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News Coverage on Nature Comms Article

Christopher Bergland, How Does Your Brain Learn Through Trial and Error? Problem-solving and critical thinking can rewire the orbitofrontal cortex (OFC), Psychology Today, Mar. 6, 2016.

In a groundbreaking discovery, neurocientists at the University of California, Berkeley, have captured brain images of active learning in real-time by photographing the brains of mice as they learn how-to problem solve through trial and error.

[…]

Yasmin Anwar, Scientists tap the smarts of mice, capture problem-solving in action, UC Berkeley Press Release, March 7, 2016.

 

News Coverage on Nature Comms Article2016-03-07T10:54:05+00:00

Long-range orbitofrontal and amygdala axons show divergent patterns of maturation in the frontal cortex across adolescence

The adolescent transition from juvenile to adult is marked by anatomical and functional remodeling of brain networks. Currently, the cellular and synaptic level changes underlying the adolescent transition are only coarsely understood. Here, we use two-photon imaging to make time-lapse observations of long-range axons that innervate the frontal cortex in the living brain. We labeled cells in the orbitofrontal cortex (OFC) and basolateral amygdala (BLA) and imaged their axonal afferents to the dorsomedial prefrontal cortex (dmPFC). We also imaged the apical dendrites of dmPFC pyramidal neurons. Images were taken daily in separate cohorts of juvenile (P24–P28) and young adult mice (P64–P68), ages where we have previously discovered differences in dmPFC dependent decision-making. Dendritic spines were pruned across this peri-adolescent period, while BLA and OFC afferents followed alternate developmental trajectories. OFC boutons showed no decrease in density, but did show a decrease in daily bouton gain and loss with age. BLA axons showed an increase in both bouton density and daily bouton gain at the later age, suggesting a delayed window of enhanced plasticity. Our findings reveal projection specific maturation of synaptic structures within a single frontal region and suggest that stabilization is a more general characteristic of maturation than pruning.

Johnson CM, Loucks A, Peckler H, Thomas AW, Janak P, Wilbrecht L. (in press) Long-range orbitofrontal and amygdala axons show divergent patterns of maturation in the frontal cortex across adolescence. Developmental Cognitive Neuroscience (2016)

Long-range orbitofrontal and amygdala axons show divergent patterns of maturation in the frontal cortex across adolescence2016-02-03T06:01:29+00:00

Rule learning enhances structural plasticity of long range axons in frontal cortex

Rules encompass cue-action-outcome associations used to guide decisions and strategies in a specific context. Subregions of the frontal cortex including the orbitofrontal cortex (OFC) and dorsomedial prefrontal cortex (dmPFC) are implicated in rule learning, although changes in structural connectivity underlying rule learning are poorly understood. We imaged OFC axonal projections to dmPFC during training in a multiple choice foraging task and used a reinforcement learning model to quantify explore–exploit strategy use and prediction error magnitude. Here we show that rule training, but not experience of reward alone, enhances OFC bouton plasticity. Baseline bouton density and gains during training correlate with rule exploitation, while bouton loss correlates with exploration and scales with the magnitude of experienced prediction errors. We conclude that rule learning sculpts frontal cortex interconnectivity and adjusts a thermostat for the explore–exploit balance.

Johnson C, Peckler H,Tai LH, Wilbrecht L., Rule learning enhances structural plasticity of long range axons in frontal cortex. Nature Communications (2016)

Rule learning enhances structural plasticity of long range axons in frontal cortex

Rule learning enhances structural plasticity of long range axons in frontal cortex2016-02-03T05:59:56+00:00

Cell-Type-Specific Control of Brainstem Locomotor Circuits by Basal Ganglia

The basal ganglia (BG) are critical for adaptive motor control, but the circuit principles underlying their pathway-specific modulation of target regions are not well understood. Here, we dissect the mechanisms underlying BG direct and indirect pathway-mediated control of the mesencephalic locomotor region (MLR), a brainstem target of BG that is critical for locomotion. We optogenetically dissect the locomotor function of the three neurochemically distinct cell types within the MLR: glutamatergic, GABAergic, and cholinergic neurons. We find that the glutamatergic subpopulation encodes locomotor state and speed, is necessary and sufficient for locomotion, and is selectively innervated by BG. We further show activation and suppression, respectively, of MLR glutamatergic neurons by direct and indirect pathways, which is required for bidirectional control of locomotion by BG circuits. These findings provide a fundamental understanding of how BG can initiate or suppress a motor program through cell-type-specific regulation of neurons linked to specific actions.

Thomas K. Roseberry, A. Moses Lee, Arnaud L. Lalive, Linda Wilbrecht, Antonello Bonci, Anatol C. Kreitzer, Cell-Type-Specific Control of Brainstem Locomotor Circuits by Basal Ganglia, 64(3) Cell (Jan. 2016), http://www.cell.com/cell/abstract/S0092-8674%2815%2901701-8

Cell-Type-Specific Control of Brainstem Locomotor Circuits by Basal Ganglia2016-01-30T02:04:46+00:00

Early maternal separation impacts cognitive flexibility at the age of first independence in mice

Early life adversity is associated with increased risk for mental and physical health problems, including substance abuse. Changes in neural development caused by early life insults could cause or complicate these conditions. Maternal separation (MS) is a model of early adversity for rodents. Clear effects of MS have been shown on behavioral flexibility in rats, but studies of effects of MS on cognition in mice have been mixed. We hypothesized that previous studies focused on adult mice may have overlooked a developmental transition point when juvenile mice exhibit greater flexibility in reversal learning. Here, using a 4-choice reversal learning task we find that early MS leads to decreased flexibility in post-weaning juvenile mice, but no significant effects in adults. In a further study of voluntary ethanol consumption, we found that adult mice that had experienced MS showed greater cumulative 20% ethanol consumption in an intermittent access paradigm compared to controls. Our data confirm that the MS paradigm can reduce cognitive flexibility in mice and may enhance risk for substance abuse. We discuss possible interpretations of these data as stress-related impairment or adaptive earlier maturation in response to an adverse environment.

A. Wren Thomas, Natalia Caporale, Claudia Wu, Linda Wilbrecht, Early maternal separation impacts cognitive flexibility at the age of first independence in mice, Developmental Cognitive Neuroscience, Available online 19 October 2015, ISSN 1878-9293, http://dx.doi.org/10.1016/j.dcn.2015.09.005.
(http://www.sciencedirect.com/science/article/pii/S187892931530030X)
Keywords: Development; Reversal; Prefrontal; Perseveration; Stress; Neglect

Early maternal separation impacts cognitive flexibility at the age of first independence in mice2015-11-01T15:57:07+00:00

News Coverage

The Wilbrecht Lab’s recent paper appearing in Neuropharmacology, Brief cognitive training interventions in young adulthood promote long-term resilience to drug-seeking behavior, has attracted some news attention:

Intellectual pursuits may buffer the brain against addiction

Mouse on Sudoku puzzle

Challenging the idea that addiction is hardwired in the brain, a new UC Berkeley study of mice suggests that even a short time spent in a stimulating learning environment can rewire the brain’s reward system and buffer it against drug dependence.

Scientists tracked cocaine cravings in more than 70 adult male mice and found that those rodents whose daily drill included exploration, learning and finding hidden tasty morsels were less likely than their enrichment-deprived counterparts to seek solace in a chamber where they had been given cocaine.

“We have compelling behavioral evidence that self-directed exploration and learning altered their reward systems so that when cocaine was experienced it made less of an impact on their brain,” said Linda Wilbrecht, assistant professor of psychology and neuroscience at UC Berkeley and senior author of the paper just published in the journal, Neuropharmacology.

By contrast, mice who were not intellectually challenged and/or whose activities and diets were restricted, were eager to return to the quarters where they had been injected with cocaine for weeks on end.

“We know that mice living in deprived conditions show higher levels of drug-seeking behavior than those living in stimulating environments, and we sought to develop a brief intervention that would promote resilience in the deprived animals,” said study lead author Josiah Boivin, a Ph.D. student in neuroscience at UC San Francisco who conducted the research at UC Berkeley as part of his thesis work.

Drug abuse and addiction rank among the world’s more costly, destructive and seemingly insurmountable problems. Previous studies have found that poverty, trauma, mental illness and other environmental and physiological stressors can alter the brain’s reward circuitry and make us more susceptible to substance abuse.

The good news about this latest study is that it offers scalable interventions against drug-seeking behaviors, albeit through evidence based on animal behavior.

“Our data are exciting because they suggest that positive learning experiences, through education or play in a structured environment, could sculpt and develop brain circuits to build resilience in at-risk individuals, and that even brief cognitive interventions may be somewhat protective and last a relatively long time,” Wilbrecht said.

Intellectually challenged mice vs. deprived mice

Researchers compared the lure of drugs, specifically cocaine, in three sets of mice: The test or “trained” mice were put through a nine-day cognitive training program based on exploration, incentives and rewards while their “yoked-to-trained” counterparts received rewards but no challenges. The “standard-housed” mice stayed in their home cages with restricted diets and activities.

For a few hours each day, the trained mice and yoked-to-trained mice were set loose in adjacent chambers. The trained mice were free to explore and engage in enrichment activities, which included digging up Honey Nut Cheerios in a pot of scented wood shavings. The exercise kept them on their toes because the rules for how to find the treats would change on a regular basis.

Meanwhile, their yoked-to-trained counterparts received a Honey Nut Cheerio each time their trained partner hit the jackpot, but did not have to work for it. As for the standard-housed mice, they remained in their cages without enrichment opportunities or Honey Nut Cheerios. After the cognitive training phase of the experiment, all three sets of mice remained in their cages for a month.

Cocaine conditioning tests desire for drugs

Next, the mice were set loose, one by one, to explore two adjoining chambers in a plexiglass box, which differed from one another in smell, texture and pattern. The researchers recorded which chamber each mouse preferred and then set about changing their preference by giving them cocaine in the chamber that they had repeatedly not favored.

For the drug seeking test, the mice received mock injections, and were freed to explore both chambers for 20 minutes, using the open doorway to scamper back and forth. At first, all the mice overwhelmingly returned to the chamber where they had presumably enjoyed the cocaine. But in subsequent weekly drug seeking tests, the mice who had received cognitive training showed less preference for the chamber where they had been high on cocaine. And that pattern continued.

“Overall, the data suggest that deprivation may confer vulnerability to drug seeking behavior and that brief interventions may promote long-term resilience,” Wilbrecht said.

Denise Piscopo, an assistant professor at the University of Oregon and former member of Wilbrecht’s lab, is the third co-author on the paper.

News Coverage2015-07-25T18:28:04+00:00

The BDNF Val68 to Met Polymorphism Increases Compulsive Alcohol Drinking In Mice Which Is Reversed By TrkB Activation

Background

The Val66 to Met polymorphism within the brain-derived neurotrophic factor (BDNF) sequence reduces activity-dependent BDNF release, and is associated with psychiatric disorders in humans. Alcoholism is one of the most prevalent psychiatric diseases. Here, we tested the hypothesis that this polymorphism increases the severity of alcohol abuse disorders.

Methods

We generated transgenic mice carrying the mouse homolog of the human Met66BDNF allele (Met68BDNF), and used alcohol-drinking paradigms in combination with viral-mediated gene delivery and pharmacology.

Results

We found that Met68BDNF mice consumed excessive amounts of alcohol and continued to drink despite negative consequences, a hallmark of addiction. Importantly, compulsive alcohol intake was reversed by overexpression of the wild-type Val68BDNF allele in the ventromedial prefrontal cortex of the Met68BDNF mice, or by systemic administration of the TrkB agonist, LM22A-4.

Conclusions

Our findings suggest that carrying the Met66BDNF allele increases the risk of developing uncontrolled and excessive alcohol drinking that can be reversed by directly activating the BDNF receptor, TrkB. Importantly, this work identifies a potential therapeutic strategy for the treatment of compulsive alcohol drinking in humans carrying the Met66BDNF allele.

Vincent Warnault, Emmanuel Darcq, Nadege Morisot, Khanhky Phamluong, Linda Wilbrecht, Stephen M. Massa, Frank M. Longo, and Dorit Ron, The BDNF Val68 to Met Polymorphism Increases Compulsive Alcohol Drinking In Mice Which Is Reversed By TrkB Activation. Biological Psychiatry

The BDNF Val68 to Met Polymorphism Increases Compulsive Alcohol Drinking In Mice Which Is Reversed By TrkB Activation2015-05-28T06:39:54+00:00

Brief cognitive training interventions in young adulthood promote long-term resilience to drug-seeking behavior

Environmental stress and deprivation increase vulnerability to substance use disorders in humans and promote drug-seeking behavior in animal models. In contrast, experiences of mastery and stability may shape neural circuitry in ways that build resilience to future challenges. Cognitive training offers a potential intervention for reducing vulnerability in the face of environmental stress or deprivation. Here, we test the hypothesis that brief cognitive training can promote long-term resilience to one measure of drug-seeking behavior, cocaine conditioned place preference (CPP), in mice. In young adulthood, mice underwent cognitive training, received rewards while exploring a training arena (i.e. yoked control), or remained in their home cages. Beginning 4 weeks after cessation of training, we conditioned mice in a CPP paradigm and then tested them weekly for CPP maintenance or daily for CPP extinction. We found that a brief 9-day cognitive training protocol reduced maintenance of cocaine CPP when compared to standard housed and yoked conditions. This beneficial effect persisted long after cessation of the training, as mice remained in their home cages for 4 weeks between training and cocaine exposure. When mice were tested for CPP on a daily extinction schedule, we found that all trained and yoked groups that left their home cages to receive rewards in a training arena showed significant extinction of CPP, while mice kept in standard housing for the same period did not extinguish CPP. These data suggest that in early adulthood, deprivation may confer vulnerability to drug-seeking behavior and that brief interventions may promote long-term resilience.

Josiah Boivin, Denise Piscopo, Linda Wilbrecht, Brief cognitive training interventions in young adulthood promote long-term resilience to drug-seeking behavior. Neuropharmacology

Brief cognitive training interventions in young adulthood promote long-term resilience to drug-seeking behavior2015-05-28T06:34:03+00:00

Adolescent maturation of inhibitory inputs onto cingulate cortex neurons is cell-type specific and TrkB dependent

The maturation of inhibitory circuits during adolescence may be tied to the onset of mental health disorders such as schizophrenia. Neurotrophin signaling likely plays a critical role in supporting inhibitory circuit development and is also implicated in psychiatric disease. Within the neocortex, subcircuits may mature at different times and show differential sensitivity to neurotrophin signaling. We measured miniature inhibitory and excitatory postsynaptic currents (mIPSCs and mEPSCs) in Layer 5 cell-types in the mouse anterior cingulate (Cg) across the periadolescent period. We differentiated cell-types mainly by Thy1 YFP transgene expression and also retrobead injection labeling in the contralateral Cg and ipsilateral pons. We found that YFP− neurons and commissural projecting neurons had lower frequency of mIPSCs than neighboring YFP+ neurons or pons projecting neurons in juvenile mice (P21–25). YFP− neurons and to a lesser extent commissural projecting neurons also showed a significant increase in mIPSC amplitude during the periadolescent period (P21–25 vs. P40–50), which was not seen in YFP+ neurons or pons projecting neurons. Systemic disruption of tyrosine kinase receptor B (TrkB) signaling during P23–50 in TrkBF616A mice blocked developmental changes in mIPSC amplitude, without affecting miniature excitatory post synaptic currents (mEPSCs). Our data suggest that the maturation of inhibitory inputs onto Layer 5 pyramidal neurons is cell-type specific. These data may inform our understanding of adolescent brain development across species and aid in identifying candidate subcircuits that may show greater vulnerability in mental illness.

Vandenberg A, Piekarski DJ, Caporale N, Munoz-Cuevas FJ and Wilbrecht L (2015) Adolescent maturation of inhibitory inputs onto cingulate cortex neurons is cell-type specific and TrkB dependent. Front. Neural Circuits 9:5. doi: 10.3389/fncir.2015.00005

Adolescent maturation of inhibitory inputs onto cingulate cortex neurons is cell-type specific and TrkB dependent2015-02-17T12:10:30+00:00

Review: Between the Primate and “Reptilian” Brain: Rodent Models Demonstrate the Role of the Corticostriatal Circuits in Decision Making

Decision making can be defined as the flexible integration and transformation of information from the external world into action. Recently, the development of novel genetic tools and new behavioral paradigms has made it attractive to study behavior of all kinds in rodents. By some perspectives, rodents are not an acceptable model for the study of decision making due to their simpler behavior often attributed to their less extensive cortical development when compared to non-human primates. We argue that decision making can be approached with a common framework across species. We review insights from comparative anatomy that suggest the expansion of cortical-striatal connectivity is a key development in evolutionary increases in behavioral flexibility. We briefly review studies that establish a role for corticostriatal circuits in integrative decision making. Finally, we provide an overview of a few recent, highly complementary rodent decision making studies using genetic tools, revealing with new cellular and tempo- ral resolution how, when and where information can be integrated and compared in striatal circuits to influence choice.

Lee AM et al. Between the primate and ‘reptilian’ brain: Rodent models demonstrate the role of corticostriatal circuits in decision making. Neuroscience (2015), http://dx.doi.org/10.1016/j.neuroscience.2014.12.042

 

Review: Between the Primate and “Reptilian” Brain: Rodent Models Demonstrate the Role of the Corticostriatal Circuits in Decision Making2015-01-31T21:27:19+00:00