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Rabinovich, R.

Publications and source records attributed to Rabinovich, R..

6 recordsLinked to original sources

Temporal Processing during Decision Making under Uncertainty.

Time perception and decision-making are interrelated processes that are critical to much of human and animal behavior. Although the behavioral importance of this link between the processes has been established, the neural underpinnings of temporal decision-making are unclear. The current study leverages human intracranial electro-physiology to investigate the neural contribution of temporal processing to decision-making under risk. To probe temporal decision-making, we use a version of the Balloon Analogue Risk Task, in which participants inflate virtual balloons with the goal of reaching maximal balloon size but stopping inflation before the balloon pops. Points are awarded based on inflation duration of successful trials, such that points awarded are linearly related to balloon size. By decoding temporal features of the task on a trial-by-trial basis, we find neural representations of time during balloon inflation. Specifically, we find that both medial and lateral temporal regions of the brain encode the majority of this time-related signal. Importantly, we can decode the progression of time leading up to the outcome of a successful decision (pressing a button to stop inflation before the balloon pops). This encoding of time depends on an active decision to end the trial: we cannot decode time during passive observation of balloon inflation to a known maximal size. To validate these results further, we use a temporal convolution network to predict participants response (i.e., time of button press) based on the brain activity leading up to the response. We find that we can predict the moment of response with high accuracy and temporal resolution. The model predicts the timing of successful decisions but not the timing of balloon pops. Together, these findings reveal neural representations that encode the progression of time, specifically in relation to an active decision.

neuroscience↗

Asymmetric Reinforcement Learning Explains Human Choice Patterns in Decision-making Under Risk

Human decisions under uncertainty are shaped by experience, but the computations that translate expectation and experience into choice remain debated in neural and cognitive science. Prior studies highlight reinforcement learning (RL) as a unifying framework, yet it is unclear whether human behavior under risk is better captured by symmetric updating from outcomes or by asymmetric learning that weights reward and loss differently. This work examines which learning strategies better explain trial-by-trial choices given contextual uncertainty and manipulations of outcome distributions. Our results show that a Risk Sensitive (RS) model with asymmetric learning rates best explains human behavior in our novel decision-making task. Fitting candidate models to individual trial histories yielded value signals that predicted both choice and response time. These results highlight that RS model, as an asymmetric learning provides a concise and identifiable account of behavior in decision-making under risk tasks.

neuroscience↗

Increased Aperiodic Exponents Track Depression Symptom Severity

Roughly one-third of patients with major depressive disorder (MDD) fail to respond to standard treatments and develop treatment-resistant MDD. For these patients, alternative therapies ofer additional options but yield inconsistent outcomes. Progress has been limited by the absence of objective, brain-based biomarkers to guide target selection or track therapeutic response in real time. Instead, clinicians rely on behavioral assessments that evolve slowly over weeks to months, obscuring the underlying neural dynamics of symptom changes. Here, we test whether the aperiodic exponent of intracranial EEG (iEEG) local field potentials can serve as a neurophysiological marker of depression symptom severity. We leveraged a large iEEG cohort (N = 20) undergoing invasive monitoring for refractory epilepsy, yielding over 1,800 contacts spanning cortical and subcortical zones. For each contact, we estimated the aperiodic exponent (thought to reflect aspects of cortical excitability) of the power spectrum across 10-100 Hz within local brain regions and across distributed cortical association networks. Depressive symptoms were assessed with the Beck Depression Inventory-II (BDI-II) immediately before intracranial resting state recordings. With respect to the BDI-II scale, participants were identified as experiencing minimal (BDI-II [≤] 13) or elevated depression symptoms (BDI-II [≥] 14). Associations between symptom severity (BDI-II total score and Somatic-Afective, Cognitive, and Anhedonia subscales) and region- or network-level exponents were modeled with ordinary least squares (OLS) regression. The whole-brain, mean aperiodic exponent for each participant discriminated symptom status (AUC = 0.82). At the regional level, the orbitofrontal cortex, anterior cingulate cortex, insula, and amygdala showed higher exponents in the elevated depression symptom group (d = 1.18-1.71; p = 0.032-0.004). A post-hoc classification analysis across these four regions misclassified one participant per group (AUC = 0.86; 95% CI 0.64-1.00). In continuous analyses, BDI-II scores correlated positively with exponents in these same four regions (pFDR = 0.019-0.027; partial r=0.61-0.70) and at the network level in the Salience network (pFDR = 0.024; partial r = 0.63) and Default (pFDR = 0.046; partial r = 0.55) network. The Salience network significantly tracked Anhedonia symptoms (p = 0.004; partial r = 0.62). Here we report that intracranial aperiodic exponents within fronto-limbic and insular circuits, overlapping with networks implicated in contemporary accounts of depression pathophysiology, diferentiate depressive symptom status and scale with severity. These findings support the aperiodic exponent as a candidate neurophysiological marker of current depression symptom burden, with potential relevance for individualized neuromodulation in MDD.

neuroscience↗

Human brain network control of creativity

The ability to think creatively is fundamental to human cognition, shaping how we interact with the world and navigate complex problems. Creativity depends on the interaction of multiple large-scale brain networks, but how these networks represent creative thought and distinguish it from other cognitive states remains unclear. Here, we use invasive intracranial recordings in the human brain to explore the network-level representations underlying creative thinking. Our results demonstrate that cortical networks in the human brain differentially encode distinct cognitive states: we found unique brain states underlying creative thinking vs. arithmetic calculations, particularly in the default mode network. Further, in the dorsal attention network, we uncovered nonlinear, high-dimensional representations of moment-by-moment fluctuations in creative performance. These representations define a neural creativity axis shared between network-level and single-neuron computations. Our findings reveal widespread neural representations of cognitive state and suggest distinct roles of specific cortical networks in controlling creativity, with the default mode network gating access to creative states and the dorsal attention network regulating the quality of creative output.

neuroscience↗

Default mode network spatio-temporal electrophysiological signature and causal role in creativity

The default mode network (DMN) is a widely distributed, intrinsic brain network thought to play a crucial role in internally-directed cognition. It subserves self-referential thinking, recollection of the past, mind wandering, and creativity. Knowledge about the electrophysiology underlying DMN activity is scarce, due to the difficulty to simultaneously record from multiple distant cortical areas with commonly-used techniques. The present study employs stereo-electroencephalography depth electrodes in 13 human patients undergoing monitoring for epilepsy, obtaining high spatiotemporal resolution neural recordings across multiple canonical DMN regions. Our results offer a rare insight into the temporal evolution and spatial origin of theta (4-8Hz) and gamma signals (30-70Hz) during two DMN-associated higher cognitive functions: mind-wandering and alternate uses. During the performance of these tasks, DMN activity is defined by a specific pattern of decreased theta coupled with increased gamma power. Critically, creativity and mind wandering engage the DMN with different dynamics: creativity recruits the DMN strongly during the covert search of ideas, while mind wandering displays the strongest modulation of DMN during the later recall of the train of thoughts. Theta band power modulations, predominantly occurring during mind wandering, do not show a predominant spatial origin within the DMN. In contrast, gamma power effects were similar for mind wandering and creativity and more strongly associated to lateral temporal nodes. Interfering with DMN activity through direct cortical stimulation within several DMN nodes caused a decrease in creativity, specifically reducing the originality of the alternate uses, without affecting creative fluency or mind wandering. These results suggest that DMN activity is flexibly modulated as a function of specific cognitive processes and supports its causal role in creative thinking. Our findings shed light on the neural constructs supporting creative cognition and provide causal evidence for the role of DMN in the generation of original connections among concepts.

neuroscience↗

Effect of wall type, delayed mortality and mosquito age on the residual efficacy of a clothianidin-based indoor residual spray formulation (SumiShieldTM 50WG) in southern Mozambique

BackgroundIndoor residual spraying (IRS) is one of the main malaria vector control strategies in Mozambique alongside the distribution of insecticide treated nets. As part of the national insecticide resistance management strategy, Mozambique introduced SumiShield 50WG, a third generation IRS product, in 2018. Its residual efficacy was assessed in southern Mozambique during the 2018-2019 malaria season. MethodsTwo different wall surfaces, cement and mud-plastered surfaces, daily mosquito mortality up to 120 hours post-exposure, and older mosquitoes (13-26d old) were included in standard WHO (World Health Organization) cone bioassay tests. Lethal times (LT) 90, LT50 and LT10 were estimated using Bayesian models. ResultsMortality 24h post exposure was consistently below 80%, the current WHO threshold value for effective IRS, in both young and old mosquitoes, regardless of wall surface type. Considering delayed mortality, residual efficacies (mosquito mortality equal or greater than 80%) ranged from 1 to [≥]12 months, with the duration depending on mortality time post exposure, wall type and mosquito age. Looking at mortality 72h after exposure, residual efficacy was between 6 and 9 months, depending on wall type and mosquito age. Mortality of older mosquitoes was significantly higher on mud-surfaces compared to cemented-surfaces 24h post exposure, but this difference was not significant for the delayed mortalities. The LT50 and LT10 (i.e. 90% of the mosquitoes survive exposure to the insecticides) values were consistently higher for older mosquitoes using the 24h post-exposure observations and ranged from 0.2 to 5.7 months and 0.2 to 7.2 months for LT50 and LT10, respectively. ConclusionsThe present study highlights the need for assessing mosquito mortality beyond the currently recommended 24h post exposure. Failure to do so may lead to underestimation of the residual efficacy of IRS products, as delayed mortality will lead to a further reduction in mosquito vector populations and potentially negatively impact disease transmission. Monitoring residual efficacy on relevant wall surfaces, including old mosquitoes that are ultimately responsible for malaria transmission, and assessing delayed mortalities are critical to provide accurate and actionable data to guide vector control programmes.

ecology↗