Biology subjects

Barbeau, E.

Publications and source records attributed to Barbeau, E..

3 recordsLinked to original sources

bioRxiv2025

Choosing the best or avoiding the worst: complementary and opponent value signals in the human brain

Whether the brain encodes the subjective value of pleasant and unpleasant situations via a single integrated circuit or through distinct pathways remains unresolved. It is also unclear how neural value signals guide choices when the context involves choosing the most favorable option or avoiding the most unfavorable one. To address these questions, we recorded intracerebral activity from 27 participants as they first rated pleasant and unpleasant scenarios and then made binary choices across all combinations of item domain (pleasant/unpleasant) and choice frame (choose best/worst). Ventromedial prefrontal cortex (vmPFC) broadband gamma activity (BGA, 50-150 Hz) tracked the value of pleasant items during rating and pre-choice, correlating positively with the most pleasant item irrespective of choice frame. Similarly, anterior insula (aIns) BGA tracked the value of unpleasant items during rating and pre-choice, correlating negatively with the most unpleasant item irrespective of choice frame. The difference in relative value correlations between the vmPFC and aIns was larger for choices involving a conflict between item domain and choice frame, consistent with slower response times and choices less aligned with value differences in these trials. These findings reveal dissociable yet complementary neural systems for pleasant and unpleasant valuation and highlight how such signals may guide flexible decision-making across contexts.

neuroscience↗

bioRxiv2025

Optimization of the prostaglandin F2α receptor for structural biology

Prostaglandin F2[a] (PGF2[a]) is a bioactive lipid derived from arachidonic acid and is involved in many physiological and pathophysiological processes such as parturition, vascular tone regulation, glaucoma and inflammation. It acts by binding to the Prostaglandin F2[a] receptor (FP), a G Protein-Coupled Receptor (GPCR) that mediates signaling events by engaging intracellular heterotrimeric G protein effectors. The orthosteric binding site of lipid-binding receptors displays greater efficacy-dependent plasticity that hinders the design of ligands. Solving the structure of FP with ligands of different efficacies at an atomic level is important to fully understand its mechanism of activation and inhibition. Most purified FP-ligand complexes are unstable in vitro. The development of new X-ray crystallography and single particle cryo-electron (cryoEM) strategies to understand receptors signal transduction requires improved purification yield and in vitro stability of the receptor. Here, we present a protein engineering effort to optimize the FP protein sequence for use in structural biology. Strategies involve protein insertion sites in the third intracellular loop (ICL3), N-terminal and C-terminal deletions, and single-point mutations that favorably affect receptor purification yield and stability in vitro. The best FP construct displays a yield of 1.5 mg/L and a stability of 59{degrees}C that constitute a threefold improvement in purification yield and 9{degrees}C increase in stability over the wild-type receptor. These modifications in the receptor are suitable for pursuing alternative strategies for improving FP purification yield and for studying FP binding efficacy to its ligands through structural biology approaches.

pharmacology and toxicology↗

bioRxiv2021

Intracerebral mechanisms explaining the impact of incidental feedback on mood state and risky choice

Identifying factors whose fluctuations are associated with choice inconsistency is a major issue for rational decision theory. Here, we investigated the neuro-computational mechanisms through which mood fluctuations may bias human choice behavior. Intracerebral EEG data were collected in a large group of participants (n = 30), while they were performing interleaved quiz and choice tasks. Neural baseline activity preceding choice onset was confronted first to mood level, estimated by a computational model integrating the feedbacks received in the quiz task, and then to the weighting of option attributes, in a computational model predicting risk attitude in the choice task. Results showed that 1) elevated broadband gamma activity (BGA) in the ventromedial prefrontal cortex (vmPFC) and dorsal anterior insula (daIns) was respectively signaling periods of high and low mood, 2) increased vmPFC and daIns BGA respectively promoted and tempered risk taking by overweighting gain versus loss prospects. Thus, incidental feedbacks induce brain states that correspond to different moods and bias the comparison of safe and risky options. More generally, these findings might explain why people experiencing positive (or negative) outcome in some part of their life tend to expect success (or failure) in any other.

neuroscience↗