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Surendran, D.

Publications and source records attributed to Surendran, D..

2 recordsLinked to original sources

From Exploration to Structured Navigation: Learning Dynamics of Freely Moving Marmosets during Foraging

How do structured, memory-guided behaviors emerge in freely moving primates? We addressed this question by training common marmosets to perform a foraging task in a semi-naturalistic environment, where they retrieved food from eight dispensers over multiple sessions. Animals received no instruction or shaping and were free to visit dispensers in any order. We found that animals engaged with the task in most trials and, within engaged trials, transitioned from exploratory to efficient foraging behavior. Learning was marked by performance gains and the emergence of reproducible movement patterns between specific dispensers. Using trajectory analyses and probabilistic modeling, we found that animals formed stable route segments linking specific dispensers, reflecting the emergence of local navigation motifs. These segments became increasingly regular and predictable with experience. Yet rather than being rigidly replayed, they were flexibly recombined into variable global sequences. This indicates that animals adopted a hybrid navigation strategy, in which reusable route segments are embedded within a topological structure. These findings demonstrate how efficient, adaptive navigation can emerge through self-guided experience in complex environments. Our approach provides a naturalistic and longitudinal framework for studying the formation of structured spatial strategies in non-human primates, bridging ecological behavior with theoretical models of learning and memory.

animal behavior and cognition↗

Receptor-independent membrane mediated pathways of serotonin action

Serotonin is a neurotransmitter as well as a somatic signaling molecule, and the serotonergic system is a major target for psychotropic drugs. Serotonin, together with a few related neurotransmitters, has recently been found to exhibit an unexpectedly high lipid membrane affinity1–3. It has been conjectured that extrasynaptic serotonin can diffuse in the lipid membrane to efficiently reach remote receptors (and receptors with buried ligand-binding sites)4, providing a mechanism for the diffuse ‘volume’ neurotransmission that serotonin is capable of5–10. Here we show that membrane binding by serotonin can directly modulate membrane properties and cellular function, independent of its receptor-mediated actions. Atomic force microscopy shows that serotonin binding makes artificial lipid bilayers softer. It induces nucleation of liquid disordered domains inside the raft-like liquid-ordered domains in a ternary bilayer displaying phase separation. Solid-state NMR spectroscopy corroborates this data, revealing a rather homogeneous decrease in the order parameter of the lipid chains in the presence of serotonin. In the RN46A immortalized serotonergic neuronal cell line, extracellular serotonin enhances transferrin receptor endocytosis, an action exerted even in the presence of both broad-spectrum serotonin receptor and transporter inhibitors. Similarly, it increases the binding and internalization of Islet Amyloid Polypeptide (IAPP) oligomers, suggesting a connection between serotonin, which is co-secreted with IAPP by pancreatic beta cells, and the cellular effects of IAPP. Our results uncover a hitherto unknown serotonin-bilayer interaction that can potentiate key cellular processes in a receptor-independent fashion. Therefore, some pathways of serotonergic action may escape potent pharmaceutical agents designed for serotonin transporters or receptors. Conversely, bio-orthogonal serotonin-mimetics may provide a new class of cell-membrane modulators.Competing Interest StatementThe authors have declared no competing interest.View Full Text

biophysics↗