to SCI. We then used imaging and behavioral analysis to evaluate whether differences existed based on the age of injury. Injury led to increased expression of cytokines associated with the immune response; however, we found that the timing of specific inflammatory markers changed with the age of the injury. We also observed changes in glial and axonal bridging with age. Young larvae (3 dpf) were better able to regenerate axons independent of the glial bridge, unlike older larvae (7 dpf), consistent with results seen in adult zebrafish. Finally, locomotor experiments demonstrated that some swimming behavior occurs independent of glial bridge formation, further highlighting the need for standardization of this model and functional recovery assays. Overall, we found differences based on the age of transection in larval zebrafish, underlining the importance of considering age when designing experiments aimed at understanding regeneration.

developmental biology↗