TY - GEN A1 - He, Yangyang A1 - Wuertz-Kozak, Karin A1 - Kuehl, Linn K. A1 - Wippert, Pia-Maria T1 - Extracellular vesicles: potential mediators of psychosocial stress contribution to osteoporosis? T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Osteoporosis is characterized by low bone mass and damage to the bone tissue’s microarchitecture, leading to increased fracture risk. Several studies have provided evidence for associations between psychosocial stress and osteoporosis through various pathways, including the hypothalamic-pituitary-adrenocortical axis, the sympathetic nervous system, and other endocrine factors. As psychosocial stress provokes oxidative cellular stress with consequences for mitochondrial function and cell signaling (e.g., gene expression, inflammation), it is of interest whether extracellular vesicles (EVs) may be a relevant biomarker in this context or act by transporting substances. EVs are intercellular communicators, transfer substances encapsulated in them, modify the phenotype and function of target cells, mediate cell-cell communication, and, therefore, have critical applications in disease progression and clinical diagnosis and therapy. This review summarizes the characteristics of EVs, their role in stress and osteoporosis, and their benefit as biological markers. We demonstrate that EVs are potential mediators of psychosocial stress and osteoporosis and may be beneficial in innovative research settings. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1166 KW - allostatic load KW - bone remodeling KW - microRNA KW - osteoblast KW - osteoclast Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-523007 SN - 1866-8372 IS - 11 ER - TY - JOUR A1 - Schultebraucks, Katharina A1 - Deuter, Christian E. A1 - Duesenberg, Moritz A1 - Schulze, Lars A1 - Hellmann-Regen, Julian A1 - Domke, Antonia A1 - Lockenvitz, Lisa A1 - Kuehl, Linn K. A1 - Otte, Christian A1 - Wingenfeld, Katja T1 - Selective attention to emotional cues and emotion recognition in healthy subjects: the role of mineralocorticoid receptor stimulation JF - Psychopharmacology N2 - Selective attention toward emotional cues and emotion recognition of facial expressions are important aspects of social cognition. Stress modulates social cognition through cortisol, which acts on glucocorticoid (GR) and mineralocorticoid receptors (MR) in the brain. We examined the role of MR activation on attentional bias toward emotional cues and on emotion recognition. We included 40 healthy young women and 40 healthy young men (mean age 23.9 +/- 3.3), who either received 0.4 mg of the MR agonist fludrocortisone or placebo. A dot-probe paradigm was used to test for attentional biases toward emotional cues (happy and sad faces). Moreover, we used a facial emotion recognition task to investigate the ability to recognize emotional valence (anger and sadness) from facial expression in four graded categories of emotional intensity (20, 30, 40, and 80 %). In the emotional dot-probe task, we found a main effect of treatment and a treatment x valence interaction. Post hoc analyses revealed an attentional bias away from sad faces after placebo intake and a shift in selective attention toward sad faces compared to placebo. We found no attentional bias toward happy faces after fludrocortisone or placebo intake. In the facial emotion recognition task, there was no main effect of treatment. MR stimulation seems to be important in modulating quick, automatic emotional processing, i.e., a shift in selective attention toward negative emotional cues. Our results confirm and extend previous findings of MR function. However, we did not find an effect of MR stimulation on emotion recognition. KW - Selective attention KW - Emotion recognition KW - Fludrocortisone KW - Mineralocorticoid receptor KW - Stress KW - Cortisol Y1 - 2016 U6 - https://doi.org/10.1007/s00213-016-4380-0 SN - 0033-3158 SN - 1432-2072 VL - 233 SP - 3405 EP - 3415 PB - Springer CY - New York ER -