Marc Ten-Blanco, María Ponce-Renilla, Inmaculada Pereda-Pérez, Cristina Izquierdo-Luengo, Carlo Bressa, Olga Zafra, Rosa María Tolón, Fernando Berrendero
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引用次数: 0
Abstract
Exposure to traumatic life events may compromise physical and mental health of specific subjects. While some individuals extinguish fear appropriately, others exhibit an inefficient and persistent fear response, with remarkable differences between sexes. Understanding the heterogeneity in fear extinction responses is essential for elucidating the underlying mechanisms of fear-related disorders. We used a multidisciplinary approach analyzing the hypothalamic-pituitary-adrenal (HPA) axis tone, the microbiota composition, and the transcriptome of the amygdala (primary brain region involved in fear regulation) in adult male and female mice that were exposed to the Pavlovian fear conditioning and extinction paradigm. This model allowed us to stratify the mice population into two extreme phenotypic subgroups (resilient and susceptible), based on their individual fear extinction behavior. Characterization of some components of the HPA axis revealed strong disturbances in vulnerable males (e.g., increased hypothalamic CRF mRNA and corticosterone plasma levels), whereas softer changes were found in female animals. Several bacterial groups such as the genera Parvibacter, Alloprevotella and Limosilactobacillus and the family Christensenellaceae were enriched in the microbiota of resilient males, as well as relevant bacterial taxa enrichment was also observed in resilient (genus Muribaculum) and susceptible (family Eggerthellaceae) female mice. We also identified clear differences in the transcriptomic profile of the amygdala (31 differentially expressed genes) in male animals. These findings underscore the intricate involvement of multiple factors shaping the inter-individual variability of fear extinction response in a sex-dependent manner, thus paving the way for new potential targets for fear-related disorders.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.