• Applied Microscopy
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• 제34권4호
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• pp.223-230
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• 2004

초파리 돌연변이를 이용한 신경연접에서의 신경충격의 전달을 알아보기 위하여 배양한 초파리 배자 신경세포의 신경연접 미세구조를 관찰하여 분석하였다. 배양된 Wild-type 초파리 배자 신경세포의 신경연접(synapse)은 신경연접간극(synaptic cleft)에 의해 구분되면서 평행하게 뻗어있는 신경연접전 돌기(presynaptic area)의 세포막과 신경연접후 세포(postsynaptic cell)의 세포막 구조에 의해서 확인하였다. Presynaptic active zones과 postsynaptic densities는 각 세포막부분의 전자밀도에 의해 구분하였다. 특히 두 개의 세포막이 서로 근접하여 있으면서, 하나 또는 그 이상의 전자밀도가 높은 presynaptc densities 를 가지고 있고 그 주위에 투명한 신경연접소포들(clear core synaptic vesicles)이 모여있을 경우 이를 신경연접전 돌기로 보았다. 신경연접전 돌기에는 평균 $35.1{\pm}1.44$ nm 직경의 작고 투명한 신경연접소포들이 모여있었다. 신경연접소포들 중 일부는 세포막이나 세포막의 전자밀도가 높은 부분에 직접 접촉하고 있었는데 이를 신경전달물질이 방출되기 직전인 morphologically docked vesicles로 보았다. 이외에도 신경연접전 돌기에서는 내부가 전자밀도가 높은 물질로 채워져 있고 직경이 큰 dense core 신경연접소포들도 관찰할 수 있었다.

• The Korean Journal of Physiology and Pharmacology
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• 제23권5호
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• pp.317-328
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• 2019

It is known that top-down associative inputs terminate on distal apical dendrites in layer 1 while bottom-up sensory inputs terminate on perisomatic dendrites of layer 2/3 pyramidal neurons (L2/3 PyNs) in primary sensory cortex. Since studies on synaptic transmission in layer 1 are sparse, we investigated the basic properties and cholinergic modulation of synaptic transmission in layer 1 and compared them to those in perisomatic dendrites of L2/3 PyNs of rat primary visual cortex. Using extracellular stimulations of layer 1 and layer 4, we evoked excitatory postsynaptic current/potential in synapses in distal apical dendrites (L1-EPSC/L1-EPSP) and those in perisomatic dendrites (L4-EPSC/L4-EPSP), respectively. Kinetics of L1-EPSC was slower than that of L4-EPSC. L1-EPSC showed presynaptic depression while L4-EPSC was facilitating. In contrast, inhibitory postsynaptic currents showed similar paired-pulse ratio between layer 1 and layer 4 stimulations with depression only at 100 Hz. Cholinergic stimulation induced presynaptic depression by activating muscarinic receptors in excitatory and inhibitory synapses to similar extents in both inputs. However, nicotinic stimulation enhanced excitatory synaptic transmission by ~20% in L4-EPSC. Rectification index of AMPA receptors and AMPA/NMDA ratio were similar between synapses in distal apical and perisomatic dendrites. These results provide basic properties and cholinergic modulation of synaptic transmission between distal apical and perisomatic dendrites in L2/3 PyNs of the visual cortex, which might be important for controlling information processing balance depending on attentional state.

• 한국동물학회:학술대회논문집
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• 한국동물학회 2001년도 공동 춘계학술대회
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• pp.84.2-84
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• 2001

No Abstract, See Full Text

• 전자공학회논문지CI
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• 제40권6호
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• pp.56-68
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• 2003

범용 신경망 연산기를 디지털 회로로 구현함에 있어 가장 까다로운 문제들 중 하나는 시냅스의 확장과 해당 네트워크에 맞게 뉴런들을 재배치하는 재구성 문제일 것이다. 본 논문에서는 이러한 문제들을 해결하기 위한 새로운 하드웨어 구조를 제안한다. 제안된 구조는 시냅스의 확장과 네트워크 구조의 변경을 위해 오리지날 디자인의 변경이 필요치 않으며, 모듈러 프로세싱 유니트의 확장을 통한 뉴런의 개수 및 레이어의 확장이 가능하다. 이 구조의 범용성 및 확장성에 대한 검증을 위해 다양한 종류의 다층 퍼셉트론 및 코호넨 네트워크를 구성하여 HDL 시뮬레이터를 통한 결과와 C 언어로 작성된 소프트웨어 시뮬레이터 결과를 비교하였으며 그 결과 성능이 거의 일치함을 확인하였다.

• The Korean Journal of Physiology and Pharmacology
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• 제21권4호
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• pp.423-428
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• 2017

Vestibular compensation is a recovery process from vestibular symptoms over time after unilateral loss of peripheral vestibular end organs. The aim of the present study was to observe time-dependent changes in long-term potentiation (LTP) at Schaffer collateral-CA1 synapses in the CA1 area of the hippocampus during vestibular compensation. The input-output (I/O) relationships of fEPSP amplitudes and LTP induced by theta burst stimulation to Schaffer's collateral commissural fibers were evaluated from the CA1 area of hippocampal slices at 1 day, 1 week, and 1 month after unilateral labyrinthectomy (UL). The I/O relationships of fEPSPs in the CA1 area was significantly reduced within 1 week post-op and then showed a non-significant reduction at 1 month after UL. Compared with sham-operated animals, there was a significant reduction of LTP induction in the hippocampus at 1 day and 1 week after UL. However, LTP induction levels in the CA1 area of the hippocampus also returned to those of sham-operated animals 1 month following UL. These data suggest that unilateral injury of the peripheral vestibular end organs results in a transient deficit in synaptic plasticity in the CA1 hippocampal area at acute stages of vestibular compensation.

• 대한전자공학회논문지
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• 제26권7호
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• pp.140-145
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• 1989

이 논문에서는 ASIC 칩의 설계도면에서 발생하는 임의의 모양을 갖는 영역에서의 효과적인 회로배치 방법인 SOAP (self-organization assisted placement) 를 제안한다. 자율조직이란 Kohonen[1]이 제안한 신경회로망의 학습방법으로 가까이 위치하고 있는 신경소자들이 물리적으로 유사한 외부입력에 민감하도록 소자에 연결된 시냅스 (synapse)의 가중치들을 조절하는 것이다. SOAP에서는 회로 블럭을 신경소자에 회로 블럭의 위치 (x, y좌표)를 해당 신경소자에 연결된 2개의 학습입력으로부터의 시냅스의 가중치 쌍으로 대응시킴으로써 임의의 영역에서의 좋은 회로 배치 결과를 얻을 수 있었다. 이 방법은 또한 입체 표면에서의 회로 배치에도 확장될 수 있다.

• 센서학회지
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• 제18권2호
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• pp.128-134
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• 2009

Integrated circuit of a new neuron chain with a synapse function for Hodgkin-Huxley model which is a good electrical model about a real biological neuron is implemented in a $0.5{\mu}m$ 1 poly 2 metal CMOS technology. Pulse type neuron chain consist of series connected current controlled single neurons through synapses. For the realization of the single neuron, a pair of voltage mode oscillators using operational transconductance amplifiers and capacitors is used. The synapse block which is a connection element between neurons consist of a voltage-current conversion circuit using current mirror. SPICE simulation results of the proposed circuit show 160 mV amplitude pulse output and propagation of the signal through synapses. Measurements of the fabricated pulse type neuron chip in condition of ${\pm}2.5\;V$ power supply are shown and compared with the simulated results.

• JSTS:Journal of Semiconductor Technology and Science
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• 제14권4호
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• pp.383-390
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• 2014

This paper presents an excitatory CMOS neuron oscillator circuit design, which can synchronize two neuron-bursting patterns. The excitatory CMOS neuron oscillator is composed of CMOS neurons and CMOS excitatory synapses. And the neurons and synapses are connected into a close loop. The CMOS neuron is based on the Hindmarsh-Rose (HR) neuron model and excitatory synapse is based on the chemical synapse model. In order to fabricate using a 0.18 um CMOS standard process technology with 1.8V compatible transistors, both time and amplitude scaling of HR neuron model is adopted. This full-chip integration minimizes the power consumption and circuit size, which is ideal for motion control unit of the proposed bio-mimetic micro-robot. The experimental results demonstrate that the proposed excitatory CMOS neuron oscillator performs the expected waveforms with scaled time and amplitude. The active silicon area of the fabricated chip is $1.1mm^2$ including I/O pads.

• Genes and Genomics
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• 제40권12호
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• pp.1339-1349
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• 2018

Cerebral palsy (CP) is a non-progressive neurological disease, of which susceptibility is linked to genetic and environmental risk factors. More and more studies have shown that CP might be caused by multiple genetic factors, similar to other neurodevelopmental disorders. Due to the high genetic heterogeneity of CP, we focused on investigating related molecular pathways. Ten children with CP were collected for whole-exome sequencing by next-generation sequencing (NGS) technology. Customized processes were used to identify potential pathogenic pathways and variants. Three pathways (axon guidance, transmission across chemical synapses, protein-protein interactions at synapses) with twenty-three genes were identified to be highly correlated with CP. This study showed that the three pathways associated with CP might be the molecular mechanism of pathogenesis. These findings could provide useful clues for developing pathway-based pharmacotherapies. Further studies are required to confirm potential roles for these pathways in the pathogenesis of CP.

• Molecules and Cells
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• 제45권2호
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• pp.84-92
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• 2022

To understand the microcircuitry of the brain, the anatomical and functional connectivity among neurons must be resolved. One of the technical hurdles to achieving this goal is that the anatomical connections, or synapses, are often smaller than the diffraction limit of light and thus are difficult to resolve by conventional microscopy, while the microcircuitry of the brain is on the scale of 1 mm or larger. To date, the gold standard method for microcircuit reconstruction has been electron microscopy (EM). However, despite its rapid development, EM has clear shortcomings as a method for microcircuit reconstruction. The greatest weakness of this method is arguably its incompatibility with functional and molecular analysis. Fluorescence microscopy, on the other hand, is readily compatible with numerous physiological and molecular analyses. We believe that recent advances in various fluorescence microscopy techniques offer a new possibility for reliable synapse detection in large volumes of neural circuits. In this minireview, we summarize recent advances in fluorescence-based microcircuit reconstruction. In the same vein as these studies, we introduce our recent efforts to analyze the long-range connectivity among brain areas and the subcellular distribution of synapses of interest in relatively large volumes of cortical tissue with array tomography and superresolution microscopy.