• Applied Microscopy
• /
• 제24권2호
• /
• pp.48-62
• /
• 1994

The acute irradiation effect on rat Purkinje cell was carried out. Anesthetized rats, weighing 200-250g each, were exposed their heads to the linear accelerator (ML-4MV) with the doses of 3,000 rads or 6,000 rads respectively. Irradiated rats were sacrificed by perfusion fixation under anesthesia, six hours, two days and six days following the irradiations. Rats were perfused with the fixative of 1% glutaraldehyde-1% paraformaldehyde solution (pH 7.4). Small pieces of cerebellar cortices were taken out. Tissue blocks were washed out, and were refixed in the 2% osmium tetroxide solution. After dehydration, tissues were embedded in the araldite mixture. Ultrathin sections stained with uranyl acetate-lead citrate solution, were examined with an electron microscope. The results observed were as follow; 1. Many dark Purkinje cells exhibited most severe cellular alterations on 6 hours. But after the 2 or 6 days, the cells exhibited only some alterations of cytoplasmic organelles. 2. Many granular and agranular endoplasmic reticula exhibited the fusion of cisterns. These reticular alterations were most severe on 6 hours following irradiation. But the alterations were hardly found on 6 days. 3. In the Golgi region, alterations including the adhesion of lamelliform cisterns, enlarged saccules, and increased number of vesicles, etc, were seen on 6 hours. But the Golgi complexes were almost recovered on 6 days. 4. Lysosomes were abundant on 6 hours or 2 days, but some residual bodies were found on 6 days. 5. Mitochondrial changes were also most severe at on hours, and they were recovered thereafter. From the results, it was concluded that the cerebellar Purkinje cells reacted to the high doses of irradiation by hyperactive protein synthesis, autolytic activities and energy metabolism. The reaction was most active in the early stage. It implies that motor-control function of Purkinje cells are severely disturbed in the early stage of irradiation.

• The Korean Journal of Physiology and Pharmacology
• /
• 제1권5호
• /
• pp.477-484
• /
• 1997

Intracellular recordings of oscillatory firing (bursting activity) were obtained from Purkinje cells (PCs) in rat cerebellar slices. Apamin inhibited post-burst hyperpolarizations (PBHs) progressively and finally terminated oscillatory firing activity of PCs. Apamin did not affect the amplitude or duration of the after-hyperpolarization (AHP) between spikes within the burst. In the voltage clamp mode, apamin shifted the whole-cell, quasi-steady state I/V relationship in an inward direction and abolished the zero slope resistance (ZSR) region by blocking outward current. Nickel ($Ni^{2+}$) terminated oscillatory activity and also abolished the ZSR region. However, $Ni^{2+}$ did not have progressive blocking action on the post-burst hyperpolarization before it blocked oscillatory activity. $Ni^{2+}$ blocked an inward current at potentials positive to approximately -65 mV, which was responsible for the ZSR region and outward current at more negative potentials. These data indicated that oscillatory activity of PCs is sustained by a balance between a slow $Ni^{2+}$-sensitive inward current and an apamin-sensitive outward current in the region of ZSR of the whole-cell I/V curve.

• 한국체육학회지인문사회과학편
• /
• 제58권4호
• /
• pp.481-492
• /
• 2019

본 연구는 12주간의 트레드밀 운동이 노화 흰쥐 소뇌의 성상세포 활성과 퍼킨제 세포 발현 및 운동기능 변화에 미치는 영향에 대해 알아보았다. Sprague-Dawley(SD) 흰쥐를 실험처치에 따라 (1)젊은 통제집단 (Young Control Group; YCG; 3months aged; n=10), (2) 노화 통제집단 (Old Control Group; OCG; 24months aged; n=10), (3) 노화 운동집단 (Old Exercise Group; OEG; 24months aged; n=10)으로 구분한 후 OEG는 트레드밀 운동을 시간과 강도를 점증적으로 증가하여 12주간, 주 5회 실시하였다. 실험결과 rota-rod 검사에서 운동기능이 OCG에 비해 OEG에서 증가하는 것으로 나타났으며(p<.05) 그 수준은 YCG와 유사한 것으로 나타났다. calbindin-양성 퍼킨제 세포의 발현도 OCG에 비해 OEG의 소뇌 충부에서 증가하였으며(p<.05), 그 수준은 YCG와 유사하였다. GFAP-, NMDAR-양성세포의 발현도 OEG에서 증가하였다(각각 p<.001). GFAP, GLAST 단백질 수준은 OCG에 비해 OEG에서 증가하였으며(p<.05, p<.001) 그 수준은 YCG와 유사하였다. BDNF, NGF 수준은 YCG에서 가장 높았으며 OCG에 비해 OEG에서 증가하는 것으로 나타났다(p<.001, p<.05). 이상의 결과를 종합하면 규칙적인 운동은 성상세포의 활성을 향상시킬 뿐만 아니라 신경영양인자의 증가를 통하여 소뇌의 퍼킨제 세포 발현과 운동기능을 개선시키는 것으로 판단된다.

• The Korean Journal of Physiology
• /
• 제29권1호
• /
• pp.103-111
• /
• 1995

Intracellular recordings were obtained from Purkinje cells in rat cerebellar slices maintained in vitro. Adding tetrodotoxin to the superfusion solution produced a typical pattern of repetitive burst firing consisting of a cluster of action potentials followed by a long hyperpolarization. TTX-induced oscillatory activity was not due to modulation of membrane potential although underlying mechanisms for maintenance of oscillatory activity were influenced by membrane voltage. The mechanism of TTX-induced oscillation was not related to the presence or amplitude of $I_h$ and could still induce the oscillatory activity after blockade of $I_h$ by cesium. The result from an experiment in which QX-314 was injected intracellularly strongly suggested that TTX-induced oscillatory firing activity was due to blockade of post-synaptic $Na^{+}$ currents intrinsic to PCs.

• The Korean Journal of Physiology and Pharmacology
• /
• 제16권2호
• /
• pp.139-144
• /
• 2012

It has been reported that activation of metabotropic glutamate receptor 1 (mGluR1) can mediate endocannabinoid-induced short-term depression of synaptic transmission in cerebellar parallel fiber (PF)-Purkinje cell (PC) synapse. mGluR1 has signaling pathways involved in intracellular calcium increase which may contribute to endocannabinoid release. Two major mGluR1-evoked calcium signaling pathways are known: (1) slow-kinetic inward current carried by transient receptor potential canonical (TRPC) channel which is permeable to $Ca^{2+}$; (2) $IP_3$-induced calcium release from intracellular calcium store. However, it is unclear how much each calcium source contributes to endocannabinoid signaling. Here, we investigated whether calcium influx through mGluR1-evoked TRPC channel contributes to endocannabinoid signaling in cerebellar Purkinje cells. At first, we applied SKF96365 to inhibit TRPC, which blocked endocannabinoid-induced short-term depression completely. However, an alternative TRP channel inhibitor, BTP2 did not affect endocannabinoid-induced short-term depression although it blocked mGluR1-evoked TRPC currents. Endocannabinoid signaling occurred normally even though the TRPC current was mostly blocked by BTP2. Our data imply that TRPC current does not play an important role in endocannabinoid signaling. We also suggest precaution in applying SKF96365 to inhibit TRP channels and propose BTP2 as an alternative TRPC inhibitor.

• 한국전자현미경학회:학술대회논문집
• /
• 한국현미경학회 1999년도 제30차 추계학술대회
• /
• pp.32-33
• /
• 1999

• 생물정신의학
• /
• 제7권2호
• /
• pp.164-173
• /
• 2000

This study was carried out to investigate the direct neurotoxicity of alcohol on CNS and the effects of piracetam or vitamins on ultrastructural changes of the rat cerebellar and hippocampal neurons during long-term alcohol treatment. To evaluate the results, quantitative analysis were done for light and electronic microscopic findings. On the light microscopy, red degeneration of pyramidal cells and Purkinje cells was found more apparently in the alcohol only treated group than in the control group. On the electron microscopy, increased lipofuscin pigments were found in cerebellum and hippocampus. In quantitative analysis, vitamins significantly reduced red degeneration in both hippocampus and cerebellum. However, piracetam significantly reduced red degeneration in cerebellum but not in hippocampus. Lipofuscin pigments in Purkinje cells and pyramidal cells were significantly reduced in the alcohol with piracetam treated group than the alcohol only treated group. However, vitamins had no significant reducing effect of lipofuscin pigments in Purkinje cells and pyramidal cells. According to the results, it is concluded that vitamins deficiency might cause red degeneration of pyramidal cell after long-term alcohol treatment, but increment of lipofuscin pigments in pyramidal and Purkinje cell may be caused by alcohol itself or its metabolite rather than vitamins deficiency. Piracetam seems to improve cognitive function impairment caused by alcohol consumption.

• 생명과학회지
• /
• 제8권1호
• /
• pp.14-26
• /
• 1998

본 연구에서는 SDS/polyacrylamide 젤 전기영동에 의한 쥐의 성장과정에 따른 소뇌의 단백질양상의 변화양상과 immunocytochemistry를 이용하여 c-raf a-raf kinase의 정상 소뇌에서의 분포에 대해 관찰 하였으며 western blot을 이용하여 소뇌의 단백질들에서 c-raf의 존재에 대해 살펴보았다. 단백질 양상에서 쥐의 성장에 따라 crude에선,ㄴ 49,200 dalton과 169,000 dalton 사이의 bands가 양적 증가를 보였으며 cytosolic fraction 에서는 37,800 dalton의 band가 양적 증가를 보이는데 비해 membrane fraction 에서는 260,600 dalton의 band가 증가하였다. 이러한 결과로 성장 발달에 따라 고분자 량의 물질들이 이들 소뇌 부위에서 기여하였을 것으로 추정할 수 있었다. Immunocytochemistry에 의한 분석에서는 c-raf와 a-raf가 소뇌의 피질주위에서 조롱박 세포(Purkinje cell) 의 세포질 특히 핵 주변부위에서 강하게 검출되었으며 a-raf에 비해 c-raf가 더 강하게 나타났었다. 그리고 그 외에 Nucleus embolifornis의 큰 neuronal cell의 세포질 부위의 나타남을 볼 수 있었다. Immunoblot에 의한 분석에서는 crude와 cytosolic fraction에서 raf protein kinase의 존재를 확인할 수 있었으며, 이상의 결과들을 종합해 보았을 때 소뇌의 정상의 많은 신경세포(neuronal cell)에 raf protein kinase가 분포되어 있으며 이들이 정상의 cell에서 기능을 가질 것으로 추정된다.

• PNF and Movement
• /
• 제4권1호
• /
• pp.51-62
• /
• 2006

Purpose : The purposes of this study were to test the effect of proprioceptive and vestibular sensory input on expression of BDNF after traumatic brain injury in the rat. Subject : The control group was sacrificed at 24 hours after traumatic brain injury. The experimental group I was housed in standard cage for 7 days. The experimental group II was housed in standard cage after intervention to proprioceptive and vestibular sensory(balance training) for 7 days. Method : Traumatic brain injury was induced by weight drop model and after operation they were housed in individual standard cages for 24 hours. After 7th day, rats were sacrificed and cryostat coronal sections were processed individual1y in goat polyclonal anti-BDNF antibody. The morphologic characteristics and the BDNF expression were investigated in injured hemisphere section and contralateral brain section from immunohistochemistry using light microscope. Result : The results of this experiment were as follows: 1. In control group, cell bodies in lateral nucleus of cerebellum, superior vestibular nucleus, purkinje cell layer of cerebellum and pontine nucleus changed morphologically. 2. The expression of BDNF in contralateral hemisphere of group II were revealed. 3. On 7th day after operation, immunohistochemical response of BDNF in lateral nucleus, superior vestibular nucleus, purkinje cell layer and pontine nucleus appeared in group II. Conclusion : The present results revealed that intervention to proprioceptive and vestibular sensory input is enhance expression of BDNF and it is useful in neuronal reorganization improvement after traumatic brain injury.

• Applied Microscopy
• /
• 제31권1호
• /
• pp.1-8
• /
• 2001

신경세포 가지돌기가시의 형태를 분석하는 것은 신경세포의 기능을 이해하는데 중요하다. 가지돌기가시는 광학현미경 해상도의 한계근처에 있는 구조물로 투과전자현미경 및 공초점헌미경 등을 이용한 연구들이 보고 되고 있다. 고압전자현미경은 높은 해상도와 투과능력 덕분에 두꺼운 절편의 관찰이 용이하여 신경세포의 가지돌기가시 등을 관찰하는데 유용한 것으로 알려져 있다. 고압전자현미경을 이용하여 신경세포의 가지돌기가시를 효과적으로 관찰하는방법을 확인하고 기본적인 형태학적 자료를 축적하고자 하였다. 생쥐 소뇌에 위치하는 조롱박세포의 가지돌기가시를 anti-calbindin 28kD항체 및 Golfi 염색으로 표지한 후 $4{\mu}m$두께의 절편을 제작하여 impregnation방법으로 각각 처리하여 표본을 제작한 후, 초고압전자현미경으로 관찰하여 효과적인 관찰방법을 찾고, 영상분석 기법을 이용하여 가지돌기가시의 밀도와 가시의 길이를 측정하였다. 초고압전자현미경 관찰 결과, 면역조직화학법과 Golgi법 모두 조롱박세포의 가지돌기가시를 관찰할 수 있었으나 Golgi법으로 준비된 표본이 가시를 정량적으로 분석하기에 더욱 적합하였다. 명상분석 결과로는 가지돌기 가시의 평균밀도가 $24.5{\pm}3.6$개/$10{\mu}m$였고, 가시의 평균길이는 $1.12{\pm}0.22{\mu}m$였다. 본 연구를 통해서 Gogli 법으로 염색된 조롱박세포를 고압전자현미경으로 관찰할 경우, 가지돌기가시를 정량적으로 관찰할만한 만족스러운 영상을 얻을 수 있었고, 추후 경사를 주어 촬영한 두 장의 사진을 이용하여 3차원적으로 분석하면 좀 더 정확한 결과를 얻을 수 있을 것으로 판단되며, 이는 소뇌의 신경가소성을 이해하는데 중요한 자료가 될 것이다.