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Background: Hyperactivity related behaviors as well as inattention and impulsivity are regarded as the nuclear symptoms of attention-deficit/hyperactivity disorder (ADHD).
Purpose: To investigate the therapeutic effects of atomoxetine on the motor activity in relation to the expression of the dopamine (DA) D2 receptor based on the hypothesis that DA system hypofunction causes ADHD symptoms, which would correlate with extensive D2 receptor overproduction and a lack of DA synthesis in specific brain regions: prefrontal cortex (PFC), striatum, and hypothalamus.
Methods: Young male spontaneously hypertensive rats (SHR), animal models of ADHD, were randomly divided into four groups according to the daily dosage of atomoxetine and treated for 21 consecutive days. The animals were assessed using an open-field test, and the DA D2 receptor expression was examined.
Results: The motor activity improved continuously in the group treated with atomoxetine at a dose of 1 mg/Kg/day than in the groups treated with atomoxetine at a dose of 0.25 mg/Kg/day or 0.5 mg/Kg/day. With respect to DA D2 receptor immunohistochemistry, we observed significantly increased DA D2 receptor expression in the PFC, striatum, and hypothalamus of the SHRs as compared to the WKY rats. Treatment with atomoxetine significantly decreased DA D2 expression in the PFC, striatum, and hypothalamus of the SHRs, in a dose-dependent manner.
Conclusion: Hyperactivity in young SHRs can be improved by treatment with atomoxetine via the DA D2 pathway.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182750 | PMC |
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0108918 | PLOS |
Int J Eat Disord
September 2025
Department of Physiology, Monash University, Clayton, Victoria, Australia.
Objective: Converging evidence from neuroimaging studies and genome-wide association study (GWAS) suggests the involvement of prefrontal cortex (PFC) and striatum dysfunction in the pathophysiology of anorexia nervosa (AN). However, identifying the causal role of circuit-specific genes in the development of the AN-like phenotype remains challenging and requires the combination of novel molecular tools and preclinical models.
Methods: We used the activity-based anorexia (ABA) rat model in combination with a novel viral-based translating ribosome affinity purification (TRAP) technique to identify transcriptional differences within a specific neural pathway that we have previously demonstrated to mediate pathological weight loss in ABA rats (i.
Front Behav Neurosci
August 2025
Henan Provincial Key Laboratory of Rehabilitation Medicine, The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by impaired social interaction and restricted, repetitive behaviors (RRBs). These symptoms may stem from cognitive flexibility deficits, with dysfunction in the prefrontal cortex (PFC) and related neural circuits proposed as underlying mechanisms.
Objectives: This study examined whether transcranial direct current stimulation (tDCS) could enhance PFC activity and functional connectivity, thereby improving cognitive flexibility in a valproic acid (VPA)-induced ASD rat model.
Neuropathol Appl Neurobiol
October 2025
Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Aims: Despite the critical role of mitochondria in confronting alcohol challenges and providing energy, to date, there are no studies describing the effect of alcohol on mitochondrial epigenetics in energy-craving brain tissues. Focusing on the human nucleus accumbens (NAcc) and prefrontal cortex (PFC), we aimed to examine the effect of alcohol on mitochondrial DNA methylation.
Methods: We collected 105 brain tissue samples from 53 deceased individuals, classified into no antemortem alcohol use (n = 34), alcohol-ingested (n = 9) and alcohol-fermented (n = 10).
Prog Neuropsychopharmacol Biol Psychiatry
August 2025
Department of Physiology, Kerman University of Medical Sciences, Kerman Neuroscience Research Center, Kerman, Iran. Electronic address:
Clinical evidence suggests that the cerebellum is one of the brain areas most vulnerable to the effects of psychostimulants. Functional neuroimaging studies support the idea that the cerebellum is involved in the neural circuits affected by these drugs. The cerebellum plays a vital role in the brain's reward mechanisms, working in conjunction with the striatum, ventral tegmental area (VTA), and prefrontal cortex (PFC).
View Article and Find Full Text PDFAlthough there is a rapidly growing interest in reward-emotion interactions, our current understanding of how negative emotion influences reward motivation and modulates reward-driven enhancements in visual perception remains limited. To address these gaps, we conducted a fMRI study using a novel variant of the monetary incentive delay task where the valence (negative or neutral) of an emotional scene image served as a cue to indicate a reward or no-reward prospect in the subsequent house-building discrimination task. During the initial cue stage, we hypothesized competitive interactions between reward anticipation and negative emotion along the common value/valence dimension.
View Article and Find Full Text PDF