Being the chosen one: social inclusion modulates decisions in the ultimatum game. An ERP study

International audienceIn the present study, participants played a modified ultimatum game simulating a situation of inclusion/exclusion, in which either the participant or a rival could be selected to play as the responder. This selection was made either randomly by a computer (i.e. random pairing mode) or by the proposer (i.e. choice mode), based on physical appearance. Being chosen by the proposer triggered positive reciprocal behavior in participants, who accepted unfair offers more frequently than when they had been selected by the computer. Independently of selection mode, greater P200 amplitudes were found when participants received fair offers than when they received unfair offers and when unfair shares were offered to their rivals rather than to them, suggesting that receiving fair offers or observing a rival's misfortune was rewarding for participants. While participants generally showed more interest in the offers they themselves received (i.e. greater P300 responses to these offers), observing their rivals receive fair shares after the latter had been chosen by the proposer triggered an increase in P300 amplitude likely to ref lect a feeling of envy. This study provides new insights into both the cognitive and affective processes underpinning economic decision making in a context of social inclusion/exclusion

Fragile temporal prediction in patients with schizophrenia is related to minimal self disorders

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Histological and transcriptional study of angiogenesis and lymphangiogenesis in uninvolved skin, acute pinpoint lesions and established psoriasis plaques: an approach of vascular development chronology in psoriasis

Background Dysregulation of angiogenesis and lymphangiogenesis could participate in psoriasis pathogenesis. Analysis of nascent psoriasis lesions should help at identifying early vascular anomalies. Objective To analyse vascular development, angiogenesis and lymphangiogenesis markers expression in uninvolved skin in psoriatic patients (N), early psoriasis lesions or pinpoints (PP) and psoriasis plaques (PSO). Methods Skin biopsies were taken in 17 patients in N and in PSO and/or PP. The mRNA steady-state level of angiogenesis and lymphangiogenesis markers was measured by RT-PCR. Immunohistochemistry was performed for von Willebrand factor, podoplanin, Ki-67 and VEGFR3. Blood (BV) and lymphatic (LV) vessels expansion was measured by computer-assisted morphometry. Results Clinical and epidermal aspects indicated that PP are intermediate between N and PSO. While total BV area was already increased in PP similarly to PSO as compared to N, LV area in PP was intermediate between N and PSO. Mean LV size was identical in N and PP and increased in PSO, mean BV size in PP being intermediate between N and PSO. VEGF-A 189 variant was increased in PP as compared to N and PSO. As compared to N, angiogenesis markers (VEGF-A isoforms, PlGF, VEGFR2, NRP-1), VEGF-C and NRP-2 were similarly increased in PP and PSO. Keratin 16 and the lymphangiogenesis markers (VEGFR3, prox-1) were intermediate in PP. Conclusion These data suggest that the expansion of lymphatic vessels occurs after blood vascular development in psoriasis. Expansion of BV in PP could be followed by vessel enlargement during progression to PSO, in parallel with a decreased VEGF-A 189/VEGF-A 121 balance in plaque