The patch clamp recording technique in vivois a blind patch clamp recording methods to record the current of the spinal or cereral neurons of anaes：hesia （ or awake） animals. This technique can be used to study the...The patch clamp recording technique in vivois a blind patch clamp recording methods to record the current of the spinal or cereral neurons of anaes：hesia （ or awake） animals. This technique can be used to study the synaptic function and plasticity in central nervous system in vivoin order to understand the physiological properties of the ion channels from an integrated point of view. The advantage of this technique have already presented itself in the study of the synaptic transmission and nervous network. Nowadays, in vivo patch whole-cell recording technique in combination with other techniques is becoming a common method in the research fields.展开更多
In this paper, we conduct research on the developmental trend of the computer music technology under the background of multichannelstereo recording. Surround sound is not only used in the fi lm, home theater, also pen...In this paper, we conduct research on the developmental trend of the computer music technology under the background of multichannelstereo recording. Surround sound is not only used in the fi lm, home theater, also penetrated the digital TV and digital broadcasting.But because of the limitation of storage media capacity and transmission bandwidth must use all kinds of that audio compression technologyto transmit audio data. As a more general and more practical signifi cance, as masking and by masking sound are not limited to their respectiveresend by a single speaker, but in different proportion to their respective ‘channel sound level is poor. To deal with this issue, this paperintegrates the signal denoising method as the optimization and achieves better performance.展开更多
A series of experiments are conducted to confirm whether the vectors calculated for an early section of a continuous non-invasive fetal electrocardiogram （fECG） recording can be directly applied to subsequent sectio...A series of experiments are conducted to confirm whether the vectors calculated for an early section of a continuous non-invasive fetal electrocardiogram （fECG） recording can be directly applied to subsequent sections in order to reduce the computation required for real-time monitoring. Our results suggest that it is generally feasible to apply the initial optimal maternal and fetal ECG combination vectors to extract the fECG and maternal ECG in subsequent recorded sections.展开更多
Biodynamical processes,especially in system biology,that occur far apart in space may be highly correlated.To study such biodynamics,simultaneous imaging over a large span at high spatio-temporal resolutions is highly...Biodynamical processes,especially in system biology,that occur far apart in space may be highly correlated.To study such biodynamics,simultaneous imaging over a large span at high spatio-temporal resolutions is highly desired.For example,large-scale recording of neural network activities over various brain regions is indispensable in neuroscience.However,limited by the field-of-view(FoV)of conventional microscopes,simultaneous recording of laterally distant regions at high spatio-temporal resolutions is highly challenging.Here,we propose to extend the distance of simultaneous recording regions with a custom micro-mirror unit,taking advantage of the long working distance of the objective and spatio-temporal multiplexing.We demonstrate simultaneous dual-region two-photon imaging,spanning as large as 9 mm,which is 4 times larger than the nominal FoV of the objective.We verify the system performance in in vivo imaging of neural activities and vascular dilations,simultaneously,at two regions in mouse brains as well as in spinal cords,respectively.The adoption of our proposed scheme will promote the study of systematic biology,such as system neuroscience and system immunology.展开更多
A multi-channel, fully differential programmable chip for neural recording application is presented. The integrated circuit incorporates eight neural recording amplifiers with tunable bandwidth and gain, eight 4thorde...A multi-channel, fully differential programmable chip for neural recording application is presented. The integrated circuit incorporates eight neural recording amplifiers with tunable bandwidth and gain, eight 4thorder Bessel switch capacitor filters, an 8-to-1 analog time-division multiplexer, a fully differential successive approximation register analog-to-digital converter （SAR ADC）, and a serial peripheral interface for communication. The neural recording amplifier presents a programmable gain from 53 dB to 68 dB, a tunable low cut-off frequency from 0.1 Hz to 300 Hz, and 3.77μVrms input-referred noise over a 5 kHz bandwidth. The SAR ADC digitizes signals at maximum sampling rate of 20 μS/s per channel and achieves an ENOB of 7.4. The integrated circuit is designed and fabricated in 0.18-μm CMOS mix-signal process. We successfully performed a multi-channel in-vivo recording experiment from a rat cortex using the neural recording chip.展开更多
Vision formation is classically based on projections from retinal ganglion cells(RGC)to the lateral geniculate nucleus(LGN)and the primary visual cortex(V1).Neurons in the mouse V1 are tuned to light stimuli.Although ...Vision formation is classically based on projections from retinal ganglion cells(RGC)to the lateral geniculate nucleus(LGN)and the primary visual cortex(V1).Neurons in the mouse V1 are tuned to light stimuli.Although the cellular information of the retina and the LGN has been widely studied,the transcriptome profiles of single light-stimulated neuron in V1 remain unknown.In our study,in vivo calcium imaging and whole-cell electrophysiological patch-clamp recording were utilized to identify 53 individual cells from layer 2/3 of V1 as lightsensitive(LS)or non-light-sensitive(NS)by single-cell light-evoked calcium evaluation and action potential spiking.The contents of each cell after functional tests were aspirated in vivo through a patch-clamp pipette for mRNA sequencing.Moreover,the three-dimensional(3-D)morphological characterizations of the neurons were reconstructed in a live mouse after the whole-cell recordings.Our sequencing results indicated that V1 neurons with a high expression of genes related to transmission regulation,such as Rtn4r and Rgs7,and genes involved in membrane transport,such as Na+/K+ATPase and NMDA-type glutamatergic receptors,preferentially responded to light stimulation.Furthermore,an antagonist that blocks Rtn4r signals could inactivate the neuronal responses to light stimulation in live mice.In conclusion,our findings of the vivo-seq analysis indicate the key role of the strength of synaptic transmission possesses neurons in V1 of light sensory.展开更多
文摘The patch clamp recording technique in vivois a blind patch clamp recording methods to record the current of the spinal or cereral neurons of anaes：hesia （ or awake） animals. This technique can be used to study the synaptic function and plasticity in central nervous system in vivoin order to understand the physiological properties of the ion channels from an integrated point of view. The advantage of this technique have already presented itself in the study of the synaptic transmission and nervous network. Nowadays, in vivo patch whole-cell recording technique in combination with other techniques is becoming a common method in the research fields.
文摘In this paper, we conduct research on the developmental trend of the computer music technology under the background of multichannelstereo recording. Surround sound is not only used in the fi lm, home theater, also penetrated the digital TV and digital broadcasting.But because of the limitation of storage media capacity and transmission bandwidth must use all kinds of that audio compression technologyto transmit audio data. As a more general and more practical signifi cance, as masking and by masking sound are not limited to their respectiveresend by a single speaker, but in different proportion to their respective ‘channel sound level is poor. To deal with this issue, this paperintegrates the signal denoising method as the optimization and achieves better performance.
基金supported by the National Natural Science Foundation of China(Grant No.61271079)
文摘A series of experiments are conducted to confirm whether the vectors calculated for an early section of a continuous non-invasive fetal electrocardiogram （fECG） recording can be directly applied to subsequent sections in order to reduce the computation required for real-time monitoring. Our results suggest that it is generally feasible to apply the initial optimal maternal and fetal ECG combination vectors to extract the fECG and maternal ECG in subsequent recorded sections.
基金STI2030-Major Projects(2022ZD0212000)National Natural Science Foundation of China(32021002,61831014)"Bio-Brain+X”Advanced Imaging Instrument Development Seed Grant。
文摘Biodynamical processes,especially in system biology,that occur far apart in space may be highly correlated.To study such biodynamics,simultaneous imaging over a large span at high spatio-temporal resolutions is highly desired.For example,large-scale recording of neural network activities over various brain regions is indispensable in neuroscience.However,limited by the field-of-view(FoV)of conventional microscopes,simultaneous recording of laterally distant regions at high spatio-temporal resolutions is highly challenging.Here,we propose to extend the distance of simultaneous recording regions with a custom micro-mirror unit,taking advantage of the long working distance of the objective and spatio-temporal multiplexing.We demonstrate simultaneous dual-region two-photon imaging,spanning as large as 9 mm,which is 4 times larger than the nominal FoV of the objective.We verify the system performance in in vivo imaging of neural activities and vascular dilations,simultaneously,at two regions in mouse brains as well as in spinal cords,respectively.The adoption of our proposed scheme will promote the study of systematic biology,such as system neuroscience and system immunology.
基金supported by the National Basic Research Program of China(No.2011CB933203)the National Natural Science Foundation of China(Nos.61076023,61178051)the National High Technology Research & Development Program of China(No.2012AA030608)
文摘A multi-channel, fully differential programmable chip for neural recording application is presented. The integrated circuit incorporates eight neural recording amplifiers with tunable bandwidth and gain, eight 4thorder Bessel switch capacitor filters, an 8-to-1 analog time-division multiplexer, a fully differential successive approximation register analog-to-digital converter （SAR ADC）, and a serial peripheral interface for communication. The neural recording amplifier presents a programmable gain from 53 dB to 68 dB, a tunable low cut-off frequency from 0.1 Hz to 300 Hz, and 3.77μVrms input-referred noise over a 5 kHz bandwidth. The SAR ADC digitizes signals at maximum sampling rate of 20 μS/s per channel and achieves an ENOB of 7.4. The integrated circuit is designed and fabricated in 0.18-μm CMOS mix-signal process. We successfully performed a multi-channel in-vivo recording experiment from a rat cortex using the neural recording chip.
基金This work was supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB32010100)National Basic Research Program of China(2019YFA0110101,2017YFA0103303,2017YFA0102601)+2 种基金the National Natural Science Foundation of China(NSFC)(31671072,31771140,81891001)the Beijing Brain Initiative of Beijing Municipal Science&Technology Commission(Z181100001518004)Open Research Fund of the State Key Laboratory of Cognitive Neuroscience and Learning.
文摘Vision formation is classically based on projections from retinal ganglion cells(RGC)to the lateral geniculate nucleus(LGN)and the primary visual cortex(V1).Neurons in the mouse V1 are tuned to light stimuli.Although the cellular information of the retina and the LGN has been widely studied,the transcriptome profiles of single light-stimulated neuron in V1 remain unknown.In our study,in vivo calcium imaging and whole-cell electrophysiological patch-clamp recording were utilized to identify 53 individual cells from layer 2/3 of V1 as lightsensitive(LS)or non-light-sensitive(NS)by single-cell light-evoked calcium evaluation and action potential spiking.The contents of each cell after functional tests were aspirated in vivo through a patch-clamp pipette for mRNA sequencing.Moreover,the three-dimensional(3-D)morphological characterizations of the neurons were reconstructed in a live mouse after the whole-cell recordings.Our sequencing results indicated that V1 neurons with a high expression of genes related to transmission regulation,such as Rtn4r and Rgs7,and genes involved in membrane transport,such as Na+/K+ATPase and NMDA-type glutamatergic receptors,preferentially responded to light stimulation.Furthermore,an antagonist that blocks Rtn4r signals could inactivate the neuronal responses to light stimulation in live mice.In conclusion,our findings of the vivo-seq analysis indicate the key role of the strength of synaptic transmission possesses neurons in V1 of light sensory.
