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Dadam, F.

Publications and source records attributed to Dadam, F..

2 recordsLinked to original sources

Sex-specific effects of psychoactive drugs on memory performance in an animal model of Attention-Deficit Hyperactivity Disorder

Attention-Deficit/Hyperactivity Disorder (ADHD) is a prevalent neurodevelopmental condition characterized by persistent deficits in working memory (WM) and executive control. Dysregulation of the Cyclin-dependent kinase 5 (Cdk5)/p35 signaling pathway has been implicated in ADHD pathophysiology due to its impact on neuronal connectivity and dopamine regulation. Using p35 knockout (p35KO) mice--an animal model exhibiting ADHD-like phenotypes--we investigated WM performance, task-related c-Fos-IR expression under basal conditions as a function of sex and genotype, as well as WM responses to acute treatment with methylphenidate (MPH) or fluoxetine (FLX), administered alone or in combination. Under basal conditions, p35KO mice exhibited significantly reduced spontaneous alternation in the Y-maze test compared with wild type (WT), whereas recognition memory remained intact. Analysis of c-Fos-IR expression, used as a marker of task-related neuronal activity, revealed region- and genotype-dependent differences, with effects of sex. p35KO animals showed reduced c-Fos-IR expression in prefrontal cortical regions and increased expression in hippocampal regions. Acute MPH or FLX treatment significantly increased spontaneous alternation in p35KO males, whereas this effect was not observed following combined treatment (MPH+FLX). In WT mice, treatment with MPH, FLX, or MPH+FLX reduced spontaneous alternation, particularly evident in females. Exploratory activity was increased in p35KO mice independently of treatment. These findings support a role for Cdk5/p35 signaling in the prefrontal-hippocampal activation patterns associated with WM testing and indicate that behavioral and pharmacological responses in this model vary according to sex and neurobiological background, highlighting the importance of considering sex as a biological variable in preclinical and translational ADHD research. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/696253v3_ufig1.gif" ALT="Figure 1"> View larger version (36K): org.highwire.dtl.DTLVardef@10f3aeorg.highwire.dtl.DTLVardef@ee28a5org.highwire.dtl.DTLVardef@1ae7152org.highwire.dtl.DTLVardef@191c061_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

SEX DIFFERENCES IN BLOOD PRESSURE RESPONSE TO CONTINUOUS ANG II INFUSION: ARE ONLY SEX HORMONES TO BLAME?

To investigate the involvement of the sex chromosome complement (SCC), organizational and activational hormonal effects in changes in mean arterial pressure during acute Ang II infusion, we used gonadectomized (GDX) mice of the "four core genotypes" model, which dissociates the effect of gonadal sex and SCC, allowing comparisons of sexually dimorphic traits between XX and XY females as well as XX and XY males. Additionally, {beta}-estradiol and testosterone propionate (2ug/g) were daily injected for 4 days to evaluate activational hormonal effects. Statistical analysis of the changes in mean arterial pressure revealed an interaction of SCC, organizational and activational hormonal effects during Ang II infusion {F(7,39=2,60 p<0.01)}. Our results indicate that, in absence of activational hormonal effects, interaction between the SCC and organizational hormonal action differentially modulates changes in arterial pressure. In GDX mice without hormone replacement, Ang II infusion resulted in an increase in mean arterial pressure in XX-male, XX-female and XY-female mice, while no changes were observed in XY-male mice. Furthermore, {beta}-estradiol replacement (GDX+E2 group) resulted in a decrease in blood pressure in XX-males, XX-females and XY-females (indicating an activational {beta}-estradiol effect), while no changes were observed in the XY-male group. Moreover, testosterone propionate replacement (GDX+TP group) showed a greater increase in blood pressure in XY-male mice than in XX-males and XX-females, demonstrating an activational hormonal effect of testosterone in XY-male mice. Our data isolates and highlights the contribution and interaction of SCC, activational and organizational hormonal effects in sex differences in Ang II blood pressure regulation.

physiology↗