Miniscope-LFOV: A large field of view, single cell resolution, miniature microscope for wired and wire-free imaging of neural dynamics in freely behaving animals DOI Creative Commons
Changliang Guo, Garrett J. Blair, Megha Sehgal

et al.

bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2021, Volume and Issue: unknown

Published: Nov. 22, 2021

Abstract Imaging large-population, single-cell fluorescent dynamics in freely behaving animals larger than mice remains a key endeavor of neuroscience. We present large field view open-source miniature microscope (MiniLFOV) designed for large-scale (3.6 × 2.7 mm), single cell resolution neural imaging rats. It has an electrically adjustable working distance up to 3.5 mm±100 μm, incorporates absolute head-orientation sensor, and weighs only 13.9 grams. The MiniLFOV is capable both deep brain cortical been validated rats by simultaneously >1000 GCaMP7s expressing neurons the hippocampal CA1 layer head-fixed ~2000 dorsal cortex through cranial window. also supports optional wire-free operation using novel, data acquisition expansion board. expect this new implementation UCLA Miniscope platform will enable researchers address novel hypotheses concerning function animals.

Language: Английский

Miniscope-LFOV: A large-field-of-view, single-cell-resolution, miniature microscope for wired and wire-free imaging of neural dynamics in freely behaving animals DOI Creative Commons
Changliang Guo, Garrett J. Blair, Megha Sehgal

et al.

Science Advances, Journal Year: 2023, Volume and Issue: 9(16)

Published: April 21, 2023

Imaging large-population, single-cell fluorescent dynamics in freely behaving animals larger than mice remains a key endeavor of neuroscience. We present large-field-of-view open-source miniature microscope (MiniLFOV) designed for large-scale (3.6 mm × 2.7 mm), cellular resolution neural imaging rats. It has an electrically adjustable working distance up to 3.5 ± 100 μm, incorporates absolute head orientation sensor, and weighs only 13.9 g. The MiniLFOV is capable both deep brain cortical been validated rats by simultaneously >1000 GCaMP7s-expressing neurons the hippocampal CA1 layer head-fixed ~2000 dorsal cortex through cranial window. also supports optional wire-free operation using novel, data acquisition expansion board. expect that this new implementation UCLA Miniscope platform will enable researchers address novel hypotheses concerning function animals.

Language: Английский

Citations

70

Understanding the Neural Mechanisms of General Anesthesia from Interaction with Sleep–Wake State: A Decade of Discovery DOI

Wei-Wei Bao,

Shan Jiang, Wei‐Min Qu

et al.

Pharmacological Reviews, Journal Year: 2023, Volume and Issue: 75(3), P. 532 - 553

Published: Jan. 10, 2023

The development of cutting-edge techniques to study specific brain regions and neural circuits that regulate sleep–wake states general anesthesia (GA), has increased our understanding these exhibit similar neurophysiologic traits. This review summarizes current knowledge focusing on cell subtypes control wakefulness, rapid eye movement (REM) sleep, non-REM GA. We also novel insights into their interactions raise unresolved questions challenges in this field. Comparisons the overlapping substrates GA regulation will help us understand transitions how anesthetics cause reversible loss consciousness.

Significance Statement

General sharing numerous traits with process natural is administered millions surgical patients annually. In past decade, studies exploring mechanisms underlying have advanced Pharmacotherapies targeting associated regulations significance for clinical practice sleep medicine.

Language: Английский

Citations

44

A molecularly defined amygdala-independent tetra-synaptic forebrain-to-hindbrain pathway for odor-driven innate fear and anxiety DOI
Hao Wang, Qin Wang,

Liuzhe Cui

et al.

Nature Neuroscience, Journal Year: 2024, Volume and Issue: 27(3), P. 514 - 526

Published: Feb. 12, 2024

Language: Английский

Citations

17

Neuro-orchestration of sleep and wakefulness DOI
Bibi A. Sulaman, Su Wang, Jean Tyan

et al.

Nature Neuroscience, Journal Year: 2022, Volume and Issue: 26(2), P. 196 - 212

Published: Dec. 29, 2022

Language: Английский

Citations

68

Defensive responses: behaviour, the brain and the body DOI
Yu-Ting Tseng, Bernhard Schaefke, Pengfei Wei

et al.

Nature reviews. Neuroscience, Journal Year: 2023, Volume and Issue: 24(11), P. 655 - 671

Published: Sept. 20, 2023

Language: Английский

Citations

34

Reversal of hyperactive higher-order thalamus attenuates defensiveness in a mouse model of PTSD DOI Creative Commons
Kaiwen Xi, Haoxiang Xiao, Xin Huang

et al.

Science Advances, Journal Year: 2023, Volume and Issue: 9(5)

Published: Feb. 3, 2023

Posttraumatic stress disorder (PTSD) is a highly prevalent and debilitating psychiatric disease often accompanied by severe defensive behaviors, preventing individuals from integrating into society. However, the neural mechanisms of defensiveness in PTSD remain largely unknown. Here, we identified that higher-order thalamus, posteromedial complex thalamus (PoM), was overactivated mouse model PTSD, suppressing PoM activity alleviated excessive behaviors. Moreover, found diminished thalamic inhibition derived reticular nucleus major cause hyperactivity mice. Overloaded innervation to downstream cortical area, frontal association cortex, drove abnormal defensiveness. Overall, our study revealed malfunction mediates behaviors highlighted thalamocortical circuit as potential target for treating PTSD-related overreactivity symptoms.

Language: Английский

Citations

17

Neural Control of Action Selection Among Innate Behaviors DOI Creative Commons
Xinyu Jiang, Yufeng Pan

Neuroscience Bulletin, Journal Year: 2022, Volume and Issue: 38(12), P. 1541 - 1558

Published: May 28, 2022

Abstract Nervous systems must not only generate specific adaptive behaviors, such as reproduction, aggression, feeding, and sleep, but also select a single behavior for execution at any given time, depending on both internal states external environmental conditions. Despite their tremendous biological importance, the neural mechanisms of action selection remain poorly understood. In past decade, studies in model animal Drosophila melanogaster have demonstrated valuable underlying innate behaviors. this review, we summarize circuit with particular focus small number sexually dimorphic neurons controlling among sex, fight, sleep behaviors sexes flies. We discuss potentially conserved configurations neuromodulation fly mouse models, aiming to provide insights into prioritization

Language: Английский

Citations

27

Behavioral and cortical arousal from sleep, muscimol-induced coma, and anesthesia by direct optogenetic stimulation of cortical neurons DOI Creative Commons

Rong Mao,

Matías Cavelli, Graham Findlay

et al.

iScience, Journal Year: 2024, Volume and Issue: 27(6), P. 109919 - 109919

Published: May 7, 2024

Highlights•Optogenetic activation of cortical neurons wakes up mice from NREM and REM sleep•Awakenings are induced more effectively in posterior parietal than prefrontal cortex•Cortical opto stimulation causes EEG behavioral arousal coma•Cortical during deep sevo-dex anesthesiaSummaryThe cerebral cortex is widely considered part the neural substrate consciousness, but direct causal evidence missing. Here, we tested whether optogenetic (PtA) or medial (mPFC) sufficient for three states characterized by progressively deeper unresponsiveness: sleep, a coma-like state muscimol injection midbrain, sevoflurane-dexmedetomidine anesthesia. We find that always awakens both sleep with PtA requiring weaker/shorter light pulses mPFC. Moreover, most cases produce (decrease low frequencies) (recovery righting reflex) brainstem coma, as well These findings provide and/or anesthesia.Graphical abstract

Language: Английский

Citations

6

A REM-active basal ganglia circuit that regulates anxiety DOI Creative Commons
Wei Ba, Mathieu Nollet,

Chunyu Yin

et al.

Current Biology, Journal Year: 2024, Volume and Issue: 34(15), P. 3301 - 3314.e4

Published: June 28, 2024

Rapid eye movement (REM) sleep has been hypothesized to promote emotional resilience, but any neuronal circuits mediating this have not identified. We find that in mice, somatostatin (Som) neurons the entopeduncular nucleus (EP

Language: Английский

Citations

5

A potentiation of REM sleep-active neurons in the lateral habenula may be responsible for the sleep disturbance in depression DOI

Zehui Zhang,

Wei Zhang,

Yuanyuan Fang

et al.

Current Biology, Journal Year: 2024, Volume and Issue: 34(15), P. 3287 - 3300.e6

Published: June 28, 2024

Language: Английский

Citations

5