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The preschool years are a critical time for the development of emotion regulation, which is vital for children’s intellectual and social growth. Children with behavior problems are at particular risk of developing poor regulatory skills. Understanding factors underlying emotion dysregulation in children with behavior problems is therefore important for fostering children’s emotional development. Although theory and research suggest executive function may be important in this regard, its role among children at-risk for emotion dysregulation remains unclear. The goal of the current study was to examine whether executive function predicted trajectories of emotion dysregulation from age 3 to age 5 among children with behavior problems. This study focused on 199 3-year-old children with behavior problems who took part in a larger longitudinal study. Results revealed that response inhibition and working memory were not predictive of later emotion dysregulation. However, children who exhibited worse delay of gratification at ages 3 and 4 had greater symptoms of externalizing emotion dysregulation at age 5. In addition, children who made more omission errors on a test of attentional control at ages 3 and 4 exhibited greater externalizing emotion dysregulation at age 5. Gender differences emerged on two measures of delay of gratification and one measure of attentional control. Results suggest that specific facets of executive function may play an important role in difficulties with emotion dysregulation across the preschool years and that this pattern may differ across boys and girls.

Le traitement médicamenteux de la maladie de Parkinson idiopathique (MPI) repose essentiellement,t sur la restauration de la transmission dopaminergique par la L-Dopa et par les agonistes dopaminergiques (DARAs) agissant sur les récepteurs dopaminergiques de la classe D2R et D3R. Cependant au cours du traitement apparaissent des comportements addictifs (addiction aux médicaments dopaminergiques, hyper-sexualité, addiction aux jeux, addiction aux achats impulsifs...). Ces troubles du comportement impulsifs (TCI) observés chez les patients parkinsoniens traités aux agonistes dopaminergiques ressemblent bien à ceux observés chez les utilisateurs chroniques de drogues d'abus telles que la morphine, les amphétamines ou la cocaïne. [...] Dans le but de comprendre la physiopathologie des manifestations addictives chez le patient parkinsonien, notre étude s'est proposée d'étudier les effets renforçateurs ou motivationnels des agonistes dopaminergiques chez l'animal dont l'ATV postérieur ou antérieure ont été bilatéralement lésés. Les manifestations addictives seront investies en utilisant le test de préférence de place conditionnée (PPC), un paradigme qui étudie l'effet motivationnel / renforçateur des agonistes utilisés. Une particularité de notre étude est qu'elle a été réalisée chez l'animal naïf sans être au préalable sensibilisé à une drogue d'abus. Son intérêt est de montrer l'effet direct des agonistes dopaminergiques sur le comportement recherché. / Néant

High prevalence rates exist for physical (i.e., threatened or actual physical force) and relational (i.e., actions meant to harm another’s social relationships) aggression within early adolescence, and these behaviors lead to detrimental social, physical, and mental health outcomes. Thus, there is a need to identify risk and protective processes related to these subtypes of aggression, especially those that can inform violence prevention efforts. Prior studies including early adolescents have shown emotion dysregulation to be a risk factor for aggression. However, few studies have incorporated the emotional competence process of poor emotional awareness, which may be a risk factor for emotion dysregulation and, in turn, for aggression. Furthermore, little research has assessed relations between subtypes of emotion dysregulation (i.e., anger and sadness) and physical and relational aggression. The current study examined longitudinal relations between poor emotional awareness and these subtypes of emotion dysregulation and aggression, as well as concurrent pathways between the emotion dysregulation and aggression variables. Exploratory tests for gender differences were also conducted. Rating scales were collected from 528 sixth graders (51% girls, 49% boys; missing data n = 8) and their teachers over a six month period in the fall and spring of the school year. Across the full sample, 65% of students identified as African-American, 19% European-American, 2%, Hispanic Latino, 11% Multiracial, and 3% as “Other”(missing data n = 8). Results indicated no significant differences by gender in the strength of relations between study variables. Poor emotional awareness was not directly related to changes in subsequent frequency of physical or relational aggression. However, poor emotional awareness at Time 1 was associated with later rates of anger and sadness dysregulation. Furthermore, an indirect effect was found for poor emotional awareness on both physical and relational aggression via anger dysregulation, and this was true for student- and teacher-rated outcomes. Sadness dysregulation showed a negative concurrent association with teacher-rated physical aggression; and there was an indirect effect of poor emotional awareness on teacher-rated physical aggression via sadness dysregulation. Study findings have important implications for theoretical treatises, youth violence prevention programs, and future directions for research, which are all discussed.

Le trouble bipolaire (TB) est un trouble psychiatrique qui toucherait au minimum 1% à 2% de la population adulte. Si l'étiologie de ce trouble reste complexe et multifactorielle, le poids des facteurs génétiques est conséquent avec une héritabilité estimée entre 70% et 80%. Le fait d'avoir un parent bipolaire apparaît comme le premier facteur de risque de développer soi-même un trouble bipolaire. Egalement, ces enfants présentent un très haut risque d’avoir des psychopathologies. Un marqueur intéressant chez ces enfants pour identifier ce risque est le profil de dysrégulation obtenu au CBCL-DP. Ainsi, l'accès à des programmes de prévention ciblés, avant même l’apparition des troubles de ces enfants « à risque » (enfants de parents bipolaires ayant des symptômes sub-cliniques et un profil au CBCL-DP élevé) est une démarche prometteuse. Les programmes centrés sur la famille (Family Focused Therapy, FFT) dont l'efficacité est établie dans le TB à début précoce pourraient servir de base à des actions de prévention. En France, à ce jour aucune étude ne s’est intéressée à ces enfants.Méthode : Ce protocole exploratoire a été écrit dans le cadre d’une collaboration entre le service de pédopsychiatrie et le Centre Expert Bipolaire au sein du CHU de Montpellier. Nous proposons de faire participer 17 enfants « à risque » (moyenne age = 9,6 ans) à un programme de TCC multifamilles centré sur la gestion émotionnelle et la résolution de problèmes afin de voir si la dimension de dysrégulation est améliorée en fin de groupe. Au terme de ce groupe et à 12 mois, une réévaluation est proposée afin d’en mesurer les éventuels bénéfices par rapport à l’évaluation initiale.Résultats : Une amélioration significative est montrée sur la dimension de dysrégulation à la fin du groupe (p = 0,007) et en phase de suivi (p = <.001). Toutefois, compte tenu des limites méthodologiques de notre étude et en l’absence de groupe contrôle, il faut être prudent quant aux conclusions et répliquer cette étude avec un groupe contrôle. / Bipolar disorder (BD) is a psychiatric disorder that affects about 1% to 2% of adults. Its aetiology is complex and multifactorial but the genetic factors play an important role, with an estimated heritability between 70% and 80%. Having a bipolar parent appears to be the first risk factor for self-development of BD. Also, these children present a very high risk of having disorders.In this context, a high score in the Child Behavior Check-List-Dysregualtion Profile (CBCL-DP) is constantly reported as a reliable screener. Offering the identified children targeted prevention programs, in order to provide them strategies to face the developing symptoms, is a promising approach. The Family Focused Therapy (FFT) is a multifamily, parents-children CBT program. Its effectiveness was proved in early-onset BD and it is now considered as a possible preventive action for BD offsprings. In France, no study have been conducted on this population Method : The aim of our research is to test the efficacy of a FFT program on a French sample of 17 parents and BD offsprings (mean age = 9,6 years). The protocol was written in the context of a collaboration between the Child and Adolescent Mental Health Service (CAMHS) St Eloi and the Bipolar Expert Centre, within the University Hospital of Montpellier. Families were involved in a CBT program that focuses on emotion and problem solving strategies. Assessment was conducted at the end of this group and after 12 months, in order to measure the benefits compared to the first evaluation. Results: A significant decrease is shown on the dysregulation dimension at the end of the group (p = 0,007) and in the follow-up phase (p = <.001). However, given the methodological limitations of our study and in the absence of a control group, one should be cautious when considering caution should be exercised in making the findings. A replication of this first exploratory study, including a control group, is now necesary.

Insulin plays a vital role in whole-body metabolism and provides a major anabolic stimulus for cellular signaling pathways, including those involved in the metabolism of glucose and protein. Consequently, insulin dysregulation (ID) is known to alter molecular signal transduction in insulin-sensitive tissues such as skeletal muscle, thereby disrupting glucose metabolism and compromising protein synthetic capacity. Our first objective was to induce ID in healthy horses by administering dexamethasone (DEX), a potent glucocorticoid, for 21 days. We evaluated the effects on insulin-stimulated muscle protein signaling components involved in the mammalian target of rapamycin (mTOR) pathway. DEX-induced ID reduced insulin-stimulated activation of downstream (rpS6, 4EBP-1) mTOR signaling and increased atrogin-1 abundance, a marker for protein breakdown (P < 0.05). Additionally, 21 days of DEX elevated plasma amino acids levels in insulin-stimulated conditions, indicative of reduced uptake or increase release into circulation (P < 0.05). The second objective was to evaluate the short-term effects of DEX treatment in healthy horses. Plasma insulin, glucose and amino acid dynamics and activation of mTOR signaling pathways following an oral sugar test (OST) or intake of a high protein meal were evaluated before and after 7 days of DEX treatment, and after 7 days of no treatment. Seven days of DEX treatment increased basal levels of glucose, insulin and several amino acids (P < 0.05). Additionally horses treated with DEX had an exacerbated insulin response to the OST and consumption of the high protein meal in comparison to control horses (P < 0.05). The majority of blood metabolites returned to basal levels after 7 days of recovery from DEX treatment, indicating these effects were transient. Short-term DEX treatment decreased overall activation of mTOR and FoxO3 but increased total FoxO3 and IRS-1 abundance (P < 0.05). Postprandial activation of rpS6 was greater in horses treated with DEX for 7 days but was lower in those horses after 7 days of recovery from treatment (P < 0.05). Postprandial activation of ULK and AMPK tended to be greater in DEX treated horses (P < 0.1). Akt phosphorylation and mysotatin abundance were lower after the OST in DEX treated horses (P < 0.05). The final objective was to evaluate whether similar changes in postprandial metabolic responses would be seen in horses with naturally occurring ID. Plasma insulin, glucose and amino acid responses following ingestion of a high protein meal were determined in mature horses with equine metabolic syndrome (EMS). Horses with EMS had higher basal plasma insulin concentrations but lower levels of aspartate, glutamate, asparagine and plasma urea nitrogen in comparison to healthy controls (P < 0.05). Consumption of a high protein meal resulted in a 9-fold greater insulin response and higher postprandial levels of various amino acids (P < 0.05). Together this research indicates that ID affects whole body protein metabolism by altering cellular signaling pathways in healthy and diseased horses.

Background: Approximately 7% of clinically referred youth exhibit profound impairment in the ability to regulate their affect, behavior, and cognition. This phenotype – often referred to as dysregulation – has been associated with a multitude of negative outcomes. Symptom overlap between dysregulation and other psychological disorders has generated debate regarding whether DP constitutes a distinct syndrome characterized by intense, persistent irritability or is merely the combination of symptoms from disruptive or mood disorders. In order to elucidate this question, the current study examined the transdiagnostic continuities and discontinuities in three RDoC constructs (frustrative non-reward, acute threat, and cognitive control) proposed to be mechanisms of irritability Method: Participants were 294 children ages 7-17 (M=10.94; 67% male). Emotional and behavioral symptoms were measured using the Child Behavior Checklist and the Kiddie Schedule for Affective Disorders and Schizophrenia. Frustrative non-reward was measured using a frustration-induction Go/No-Go paradigm during which heart rate variability was indexed by respiratory sinus arrhythmia (RSA) and pre-ejection period (PEP). Acute threat was measured using an Emotional Faces computer paradigm in conjunction with an eyetracker/pupilometer. Cognitive control was assessed with the Behavioral Rating Inventory of Executive Function (BRIEF), Delis-Kaplan Executive Function System (D-KEFS) and Stop Signal Task (SST). Results: Symptoms of dysregulation and non-episodic irritability were strongly, positively related. Due to a lack of demonstrated construct validity for the hypothesized RDoC constructs of frustrative non-reward, acute threat, and cognitive control, two alternative mechanisms—SNS response and cognitive dyscontrol of emotion—were derived from the data. Results showed that blunted sympathetic responsivity and poor executive control in response to emotion were predictive of more severe irritability symptoms. Finally, moderation analyses showed that among highly dysregulated children, low levels of sympathetic responsiveness were associated with more severe irritability symptoms. Conclusions: Despite phenotypic overlap with other forms of developmental psychopathology, dysregulated children can be distinguished based on the severity of their irritability symptoms. This supports the conceptualization of dysregulation as a unique syndrome characterized by intense and persistent irritability and lends credence to the novel diagnosis of DMDD. Furthermore, cognitive, behavioral and physiological patterns identified in this study suggest that difficulties with processing negative emotion—as opposed to frustration or threat specifically—may constitute a vulnerability for irritability.