1.An effect of IV methylprednisolone in acute idiopathic thrombocytopenic purpura.
Jin Kuk KIM ; Kyeong Hee HONG ; Tae Gyu WHANG ; Soon Yong LEE
Journal of the Korean Pediatric Society 1991;34(9):1240-1245
No abstract available.
Methylprednisolone*
;
Purpura, Thrombocytopenic, Idiopathic*
2.A case of Weber-Christian disease.
Doo Kweon KIM ; Sang Jo PARK ; Tae Gyu WHANG ; Soon Yong LEE
Journal of the Korean Pediatric Society 1991;34(8):1157-1162
No abstract available.
Panniculitis
;
Panniculitis, Nodular Nonsuppurative*
3.A Case of Spontaneous Thoracic Epidural Hematoma.
Sung Gyun PARK ; Dong Gyu KIM ; Shin Tae KIM ; Sung Nam WHANG ; Hwa Young RHEE
Journal of Korean Neurosurgical Society 1985;14(2):437-442
Spontaneous thoracic epidural hematoma occur rarely. We present a case of spontaneous thoracic epidural hematoma without any identified etiology and discuss the symptoms, signs and pathophysiology of this disorder. Early diagnosis and treatment by surgery can result in good recovery.
Early Diagnosis
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Hematoma*
4.A Case of Neurofibromatosis with Multiple Neurofibromas on Mesentery.
Pil Geung HWANG ; Sun Young PARK ; Tae Gyu WHANG ; Soon Yong LEE
Journal of the Korean Pediatric Society 1997;40(2):270-273
Neurofibromatosis originally described by von-Recklinhausen in 1882, is often depicted as a chronic progressive hereditary disease characterized by pigmentation of the skin, cutaneus lesions, and numerous tumors developing in association with elements of both the central and peripheral nervous tissue. Mesenteric involvements in neurofibromatosis are very rare in childrens. We experienced a case of neurofibromatosis with multiple neurofibromas on mesentery in 6 years old male who presented with abdominal pain. The diagnosis was confirmed by clinical manifestations, abdominal CT, and histopathologic findings. Brief review of literatures was made.
Abdominal Pain
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Child
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Diagnosis
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Genetic Diseases, Inborn
;
Humans
;
Male
;
Mesentery*
;
Neurofibroma
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Neurofibromatoses*
;
Pigmentation
;
Skin
;
Tomography, X-Ray Computed
5.Natural compounds, fraxin and chemicals structurally related to fraxin protect cells from oxidative stress.
Wan Kyunn WHANG ; Hyung Soon PARK ; InHye HAM ; Mihyun OH ; Hong NAMKOONG ; Hyun Kee KIM ; Dong Whi HWANG ; Soo Young HUR ; Tae Eung KIM ; Yong Gyu PARK ; Jae Ryong KIM ; Jin Woo KIM
Experimental & Molecular Medicine 2005;37(5):436-446
Coumarins comprise a group of natural phenolic compounds found in a variety of plant sources. In view of the established low toxicity, relative cheapness, presence in the diet and occurrence in various herbal remedies of coumarins, it appears prudent to evaluate their properties and applications further. The purpose of this study is to investigate cellular protective activity of coumarin compound, fraxin extracted from Weigela florida var. glabbra, under oxidative stress, to identify genes expressed differentially by fraxin and to compare antioxidative effect of fraxin with its structurally related chemicals. Of the coumarins, protective effects of fraxin against cytotoxicity induced by H2O2 were examined in human umbilical vein endothelial cells (HUVECs). Fraxin showed free radical scavenging effect at high concentration (0.5 mM) and cell protective effect against H2O2-mediated oxidative stress. Fraxin recovered viability of HUVECs damaged by H2O2- treatment and reduced the lipid peroxidation and the internal reactive oxygen species level elevated by H2O2 treatment. Differential display reverse transcription-PCR revealed that fraxin upregulated antiapoptotic genes (clusterin and apoptosis inhibitor 5) and tumor suppressor gene (ST13). Based on structural similarity comparing with fraxin, seven chemicals, fraxidin methyl ether (29.4% enhancement of viability), prenyletin (26.4%), methoxsalen (20.8 %), diffratic acid (19.9%), rutoside (19.1%), xanthyletin (18.4%), and kuhlmannin (18.2%), enhanced more potent cell viability in the order in comparison with fraxin, which showed only 9.3% enhancement of cell viability. These results suggest that fraxin and fraxin-related chemicals protect HUVECs from oxidative stress.
Catalase/metabolism
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Cell Survival/drug effects
;
Cells, Cultured
;
Coumarins/*chemistry/*pharmacology
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Endothelial Cells/drug effects/metabolism
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Humans
;
Hydrogen Peroxide/pharmacology
;
Lipid Peroxidation/drug effects
;
Molecular Structure
;
Oxidative Stress/*drug effects
;
Reactive Oxygen Species/metabolism
;
Research Support, Non-U.S. Gov't
;
Structure-Activity Relationship
;
Superoxide Dismutase/metabolism
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Umbilical Cord/drug effects/metabolism
6.Methyl gallate and chemicals structurally related tomethyl gallate protect human umbilical vein endothelial cells from oxidative stress.
Wan Kyunn WHANG ; Hyung Soon PARK ; In Hye HAM ; Mihyun OH ; Hong NAMKOONG ; Hyun Kee KIM ; Dong Whi HWANG ; Soo Young HUR ; Tae Eung KIM ; Yong Gyu PARK ; Jae Ryong KIM ; Jin Woo KIM
Experimental & Molecular Medicine 2005;37(4):343-352
Methyl gallate (meGAL) is known as one of major antioxidants. To investigate whether meGAL protects human cells from oxidative stress, meGAL extracted from Korean medicinal plant, Cercis chinensis leaves, was primarily screened using cell viability assay against oxidative stress. Human umbilical vein endothelial cells (HUVECs) were treated with three different concentrations of meGAL for indicated time. After or during meGAL treatment, H2O2 was added and incubated. meGAL showed free radical scavenging effect at low concentration (0.02 mM) and cell protective effect against H2O2-mediated oxidative stress. meGAL recovered viability of HUVECs damaged by H2O2-treatment, reduced the lipid peroxidation (LPO) and decreased the internal reactive oxygen species (ROS) level elevated by H2O2-treatment. Free radical scavenging effect of meGAL was proven to be very high. Differential display reverse transcription-PCR analysis showed that meGAL upregulated the levels of regulator of chromatin condensation 1, type 1 sigma receptor and phosphate carrier protein expressions, respectively. Based on structural similarity compared with meGAL, 14 chemicals were chosen and viability assay was performed. Four chemicals, haematommic acid (56.2% enhancement of viability), gallic acid (35.0%), methylorsellinic acid (23.7%), and syringic acid (20.8%), enhanced more potent cell viability than meGAL, which showed only 18.1% enhancement of cell viability. These results suggest that meGAL and four meGAL-related chemicals protect HUVECs from oxidative stress.
Antioxidants/*chemistry/*pharmacology
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Biological Assay
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Catalase/analysis
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Endothelial Cells/*drug effects/enzymology
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Fabaceae/*metabolism
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Free Radical Scavengers/chemistry/pharmacology
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Gallic Acid/*analogs & derivatives/chemistry/pharmacology
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Gene Expression/drug effects
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Humans
;
Molecular Structure
;
Oxidative Stress/*drug effects/genetics
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Plant Extracts/chemistry/pharmacology
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Plant Leaves/metabolism
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Research Support, Non-U.S. Gov't
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Superoxide Dismutase/analysis
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Umbilical Veins/cytology
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Water/pharmacology