• 제목/요약/키워드: Cerebral neuron

검색결과 97건 처리시간 0.029초

Cerebral Infarction Presenting with Unilateral Isolated Foot Drop

  • Kim, Ki-Wan;Park, Jung-Soo;Koh, Eun-Jeong;Lee, Jong-Myong
    • Journal of Korean Neurosurgical Society
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    • 제56권3호
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    • pp.254-256
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    • 2014
  • Weakness of the dorsiflexor muscles of the ankle or toe, referred to as foot drop, is a relatively common presentation. In most cases, foot drop is caused by a lower motor neuron disease such as peroneal peripheral neuropathy, L4-5 radiculopathic sciatic neuropathy, or polyneuropathy. Although upper motor neuron lesions can present as foot drop, the incidence is very rare. Here, we report an extremely rare case in which foot drop was the only presenting symptom of cerebral infarction.

Cortical Neuronal Loss after Chronic Prenatal Hypoxia : A Comparative Laboratory Study

  • Chung, Yoon Young;Jeon, Yong Hyun;Kim, Seok Won
    • Journal of Korean Neurosurgical Society
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    • 제56권6호
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    • pp.488-491
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    • 2014
  • Objective : The purpose of this study was to investigate the prenatal hypoxic effect on the fetal brain development. Methods : We used the guinea pig chronic placental insufficiency model to investigate the effect of hypoxia on fetal brain development. We ligated unilateral uterine artery at 30-32 days of gestation (dg : with term defined as -67 dg). At 50 dg, 60 dg, fetuses were sacrificed and assigned to either the growth-restricted (GR) or control (no ligation) group. After fixation, dissection, and sectioning of cerebral tissue from these animals, immunohistochemistry was performed with NeuN antibody, which is a mature neuronal marker in the cerebral cortex. Results : The number of NeuN-immunoreactive (IR) cells in the cerebral cortex did not differ between the GR and control groups at 50 dg. However, the number of NeuN-IR cells was lesser in GR fetuses than in controls at 60 dg (p<0.05). Conclusion : These findings show that chronic prenatal hypoxia affect the number of neuron in the cerebral cortex of guinea pig fetus at 60 dg. The approach used in this study is helpful for extending our understanding of neurogenesis in the cerebral cortex, and the findings may be useful for elucidating the brain injury caused by prenatal hypoxia.

방풍당귀음(防風當歸飮)이 중대뇌동맥 폐쇄 후 재관류 모델에 미치는 영향 -육안.광학현미경 소견- (The effect of Bangpungdangkwi-eum extracts on reperfusion following the middle cerebral artery occlusion in rats)

  • 홍천표;박인식;신길조;이원철;정승현
    • 대한한방내과학회지
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    • 제21권2호
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    • pp.319-327
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    • 2000
  • To evaluate the effect of Bangpungdangkwi-eum extracts on reperfusion following the middle cerebral artery occulsion in Sprague Dawley rats, the neuron protection effect were investigated through examining the size of cerebral infarction, cerebral edema, and the morphologic change of neuron. The results were obtained as follows; 1. The size of cerabral infarction in sample group is significantly decreased compared with that in control group. Sample group has approximately 17% cerebral infarction parts induced by ischemia in cerebrum while control group has approximately 22%. 2. The volume of cerebral edema in sample group is significantly decreased compared with that in control group. The volumn in sample group is increased by approximately 4.4% compared with that in normal group while that in control group is increased by approximately 7.7%. 3. The optical microscopic examination reveals that the damage of neurons in the ischemic parts and CA1 and CA3 region of hippocampus in the same side of the ischemic parts was the most high and the damage in sample group is decreased compared with that in control group.

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활성산소로 손상된 대뇌신경세포에 대한 천오두의 영향 (Effect of Aconiti Radix on Cultured Cerebral Neurons Damaged by Reactive Oxygen Species)

  • 심재한;이은미;이종화;김대근;이영찬;강정호;박신기
    • 동의생리병리학회지
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    • 제17권2호
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    • pp.499-502
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    • 2003
  • Neurotoxicity of reactive oxygen species(ROS) and neuroprotective effect of Aconiti Radix(AR) against ROS-induced cytotoxicity were determined on cultured mouse cerebral neurons by MTT assay after cerebral neurons were cultured for 5 hours in various concentrations of GO. GO was toxic in a dose-dependent manner on cultured cerebral neurons after cerebral neurons were incubated for 5 hours in media containing 5~40mU/ml GO. While, cultures were pretreated with 180 μg/ml AR for 2 hours increased remarkably cell viability. From these results, it is suggested that GO has toxic effect on cultured mouse cerebral neurons by the decrease of cell viability. And also, herb extract such as AKR is very effective in the protection pf neurotoxicity induced by GO.

대승기탕(大承氣湯)의 사하작용이 중대뇌동맥 폐쇄 흰쥐의 뇌경색에 미치는 영향 (Effects of Daeseungkitang on Cerebral Infarct of MCAO Rats)

  • 이규식;김연섭
    • 대한본초학회지
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    • 제26권3호
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    • pp.7-14
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    • 2011
  • Object : This study evaluated the effects of Daeseungkitang(DSK) on cerebral infarct of middle cerebral artery occlusion(MCAO). Method : Sprague-Dawley rats are used for observing to induce cerebral infraction closing its middle cerebral artery temporarily and take DSK by mouth the next 5 days, observe the amount of feces and urine. It is investigated the correlation between them after examining neurological score. Results : It is resulted the below. On the 2nd day of taking DSK, the total amount of feces of the cerebral infarct rats is increased significantly. After taking DSK, the urine volume of the cerebral infarct rats does not change at all. Taking DSK significantly improves neurological score of the cerebral infarct rats. There is a significant correlation between total amount of feces of the cerebral infarct rats and neurological score, otherwise there is no significant correlation between total amount of feces and neurological score which is taken DSK. By taking DSK, the volume of cerebral infarction does not decrease significantly. Taking DSK restrains the expression of iNOS in the cerebral cortex and striatum of the cerebral infarct rats. Taking DSK restrains the expression of MMP-9 in the cerebral cortex of the cerebral infarct rats. Taking DSK restrains the edema of astrocytes of the positive reaction of GFAP in the cerebral cortex of the cerebral infarct rats. Conclusion : According to above results, Daeseungkitang(DSK) is assumed that showing reaction of protecting neuron cell by restraint brain tissue edema thorough controlling water balance.

L-NAME으로 유발된 학습.기억장애와 뇌허혈 손상에 관한 대조환의 효과 (Effects of Daejo-hwan(Tatsao-wan) on L-NAME Induced Learning and Memory Impairment and on Cerebral Ischemic Damage of the Rats)

  • 김근우;구병수
    • 대한한의학회지
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    • 제21권2호
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    • pp.25-36
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    • 2000
  • Objectives : This study demonstrates the effects of Daejo-hwan on learning and memory impairment induced by L-NAME (75 mg/kg) treatment and on cerebral ischemic damage induced by middle cerebral artery (MCA) occlusion in rats. Methods : Daejo-hwan emulsion (73.3 mg/100 g/l ml) was administered to rats along a timed study schedule. The Moms water maze was used for learning and memory test of the rats. The MCA was occluded by using the intraluminal thread method. The brain slices were stained by 2 % triphenyl tetrazolium chloride (TTC) and 1 % cresyl violet solution. Infarct size, neuron cell number and size in penumbra was measured by using computer image analysis system. Results : 1. The escape latency of the Daejo-hwan treated group decreased significantly with respect to the control group. 2.The memory score of the Daejo-hwan treated group showed increase tendency, And the swimming distance was not different between the normal, the control, and the Daejo-hwan treated group. 3. The infarct size of the Daejo-hwan treated group decreased significantly with respect to the control group. 4. The total infarct volume of the Daejo-hwan treated group showed decrease tendency. And the brain edema index of the Daejo-hwan treated group decreased significantly with respect to the control group. 5. The neuron cell number and cell size in penumbra of the Daejo-hwan treated group increased significantly with respect to the control group. Conclusions : According to the above results, it is supposed that Daejo-hwan is clinically applicable to the vascular dementia.

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초저체온하 완전순환정지 시에 이용되는 역행성 뇌관류의 시간에 따른 뇌대사 지표, 혈청 내 neuron-specific enolase, 및 S-100 베타단백의 변화 (The Changes of Cerebral Metabolic Parameters, Serum Levels of Neuron-Specific Enolase and S-100$\beta$ Protein During Retrograde Cerebral Perfusion Under Profound Hypothermic Total Circulatory Arrest)

  • 김경환
    • Journal of Chest Surgery
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    • 제34권9호
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    • pp.653-661
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    • 2001
  • 배경 : 역행성 뇌관류는 대동맥궁 수술에서 이용되는 뇌보호법중의 하나이다. 저자는 이에 대한 연구결과를 이미 발표한 바 있으나, 그 안전성 여부에 대하여는 아직 논의가 필요한 부분이다. 역행성 뇌관류 연구를 진행하면서, 조기 뇌손상을 시사한다고 알려진 여러 인자들을 조사하였다. 대상 및 방법 : 25~30kg 돼지를 이용하여 120분간 역행성 뇌관류를 시행하였다. 심폐기 이탈을 시행하고 2시간 동안 생존을 유도하였으며, 전기간에 걸쳐 직장체온, 내경정맥 산소포화도, 중심정맥압 등을 관찰하였다. 조직학적 소견을 관찰하였고, 혈중 neuron-specific enolose(NSE) 및 S100베타 단백치를 측정하였다. 역행성 뇌관류 시행 중 중심정맥압은 20~25mmHg를 유지하였다. 결과 : 역행성 뇌관류 속도 (ml/min)는 224.3$\pm$87.5(20분), 227.1$\pm$111.0(40분), 221.4$\pm$119.5(60분), 230.0$\pm$136.5(80분), 234.3$\pm$146.1(100분), 184.3$\pm$50.5(120분)으로 나타났으며 혈중 NSE 농도는 역행성 뇌관류 후에 관류전에 비해 유의한 증가를 보이지 않았다. 혈중 S100 베타 단백치(ng/ml)는 0.12$\pm$0.07(마취시작), 0.12$\pm$0.07(심폐바이패스직후), 0.19$\pm$0.12(심폐기가동 20분), 0.25$\pm$0.06(역행성뇌관류 20분), 0.29$\pm$0.08(40분), 0.41$\pm$0.05(60분), 0.49$\pm$0.03(80분), 0.51$\pm$0.10(100분), 0.46$\pm$0.11(120분), 0.52$\pm$0.15(심폐기 재가동 30분), 0.62$\pm$0.15(60분), 0.76$\pm$0.17(심폐기이탈 30분), 0.81$\pm$0.20(60분), 0.84$\pm$0.23(90분) and 0.94$\pm$0.33(120분)를 보였고 이는 역행성 뇌관류 전에 비해 유의하게 증가된 소견이었다(p<0.05). 뇌신피질, 기저핵, 해마에서 전자현미경 조직 소견을 관찰하였으며 마이토콘드리아의 부종을 관찰할 수 있었다. 결론 : 역행성 뇌관류 120분 후에 S100 베타 단백의 유의한 증가를 관찰할 수 있었으며 뇌조직 손상과의 관련성은 좀 더 연구되어야 할 부분으로 생각된다. 장기 생존 모델을 통한 재평가가 필요하다고 사료되며 심폐바이패스 시행 등의 교란 인자도 고려해야 할 것이다.

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하수오가 유기수은으로 손상된 생쥐의 배양대뇌신경세포에 미치는 영향에 관한 연구 (Study on the Effect of Radix polygoni Multiflori on Cultured Mouse Cerebral Neurons Damaged by Organic Mercury)

  • 유교상;이용석;손영우;홍기연
    • 동의생리병리학회지
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    • 제16권6호
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    • pp.1134-1137
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    • 2002
  • To investigate the neurotoxic effect of organic chloride on cultured mouse cerebral neurons, cytotoxic effect was measured by MTT assay after cultured cerebral neurons were incubated with various concentrations of methyl mercuric chloride(MMC) for 24 hours. The protective effect of Radix Polygoni Multiflori(RPM) on MMC-induced neurotoxicity was also examined in these cultures. MMC decreased cell viability of cultured mouse cerebral neurons remarkably in a dose- and time-dependent manners. In protective effect of RPM it was remarkably effective in blocking the neuroxicity induced by MMC. From aboved the results, it is suggested that MMC induce neurotoxicity, and the herba extract, RPM is very effective in preventing MMC-induced cytotoxicity on cultured mouse cerebral neurons.

돼지에서 초저체온 순환정지 하의 역행성 뇌관류시 뇌대사, 혈류역학 지표, 뇌조직 소견 및 혈청 내 neuron-specific enolase의 변화 (The Changes of Cerebral Metabolic and Hemodynamic Parameters, Brain Histology, and Serum Levels of Neuron-Specific Enolase During Retrograde Cerebral Perfusion Under Pofound Hypothermic total Circulatory Arrest in Pigs)

  • 김경환;안혁
    • Journal of Chest Surgery
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    • 제33권6호
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    • pp.445-468
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    • 2000
  • Background: Retrograde cerebral perfusion(RCP) is currently used for brain protection during aorta surgery, however, for the safety of it, various data published so far are insufficient. We performed RCP using pig and investiaged various parameters of cerebral metabolism and brain injury after RCP under deep hypothermia. Material and Method: We used two experimental groups: in group I(7 pigs, 20 kg), we performed RCP for 120 minutes and in group II (5 pigs, 20 kg), we did it for 90 minutes. Nasopharyngeal temperature, jugular venous oxygen saturation, electroencephalogram were continuously monitored, and we checked the parameters of cerebral metabolism, histological changes and serum levels of neuron-specific enolose(NSE) and lactic dehydrogenase(LDH). Central venous pressure during RCP was mainained in the range of 25 to 30 mmHg. Result: Perfusion flow rates(ml/min) during RCP were 130$\pm$57.7(30 minutes), 108.6$\pm$55.2(60 minutes), 107.1$\pm$58.8(90 minutes), 98.6$\pm$58.7(120 minutes) in group I and 72$\pm$11.0(30 minutes), 72$\pm$11.0(60 minutes), 74$\pm$11.4(90 minutes) in group II. The ratios of drain flow to perfusion flow were 0.18(30 minutes), 0.19(60 minutes), 0.17(90 minutes), 0.16(120 minutes) in group I and 0.21, 0.20, 0.17 in group II. Oxygen consumptions(ml/min) during RCP were 1.80$\pm$1.37(30 minutes), 1.72$\pm$1.23(60 minutes), 1.38$\pm$0.82(90 minutes), 1.18$\pm$0.67(120 minutes) in group I and 1.56$\pm$0.28(30 minutes), 1.25$\pm$0.28(60 minutes), 1.13$\pm$0.26(90 minutes). We could observe an decreasing tendency of oxygen consumption after 90 minutes of RCP in group I. Cerebrovascular resistance(dynes.sec.cm-5) during RCP in group I incrased from 71370.9$\pm$369145.5 to 83920.9$\pm$49949.0 after the time frame of 90 minutes(p<0.05). Lactate(mg/min) appeared after 30 minutes of RCP and the levels were 0.15$\pm$0.07(30 minutes), 0.18$\pm$0.10(60 minutes), 0.19$\pm$0.19(90 minutes), 0.18$\pm$0.10(120 minutes) in group I and 0.13$\pm$0.09(30 minutes), 0.19$\pm$0.03(60 minutes), 0.29$\pm$0.11(90 minutes) in group II. Glucose utilization, exudation of carbon dioxide, differences of cerebral tissue acidosis between perfusion blood and drain blood were maintained constantly during RCP. Oxygen saturation levels(%) in drain blood during RCP were 22.9$\pm$4.4(30 minutes), 19.2$\pm$4.5(60 minutes), 17.7$\pm$2.8(90 minutes), 14.9$\pm$2.8(120 minutes) in group I and 21.3$\pm$8.6(30 minutes), 20.8$\pm$17.6(60 minutes), 21.1$\pm$12.1(90 minutes) in group II. There were no significant changes in cerebral metabolic parameters between two groups. Differences in serum levels of NSE and LDH between perfusion blood and drain blood during RCP showed no statistical significance. Serum levels of NSE and LDH after resuming of cardipulmonary bypass decreased to the level before RCP. Brain water contents were 0.73$\pm$0.03 in group I and 0.69$\pm$0.06 in group II and were higher than those of the controls(p<0.05). The light microscopic findings of cerebral neocortex, basal ganglia, hippocampus(CA1 region) and cerebellum showed no evidence of cerebral injury in two groups and there were no different electron microscopy in both groups(neocortex, basal ganglia and hippocampus), but they were thought to be reversible findings. Conclusion: Although we did not proceed this study after survival of pigs, we could perform the RCP successfully for 120 minutes with minimal cerebral metabolism and no evidence of irreversible brain damage. The results of NSE and LDH during and after RCP should be reevaluated with survival data.

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