Adolescent neurostimulation of dopamine circuit reverses genetic deficits in frontal cortex function

Dopamine system dysfunction is commonly implicated in adolescent-onset neuropsychiatric disorders. Although psychosis symptoms can be alleviated by antipsychotics, cognitive symptoms remain unresponsive to such pharmacological treatments and novel research paradigms investigating the circuit substrates underlying cognitive deficits are critically needed. The frontal cortex and its dopaminergic input from the midbrain are implicated in cognitive functions and undergo maturational changes during adolescence. Here, we used mice carrying mutations in the Arc or DISC1 genes to model mesofrontal dopamine circuit deficiencies and test circuit-based neurostimulation strategies to restore cognitive functions. We found that in a memory-guided spatial navigation task, frontal cortical neurons were activated coordinately at the decision-making point in wild-type but not Arc mutant mice. Chemogenetic stimulation of midbrain dopamine neurons or optogenetic stimulation of frontal cortical dopamine axons in a limited adolescent period consistently reversed genetic defects in mesofrontal innervation, task-coordinated neuronal activity, and memory-guided decision-making at adulthood. Furthermore, adolescent stimulation of dopamine neurons also reversed the same cognitive deficits in DISC1 mutant mice. Our findings reveal common mesofrontal circuit alterations underlying the cognitive deficits caused by two different genes and demonstrate the feasibility of adolescent neurostimulation to reverse these circuit and behavioral deficits. These results may suggest developmental windows and circuit targets for treating cognitive deficits in neurodevelopmental disorders.


INTRODUCTION
Dysfunctions of the dopamine system are commonly implicated in neuropsychiatric disorders such as schizophrenia and substance-use disorders [1][2][3] . In addition, the treatment effect of antipsychotic medication is related to its effectiveness in blocking dopamine D2 receptors 4,5 .
However, psychiatric symptoms include not only psychosis that can be treated by antipsychotics, but also cognitive disabilities in executive functions and memory [5][6][7] . While current antipsychotic therapies based on D2 antagonism have little effect on cognitive disabilities 7-10 , frontal cortical dopamine deficits are reported in schizophrenia and the role of frontal cortical dopamine D1 receptor activation in cognitive function has been demonstrated in animal studies [11][12][13][14] .
Unfortunately, due to safety and bioavailability issues, very few D1 receptor agonists have progressed to clinical testing [15][16][17] . The long-standing difficulty of developing effective pharmacological treatments for cognitive symptoms suggests the necessity of new investigative approaches, such as evaluating the underlying neural circuitry and its potential for modification.
Dopamine regulates a multitude of behavioral functions through different anatomical pathways from dopaminergic neurons in the midbrain ventral tegmental area (VTA) and substantia nigra to cortical and subcortical target regions [18][19][20][21] . The mesofrontal pathway innervates the frontal cortex and an optimal level of dopamine is important for normal frontal circuit functions [22][23][24][25] . The frontal cortical circuit integrates dopaminergic signals with multisensory and memory information to control behavioral actions [26][27][28][29] . Together, the frontal cortex and its dopaminergic input form a critical substrate for cognitive functions and a hypoactive frontal cortical dopamine system is found in schizophrenia patients 5,14 . Genetic disruptions of several genes involved in synaptic functions related to psychiatric disorders, such as Arc and DISC1, lead to hypoactive mesofrontal dopaminergic input in mice [30][31][32][33][34][35] . Although there are many differences between these mouse lines . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint and specific human disease states, these mice offer opportunities to test whether genetic deficits in frontal cortex function can be reversed through circuit interventions.
Adolescence is an important period for the development of cognitive control functions and exploration behaviors [36][37][38] . Cognitive control deficits often emerge during adolescence as a characteristic manifestation of several psychiatric disorders including schizophrenia and substance-use disorders 2,3,39 . Developmental studies of the mesofrontal dopamine projection in both non-human primates and rodents suggest that this pathway exhibits a protracted maturation through adolescence [40][41][42][43][44] . Importantly, the structure and function of the mesofrontal circuit are malleable to experience; activity-dependent modification during adolescence and adolescent exposure to substances of abuse can produce long-lasting deficits [45][46][47][48] . However, it is unknown whether adolescent intervention in this pathway can induce long-lasting circuit changes conducive for the recovery of cognitive function from genetic deficits.
Mouse genetic models of frontal dopamine deficits and the adolescence malleability of this circuit present opportunities to investigate the cellular substrates underlying cognitive deficits and test potential intervention strategies [30][31][32] . In this study, using single-cell resolution neuronal ensemble imaging in freely behaving animals, we identified a disruption of neuronal coordination in frontal cortex that is associated with cognitive impairment in mouse models. Furthermore, taking advantage of the activity-dependent adolescent plasticity in the mesofrontal circuit, we developed targeted chemogenetic and optogenetic neuromodulation techniques that are able to reverse the neural coordination and cognitive behavioral deficits in adult animals. Our results demonstrate the capability of adolescent frontal dopamine circuit stimulation to achieve long-term reversal of cognitive deficits and suggest potential translational targets and strategies for psychiatric treatments.
. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint

Characterization of cognitive and mesofrontal innervation deficits in Arc mutant mice
We first used an Arc mutant model of a hypo-functioning mesofrontal circuit 32 for behavioral, anatomical tracing and neural activity imaging studies. To assess whether genetic disruption of Arc (by knocking-in a GFP reporter cassette 49 ) affects cognitive control of behavior, we examined wild-type and Arc homozygous mutant mice in a Y-maze spatial navigation task. This task takes advantage of the innate spatial navigation ability of mice and does not require extensive pretraining, making it well suited for both developmental and adult testing [50][51][52] . Wildtype mice explore the three arms of the maze using a memory-based decision-making strategy, preferring to visit a new arm instead of the most recently visited arm (Fig. 1a). The percentage of new arm visits out of the total arm visits is referred to as "alternation percentage", which is approximately 67% in wild-type mice and significantly above the chance level from random exploration (50%). By contrast, the alternation percentage in Arc mutant mice is significantly reduced towards the chance level (p = 0.001, t-test, t(15) = 3.975, WT: 67.2±2.6%, vs. Arc-/-: 53.4±2.3%, N = 8 and 9 mice, respectively; Fig. 1b). Arc mutant mice showed a similar number of total arm entries as the wild-type mice (Fig. 1c), suggesting that the Arc mutation did not affect overall locomotor activity or motivation level. Taken together, these results suggest that Arc mutant mice have a deficit in memory-guided choice behaviors.
Optimal performance in the Y-maze requires an intact frontal cortex and ventral tegmental area [53][54][55] . The M2 region of the frontal cortex plays an important role in action planning, generating the earliest neural signals among frontal cortical regions that are related to upcoming choice during spatial navigation 56,57 . To verify the involvement of the M2 cortex in Y-maze alternation, we . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint expressed the chemogenetic inhibitor DREADD-Gi 58 in M2 with an Adeno-Associated Viral (AAV) vector and used Clozapine-N-Oxide (CNO) injection to inhibit M2 neural activity in wildtype mice ( Supplementary Fig. 1a). We found that the alternation percentage was significantly reduced in the DREADD-Gi animals compared with control animals (p = 0.017, t-test, t(10)=2.845, Ctrl: 64.6±1.8%, Gi:54.1±3.2%, N=6 for each group, Supplementary Fig. 1b), while other aspects of motor behaviors in this task were not affected (Supplementary Fig. 1c and 1d).
These results confirm the involvement of M2 frontal cortical neurons in memory-guided decisionmaking during the Y-maze task.
Dopaminergic input from the ventral tegmental areas is critical to optimal frontal cortical function in controlling cognitive processes [22][23][24] . While the prelimbic area has the highest level of dopaminergic terminals among frontal cortical regions, a robust presence of midbrain dopaminergic projections and dopamine release in the M2 frontal cortex have been well established by immunostaining, viral labeling, single-cell axon-tracing, and in vivo imaging of dopamine biosensors 45,[59][60][61] . We therefore examined the anatomical structure of the M2 dopaminergic projection to determine if this input was altered in Arc mutant mice.
Mesocortical dopamine neurons have much stronger tyrosine hydroxylase (TH) expression than dopamine transporter (DAT) expression, which is different from mesostriatal dopamine neurons [62][63][64][65] . In addition, TH immunoreactivity in the frontal cortex can label dopaminergic axons originated from the VTA, and ablation of VTA dopaminergic neurons removes this labeling 31,44 .
Accordingly, TH-Cre transgenic lines have been frequently used to label these neurons and study the mesocortical pathway 25,66-69 .
We injected Cre-dependent AAV vectors into the VTA of TH-Cre mice to label dopaminergic axons with a cytoplasmic marker tdTomato, and the dopamine release sites in axonal . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint boutons with a GFP reporter fused to synaptic vesicle protein synaptophysin ( Fig. 1d and e) 45,[70][71][72] . Although the dopaminergic axon length in the M2 frontal cortex (normalized by the number of labeled cells in VTA) was not significantly different between Arc mutant and wildtype animals ( Fig. 1f), we found a significant reduction in the dopaminergic bouton density in this region in Arc mutant mice compared to wildtype animals (p = 0.034, t-test, t(12)=2.393, WT: 100±5%, Arc -/-:84±5%, N=7 for each group; bouton density normalized by axon length ; Fig. 1g). These results suggest that dopaminergic innervations of the M2 frontal cortex are reduced in Arc mutant mice, which agrees with our previous findings of reduced frontal dopamine release and mesofrontal activity in Arc-/-mice 32 . Our new results provide further anatomical evidence for a hypofunctional mesofrontal dopamine circuit in these mice.

Task-coordinated frontal neuronal ensemble activity is disrupted in Arc mutant mice
To determine how M2 neuronal activities during Y-maze performance might be affected by Arc mutation and reduced dopaminergic input, we expressed a genetically encoded calcium indicator GCaMP6 73 in superficial layer (L2/3) M2 neurons and used a head-mounted miniaturized microscope 70,74-76 to image task-related neuronal ensemble activity in adult wild-type and Arc-/-mice (Fig. 2a). The microscope lens was placed above the pial surface rather than inserted into the cortex to avoid damage of M2 neurons, and neuronal activities in superficial cortical layers were imaged (Supplementary Fig. 2a-2c, Supplementary Movie 1). We found that the activity of individual M2 neurons occurred at various positions along the track during Y-maze navigation (Fig. 2b). An increased proportion of neurons showed peak activation when the wildtype animal was near the center of the maze before making an arm entry (Fig. 2c). In contrast, this proportion was significantly reduced in Arc mutant mice compared to wild type animals (p < 0.0001, chi-square test, WT 938 cells from 8 mice, Arc-/-1338 cells from 7 mice). This effect is . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint not due to a general reduction of neural activity in Arc-/-mice, because there is no difference between wild-type and Arc-/-mice in the average activity of neurons throughout the task period ( Supplementary Fig. 2d-f). In addition, there is no correlation between the average activity of neurons with alteration behaviors in Y-maze ( Supplementary Fig. 2j). Thus, these results suggest that the coordinated activation of M2 neurons before making a choice is disrupted in Arc mutant mice.
To further examine how exploratory choices may be encoded in the activities of individual M2 neurons, we compared the neuronal activity patterns along the navigation trajectories leading to new arm visits versus old arm visits. Neurons selective for alternation were identified by differential neural activation between alternating and non-alternating paths (Fig. 2d). This analysis showed that the proportion of alternation-selective neurons increased in the wild type mice as the animal approached the maze center, but this increase was blunted in the Arc mutant animals (p < 0.0001, chi-square test, Fig. 2e). These same mutant animals also showed a specific reduction of alternation choices in the Y-maze (p = 0.047, t-test, t(13)=2.196, WT: 67.8 ± 4.4%, N = 8 mice; Arc-/-: 54.5 ± 4.1%, N = 7 mice, Supplementary Fig. 2g-i), replicating the deficit we observed in separate groups of animals that did not carry the miniaturized microscope (Fig. 1b). Together, these results demonstrate that both task-related frontal cortical activity and memory-guided decision behavior are impaired in Arc mutant mice.

Adolescent dopamine neuron stimulation leads to long-term reversal of mesofrontal circuit deficits
Given the hypo-functioning mesofrontal dopaminergic circuit in Arc mutant mice, we next investigated the possibility of developing neurostimulation strategies to restore normal circuit functions. The dopaminergic innervation in the mesofrontal circuit exhibits a protracted maturation . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint from postnatal day 21 (P21) to P56 30,40,77,78 . P35-42 is in the center of this period and captures the mid-adolescent stage in rodents 79 . We have previously shown that increasing dopamine neuron activity by wheel running or optogenetic stimulation during this period, but not adulthood, can induce formation of mesofrontal dopaminergic boutons and enhance mesofrontal circuit activity in wild-type mice 45 . We therefore chose the P35-P42 adolescent window to stimulate the mesofrontal dopamine circuit and test the long-term effect of this intervention on the frontal circuit and memory-guided decision-making deficits in adult Arc mutant mice.
To stimulate dopamine neuron activity, we expressed chemogenetic activator DREADD-Gq 80 in the VTA dopamine cells using a combination of stereotaxically injected Cre-dependent AAV vectors and a TH-Cre transgenic mouse line 45 (Fig. 3a, Supplementary Fig. 3a). CNO (1mg/kg) was injected systemically to enhance the activity of DREADD-Gq-expressing dopamine neurons. To control for any potential off-target effect of CNO, another group of TH-Cre mice that expressed AAV-mCherry reporter in dopamine neurons also received CNO injection. Previous studies have shown that DREADD-Gq induced neural activation reaches its peak approximately 1 hr after CNO injection and returns to baseline approximately 9 hr after injection 80 . Increased VTA dopamine activity is known to enhance frontal cortical activity, which can be measured with calcium indicator GCaMP6 32,45,81 . We validated the DREADD-Gq induced enhancement of mesofrontal activity by examining M2 cortical activity with GCaMP6 before and after CNO injection in these mice ( Fig. 3a and b, Supplementary Fig. 3b). There was a significant increase in the M2 cortical activity measured 1 hr after the injection of CNO in DREADD-Gq animals, whereas no significant effect occurred in control mCherry animals (DREADD-Gq: 82±17% vs. mCherry Ctrl: 20±14%, p = 0.018, t-test, t(10)=2.814, N=6 for each group; Fig. 3c). In addition, saline injection in DREADD-Gq expressing mice did not alter M2 neural activity, and CNO-. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint induced increase in M2 neural activity was suppressed by D1 antagonist SCH23390 ( Supplementary Fig. 3c). These results confirmed CNO-induced activation of the mesofrontal dopaminergic circuit in DREADD-Gq animals.
After the validation of activity enhancement by chemogenetic stimulation of dopamine neurons, we examined if this treatment would have any long-term effect on the circuit deficits in Arc mutant mice. Our previous work in wild-type adolescent mice showed that a single optogenetic stimulation session or a 2-hr wheel running session is sufficient to induce bouton formation in mesofrontal dopaminergic axons 45 . In this study, we sought to rescue existing structural and functional deficits in the mesofrontal dopaminergic circuits due to genetic mutations. Because previous studies suggested that an optimal level of dopamine is important for normal cognitive function [22][23][24] , we elected to do multiple stimulation sessions to boost the potential rescue effects.
We first tested whether the structural deficits in the mesofrontal dopaminergic circuit would be affected by adolescent dopamine neuron stimulation. DREADD-Gq or mCherry expression was combined with tdTomato and synaptophysin-GFP to label dopaminergic axons and boutons in the Arc mutant animals (Arc-/-;TH-Cre). After three CNO treatments in adolescence (one injection per day for three days in mice 5 weeks of age in their home cages), the mice were kept in their regular home cage until adulthood (8 weeks) for histological assessment (Fig. 3d).
Although the mesofrontal dopamine axon length did not show any difference (Fig. 3e), we found a significant increase in dopaminergic bouton density in DREADD-Gq mice compared to control animals (Ctrl:100±4% vs. Gq:120±6%, p = 0.013, t-test, t(18)=2.763, N=10 for each group; Fig.   3f). These results suggest that adolescent dopamine neuron stimulation in Arc mutant mice led to a long-term enhancement of the connection between dopaminergic axons and M2 frontal cortical neurons, thereby ameliorating the structural deficits in these mice.
. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint We next tested whether adolescent dopamine neuron stimulation would also lead to longterm improvement of the functional deficits in the mesofrontal circuit of Arc mutant mice. Our previous work indicated that Arc mutants have reduced frontal cortical response to VTA stimulation 32 . Using the same assay in adult mice, we found that the cortical calcium activity in response to VTA electrical stimulation was significantly enhanced in DREADD-Gq mice compared to control mCherry mice after adolescence CNO treatment ( Fig. 3g-i). These results suggest that adolescent dopamine neuron stimulation also leads to long-term improvement of the functional deficits in the mesofrontal dopaminergic circuit of Arc mutants.

Adolescent dopamine neuron stimulation leads to restoration of coordinated frontal neuronal activity and cognition in adulthood
To further examine whether the uncoordinated frontal neural activity patterns in Arc mutant mice during the Y-maze task would be renormalized by this adolescent dopamine neuron stimulation strategy, we conducted calcium imaging using the head-mounted miniature microscope in these mice (Fig. 4a). We found that the coordinated activation of neurons near the maze center (Fig. 4b) and the proportion of alternation-selective neurons (Fig. 4c) were both significantly enhanced in Arc mutant mice that received the DREADD-Gq activation compared to the mCherry control group (p < 0.0001, chi-square tests, DREADD-Gq 1008 cells from 7 mice, mCherry 1286 cells from 7 mice). In contrast, the average activity of M2 neurons throughout the task period was not affected by adolescent DREADD-Gq stimulation ( Supplementary Fig. 4a-c).
Strikingly, the DREADD-Gq stimulated animals also showed an enhancement of behavioral alternation (p = 0.010, t-test, t(12)=3.043, Ctrl:56.8±2.8%, Gq:67.6±2.2%, N=7 each group, Fig   4d), reaching a level comparable to that in the wild-type mice (Fig. 1b). Total arm entries were not affected (Fig. 4e), suggesting no alternations in general locomotor activity. These results indicate . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint that adult task-related functional activity in the M2 frontal cortex is restored by adolescent dopamine neuron stimulation in Arc mutant mice.

Efficacy requirements for adolescent dopamine neuron stimulation
To further characterize the experimental conditions that are important for the restoration of memory-guided decision-making behavior in Arc mutant mice, we examined several variables including post-stimulation test interval, stimulation duration, and the age of stimulation. First, we replicated the effects of adolescent dopamine neuron stimulation on Y-maze navigation in adulthood in another cohort of Arc mutant mice (p = 0.023, t-test, t(12)=2.598, Ctrl:59.5±2.4%, Gq:68.5±2.5%, N=7 for each group) (Fig. 5a). Furthermore, when tested only one day after the three-day CNO treatment procedure (one injection per day) in adolescence, Arc mutant mice already showed an increased alternation percentage (p = 0.031, t-test, t(20)=2.322, Ctrl:55.8±2.9%, Gq:64.7±2.5%, N=11 for each group) (Fig. 5b), which is comparable to the effect observed one-month after treatment in adult mice (Fig. 5a). These results suggest that the adolescent neurostimulation effect on cognitive behavioral improvement is both fast acting and long lasting.
Second, we also tested a more intense CNO stimulation procedure involving two injections per day for three weeks (5 days per week) starting in adolescence. However, this strong three-week stimulation did not enhance behavioral alternation and appeared to decrease it even further (Fig.   5c). These results indicate that moderate but not excessive stimulation of dopamine neurons can provide functional improvement of a deficient mesofrontal circuit, consistent with previous studies showing that an optimal level of dopamine is important for normal cognitive function [22][23][24] .
Third, we found that in adult Arc mutant mice with DREADD-Gq expression, three-day CNO injection did not lead to any effects on Y-maze alternation behavior assayed one-month later . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint (Fig. 5d). These results indicate that adolescent, but not adult, intervention is critical for reversing this behavioral dysfunction, in agreement with the elevated adolescent structural and functional plasticity reported for the mesofrontal circuit 45 . In addition, because 3 weeks of adolescent CNO treatment or 3 days of adult CNO treatment in DREADD-Gq mice did not lead to any rescue effects, DREADD-Gq expression alone is unlikely to generate any behavior improvement. Taken together, our findings suggest that a brief stimulation of midbrain dopamine neurons in adolescence has a long-lasting effect to reverse the memory-guided decision-making deficits in Arc mutant mice, while not affecting other aspects of motor behaviors in the Y-maze ( Supplementary Fig. 5).

Specific stimulation of adolescent frontal dopaminergic axons reverses both cognitive and psychomotor deficits
To further evaluate the impact of adolescent dopamine neuron stimulation on another frontal cortex-dependent behavioral deficit in Arc mutant mice, we subjected these mice to an amphetamine-induced hyperactivity test, which is considered an animal model for drug-induced psychomotor symptoms 32,82 . Classical neuropharmacological studies have shown that amphetamine-induced locomotor activity is facilitated by dopaminergic input to the nucleus accumbens but inhibited by dopaminergic input to the frontal cortex [83][84][85] . Consistent with a hypoactive frontal dopamine input, Arc mutant mice showed hyper-reactivity to amphetamine compared to the wild-type mice ( Figure Supplementary Fig. 6a) as reported before 32 .
However, we found that adolescent stimulation of VTA dopamine neurons through DREADD-Gq did not reduce the hyper-reactivity to amphetamine in adult Arc mutant mice ( Supplementary Fig. 6b). Dopamine neurons in the VTA include separate neuronal populations that project to the frontal cortex and the nucleus accumbens, respectively 18,62 . Our results suggest . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint that adolescent stimulation of both populations of VTA neurons in mesofrontal and mesoaccumbens pathways, which have opposing effects on amphetamine-induced locomotor activity, result in no net change in this behavioral phenotype at adulthood. Subsequently, we tested whether targeted stimulation of dopaminergic axons projecting to the frontal cortex would be a better strategy to reinstate memory-guided decision-making in the Y-maze task and prevent amphetamine hyper-reactivity in Arc mutant mice. Although CNO in principle could be injected directly into the frontal cortex to stimulate DREADD-Gq labeled dopaminergic axons, we found in preliminary experiments that repeated injections (three times) in adolescent brain led to tissue deformation and damage. Therefore, we turned to a less invasive optogenetic method to enhance the activity of labeled axons using Stabilized Step Function Opsins neural activity using calcium reporter GCaMP6 before and 30 min after light activation. Similar to the DREADD-Gq mediated activity changes in the mesofrontal circuit, frontal cortical activity was increased after light activation compared to before in SSFO animals, and this increase was significantly higher than the control EGFP animals that were also exposed to the light (p = 0.001, t-test, t(8)=5.135, Ctrl: 7.5±3.1%, SSFO: 46.7±6.9%, N=5 each group, Fig. 6b-c, Supplementary   Fig. 6e). These results indicate that light stimulation of SSFO-labeled frontal dopamine axons can enhance the activity in the mesofrontal circuit.
. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint To determine whether adolescent stimulation of mesofrontal dopamine axons would be sufficient to reinstate memory-guided decision-making in Arc mutant mice, we stimulated SSFOlabeled dopamine axons in the frontal cortex once per day for three days in adolescence (Fig. 6d).
When tested either one day after light stimulation or one month after in adulthood, SSFO-labeled mice showed a significant increase in the Y-maze alternation percentage compared to control EGFP animals (Fig. 6e, 1

Adolescent dopamine neuron stimulation reverses cognitive deficits in DISC1 mutant mice
Finally, we sought to determine if this adolescent neurostimulation strategy would be applicable to another genetic model with a hypoactive mesofrontal circuit. Previous studies showed that knocking-down DISC1 or overexpressing a dominant negative DISC1 reduced mesofrontal dopaminergic innervation, dopamine release and cognitive dysfunction 30,31 . Using a DISC1 mouse model that contains a knocked-in mutation identified from a subset of human patients 35,87 , we first examined whether mesofrontal activity is also impaired in this model by . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint imaging the calcium activity of M2 frontal cortex with two-photon microscopy in response to VTA stimulation (Fig. 7a). Our results showed a reduction of VTA-induced frontal cortical activity in DISC1 mutants compared to wildtype animals (10 pulse F(1,10)=16.5, p=0.002, Two-way ANOVA, N=6 mice per group, Fig. 7b We then tested whether the same adolescent neurostimulation strategy used in the Arc mutant mice would also reverse the cognitive deficits in DISC1 mutants. Remarkably, we found that the alternation percentage in adult DISC1 animals was significantly increased after adolescent neurostimulation (p = 0.012, t-test, t(9)=3.139, Ctrl:60.7±2.4%, N=5, Gq:69.3±1.5% N=6, Fig.   7d), reaching a level similar to the wild-type mice. Other aspects of motor behaviors in the Y-maze were not affected ( Supplementary Fig. 7). Taken together, these results suggest that adolescent dopamine neuron stimulation is effective for long-term cognitive improvement in two different genetic models of mesofrontal hypofunction.

Fast-acting and long-lasting cognitive rescue by adolescent dopamine circuit stimulation
. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. We used both chemogentic (DREADD-Gq) and optogenetic (SSFO) methods to deliver adolescent dopamine circuit stimulation. We did not measure the precise firing patterns of the dopaminergic neurons targeted by SSFO but evaluated the effects of SSFO activation on the frontal cortex. Similar to DREADD-Gq mediated activity changes in the mesofrontal circuit, which was blocked by D1 antagonist, we found increased frontal cortical activity post-light stimulation of frontal dopamine axons in our SSFO treated animals. While quantitatively the firing patterns of DREADD-Gq and SSFO activated dopaminergic neurons likely differ, qualitatively both of these manipulations lead to increased mesofrontal circuit activity and improvements in cognitive . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint behaviors. In our previous work with wild-type adolescent mice, both wheel running and a single 10-min session of phasic optogenetic stimulation of the VTA resulted in dopaminergic bouton outgrowth in the frontal cortex 45 . Taken together, these results suggest that adolescent dopaminergic mesofrontal projections are highly responsive to neural activity changes and a variety of adolescent stimulation paradigms are sufficient to elicit lasting changes in this circuit.
As dopamine's effects often display an inverted-U dose-response curve 12,24 , it will be interesting for future research to compare the effects of specific stimulation methods between wild-type mice and mutant mice with underlying dopamine deficiency. In addition, although we targeted dopamine neurons in our adolescent stimulation, the final behavioral outcome likely includes contributions from co-released neurotransmitters such as glutamate and non-dopaminergic neurons via network effects 69,93 , which will be interesting directions for future research.

Cellular alterations in the mesofrontal circuit underlying cognitive dysfunction and rescue
Our examination across different mechanistic levels suggests a coherent picture in which increased dopamine neuron activity in adolescence leads to enhanced frontal dopaminergic innervation and cortical response to dopamine. Although many of dopamine boutons are not associated with defined postsynaptic structures, these axonal boutons and the active zones they contain are the major release sites for dopamine [94][95][96][97] . Past studies have established a consistent association between increased dopaminergic innervation in the frontal cortex and an increase in dopamine levels 30,77 . Our previous work also found that increasing dopaminergic boutons through adolescent VTA stimulation led to prolonged frontal local field potential responses with highfrequency oscillations 45 , which is characteristic of increased dopaminergic signaling 69,98-100 .
Importantly, in our quantification of the structural changes in this study, we evaluated boutons which were labeled with synaptophysin, a molecular marker indicating the presence of synaptic . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint underlying adolescent dopamine stimulation induced changes, particularly in the GABAergic inhibitory neurons, will be an exciting direction for future research.

Reversal of cognitive deficits in independent genetic models
Our studies have shown that the mesofrontal dopamine circuit is a common target disrupted by mutations in Arc and DISC1. The initial motivation of this study was to test if adolescent dopamine stimulation can rescue the deficits in the mesofrontal dopaminergic circuit and cognitive function of Arc-/-mice, which were identified in our previous studies 32 . We first conducted multiple levels of analyses including viral tracing, in vivo calcium imaging, and behavioral tests to establish the coherent impacts of adolescent dopamine neuron stimulation on circuits and behaviors. We then examined a range of stimulation protocols to assess the efficacy requirements for cognitive improvement, which is our primary goal. Finally, we included DISC1 mice in our study to test if adolescent dopamine stimulation can also reverse the cognitive deficit in another genetic model for mesofrontal dopamine deficiency. By demonstrating a similar cognitive recuse effect of adolescent VTA stimulation in an independent mouse model, this study provides a foundation for future research to compare the detailed cellular mechanisms that underlie the functional rescue in different genetic models.
Arc and DISC1 have different protein interaction partners and function in distinct molecular pathways. Arc is best understood for its role in regulating the trafficking of excitatory neurotransmitter receptors at synapses, whereas DISC1 has been shown to act as a scaffold protein to interact with multiple cytoskeletal proteins and synaptic molecules [111][112][113][114] . Dopamine-related deficits have been reported in multiple Arc and DISC1 mutant lines or direct knockdown of these molecules [30][31][32][115][116][117] , but the exact molecular mechanisms underlying these deficits and the varying severity in different models remain to be elucidated in future studies. Considering the . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint widely reported roles of Arc and DISC1 in regulating activity-dependent synaptic plasticity 118,119 , mutations in these genes may compromise activity-dependent maturation of the mesofrontal dopaminergic circuit. In the two mouse lines we tested, both Arc and DISC1 mutations lead to a hypoactive mesofrontal circuit and deficits in memory-guided decision-making behaviors. Our study demonstrates that the cognitive behavioral phenotypes arising from distinct genetic origins can be effectively rescued by the same neurostimulation strategy targeting a convergent mesofrontal circuit phenotype during a critical adolescent window.

Reversal of both cognitive and psychomotor deficits by targeting frontal dopamine projections
Our work reveals a specific circuit target for long-lasting restoration of cognitive control functions. Dopamine neurons projecting to the frontal cortex are located in the VTA but are distinct from those projecting to the nucleus accumbens 18,62 . Our initial chemogenetic neuromodulation strategies targeted most of the dopamine neurons in the VTA. While changes in the mesofrontal dopamine circuit were clearly induced, we cannot rule out other potential changes in the brain that might be also induced by such a targeting strategy and result in the lack of net effect related to amphetamine reactivity. The more refined optogenetic (SSFO) neurostimulation method allowed us to specifically target the dopaminergic axons projecting to the frontal cortex. Enhancing their activity transiently in adolescence is sufficient to not only restore memory-guided decision making in the Y-maze task but also prevent hyper-reactivity to amphetamine. Thus, the mesofrontal dopaminergic circuit may provide an important therapeutic target to restore both cognitive control functions and prevent psychomotor symptoms.
We did not examine the degree of bouton growth in the SSFO cohort, which is a limitation of this study. Accurate quantification of dopamine boutons requires the co-injection of another . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint AAV vector encoding Synaptophysin-GFP to label the boutons. Because we used light to directly stimulate SSFO-labeled dopaminergic axons in the frontal cortex, we were concerned that coinjecting another AAV vector may dilute SSFO-labeling of axons and reduce the efficacy of optogenetic stimulation. Given the behavioral benefits we observed, we would expect an increase in bouton density after optogenetic stimulation. A systematic optimization of viral co-labeling and optogenetic stimulation protocols will facilitate examination of the impact of SSFO stimulation at the structural level in future studies. This study focused on the M2 region of the frontal cortex because it is functionally required for memory-guided Y-maze navigation, generates behavioral choice-related neural signals during spatial navigation, and is optically most accessible. The medial prefrontal regions (anterior cingulate, prelimbic and infralimbic) ventral to M2 also receive dense dopaminergic innervation and can act in concert with M2 in decision making 56,57,120 . As dopaminergic innervations to the frontal cortical regions progress in a ventral-to-dorsal direction during development 40,78 , how the changes induced by adolescent dopamine stimulation may proceed spatial-temporally across different frontal subregions requires more extensive investigation in the future.
In conclusion, our results suggest that adolescent frontal dopaminergic projections may provide an effective target to achieve fast-acting and enduring improvement of cognitive function while avoiding psychotic exacerbation, which has been a long-standing challenge for neuroscience and psychiatric research 2,6,7,121 . Developmentally guided and circuit-based intervention strategies that use clinical brain stimulation, local pharmacological application, or behavioral training methods 36,38,105,122 to engage the adolescent mesofrontal dopamine circuit may offer new routes to treat cognitive and behavior control disorders.
. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint

Experimental Model and Subject Details
Arc-/- 49

Spontaneous alternation in the Y-maze
A three-arm plexiglass Y-maze (45cm length X 8cm width X 12cm height for each arm) was used to test spontaneous alternation. Animals were brought into the testing room at least 30min prior to the start of the session to acclimate to the room. Room lights were dimmed to ~10-15 lux.
Animals were placed in the start arm facing away from the center. Recording of the session was started when the animal started to move toward the center and the animal was allowed to freely explore the y-maze for 8 minutes. The Y-maze was cleaned with 70% ethanol between animals.
Videos of the sessions were analyzed blindly offline. Arms were identified as A, B, C.
Starting from the start arm, entry into each arm was recorded as a sequence of arm letters. Entry . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint was recorded if all four paws of the animal entered the arm. The number of alternating entries (Triplet sequences with non-repeating letters, e.g. ABC) and total entries (total number of letters) were counted. Alternation percentage was calculated as: (total alternating entries/(total entries-2)) X100.

Amphetamine induced locomotion
An animal was placed in an open field arena (50 cm x 50 cm x 25 cm) and monitored by video camera for 10 minutes. After that, d-amphetamine (1.5 mg/kg) was injected (i.p.), and the animal was monitored by video camera for another 60 min in the arena. Locomotion was automatically tracked using the animal's body position by the Limelight video tracking system (Actimetrics-Coulbourn Instruments).

Calcium imaging with head-mounted miniature microscope
WT and Arc-/-animals were prepared for surgery following previous published procedures 75,126,127 . Mice were anesthetized with Avertin (1.5% solution given at 0.01 ml/g, i.p.) and treated with dexamethasone (0.2 mg/kg, s.c.) and carprofen (5 mg/kg, s.c.) to prevent brain swelling and inflammation. A piece of skull (3.5 mm in diameter) in the frontal cortex was removed after highspeed dental drilling. AAV2/9 -Syn-GCaMP6s (3-5x10 12 copies/ml, 0.6 μl per animal) was infused into M2 frontal cortex (Bregma, AP1.7, ML0.8) from the pial surface using a micro-syringe pump 75 . A 3-mm coverslip was used to seal the cranial window and the exposed scalp was sutured after cranial window surgery. 7-10 days later, the baseplate of a miniaturized integrated fluorescent microscope (Inscopix) was fixed on top of the coverslip. Animals were habituated to the attachment of the microscope (20 minutes per day for 4 days), then imaged during the spontaneous Y maze alternation task.
. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint Calcium imaging was performed in freely moving mice using the head-attached microscope (LED power: 0.6 -1.0 mW; camera resolution: 1440 x1080 pixels). Images were acquired at 30 Hz using nVista 2.0 (Inscopix). At the beginning of each imaging session, the protective cap of the previously implanted baseplate was removed, and the microscope was attached. The imaging field of view was 900 × 600 μm 2 at 0.65 μm/pixel resolution and the imaging depth was selected by adjusting the focus of the microscope until clear neuronal signals were observed in online ΔF/F calcium video. The focal plane was 150-250 μm below the lens. Mouse behavior was recorded with a video camera (Limelight), which was synchronized with calcium imaging using the trigger-out signal from nVista.
Calcium imaging videos were analyzed by using Mosaic software (Inscopix) and customwritten scripts in Matlab following published algorithms 128,129 . Raw videos were first down- was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint neurons that showed maximal activity at each binned location was then calculated. To measure the alternation selectivity of neurons, neuronal activity difference between alternating and nonalternating trials were calculated at each track position. If the difference at a particular position is higher than 2 standard deviations of the differences at all other positions, the activity was determined as alternation-selective at the designated position.
Coronal 100 µm thick sections in the frontal cortical and midbrain regions were prepared with a . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint sliding microtome. 3 sections in the frontal cortical region (AP 1.6, 1.8, and 2.0; 25x lens, 10 µm Z-stack, 10 stacks per section) and 5 sections in the midbrain region (AP -2.9, -3.1, -3.3, -3.5 and -3.7; 10x lens, single-frame images) were imaged in both the green and red channels using confocal microscopy (Olympus FV1000). For the frontal cortex, each image stack was maximum projected, and the 10 stacks were stitched together for each section. Animals that did not show VTA labeling were excluded from further analysis.
Image analysis was carried out using custom Matlab scripts. For boutons and axons, an ROI for the M2 region was drawn in each section using the mouse brain atlas (Paxinos) as reference, and boutons and axons were identified within this region. SypGFP labeled green channel images were used for bouton quantification. Boutons were detected automatically using a Laplacian filter and thresholded at 5 standard deviations above background. tdTomato labeled red channel images were used for the axon quantification. Axons were detected automatically using a Hessian filter, thresholded at 2 standard deviations above background, and skeletonized. For the midbrain sections, cells were detected automatically using a Laplacian filter and thresholded at 2 standard deviations above background. For each animal, the bouton density was normalized by the total axon length, and the total axon length was normalized by the total number of tdTomato labeled midbrain dopamine cells.
After ~2 weeks, a cranial window was opened above the AAV-GCaMP6 injected region in the frontal cortex (from Bregma: AP 1.0-3.0 mm, ML 0.3-1.3 mm, covering the M2 region) in animals anesthetized with isofluorane (~1.5%). The cranial window was filled with silicone gel, covered with a glass cover slip, and sealed with dental cement. A head plate was glued on the skull for fixation during imaging. The animals were then taken off the anesthesia and allowed to recover for ~1hr before imaging. A two-photon microscope (FV1000, Olympus) was used to image the brain under the cranial window (excitation laser: 900 nm) using a 20x water immersion lens (NA 0.95) in the head fixed awake animal. Animals were imaged before and 1hr after CNO (1mg/kg, ip) injection. After imaging, animals were perfused, and DREADD-Gq expression was confirmed in the midbrain regions. Animals that did not show VTA labeling were excluded from further analysis.
Images were analyzed using NIH ImageJ. Two 2-min movies of spontaneous activity before and after CNO were analyzed. The mean pixel intensity in each image frame of the movie was calculated as Ft. Baseline fluorescence (F0) was defined as the average of the fluorescent signals (Ft) in the time series. Changes in calcium signals (ΔF/F) are calculated as (Ft-F0)/F0. The standard deviation of the (ΔF/F) was used as a quantitative measure of overall cortical activity.

CNO stimulation of DREADD-Gq in midbrain dopamine neurons and behavior testing
Animals were prepared for surgery as above. 0.7 µl of pAAV8-hSyn-DIO-hM3D(Gq)-mCherry or pAAV8-hSyn-DIO-mCherry was bilaterally injected into the midbrain region (from bregma: AP -3.2, ML0.5, DV4.4mm) of Arc-/-;TH-Cre or DISC1+/-;TH-Cre animals within postnatal days P21-P25. CNO (1mg/kg, ip) was injected 1 time per day for three days into the . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint animals within postnatal days P35-P42. For one-day-after tests, animals were tested on the Y-maze 1 day after the last injection day. For adulthood tests, animals were tested at 2~3-month age on the Y-maze. Some of the adult animals were also tested for amphetamine induced locomotion as described above. After behavior testing, animals were perfused, and DREADD-Gq expression was confirmed in the ventral midbrain region. Animals that did not show VTA labeling were excluded from further analysis.

CNO stimulation of DREADD-Gq in midbrain dopamine neurons and in vivo imaging of cortical activity
Animals were prepared for surgery as described above. 0.7 µl of pAAV8-hSyn-DIO-hM3D(Gq)-mCherry or pAAV8-hSyn-DIO-mCherry was bilaterally injected into the midbrain region (from bregma: AP -3.2, ML0.5, DV4.4mm) of Arc-/-;TH-Cre animals within postnatal days P21-P25. CNO (1mg/kg, ip) was injected 1 time daily for three days into the animals for activation within postnatal days P35-P42. At adulthood, GCaMP6 labeling, cranial window opening, and imaging during Y-maze were carried out as described above. After an interval of at least 1 day after miniscope imaging, animals were used for VTA electrical stimulation coupled with in vivo two-photon imaging. A bipolar stimulation electrode was placed into the VTA (from bregma: AP -3.2, ML 0.5, and DV 4.5mm) and glued in place in animals anesthetized with isofluorane (~1.5%).
A head plate was also glued on to the skull. The animals were then taken off the anesthesia and allowed to recover for ~1hr before imaging. Time series images lasting ~40s (115 frames at 0.351 s/frame) were taken for each stimulus train, with the VTA stimulus delivered at 20s after the start of imaging. Image analysis was carried out as described above. Baseline fluorescence ( Animals were allowed to wake and recover for at least 2 hrs. Animals were then head fixed and an . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint optical fiber (200 μm in diameter, Thor Labs) connected to a 473 nm solid-state laser diode (CrystaLaser) with ~10 mW output from the fiber was used to deliver 2 s light pulses to the frontal cortex. Three spots separated by around 200 µm anterior posterior in the center of the window were activated in each hemisphere. The light activation was repeated for two more days. For oneday-after tests, animals were tested in the Y-maze 1 day after the last injection day. For adulthood tests, animals of 2~3-month age were first tested in the Y-maze, then tested for amphetamine induced locomotion as described above. After behavior testing, animals were perfused, and SSFO expression was confirmed in the midbrain regions. Animals that did not show VTA labeling were excluded from further analysis.

Quantification and statistical analysis
Statistical analyses were performed in Prism 9 or Matlab. No statistical methods were used to predetermine sample size. Sample sizes were chosen based on previous studies using similar techniques to determine biological effects 32,45,70,76 . Statistical differences between the means of two groups were evaluated with two-tailed t-test and normality was confirmed with Shapiro-Wilk test. Statistical differences between the means of multiple groups were determined using ANOVA.
Statistical differences between two proportions were evaluated with chi-squared test.
. CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint . CC-BY 4.0 International license available under a was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprint (which this version posted July 12, 2023. ; https://doi.org/10.1101/2023.02.03.526987 doi: bioRxiv preprint    Cortical activity is summarized by the standard deviation (SD) of the spontaneous activity traces.