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1.
Nat Neurosci ; 27(1): 148-158, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-38036743

RESUMO

Experimental work across species has demonstrated that spontaneously generated behaviors are robustly coupled to variations in neural activity within the cerebral cortex. Functional magnetic resonance imaging data suggest that temporal correlations in cortical networks vary across distinct behavioral states, providing for the dynamic reorganization of patterned activity. However, these data generally lack the temporal resolution to establish links between cortical signals and the continuously varying fluctuations in spontaneous behavior observed in awake animals. Here, we used wide-field mesoscopic calcium imaging to monitor cortical dynamics in awake mice and developed an approach to quantify rapidly time-varying functional connectivity. We show that spontaneous behaviors are represented by fast changes in both the magnitude and correlational structure of cortical network activity. Combining mesoscopic imaging with simultaneous cellular-resolution two-photon microscopy demonstrated that correlations among neighboring neurons and between local and large-scale networks also encode behavior. Finally, the dynamic functional connectivity of mesoscale signals revealed subnetworks not predicted by traditional anatomical atlas-based parcellation of the cortex. These results provide new insights into how behavioral information is represented across the neocortex and demonstrate an analytical framework for investigating time-varying functional connectivity in neural networks.


Assuntos
Neocórtex , Neurônios , Camundongos , Animais , Neurônios/fisiologia , Imageamento por Ressonância Magnética , Vigília , Neocórtex/diagnóstico por imagem , Mapeamento Encefálico/métodos , Vias Neurais/fisiologia
2.
Trends Neurosci ; 46(7): 508-524, 2023 07.
Artigo em Inglês | MEDLINE | ID: mdl-37164869

RESUMO

The rapid and coordinated propagation of neural activity across the brain provides the foundation for complex behavior and cognition. Technical advances across neuroscience subfields have advanced understanding of these dynamics, but points of convergence are often obscured by semantic differences, creating silos of subfield-specific findings. In this review we describe how a parsimonious conceptualization of brain state as the fundamental building block of whole-brain activity offers a common framework to relate findings across scales and species. We present examples of the diverse techniques commonly used to study brain states associated with physiology and higher-order cognitive processes, and discuss how integration across them will enable a more comprehensive and mechanistic characterization of the neural dynamics that are crucial to survival but are disrupted in disease.


Assuntos
Encéfalo , Neurociências , Humanos , Encéfalo/fisiologia , Cognição/fisiologia
3.
Nat Commun ; 12(1): 2449, 2021 04 27.
Artigo em Inglês | MEDLINE | ID: mdl-33907194

RESUMO

In the developing auditory system, spontaneous activity generated in the cochleae propagates into the central nervous system to promote circuit formation. The effects of peripheral firing patterns on spontaneous activity in the central auditory system are not well understood. Here, we describe wide-spread bilateral coupling of spontaneous activity that coincides with the period of transient efferent modulation of inner hair cells from the brainstem medial olivocochlear system. Knocking out α9/α10 nicotinic acetylcholine receptors, a requisite part of the efferent pathway, profoundly reduces bilateral correlations. Pharmacological and chemogenetic experiments confirm that the efferent system is necessary for normal bilateral coupling. Moreover, auditory sensitivity at hearing onset is reduced in the absence of pre-hearing efferent modulation. Together, these results demonstrate how afferent and efferent pathways collectively shape spontaneous activity patterns and reveal the important role of efferents in coordinating bilateral spontaneous activity and the emergence of functional responses during the prehearing period.


Assuntos
Vias Auditivas/fisiologia , Cóclea/fisiologia , Vias Eferentes/fisiologia , Retroalimentação Fisiológica , Receptores Nicotínicos/genética , Estimulação Acústica , Animais , Vias Auditivas/citologia , Cóclea/citologia , Lateralidade Funcional/fisiologia , Expressão Gênica , Células Ciliadas Auditivas Internas/citologia , Células Ciliadas Auditivas Internas/fisiologia , Colículos Inferiores/citologia , Colículos Inferiores/fisiologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Núcleo Olivar/citologia , Núcleo Olivar/fisiologia , Receptores Nicotínicos/deficiência
4.
Nat Methods ; 17(1): 107-113, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31686040

RESUMO

Spontaneous and sensory-evoked activity propagates across varying spatial scales in the mammalian cortex, but technical challenges have limited conceptual links between the function of local neuronal circuits and brain-wide network dynamics. We present a method for simultaneous cellular-resolution two-photon calcium imaging of a local microcircuit and mesoscopic widefield calcium imaging of the entire cortical mantle in awake mice. Our multi-scale approach involves a microscope with an orthogonal axis design where the mesoscopic objective is oriented above the brain and the two-photon objective is oriented horizontally, with imaging performed through a microprism. We also introduce a viral transduction method for robust and widespread gene delivery in the mouse brain. These approaches allow us to identify the behavioral state-dependent functional connectivity of pyramidal neurons and vasoactive intestinal peptide-expressing interneurons with long-range cortical networks. Our imaging system provides a powerful strategy for investigating cortical architecture across a wide range of spatial scales.


Assuntos
Encéfalo/fisiologia , Cálcio/metabolismo , Córtex Cerebral/fisiologia , Rede Nervosa/fisiologia , Neuroimagem/métodos , Neurônios/fisiologia , Fótons , Animais , Comportamento Animal , Encéfalo/citologia , Córtex Cerebral/citologia , Interneurônios/citologia , Interneurônios/fisiologia , Camundongos , Neurônios/citologia , Células Piramidais/citologia , Células Piramidais/fisiologia , Peptídeo Intestinal Vasoativo/metabolismo
5.
Nat Commun ; 5: 4294, 2014 Jul 11.
Artigo em Inglês | MEDLINE | ID: mdl-25014177

RESUMO

The role of remote astrocyte (AC) reaction to central or peripheral axonal insult is not clearly understood. Here we use a transgenic approach to compare the direct influence of normal with diminished AC reactivity on neuronal integrity and synapse recovery following extracranial facial nerve transection in mice. Our model allows straightforward interpretations of AC-neuron signalling by reducing confounding effects imposed by inflammatory cells. We show direct evidence that perineuronal reactive ACs play a major role in maintaining neuronal circuitry following distant axotomy. We reveal a novel function of astrocytic signal transducer and activator of transcription-3 (STAT3). STAT3 regulates perineuronal astrocytic process formation and re-expression of a synaptogenic molecule, thrombospondin-1 (TSP-1), apart from supporting neuronal integrity. We demonstrate that, through this new pathway, TSP-1 is responsible for the remote AC-mediated recovery of excitatory synapses onto axotomized motor neurons in adult mice. These data provide new targets for neuroprotective therapies via optimizing AC-driven plasticity.


Assuntos
Astrócitos/fisiologia , Neurônios Motores/fisiologia , Plasticidade Neuronal/fisiologia , Fator de Transcrição STAT3/fisiologia , Transdução de Sinais/fisiologia , Sinapses/fisiologia , Trombospondina 1/fisiologia , Animais , Astrócitos/citologia , Axotomia , Células Cultivadas , Traumatismos do Nervo Facial/fisiopatologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Camundongos Transgênicos , Modelos Animais , Regeneração Nervosa/fisiologia , Técnicas de Patch-Clamp , Fator de Transcrição STAT3/deficiência , Fator de Transcrição STAT3/genética , Trombospondina 1/deficiência , Trombospondina 1/genética
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