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Biology subjects

Dias, B.

Publications and source records attributed to Dias, B..

2 recordsLinked to original sources

Demonstrating the ability of GABAergic cells in the zona incerta to modulate motivation

Motivation to engage in goal-directed actions is crucial for survival and well-being. Dopaminergic and serotonergic systems have been the focus of efforts to understand neurobiological etiologies of normative and disrupted motivation. Understanding how the brain incorporates salient sensory cues into motivational drive outside of these neuromodulatory systems is less appreciated. We posited that given their afferent and efferent connections, GABAergic cells in the zona incerta (ZI) are ideally positioned to perform this function. Combining behavioral tasks in mice with chemogenetics we show that GABAergic ZI neurons are capable of modulating effort-based motivation and that chemogenetic activation of this cell population can rescue motivational deficits induced by chronic stress - without affecting attention, memory, locomotion, or appetite. Next, using fiber photometry we report that GABAergic cells in the ZI robustly respond to sensory cues and their response to a cue increases as reward-predictive associations are formed. Inhibiting GABAergic cells in the ZI did not abolish cue-associated motivational behavior while cue-locked optogenetic activation of these cells robustly enhanced cue-associated motivated behavior demonstrating that these cells are not necessary but sufficient to allow for sensory cues to influence action selection. These findings establish GABAergic cells in the ZI as modulators of motivation and afford us a neuroanatomical hub that could be targeted to potentially remedy treatment-resistant deficits in motivation.

neuroscience↗

Early life exposure to high fructose diet induces metabolic dysregulation associated with sex-specific cognitive impairment in adolescent rats.

BackgroundThe incidence of adolescent mental health disorders is on the rise. Epidemiological studies suggest that poor nutrition is a significant contributor to this public health crisis, specifically through exposure to high level of dietary sugar, including fructose, during critical periods of development. Previous studies have shown that elevated fructose exposure during adolescence disrupts mental health. Further, it seems that infants display the highest level of exposure to fructose based on nutritional surveys. Despite these data, it is currently unknown how fructose exposure, specifically during infancy, may impact adolescent mental health. MethodsWe developed an experimental protocol in rats to investigate the effects of fructose exposure during infancy on behavioral, cognitive and metabolic endpoints in adolescence. Specifically, rat pups were exposed to fructose from birth until weaning through maternal diet. Metabolic assays, quantitative PCR and behavioral protocols such as open field, elevated O maze and a Go/ No-Go operant task, were used to determine whether high fructose exposure during infancy may set the stage for behavioral and metabolic dysfunction in adolescence. ResultsWe found that exposing rats to high fructose from birth to weaning resulted in higher circulating glucose, insulin and leptin levels in adolescence. High fructose during infancy also increased bodyweight, disrupted metabolic homeostasis in the basolateral amygdala (BLA) as indicated by decreased activity of the cellular energy sensor AMPK, and impaired attention and impulsivity in a male-specific manner. This impaired attention observed in adolescent male rats following neonatal fructose exposure was partially rescued by viral-mediated, in vivo expression of a constitutively active form of AMPK in principal neurons of the BLA. ConclusionOur results suggest that exposure to high level of fructose during infancy may impact adolescent mental health in a male-specific manner and that manipulation of AMPK activity may mitigate this impact.

animal behavior and cognition↗