• 제목/요약/키워드: Cortical neuron

검색결과 47건 처리시간 0.022초

흰쥐 대뇌세포배양의 저산소증모델에서 루이보스차 침제에 의한 신경세포 보호작용 (Neuronal Protection by Rooibos (Aspalathus linearis) Tea Infusions in a Hypoxic Model of Cultured Rat Cortical Neurons)

  • Moon, Il-Soo;Ko, Bok-Hyun
    • 생명과학회지
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    • 제14권2호
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    • pp.291-295
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    • 2004
  • 루이보스(Aspalathus linearis; RB)는 콩과식물로서 남아프리카 Cape Province의 북서부 산악지역에 자생한다. 루이보스차 침제는 가는 가지와 잎의 발효산물로서 플리보노이드류와 페놀산이 있어 강한 항산화활성을 갖는 것으로 알려져 있다. 본 연구에서는 저산소증모델에서 루이보스차 침제가 배양한 흰쥐 대뇌세포의 스트레스를 완화하는지에 대한 연구하였다. 배지로 누출된 LDH의 정량실험에 의하면 루이보스는 정상산소환경 및 저산소증에서 함량 의존적으로(10-100 $\mu\textrm{g}$/ml) 각각 6-18% 및 2-24%의 세포생존율을 증가시켰다(16 DIV 세포, 처리 후 3일째). CFP-Hsc70 단백질을 표현시킨 신경세포의 모양을 관찰하였을때 루이보스(50 $\mu\textrm{g}$/ml)는 저산소처리 후 5일에 세포체에 수포가 있는 세포의 수를 대조군(55.4$\pm$4.59%)에 비하여 유의하게 감소시켰다(40.9$\pm$6.3%). 이러한 결과들은 루이보스차가 저산소증에서 신경세포를 보호함을 의미하며, 신경세포 손상을 예방 또는 치료하는데 응용될 수 있을 것으로 보인다.

전침자극이 Spontaneously Hypertensive Rat의 대뇌겉질, 뇌줄기, 소뇌 부위의 Nitric Oxide Synthase 신경세포에 미치는 영향 (Difference in NOS between 2 Hz and 100 Hz EA in cerebral cortex, brain stem and cerebellum of spontaneously hypertensive rats)

  • 김종인;김용석;김창환
    • Journal of Acupuncture Research
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    • 제18권4호
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    • pp.116-124
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    • 2001
  • Background and Objetive : The aim of this study was to investigate the effect of various electroacupuncture stimulation on NADPH-diaphorase in cerebral cortex, brain stem, cerebellum of spontaneously hypertensive rats. Materials and Methods : We evaluated the changes of NADPH-d-positive neurons using a histochemical method. The staining intensity of NADPH-d-positive neurons was assessed in a quantitative fashion using a microdensitometrical method based on optical density by means of an image analyzer. Results and Conculsion : The average optical density of NADPH-d-positive neurons of 100 Hz (bipolar square wave 0.2 ms duration and 100 Hz frequency) electroacupuncture treatment group significantly increased in most cortical areas comparison between the manual acupuncture and 2 Hz (bipolar square wave 0.2 ms duration and 2 Hz frequency) electroacupuncture groups. In the brain stem, the optical density of NADPH-d-positive neuron at only superficial gray layer of the superior colliculus area was same as cerebral cortex. We conclude that the morphological evidence for NADPH-d-positive neurons may be have regional change in cerebral cortex brain stem and cerebellum according to various electroacupuncture stimulations.

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Comparison of EEG Changes Induced by Action Execution and Action Observation

  • Kim, Ji Young;Ko, Yu-Min;Park, Ji Won
    • The Journal of Korean Physical Therapy
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    • 제29권1호
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    • pp.27-32
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    • 2017
  • Purpose: Recent electrophysiological studies have shown that the sensorymotor cortex is activated during both actual action excuted by themselves and observation of action performed by other persons. Observation of action based on mirror neuron system can be used as a cognitive intervention to promote motor learning. The purpose of this study was to investigate the brain activity changes during action observation and action execution using EEG. Methods: Thirty healthy volunteers participated and were requested to perform hand action and to observe the video of hand action performed by another person. The EEG activity was evaluated by a method which segregated the time-locked for each condition. To compare the differences between action observation and execution, the Mu suppression and the relative band power were analysed. Results: The results showed significant mu suppression during the action observation and execution, but the differences between the two conditions were not observed. The relative band power showed a significant difference during the action observation and execution, but there were no differences between the two conditions. Conclusion: These results indicate that action execution and observation involve overlapping neural networks in the sensorymotor cortical areas, proposing positive changes on neurophysiology. We are expected to provide information related to the intervention of cognitive rehabilitation.

Attenuation of β-amyloid-induced neuroinflammation by KHG21834 in vivo

  • Kim, Eun-A;Hahn, Hoh-Gyu;Kim, Tae-Ue;Choi, Soo-Young;Cho, Sung-Woo
    • BMB Reports
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    • 제43권6호
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    • pp.413-418
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    • 2010
  • Beta-Amyloid ($A{\beta}$)-induced neuroinflammation is one of the key events in the development of neurodegenerative disease. We previously reported that KHG21834, a benzothiazole derivative, attenuates $A{\beta}$-induced degeneration of cortical and mesencephalic neurons in vitro. In the present work, we show that KHG21834 reduces $A{\beta}$-mediated neuroinflammation in brain. In vivo intracerebroventricular infusion of KHG21834 leads to decreases in the numbers of activated astrocytes and microglia and level of proinflammatory cytokines such as interleukin-$1{\beta}$ and tumor necrosis factor-$\alpha$ induced by $A{\beta}$ in the hippocampus. This suppression of neuroinflammation is associated with decreased neuron loss, restoration of synaptic dysfunction biomarkers in the hippocampus to control level, and diminished amyloid deposition. These results may suggest the potential therapeutic efficacy of KHG21834 for the treatment of $A{\beta}$-mediated neuroinflammation.

A Simple Method for Combined Fluorescence In Situ Hybridization and Immunocytochemistry

  • Moon, Il Soo;Cho, Sun-Jung;Jin, IngNyol;Walikonis, Randall
    • Molecules and Cells
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    • 제24권1호
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    • pp.76-82
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    • 2007
  • By combining in situ hybridization (ISH) and immunocytochemistry (IC), microscopic topological localization of mRNAs and proteins can be determined. Although this technique can be applied to a variety of tissues, it is particularly important for use on neuronal cells which are morphologically complex and in which specific mRNAs and proteins are located in distinct subcellular domains such as dendrites and dendritic spines. One common technical problem for combined ISH and IC is that the signal for immunocytochemical localization of proteins often becomes much weaker after conducting ISH. In this manuscript, we report a simplified but robust protocol that allows immunocytochemical localization of proteins after ISH. In this protocol, we fix cultured cortical or hippocampal neurons with 4% paraformaldehyde (PFA), rinse briefly in PBS, and then further fix the cells with $-20^{\circ}C$ methanol. Our method has several major advantages over previously described ones in that (1) it is simple, as it is just consecutive routine fixation procedures, (2) it does not require any special alteration to the fixation procedures such as changes in salt concentration, and (3) it can be used with antibodies that are compatible with either methanol (MeOH-) or PFA-fixed target proteins. To our best knowledge, we are the first to employ this fixation method for fluorescence ISH + IC.

An EEG-based Brain Mapping to Determine Mirror Neuron System in Patients with Chronic Stroke during Action Observation

  • Kuk, Eun-Ju;Kim, Jong-man
    • The Journal of Korean Physical Therapy
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    • 제27권3호
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    • pp.135-139
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    • 2015
  • Purpose: The aim of this study was to compare EEG topographical maps in patients with chronic stroke after action observation physical training. Methods: Ten subjects were recruited from a medical hospital. Participants observed the action of transferring a small block from one box to another for 6 sessions of 1 minute each, and then performed the observed action for 3 minutes, 6 times. An EEG-based brain mapping system with 32 scalp sites was used to determine cortical reorganization in the regions of interest (ROIs) during observation of movement. The EEG-based brain mapping was comparison in within-group before and after training. ROIs included the primary sensorimotor cortex, premotor cortex, superior parietal lobule, inferior parietal lobule, superior temporal lobe, and visual cortex. EEG data were analyzed with an average log ratio in order to control the variability of the absolute mu power. The mu power log ratio was in within-group comparison with paired t-tests. Results: Participants showed activation prior to the intervention in all of the cerebral cortex, whereas the inferior frontal gyrus, superior frontal gyrus, precentral gyrus, and inferior parietal cortex were selectively activated after the training. There were no differences in mu power between each session. Conclusion: These findings suggest that action observation physical training contributes to attaining brain reorganization and improving brain functionality, as part of rehabilitation and intervention programs.

흰쥐의 neuronal NOS 신경세포의 activity에 대한 전침자극 효과 (Effect of Electroacupuncture Stimulation on Activity of Neuronal NOS in Rats)

  • 김후동;남상수;김창환
    • Journal of Acupuncture Research
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    • 제23권5호
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    • pp.199-206
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    • 2006
  • Objectives : The aim of this study was to investigate the effect of various electroacupuncture stimulation on neuronal nitric oxide synthase(nNOS) in cerebral cortex, brain stem, cerebellum of spontaneously hypertensive rats. Methods : We evaluated the changes of nNOS-positive neurons using a immunohistochemical method. The staining intensity of nNOS positive neurons was assessed in a quantitative fashion using a microdensitometrical method based on optical density by means of an image analyzer. Results : The average optical density of nNOS-positive neurons of 100 Hz (bipolar square wave 0.2 ms duration and 100 Hz frequency) electroacupuncture treatment group significantly decreased in most cortical areas comparison between the manual acupuncture and 2 Hz (bipolar square wave 0.2 ms duration and 2 Hz frequency) electroacupuncture groups. In the brain stem, the optical density of nNOS-positive neuron at superficial gray layer of the superior colliculus area, dorsolateral periaqueductal gray area and paralemniscal nucleus were same as cerebral cortex. Conclusion : We conclude that the morphological evidence for nNOS-positive neurons may be have regional change in cerebral cortex brain stem and cerebellum according to various electroacupuncture stimulations.

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대뇌피질 신경세포에 미치는 glutamate 독성에 대한 한약재 효능연구 (The effect of herbal medicine on cultured cerebral cortical neurons induced by glutamate neurotoxicity)

  • 이미영;강봉주;윤유식;홍성길;곽병주;조동욱
    • 한국한의학연구원논문집
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    • 제4권1호통권4호
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    • pp.99-114
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    • 1998
  • The effect of herbal medicine on glutamate mediated neurotoxicity was studied in mouse neurons in primary culture. Immature cerebral cortex neurons (ED14) were maintained for up to 2 weeks in vitro, and we investigated the expression pattern of neuron differentiation and cytotoxicity of cell death, including LDH activity. Neuronal maturation initiated on day 7 and the susceptibility to glutamate-induced cell death was highly sensitive on Day 11 (Fig. 1). Thus, the exposure of the neurons to glutamate caused a dose$(0.1mM{\sim}1mM)$ and time$(4h{\sim}24h)$-dependent neurotoxicity(Fig. 4). Glutamate-induced neurodegeneration was prevented by Shipchondaebotang(SD), Yollyounggobondan(YG), Yugmijihwangwon(YJ) and the death of neurons exposed to glutamate was blocked by the NMDA receptor antagonist MK-801 (Fig. 5).

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신경전달물질 방출 저해제 FS11052가 신경세포와 PC12 세포의 돌기신장에 미치는 영향 (Effect of FS11052, an Inhibitor of Exocytosis, on Neurite Extension in Rat Hippocampal Neurons and PC12 Cells)

  • 이윤식;김동섭
    • 생명과학회지
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    • 제16권2호
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    • pp.315-322
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    • 2006
  • 신경세포 간 정보교환이 이루어지고 있는 신경전달물질의 방출과정은 극히 복잡하여, 이 방면의 독창적인 연구를 수행하기 위해서는 신규작용을 갖는 특이적인 저분자 probe의 탐색은 필수적이다. PC12세포에 tritium-label된 norepinephrine ($[^3H]-NE$)을 incorporation시킨 후에 60 mM의 고농도의 $K^+$의 자극에 의해서 탈분극 후에 방출되는 $[^3H]-NE$의 양을 scintillation countering하여 생리 활성 물질을 탐색하기 위한 in vitro의 실험계를 세웠다. 이 탐색계를 이용하여 곰팡이, 방선균와 박테리아의 대사산물 1만 1000여 샘플을 탐색한 결과, PC12세포에서 고농도의 $K^+$의 자극에 의해서 탈분극 후에 유도되는 $[^3H]-NE$의 방출을 효과적으로 저해하는 FS11052를 방선균 유래의 대사산물로부터 얻었다. FS11052는 또한 PC12세포와 rat cortical neurons에서 동일한 고농도의 $K^+$의 자극에 의한 탈분극 후에 유도되는 신경전달 물질로서 ATP의 방출에도 유의한 저해효과를 나타냈으며, 이 저해 효과는 ionopore로 알려진 ionomycin ($1{\mu}M$)을 포함하는 저농도의 $K^+$의 버퍼를 처리하였을 때에도 보여졌다. 이틀 결과로부터 FS11052의 신경전달 물질의 방출에 대한 저해작용은 세포내 $Ca^{2+}$ 유입 이 후의 반응으로 추정하며 이 작용기구에 대한 해석을 하기위하여, 신경세포의 돌기신장 형태에 대한 영향을 관찰한 결과, 분화를 유도하는 적정 농도인 $5{\mu}g/ml$의 NGF 존재 하에서의 PC12 세포의 돌기 신장에 대하여서는 억제작용을 나타냈다. 또 rat의 대뇌 해마 세포에 대하여 특정적인 형태의 돌기를 내고 있어, FS11052 물질의 첨가에 의해 통상의 긴 축색돌기는 억제되고 얇은 침상의 돌기가 세포체로부터 돌출되어 있었으며, growth cone 를 갖고 있지 않은 뉴우런이 많이 관찰되었다. FS11052 물질의 작용에 관해서는, 탈분극된 synaptic membrane이 $Ca^{2+}$ 이온을 유입 후 활성화되어 신경전달물질을 방출에 중요한 역할을 하고 있는 synaptotagmin, syntaxin, synapsin, SNAP25 등의 synaptosome을 구성하는 단백질에 직접 혹은 이와 밀접한 관련을 갖고 있는 인자와 간접적으로 작용하며, 신경전달물질의 방출을 억제하여 growth cone의 전향과 신경세포의 가소성을 조절하는 물질로 사료되어, 이 물질이 $Ca^{2+}$ 이온을 유입 후 일어나는 exocytosis와 신경계의 기능연구를 위해 사용되어질 수 있을 것으로 기대된다.

Regulation of SPIN90 by Cell Adhesion and ERK Activation

  • Kim Sung Hyun;Kim Dae Joong;Song Woo Keun
    • 한국미생물학회:학술대회논문집
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    • 한국미생물학회 2004년도 International Meeting of the Microbiological Society of Korea
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    • pp.141-146
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    • 2004
  • SPIN90 was identified to farm molecular complex with $\betaPIX$, WASP and Nck. This complex shows that SPIN90 interacts with Nck in a manner dependent upon cell adhesion to extracellular matrix, but $SPIN90{\cdot}{\beta}PIX{\cdot}WASP$ complex was stable even in suspended cells. This suggests that SPIN90 serves as an adaptor molecule to recruit other proteins to Nck at focal adhesions. SPIN90 was phosphorylated by ERK1, which was, itself, activated by cell adhesion and platelet-derived growth factor. Such phosphorylation of SPIN90 likely promotes the interaction of the $SPIN90{\cdot}{\beta}PIX{\cdot}WASP$ complex and Nck. It thus appears that the interaction of the $SPIN90{\cdot}{\beta}PIX{\cdot}WASP$ complex with Nck is crucial for stable cell adhesion and can be dynamically modulated by SPIN90 phosphorylation that is dependent on cell adhesion and ERX activation. SPIN90 directly binds syndapin I, syndapin isoform II-1 and II-s via its PRD region in vitro, in vivo and also associates with endocytosis core components such as clathrin and dynamin. In neuron and fibroblast, SPIN90 colocalizes with syndapins as puntate form, consistent with a role for SPIN90 in clathrin-mediated endocytosis pathway. Overexpression of SPIN90 N-term inhibits receptor-mediated endocytosis. Interestingly, SPIN90 PRD, binding interface of syndapin, significantly blocks internalization of transferrin, demonstrating SPIN90 involvement in endocytosis in vivo by interacting syndapin. Depletion of endogenous SPIN90 by introducing $\alpha-SPIN90$ also blocks receptor-mediated endocytosis. Actin polymerization could generate farce facilitating the pinch-out event in endocytosis, detach newly formed endocytic vesicle from the plasma membrane or push out them via the cytosol on actin tails. Here we found that SPIN90 localizes to high actin turn over cortical area, actin-membrane interface and membrane ruffle in PDGF treated cells. Overexpression of SPIN90 has an effect on cortical actin rearrangement as filopodia induction and it is mediated by the Arp2/3 complex at cell periphery. Consistent with a role in actin organization, CFP-SPIN90 present in actin comet tail generated by PIP5 $kinase\gamma$ overexpression. Therefore this study suggests that SPIN90 is functional linker between endocytosis and actin cytoskeleton.

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