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Bohme, R.

Publications and source records attributed to Bohme, R..

2 recordsLinked to original sources

Shared Latent Decision Strategies Underlie Reward-Guided Behavior Across Species

Adaptive behavior requires that organisms learn which actions are rewarded and to update action selection when the environment changes. While human and non-human animals exhibit adaptive behavior, whether apparently similar behavior reflects common decision strategies remains unclear. Probabilistic reversal learning provides a cross-species assay of reward-guided choice, yet standard metrics such as accuracy or reward rate can obscure underlying strategies that generate choices. Here, we applied parallel probabilistic reversal learning tasks in mice and humans and used a generalized linear model-hidden Markov model to infer latent decision strategies from trial-by-trial behavior. Across species, choices were organized into stable behavioral states with differing reliance on choice history, reward history, and response bias. Among these latent states, we identify a conserved reward-learning strategy in mice and humans characterized by the greatest feedback sensitivity, reward efficiency, and adaptation after reversal. Simulating choice behavior using state-specific decision policies reproduced the empirical hierarchy of performance, confirming that the latent states capture meaningful behavioral strategies. Although mice and humans differ in the temporal dynamics of reward learning, both species ultimately converge on the same optimized strategy. These findings identify a conserved latent reward-learning strategy in mice and humans, defining a translational framework for studying how adaptive decision-making is shaped by task experience, stress, affective processes, and neural circuit function.

neuroscience↗

Oxytocin Modulation of Spinal Circuits Drives Therapeutic Benefits of Massage

Across social species, social touch enhances well-being and reduces pain -- two seemingly distinct benefits that enhance survival. Yet where and how the nervous system integrates these functions, and whether a single mechanism could serve both, remains unknown. Here we show that massage triggers oxytocin release, which shapes both pain and touch reward at the earliest stage of central processing -- the spinal cord -- through a single, state-dependent circuit mechanism. We report that in humans, massage enhances well-being, effects that correlate with endogenous oxytocin release. In mice, gentle touch activates hypothalamic oxytocin neurons that project directly to the spinal dorsal horn. Genetic manipulation of spinal oxytocin circuits alters behavioral responses to both gentle touch and noxious stimuli. Spinal calcium imaging and slice electrophysiology reveal that oxytocin acts on both excitatory and inhibitory spinal neurons to sculpt the relative activity of spinal ascending systems that convey both social touch and pain to the brain. Extending these findings to humans, we show that oxytocin receptors are also expressed on spinal excitatory and inhibitory neurons, and that endogenous oxytocin during massage correlates with altered spinal touch processing. Thus, spinal oxytocin signaling provides an evolutionarily conserved mechanism for the therapeutic benefits of massage.

neuroscience↗