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1.
J Neurosci ; 38(50): 10692-10708, 2018 12 12.
Article in English | MEDLINE | ID: mdl-30373769

ABSTRACT

The nucleus basalis (NB) projects cholinergic axons to the cortex, where they play a major role in arousal, attention, and learning. Cholinergic inputs shift cortical dynamics from synchronous to asynchronous and improve the signal-to-noise ratio (SNR) of sensory responses. However, the underlying mechanisms of these changes remain unclear. Using simultaneous extracellular and whole-cell patch recordings in layer 4 of the mouse barrel cortex, we show that electrical or optogenetic activation of the cholinergic system has a differential effect on ongoing and sensory evoked activities. Cholinergic activation profoundly reduced the large spontaneous fluctuations in membrane potential and decorrelated ongoing activity. However, NB stimulation had no effect on the response to whisker stimulation or on signal correlations. These effects of cholinergic activation provide a unified explanation for the increased SNR of sensory response and for the reduction in noise correlations and explain the shift into the desynchronized cortical state, which are the hallmarks of arousal and attention.SIGNIFICANCE STATEMENT Attention increases the signal-to-noise ratio (SNR) of cortical sensory response, which may reflect either reduction in background firing rate or increased sensory response. Extracellular recordings showed that attention also reduces the correlation in network activity. These effects are partially mediated by cholinergic axons from the nucleus basalis projecting to the entire cortex. To reveal the cellular and synaptic correlates of these cholinergic effects, we performed simultaneous intracellular and LFP recordings in the somatosensory cortex. Global or local cholinergic activation increased the SNR of sensory response mainly by reducing the rate and amplitude of background synaptic activity and also reduced network correlations. Therefore, coding of sensory information is enhanced by the cholinergic system mainly due to a reduction in spontaneous activity.


Subject(s)
Basal Nucleus of Meynert/physiology , Cholinergic Neurons/physiology , Membrane Potentials/physiology , Nerve Net/physiology , Signal-To-Noise Ratio , Somatosensory Cortex/physiology , Animals , Basal Nucleus of Meynert/chemistry , Basal Nucleus of Meynert/drug effects , Cholinergic Agents/pharmacology , Cholinergic Neurons/chemistry , Cholinergic Neurons/drug effects , Female , Male , Membrane Potentials/drug effects , Mice , Mice, 129 Strain , Mice, Inbred C57BL , Mice, Transgenic , Nerve Net/chemistry , Nerve Net/drug effects , Optogenetics/methods , Somatosensory Cortex/chemistry , Somatosensory Cortex/drug effects
2.
Dev Med Child Neurol ; 59(5): 550-556, 2017 05.
Article in English | MEDLINE | ID: mdl-27911014

ABSTRACT

AIM: Outdoor adventure programmes aim to improve interpersonal relationships using adventurous activities. The current study examined the effectiveness of an outdoor adventure programme in children with autism spectrum disorders (ASD). METHOD: The study included 51 participants (40 males, 11 females; age 3y 4mo-7y 4mo) enrolled in ASD special education kindergartens. Only the intervention group (n=30) participated in the outdoor adventure programme for 13 weeks, completing challenging physical activities that required cooperation and communication with peers and instructors. The control group (n=21) was not significantly different from the research group in age, sex, cognitive, and adaptive behaviour measures. RESULTS: Outcomes after the intervention revealed significant improvement in social-communication and different directions in the two groups in the social cognition, social motivation, and autistic mannerisms subdomains of the Social Responsiveness Scale. While the group that received an outdoor adventure programme showed a tendency toward a reduction in severity, the control group showed the opposite (p<0.010). INTERPRETATION: The outdoor adventure programme required problem-solving skills and forced the child to communicate in exciting situations. This study suggests that an outdoor adventure programme may be an effective intervention in addition to traditional treatments in young children with ASD. Future studies should examine the outcome of outdoor adventure programmes delivered for longer periods of time and maintenance of the achievements over time.


Subject(s)
Autism Spectrum Disorder/psychology , Autism Spectrum Disorder/rehabilitation , Cognitive Behavioral Therapy/methods , Interpersonal Relations , Social Behavior , Socioenvironmental Therapy/methods , Adaptation, Psychological , Analysis of Variance , Child , Child, Preschool , Communication , Female , Humans , Male , Treatment Outcome
4.
Proc Jpn Acad Ser B Phys Biol Sci ; 91(10): 560-76, 2015.
Article in English | MEDLINE | ID: mdl-26666306

ABSTRACT

This study focuses on the structure and function of the primary sensory neurons that innervate vibrissal follicles in the rat. Both the peripheral and central terminations, as well as their firing properties were identified using intracellular labelling and recording in trigeminal ganglia in vivo. Fifty-one labelled neurons terminating peripherally, as club-like, Merkel, lanceolate, reticular or spiny endings were identified by their morphology. All neurons responded robustly to air puff stimulation applied to the vibrissal skin. Neurons with club-like endings responded with the highest firing rates; their peripheral processes rarely branched between the cell body and their terminal tips. The central branches of these neurons displayed abundant collaterals terminating within all trigeminal nuclei. Analyses of three-dimensional reconstructions reveal a palisade arrangement of club-like endings bound to the ringwulst by collagen fibers. Our morphological findings suggest that neurons with club-like endings sense mechanical aspects related to the movement of the ringwulst and convey this information to all trigeminal nuclei in the brainstem.


Subject(s)
Mechanoreceptors/cytology , Trigeminal Ganglion/cytology , Vibrissae/physiology , Animals , Electrophysiological Phenomena , Imaging, Three-Dimensional , Intracellular Space/metabolism , Male , Rats , Rats, Wistar , Trigeminal Ganglion/physiology
5.
Mol Cell Neurosci ; 45(1): 1-11, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20493948

ABSTRACT

The locus coeruleus (LC) which is the major noradrenergic nucleus in the brain develops under the influence of Bmps secreted by the roof plate and Fgf8 emitted from the mid-hindbrain organizer. We studied the development of the LC in different Bmp mouse mutants and report the absence of this nucleus in Bmp5(-/-);Bmp7(-/-) double knockouts. Notably, genes marking organizers and neuronal populations adjacent to the LC precursor field are unperturbed in Bmp5(-/-);Bmp7(-/-) animals. In addition, we found that in En1(+/Otx2) mutants in which the caudal Otx2 expression domain and thereby the mid-hindbrain organizer are shifted caudally, LC neurons are concomitantly reduced along with Bmp5/7. Complementing these results, Otx1(-/-);Otx2(+/-) mutants, in which the mid-hinbrain organizer is shifted rostrally, show a rostrally extended Bmp5 expression area and an increase in LC neurons. Taken together, our data indicate that LC development requires either Bmp5 or Bmp7, and one is able to compensate for the loss of the other. In addition, we conclude that the position of the mid-hindbrain organizer determines the size of the LC and propose that Bmp5/7 play an important role in mediating this organizer function.


Subject(s)
Bone Morphogenetic Protein 5/metabolism , Bone Morphogenetic Protein 7/metabolism , Locus Coeruleus/cytology , Locus Coeruleus/embryology , Mesencephalon/physiology , Norepinephrine/metabolism , Rhombencephalon/physiology , Animals , Apoptosis , Fibroblast Growth Factor 8/genetics , Fibroblast Growth Factor 8/metabolism , Homeodomain Proteins/genetics , Homeodomain Proteins/metabolism , Locus Coeruleus/metabolism , Mesencephalon/cytology , Mice , Mice, Knockout , Neurons/cytology , Neurons/physiology , Otx Transcription Factors/genetics , Otx Transcription Factors/metabolism , Rhombencephalon/cytology , Stem Cells/cytology , Stem Cells/physiology
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