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Attlas, G.

Publications and source records attributed to Attlas, G..

2 recordsLinked to original sources

Can you run from your worries? The effects of exercise on anxiety-like behaviour and immune signaling in female and male mice

Exercise is a positive health behaviour associated with improved mood. However, the mechanisms underlying the benefits of exercise on affective health are unclear, particularly with respect to type of exercise and sex. Chronic exercise decreases neuroinflammation, which is linked to improvements in mood and anxiety. However, exercise is also a physiological stressor that can transiently upregulate systemic inflammation, and its effects on neuroinflammation are not well understood. This study examined how acute and chronic exercise affect circulating and brain cytokine levels and anxiety-related behaviour in young healthy male and female mice. In Experiment 1, mice were placed on a treadmill for a two-hour bout of moderate exercise. Two hours after exercise, animals were either tested in the open field or euthanized for measurement of cytokines (IL-1{beta}, TNF, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p70, IFN-{gamma}, KC/GRO). In Experiment 2, mice underwent an 8-week moderate treadmill exercise paradigm followed by open field testing and tissue collection. Acute exercise decreased time spent in the centre of the open field in males only, suggesting increased anxiety-like behaviour in males. Acute exercise increased IL-6 and decreased TNF in serum, and increased amygdala principal component 1 (loading IL-12p70, IL-10, IFN-{gamma}, and TNF) in both sexes. Chronic exercise increased open field centre entries, increased IL-6 in the prefrontal cortex, decreased TNF in the dorsal hippocampus, and had minimal effects on circulating cytokines in both sexes. These results demonstrate that the effects of exercise on anxiety-related behaviour and cytokine levels depend on recurrence, tissue, and brain region. NEW & NOTEWORTHYOur work highlights the contrast between anxiogenic and anxiolytic effects of acute versus chronic exercise, respectively, in healthy mice. Acute and chronic exercise differentially affected circulating and brain cytokines, providing insight into physiological adaptations to exercise. Both sexes demonstrated similar cytokine responses to exercise. These similarities are novel with respect to exercise research and noteworthy given sex differences in anxiety with respect to acute exercise.

neuroscience↗

Cross-fostering affects microglia and cell death in the hippocampus of female and male degu pups

Parental care is essential for social, behavioural, and neural development of offspring. Disruption of parental care, for example through parental separation, can negatively affect offspring development in rodents. While previous work has focused on maternal and paternal deprivation, the effects of cross-fostering, another form of parental-offspring instability, on brain development remain poorly understood. Such disruptions are thought to induce stress, which in turn can suppress neurogenesis and increases inflammation and apoptosis in the hippocampus, with effects that often differ between sexes. Given that degus (Octodon degus) are born precocial and form strong attachments with their parents early in life, this study aimed to investigate the effect of cross-fostering on hippocampal development in female and male degu pups. At postnatal day 8, degus were assigned to either control (pups remained with parents and littermates), partial cross-foster (one pup per litter was cross-fostered), or full cross-foster (the entire litter was cross-fostered) conditions. At weaning (5-weeks-old), offspring brains were collected for immunohistochemistry to examine dentate gyrus volume, density of pyknotic cells, density of immature neurons, and number and morphology of microglia. Both types of cross-fostering reduced hippocampal cell death in both sexes relative to controls, while no significant effects were observed in the dentate gyrus volume or density of immature neurons. Cross-fostering did not affect total microglia density in either sex however full cross-fostered females had fewer amoeboid microglia compared to female controls. Together, these findings indicate that cross-fostering affects hippocampal microglia and cell death in pups, potentially disrupting circuit refinement and plasticity during development, with effects that vary by cross-fostering type, sex, and hippocampal region.

neuroscience↗