1.The Development of Hippocampus: Epileptogenesis and Interneuron Dendrite.
Journal of the Korean Child Neurology Society 1999;7(2):171-180
No abstract available.
Dendrites*
;
Hippocampus*
;
Interneurons*
2.Change of optical properties and microstructure of an Ag-Pd-In alloy according to Ag content
Hyo Joung SEOL ; Su Yoen CHO ; Mi Hyang CHO
Korean Journal of Dental Materials 2018;45(3):199-208
In this study, change of optical properties and microstructure of an Ag-Pd-In alloy according to Ag content was investigated. For this purpose, specimen alloys were prepared by adding 0–100 wt.% of Ag to the 50Pd-50In (wt.%) alloy. When the content of Ag was more than 40 wt.%, the color difference with pure gold specimen was increased(p < 0.001). L* value increased as the Ag content of the specimen increased, but a* and b* value increased until the addition of 20 wt.% Ag, and then decreased with increasing Ag content(p < 0.001). Ag-free specimen was single phase in the as-cast state, but when the content of Ag was more than 20 wt.%, the phase separation occurred and two phases of matrix and dendrite or granular structure were confirmed. The dendrite or granular structure was composed of the InPd phase, and the matrix was composed of the Ag-rich phase. From these results, it can be concluded that the specimens with Ag content of 20–70 wt.% have the Ag-rich matrix which has a high L* value and low a* and b* value, and have the dendrite structure which has a low L* value and high a* and b* value. As the content of Ag increased, the color changed from light yellow to silver white due to the increase in the ratio of the matrix to the dendrite or granular structure.
Alloys
;
Dendrites
;
Silver
3.The Morphologic Changes of Interneuron Dendrites in Child Epilepsy Model.
Journal of the Korean Pediatric Society 2001;44(3):309-309
No abstract available.
Child*
;
Dendrites*
;
Epilepsy*
;
Humans
;
Interneurons*
4.Sixty years after Hsiang-Tung Chang's presentation on dendrite at the Cold Spring Harbor Symposium.
Acta Physiologica Sinica 2012;64(5):499-503
Sixty years elapsed since Chang (Hsiang-Tung Chang, Xiang-Tong Zhang) presented his seminal report "Cortical neurons with particular reference to the apical dendrite" at the Cold Spring Harbor Symposium. Thanks to the development of elaborated techniques through the 6 decades, our understanding of the dendrite has been pushed forward greatly: the backward and forward conductions during excitation, sodium and calcium conductances, chemical excitation by uncaging glutamate at a dimension of micrometer, and the quantitative study of chemical organization of postsynaptic density (PSD), etc. Though the progression is great, there are still tough problems in dendritic research, especially the integration through dendritic spine.
Calcium Signaling
;
Dendrites
;
physiology
;
Glutamic Acid
;
metabolism
5.Electrophysiological characteristics of central neuronal dendrites and roles of dendritic back-propagating action potentials in modifications of synaptic plasticity.
Jian-Tian QIAO ; Zhong-Sheng HAN ; Jin-Shun QI
Acta Physiologica Sinica 2008;60(2):293-299
For expressing the condolences on the passing away of Dr. Hsiang-Tung Chang, one of the distinguished members of the Chinese Academia of Sciences, the pioneer studies on cortical dendritic potentials that Dr. Chang carried out in the 1950s and the prosperous progresses since then, especially, concerning the modifications of synaptic plasticity by the dendritic back-propagating action potentials were briefly reviewed.
Action Potentials
;
Dendrites
;
physiology
;
Humans
;
Neuronal Plasticity
7.Ultrastructural Study of Vitiligo.
Chan Woo JEONG ; Il Yeong SON ; Un Cheol YEO ; Joungho HAN ; Eil Soo LEE
Annals of Dermatology 2001;13(3):158-162
BACKGROUND: There is a long-standing controversy whether melanocytes in vitiligo of more than 1 year duration are actually lost or still present. Resolving this matter is essential in understanding the underlying pathology and for the development of the treatment. On previous immunohistochemical and ultrastructural studies of vitiligo lesions, damage of melanocyte and keratinocyte in early lesions were reported and complete absence of melanocyte in long standing lesions were known. OBJECTIVE: This study aimed to determine the existence of the differences in pathologic changes in melanocytes according to the duration of the lesion. METHODS: We investigated the vitiliginous skin samples from 31 patients with early(less than 1 year duration) vitiligo and 30 patients with long standing(l to 5 years duration) vitiligo under the electron microscopy. RESULTS: Multiple degenerative changes in melanocytes were observed in the early and long standing lesions. In long standing lesions, degeneration of melanocytes including pyknotic, in-dented nuclei, vacuolated cytoplasms and blunted dendrites were more pronounced than early lesions. Even in long standing lesions, definite or presumptive melanocytes were observed in 16(53.3%) of 30 cases. CONCLUSION: Our results suggest that the melanocytes of vitiligo lesions were damaged and that the percentage of degenerative changes increase in accordance with the duration of the lesion. However, in long standing lesions as well as in early lesions, some residual melanocytes can be observed ultrastructurally.
Cytoplasm
;
Dendrites
;
Humans
;
Keratinocytes
;
Melanocytes
;
Microscopy, Electron
;
Pathology
;
Skin
;
Vitiligo*
8.Ultrastructural analysis of low-threshold mechanoreceptive vibrissa afferent boutons in the cat trigeminal caudal nucleus.
Sang Kyoo PAIK ; Seung Ki CHOI ; Jong Wook LEE ; Tae Heon KIM ; Dong Kuk AHN ; Atsushi YOSHIDA ; Yun Sook KIM ; Yong Chul BAE
Anatomy & Cell Biology 2010;43(4):340-346
Ultrastructural parameters related to synaptic release and their correlation with synaptic connectivity were analyzed in the low-threshold mechanoreceptive vibrissa afferent boutons in laminae III and IV of the trigeminal caudal nucleus (Vc). Rapidly adapting vibrissa afferents were intra-axonally labeled, and quantitative ultrastructural analyses with serial sections were performed on the labeled boutons and their presynaptic endings (p-endings). The volume of the labeled boutons was widely distributed from small to large ones (0.8~12.3 microm3), whereas the p-endings were small and uniform in size. The volume of the labeled boutons was positively correlated with the ultrastructural parameters such as mitochondrial volume (correlation coefficient, r=0.96), active zone area (r=0.82) and apposed surface area (r=0.79). Vesicle density (r=-0.18) showed little correlation to the volume of labeled boutons, suggesting that the total vesicle number of a bouton is proportional to its volume. In addition, the bouton volume was positively correlated with the number of p-endings (r=0.52) and with the number of dendrites postsynaptic to the labeled bouton (r=0.83). These findings suggest that low-threshold mechanoreception conveyed through vibrissa afferents is processed in a bouton size-dependent manner in the Vc, which may contribute to the sensory-motor function of laminae III/IV in Vc.
Animals
;
Cats
;
Dendrites
;
Mitochondrial Size
;
Synapses
;
Trigeminal Caudal Nucleus
9.Diclofenac Inhibits 27-hydroxycholesterol-induced Differentiation of Monocytic Cells into Mature Dendritic Cells.
Yonghae SON ; Bo Young KIM ; Young Chul PARK ; Koanhoi KIM
Immune Network 2017;17(3):179-185
We investigated whether diclofenac could influence the development of antigen-presenting cells in an oxygenated cholesterol-rich environment by determining its effects on the 27-hydroxycholesterol (27OHChol)-induced differentiation of monocytic cells into mature dendritic cells (mDCs). Treatment of human THP-1 monocytic cells with diclofenac antagonized the effects of 27OHChol by attenuating dendrite formation and cell attachment and promoting endocytic function. Diclofenac inhibited the transcription and surface expression of the mDC markers of CD80, CD83, and CD88, and reduced the 27OHChol-induced elevation of surface levels of MHC class I and II molecules to the basal levels in a dose-dependent manner. It also reduced the expression of CD197, a molecule involved in DC homing and migration. These results indicate that diclofenac inhibits the differentiation of monocytic cells into mDCs, thereby potentially modulating adaptive immune responses in a milieu rich in cholesterol oxidation products.
Antigen-Presenting Cells
;
Cholesterol
;
Dendrites
;
Dendritic Cells*
;
Diclofenac*
;
Humans
;
Oxygen
10.The DiI Staining of Interneuron Dendrites in Kainate-Treated Hippocampal Slice Culture.
Young Hoon KIM ; In Goo LEE ; Seung Yun CHUNG ; Kyung Tai WHANG
Journal of the Korean Child Neurology Society 2000;8(2):204-210
PURPOSE: Excitotoxic injury of the dendrites of inhibitory interneurons could lead to decrease in their synaptic activation, and explain subsequent local circuit hyperexcitability and epilepsy. A hallmark of dendrotoxicity at least in principal neurons of the hippocampus and cortex are focal or varicose swellings of dendritic abors. This research was designed to study morphologic changes of interneuron dendrite in kainate-treated hippocampal slice culture overtime. METHODS: Cultures aged 15-16 Equivalent Postnatal Days (EPD) were exposed to 10 microM kainic acid (KA), and analyzed at 0, 8, 24, 48, 72 hours after transient (1 hour) KA exposure. Neuronal injury was determined by morphologic changes of interneuron dendrites in area CA1 of DiI stained sections. RESULTS: 1) Transient (1 hour) exposure of hippocampal explant cultures to KA produced marked focal swellings of the dendrites of DiI stained interneurons in a highly reproducible manner. 2) The presence of focal swellings was reversible with kainate washout. The dendrites of KA treated explants were no longer beaded at 8, 24, 48, 72 hours after KA exposure. 3) There was no significant difference in the thickness of dendrites in DiI stained interneuron among 8hr, 24hr, 48hr and 72hr recovery group, compared with control group. CONCLUSION: The presence of focal swellings was reversible with kainate washout, and was not accompanied by interneuronal cell death.
Cell Death
;
Dendrites*
;
Epilepsy
;
Hippocampus
;
Interneurons*
;
Kainic Acid
;
Neurons