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Isingrini, E.

Publications and source records attributed to Isingrini, E..

5 recordsLinked to original sources

Sex-Dependent Cross-Resilience to Social Defeat and Learned Helplessness: The Role of BDNF-ERK Signaling and Norepinephrine

Major depressive disorder (MDD) and post-traumatic stress disorder (PTSD) are two of the most prevalent and disabling psychiatric conditions, both closely tied to stress exposure. While they have distinct diagnostic criteria, MDD and PTSD share considerable comorbidity, overlapping behavioral symptoms, and common neurobiological pathways. However, not all individuals exposed to chronic or traumatic stress develop these disorders, highlighting the importance of resilience, the capacity to maintain psychological and physiological stability under stress. An emerging yet understudied concept is cross-resilience: the idea that resilience to one form of stress may confer protection against another. While animal models have effectively captured individual differences in stress responses, few have explored whether resilience generalizes across distinct stress modalities or differs by sex. We examined cross-resilience using two validated rodent models: chronic social defeat stress (CSDS) and learned helplessness (LH). These paradigms model complementary aspects of stress vulnerability. We assessed how prior CSDS experience influenced subsequent responses to LH. We also evaluated the role of the noradrenergic system using wild-type and norepinephrine (NE)-deficient (VMAT2loxDBHcre KO) mice. Behavioral phenotyping was combined with molecular analyses in key brain regions involved in emotion, motivation, and fear processing: the ventral tegmental area (VTA), nucleus accumbens (NAc), and amygdala (AMY). We focused on BDNF and ERK/MAPK signaling pathways, known to mediate neuroplasticity and stress resilience. Our findings reveal sex-specific patterns of cross-resilience, with prior CSDS resilience predicting LH resilience in males but not females. Molecular results indicate distinct adaptations across brain regions and sexes, underscoring the biological complexity of resilience. These insights may inform personalized strategies for preventing and treating stress-related disorders.

animal behavior and cognition↗

Role of the locus coeruleus noradrenergic system in susceptibility and resilience following early life stress in male and female mice

Child adversity (CA), encompassing emotional, physical, and sexual maltreatment or abuse, affects a substantial number of children worldwide. Moreover, it is the leading predictor of psychiatric disorders such as major depressive disorder (MDD), anxiety, and suicidal behavior. Despite the robust link between CA and psychopathology, individual outcomes vary significantly, with some children demonstrating resilience. Resilience is an adaptive and dynamic process, which mitigates the long-term effects of CA, suggesting potential protective mechanisms that remain underexplored. This study investigates behavioural susceptibility and resilience following early life stress (ELS) and examined whether these outcomes are associated with sex-dependent alteration of the locus coeruleus-norepinephrine (LC-NE) system, a critical modulator of stress, cognition, and emotion. Using a maternal deprivation model combined with limited nesting and bedding, we examined sex-dependent behavioral, physiological, and neurobiological markers associated with ELS outcomes in mice. Behavioral clustering revealed distinct phenotypes: resilient, anxious, and anhedonic-like with sex-specific differences in distribution. Early markers, including body weight and ultrasonic vocalization (USV) patterns, were linked to long-term susceptibility. Neuroanatomical analyses identified sex-specific LC-NE activation patterns associated with resilient and susceptible phenotype, particularly within the caudal-dorsal LC. These findings highlight sex-dependent behavioural trajectories of ELS that are associated with distinct LC-NE activation patterns, offering insights into potential interventions targeting resilience mechanisms in children exposed to CA.

neuroscience↗

A post-mortem investigation of the locus coeruleus- noradrenergic system in resilience to childhood abuse

Childhood abuse (CA) is one of the strongest lifetime predictors of major depressive disorder (MDD) and suicide. However, some individuals exposed to CA are resilient, avoiding the development of psychopathology. Recently, the locus coeruleus-noradrenergic (LC-NE) system has been involved in resilience following stressful events at adulthood. We investigated how a history of CA affects the integrity of the LC-NE system at the molecular and cellular level in human post-mortem brain samples of depressed suicides, and whether differential neurobiological mechanisms can be revealed in resilient individuals. Anatomical analysis revealed that CA-induced MDD and suicide is associated with decrease in LC-NE neurons density. RNA sequencing of laser captured LC-NE neurons highlighted differentially expressed genes, principally in the RES-CA group. Resilience to CA involves specific neurobiological adaptations in the LC-NE system that potentially protect against the loss of LC-NE neurons and the negative long-term outcome of CA-induced depression and suicide. Our results provide insights into potential therapeutic targets for preventing or treating CA-induced MDD.

neuroscience↗

Behavioral and transcriptomic changes following brain-specific loss of noradrenergic transmission.

Noradrenaline (NE) plays an integral role in shaping behavioral outcomes including anxiety/depression, fear, learning and memory, attention and shifting behavior, sleep-wake state, pain, and addiction. However, it is unclear whether dysregulation of NE release is a cause or a consequence of maladaptive orientations of these behaviors, many of which associated with psychiatric disorders. To address this question, we used a unique genetic model in which the brain-specific Vesicular Monoamine Transporter-2 (VMAT2) gene expression was removed in NE-positive neurons disabling NE release in the entire brain. We engineered VMAT2 gene splicing and NE depletion by crossing floxed VMAT2 mice with mice expressing the Cre-recombinase under the DBH gene promotor. In this study, we performed a comprehensive behavioral and transcriptomic characterization of the VMAT2DBHcre KO mice to evaluate the role of central NE in behavioral modulations. We demonstrated that NE depletion induces anxiolytic and antidepressant-like effects, improves contextual fear memory, alters shifting behavior, decreases the locomotor response to amphetamine, and induces deeper sleep during the non-rapid eye movement (NREM) phase. In contrast, NE depletion did not affect spatial learning and memory, working memory, response to cocaine, and the architecture of the sleep-wake cycle. Finally, we used this model to identify genes that could be up- or down-regulated in the absence of NE release. We found an up-regulation of the Synaptic Vesicle Glycoprotein 2c (SV2c) gene expression in several brain regions, including the locus coeruleus (LC), and were able to validate this up-regulation as a marker of vulnerability to chronic social defeat.

neuroscience↗

Unexpected inhibition of motor function by dopamine activation of D1/D2 co-expressing striatal neurons.

The central function of the striatum and its dopaminergic (DA) afferents in motor control and the integration of cognitive and emotional processes is commonly explained by the two striatal efferent pathways characterized by striatal projection neurons (SPNs) expressing DA D1 receptors and D2 receptors (D1-SPNs and D2-SPNs), without regard to SPNs coexpressing both receptors (D1/D2-SPNs). We developed an approach that enables the targeting of these hybrid SPNs and demonstrated that although these SPNs are less abundant, they play a major role in guiding the motor function of the other two main populations. D1/D2-SPNs project exclusively to the external globus pallidus (GPe) and have specific electrophysiological features with distinctive integration of DA signals. Optogenetic stimulation and loss-of-function experiments indicated that D1/D2-SPNs potentiate the prokinetic and antikinetic functions of D1-SPNs and D2-SPNs, respectively, and restrain the integrated motor response to psychostimulants. Overall, our findings demonstrate the essential role of this third unacknowledged population of D1/D2 coexpressing neurons, which orchestrates the fine-tuning of DA regulation in the thalamo-cortico-striatal loops. One-Sentence SummaryD1/D2 SPNs modulate the motor function of both D1- and D2-SPNs

neuroscience↗