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1.
Neurobiol Learn Mem ; : 107951, 2024 Jun 04.
Article in English | MEDLINE | ID: mdl-38844099

ABSTRACT

We have developed a behavioral paradigm to study volitional olfactory investigation in mice over several months. We placed odor ports in the wall of a standard cage that administer a neutral odorant stimulus when a mouse pokes its nose inside. Even though animals were fed and watered ad libitum, and sampling from the port elicited no outcome other than the delivery of an odor, mice readily sampled these stimuli hundreds of times per day. This self-paced olfactory investigation persisted for weeks with only modest habituation following the first day of exposure to a given set of odorants. If an unexpected odorant stimulus was administered at the port, the sampling rate increased transiently (in the first 20 min) by an order of magnitude and remained higher than baseline throughout the subsequent day, indicating learned implicit knowledge. Thus, this system may be used to study naturalistic olfactory learning over extended time scales outside of conventional task structures.

2.
bioRxiv ; 2023 Sep 23.
Article in English | MEDLINE | ID: mdl-37790470

ABSTRACT

Sensory stimuli associated with aversive outcomes can cause multiple behavioral responses related to an animal's evolving emotional state. We employed chemogenetic inactivation and two-photon imaging to reveal how the basolateral amygdala (BLA) mediates these state changes. Mice were presented stimuli in a virtual burrow, causing two responses reflecting fear and flight to safety: tremble and ingress into the burrow. Inactivation eliminated differential tremble and ingress to aversive and neutral stimuli without eliminating responses themselves. Multiple variables, including stimulus valence and identity, and being in the tremble or ingressed state, typically modulated each neuron's activity (mixed-selectivity). BLA neural ensembles represented these variables even after neurons with apparent specialized selectivity were eliminated from analyses. Thus, implementing different readouts of BLA ensembles comprised of mixed-selectivity neurons can identify distinct emotional states defined by responses, like tremble for fear and ingress for safety. This mechanism relies on BLA's representational geometry, not its circuit specialization.

3.
Nature ; 594(7864): 541-546, 2021 06.
Article in English | MEDLINE | ID: mdl-34108681

ABSTRACT

Perceptual constancy requires the brain to maintain a stable representation of sensory input. In the olfactory system, activity in primary olfactory cortex (piriform cortex) is thought to determine odour identity1-5. Here we present the results of electrophysiological recordings of single units maintained over weeks to examine the stability of odour-evoked responses in mouse piriform cortex. Although activity in piriform cortex could be used to discriminate between odorants at any moment in time, odour-evoked responses drifted over periods of days to weeks. The performance of a linear classifier trained on the first recording day approached chance levels after 32 days. Fear conditioning did not stabilize odour-evoked responses. Daily exposure to the same odorant slowed the rate of drift, but when exposure was halted the rate increased again. This demonstration of continuous drift poses the question of the role of piriform cortex in odour perception. This instability might reflect the unstructured connectivity of piriform cortex6-12, and may be a property of other unstructured cortices.


Subject(s)
Olfactory Cortex/physiology , Olfactory Pathways , Olfactory Perception , Animals , Conditioning, Psychological , Fear , Male , Mice , Mice, Inbred C57BL , Neurons/physiology , Odorants
4.
Nature ; 509(7498): 43-8, 2014 May 01.
Article in English | MEDLINE | ID: mdl-24784215

ABSTRACT

The precision of skilled movement depends on sensory feedback and its refinement by local inhibitory microcircuits. One specialized set of spinal GABAergic interneurons forms axo-axonic contacts with the central terminals of sensory afferents, exerting presynaptic inhibitory control over sensory-motor transmission. The inability to achieve selective access to the GABAergic neurons responsible for this unorthodox inhibitory mechanism has left unresolved the contribution of presynaptic inhibition to motor behaviour. We used Gad2 as a genetic entry point to manipulate the interneurons that contact sensory terminals, and show that activation of these interneurons in mice elicits the defining physiological characteristics of presynaptic inhibition. Selective genetic ablation of Gad2-expressing interneurons severely perturbs goal-directed reaching movements, uncovering a pronounced and stereotypic forelimb motor oscillation, the core features of which are captured by modelling the consequences of sensory feedback at high gain. Our findings define the neural substrate of a genetically hardwired gain control system crucial for the smooth execution of movement.


Subject(s)
Feedback, Sensory/physiology , Motor Skills/physiology , Movement/physiology , Neural Inhibition/physiology , Presynaptic Terminals/physiology , Spinal Cord/physiology , Animals , Axons/physiology , Efferent Pathways/physiology , Female , Forelimb/physiology , GABAergic Neurons/cytology , GABAergic Neurons/metabolism , Glutamate Decarboxylase/genetics , Glutamate Decarboxylase/metabolism , Interneurons/cytology , Interneurons/metabolism , Male , Mice , Models, Neurological , Neurotransmitter Agents/metabolism
5.
Article in English | MEDLINE | ID: mdl-25699987

ABSTRACT

Skilled motor behavior emerges from interactions between efferent neural pathways that induce muscle contraction and feedback systems that report and refine movement. Two broad classes of feedback projections modify motor output, one from the periphery and a second that originates within the central nervous system. The mechanisms through which these pathways influence movement remain poorly understood, however. Here we discuss recent studies that delineate spinal circuitry that binds external and internal feedback pathways to forelimb motor behavior. A spinal presynaptic inhibitory circuit regulates the strength of external feedback, promoting limb stability during goal-directed reaching. A distinct excitatory propriospinal circuit conveys copies of motor commands to the cerebellum, establishing an internal feedback loop that rapidly modulates forelimb motor output. The behavioral consequences of manipulating these two circuits reveal distinct controls on motor performance and provide an initial insight into feedback strategies that underlie skilled forelimb movement.


Subject(s)
Feedback , Forelimb/physiology , Movement/physiology , Nerve Net/physiology , Animals , Humans , Motor Activity/physiology , Sensation/physiology
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