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Laubach, M.

Publications and source records attributed to Laubach, M..

10 recordsLinked to original sources

Active Sampling and Sex Differences in Perceptual Decision Making in Rats

Decisions are often modeled as a sequential process in which evidence accumulates until it reaches a threshold, triggering a response. Studies in freely moving animals raise questions about how ongoing behavior, not just stimulus properties, shapes this process. We trained rats of both sexes on a visual detection task with three luminance levels, each associated with the same reward outcome. Rats controlled cue duration through sustained head entries into a center port, yielding a measurable index of active sampling. Females consistently sampled longer than males. Sampling durations were shorter on error than correct trials, and reaction times were longer on error trials. We used drift diffusion models to relate these behaviors to the decision process. Luminance selectively affected the rate of evidence accumulation, with drift rate increasing monotonically across low, mid, and high luminance levels. Active sampling time was associated with the decision threshold, with longer sampling predicting higher thresholds in both sexes. The relationship between sampling time and drift rate differed by sex. Females showed a negative association between sampling duration and drift rate that was absent in males. These findings suggest that cue properties and active sampling make separable contributions to the decision process. These findings suggest that cue properties and active sampling make separable contributions to decision making, with a negative association between sampling duration and drift rate evident in females but not males.

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Visual Salience Controls the Speed of Evidence Accumulation in Value-Based Decisions by Rats

Studies of visual discrimination in rodents can confound the effects of cue salience with reward value, making it difficult to determine which factor guides choice behavior. We examined this issue by testing how changes in relative salience affect decision dynamics in rats performing a two-alternative forced-choice task in which rats chose between visual cues associated with high or low sucrose rewards. After initial training with high and low luminance cues, we introduced a novel cue of intermediate luminance as a "luminance shift" test. The intermediate luminance cue substituted for either the brighter or dimmer cue and had the same reward value as the cue that it replaced. We found that while rats maintained a preference for the higher-value option, the introduction of a perceptually more similar cue consistently reduced choice preference and eliminated latency differences compared to baseline. Using drift diffusion modeling, we determined that the luminance shifts primarily caused a reduction in the drift rate (the speed of evidence accumulation), reflecting increased difficulty in cue discrimination. This finding suggests that the relative salience of the options determines the efficiency of evidence accumulation in value-based decisions. Furthermore, this effect on drift rate shows a dissociation from our previous work (Palmer et al., 2024), where prefrontal cortex inactivation specifically affected only the decision threshold. Our results demonstrate that relative salience influences deliberation, with low-level perceptual features shaping the computational dynamics of value-based choice. Our findings clarify the distinct contributions of sensory input and prefrontal function in the decision process. Significance StatementThis study reveals that changes in the relative salience of visual stimuli shape the computational dynamics of value-based decisions. We trained rats to make visually guided choices and found that relative differences in the brightness of the stimuli affect how quickly the rats made decisions and how often they chose a higher-value option. Our findings, together with a recent study on the role of the prefrontal cortex in value-guided decisions (Palmer et al., 2024), suggest that separate factors influence choice dynamics in rodents: visual salience affects the speed of deliberation, while prefrontal activity regulates caution. This study helps clarify how sensory and higher cognitive variables relate to the distinct computational components of the decision process.

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The role of rat prelimbic cortex in decision making

The frontal cortex plays a critical role in decision-making. One specific frontal area, the anterior cingulate cortex, has been identified as crucial for setting a threshold for how much evidence is needed before a choice is made (Domenech & Dreher, 2010). Threshold is a key concept in drift diffusion models, a popular framework used to understand decision-making processes. Here, we investigated the role of the prelimbic cortex, part of the rodent cingulate cortex, in decision making. Male and female rats learned to choose between stimuli associated with high and low value rewards. Females learned faster, were more selective in their responses, and integrated information about the stimuli more quickly. By contrast, males learned more slowly and showed a decrease in their decision thresholds during choice learning. Inactivating the prelimbic cortex in female and male rats sped up decision making without affecting choice accuracy. Drift diffusion modeling found selective effects of prelimbic cortex inactivation on the decision threshold, which was reduced with increasing doses of the GABA-A agonist muscimol. Stimulating the prelimbic cortex through mu opioid receptors slowed the animals choice latencies and increased the decision threshold. These findings provide the first causal evidence that the prelimbic cortex directly influences decision processes. Additionally, they suggest possible sex-based differences in early choice learning.

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Learning to Choose: Behavioral Dynamics Underlying the Initial Acquisition of Decision Making

Current theories of decision making propose that decisions arise through competition between choice options. Computational models of the decision process estimate how quickly information about choice options is integrated and how much information is needed to trigger a choice. Experiments using this approach typically report data from well-trained participants. As such, we do not know how the decision process evolves as a decision-making task is learned for the first time. To address this gap, we used a behavioral design separating learning the value of choice options from learning to make choices. We trained male rats to respond to single visual stimuli with different reward values. Then, we trained them to make choices between pairs of stimuli. Initially, the rats responded more slowly when presented with choices. However, as they gained experience in making choices, this slowing reduced. Response slowing on choice trials persisted throughout the testing period. We found that it was specifically associated with increased exponential variability when the rats chose the higher value stimulus. Additionally, our analysis using drift diffusion modeling revealed that the rats required less information to make choices over time. Surprisingly, we observed reductions in the decision threshold after just a single session of choice learning. These findings provide new insights into the learning process of decision-making tasks. They suggest that the value of choice options and the ability to make choices are learned separately, and that experience plays a crucial role in improving decision-making performance.

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An ancient subcortical circuit decides when to orient to threat in humans

Many psychiatric symptoms have been linked to threat-related perception and learning processes. In addition, however, there may also be mechanisms for balancing effectively between threat- and reward-related behaviors and these may also vary between individuals. We investigated neural activity associated with spontaneous switching between foraging for rewards and vigilance for threats with 7T fMRI. In a virtual naturalistic environment, participants freely switched between the two modes of behavior. Switching was driven by estimates of likelihood of threat and reward. Both tracking of threat and switching to vigilance were associated with specific but distributed patterns of activity spanning habenula, dorsal raphe nucleus (DRN), anterior cingulate cortex, and anterior insula cortex. Distinct distributed patterns heralded returns to reward-oriented behavior. Individual variation in DRN activity reflected individual variation in vigilance. All activity patterns were replicated in an initially held-out portion of data.

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The rostral medial frontal cortex is crucial for engagement in consummatory behavior

The medial frontal cortex (MFC) in rodents emits rhythmic activity that is entrained to the animals licking cycle during consumption and encodes the value of consumed fluids (Horst and Laubach, 2013; Amarante et al., 2017; Amarante and Laubach, 2021). These signals are especially prominent in the rostral half of the MFC. This region is located above an orbitofrontal region where mu opioid receptors regulate intake (Mena et al., 2011; Castro and Berridge, 2017) and reversible inactivation reduces behavioral measures associated with the incentive value and palatability of liquid sucrose (Parent et al., 2015a). Here, we examined the effects of reversible inactivation and stimulation of mu opioid receptors in rostral MFC on behavior in an incentive contrast licking task. Adult male rats licked to receive access to liquid sucrose, which alternated between high (16%) and low (4%) values over 30 sec periods. Bilateral infusion of muscimol reduced the total number of licks emitted over the 30 min test sessions, the time spent actively consuming sucrose, and the ratio of licks for the higher and lower value fluids. Inactivation did not alter licking frequency or variability or microstructural measures such as the duration of licking bouts that are classically associated with the palatability of a liquid reward. Infusions of DAMGO (1g/L) at the same sites had inconsistent behavioral effects across different subjects. Our findings suggest that the rostral MFC has a distinct role in the control of consummatory behavior and contributes to peristent consumption and not to the expression of palatability. SIGNIFICANCE STATEMENTThe medial frontal cortex (MFC) of rodents has received attention in recent years and is considered as a singular cortical region with a potential unitary function. Increasing evidence suggests that MFC is composed of distinct subregions, with unique roles in the control of behavior. The present study adds to this literature by showing unique effects of reversibly inactivating the most rostral part of the medial frontal cortex and a lack of consistent effects of stimulating mu opioid receptors in the subregion. Findings are in contrast to previous reports on the more ventral orbitofrontal cortex and caudal medial frontal cortex and are important for understanding the general role of the rodent frontal cortex and how opioids may act to control behavior.

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An open source platform for presenting dynamic visual stimuli

Operant behavior procedures often rely on visual stimuli to cue the initiation or secession of a response, and to provide a means for discriminating between two or more simultaneously available responses. While primate and human studies typically use LCD or OLED monitors and touch screens, rodent studies use a variety of methods to present visual cues ranging from traditional incandescent light bulbs, single LEDs, and, more recently, touch screen monitors. Commercially available systems for visual stimulus presentation are costly, challenging to customize, and are typically closed source. We developed an open-source, highly-modifiable visual stimulus presentation platform that can be combined with a 3D-printed operant response device. The device uses an eight by eight matrix of LEDs, and can be expanded to control much larger LED matrices. Implementing the platform is low-cost (<$70 USD per device in the year 2020). Using the platform, we trained rats to make nosepoke responses and discriminate between two distinct visual cues in a location-independent manner. This visual stimulus presentation platform is a cost-effective way to implement complex visually-guided operant behavior, including the use of moving or dynamically changing visual stimuli. Significance StatementThe design of an open source and low cost device for presenting visual stimuli is described. It is capable of presenting complex visual patterns and dynamically changing stimuli. A practical demonstration of the device is also reported, from an experiment in which rats performed a luminance based visual discrimination. The device has utility for studying visual processing, psychophysics, and decision making in a variety of species.

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Noradrenergic regulation of Win-Stay/Lose-Shift policy and choice determinism in a two-armed bandit task

Reversal learning depends on cognitive flexibility. Many reversal learning studies assess cognitive flexibility based on the number of reversals that occur over a test session. Reversals occur when an option is repeatedly chosen, e.g. eight times in a row. This design feature encourages win-stay behavior and thus makes it difficult to understand how win-stay decisions influence reversal performance. We used an alternative design, reversals over blocks of trials independent of performance, to study how perturbations of the medial orbital cortex and the noradrenergic system influence reversal learning. We found that choice accuracy varies independently of win-stay behavior and the noradrenergic system controls sensitivity to positive feedback during reversal learning.

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Rhythmic activity in the medial and orbital frontal cortices tracks reward value and the vigor of consummatory behavior

This study examined how the medial frontal (MFC) and orbital frontal (OFC) cortices process reward information. We simultaneously recorded local field potentials in the two areas as rats consumed liquid sucrose rewards. Both areas exhibited a 4-8 Hz "theta" rhythm that was phase locked to the lick cycle. The rhythm tracked shifts in sucrose concentrations and fluid volumes, demonstrating that it is sensitive to differences in reward magnitude. The coupling between the rhythm and licking was stronger in MFC than OFC and varied with response vigor and absolute reward value in the MFC. Spectral analysis revealed zero-lag coherence between the cortical areas, and found evidence for a directionality of the rhythm, with MFC leading OFC. Our findings suggest that consummatory behavior generates simultaneous theta range activity in the MFC and OFC that encodes the value of consumed fluids, with the MFC having a top-down role in the control of consumption.

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Rhythmic Activity In The Medial Frontal Cortex Encodes Relative Reward Value

Rodents lick to consume fluids. The reward value of ingested fluids is likely to be encoded by neuronal activity entrained to the lick cycle. Here, we investigated relationships between licking and reward signaling by the medial frontal cortex [MFC], a key cortical region for reward-guided learning and decision-making. Multi-electrode recordings of spike activity and field potentials were made in male rats as they performed an incentive contrast licking task. Rats received access to higher and lower value sucrose rewards over alternating 30 sec periods. They learned to lick persistently when higher value rewards were available and to suppress licking when lower value rewards were available. Spectral analysis of spikes and fields revealed evidence for reward value being encoded by the strength of phase-locking of a 6-12 Hz theta rhythm to the rats lick cycle. Recordings during the initial acquisition of the task found that the strength of phase-locking to the lick cycle was strengthened with experience. A modification of the task, with a temporal gap of 2 sec added between reward deliveries, found that the rhythmic signals persisted during periods of dry licking, a finding that suggests the MFC encodes either the value of the currently available reward or the vigor with which rats act to consume it. Finally, we found that reversible inactivations of the MFC in the opposite hemisphere eliminated the encoding of reward information. Together, our findings establish that a 6-12 Hz theta rhythm, generated by the rodent medial frontal cortex, is synchronized to rewarded actions.\n\nSignificance StatementThe cellular and behavioral mechanisms of reward signaling by the medial frontal cortex [MFC] have not been resolved. We report evidence for a 6-12 Hz theta rhythm that is generated by the MFC and synchronized with ongoing consummatory actions. Previous studies of MFC reward signaling have inferred value coding upon temporally sustained activity during the period of reward consumption. Our findings suggest that MFC activity is temporally sustained due to the consumption of the rewarding fluids, and not necessarily the abstract properties of the rewarding fluid. Two other major findings were that the MFC reward signals persist beyond the period of fluid delivery and are generated by neurons within the MFC.

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