1.Retrovirus-Mediated Herpes Simplex Virus Thymidine Kinase Gene Therapy for the Prevention of Stenosis in Rat Carotid Artery Injury Model.
Dong Woon KIM ; Young Gyu KIM ; Tae Geun OH ; Myeong Chan CHO ; Seung Taik KIM
Korean Circulation Journal 1998;28(6):977-989
BACKGROUND: Herpes simplex virus thymidine kinase (HSVtk) phosphorylates the prodrug ganciclovir to a nucleoside analog that inhibits DNA synthesis, causing cell death. Neighbouring nontransfected cells may be affected through a 'bystander effect', thereby amplifying the antiproliferative actions. This study was carried out to determine whether retrovirus-mediated HSVtk gene therapy could reduce intimal hyperplasia and prevent stenosis following balloon injury of the rat carotid artery. METHODS: A replication-defective recombinant retroviral vector containing HSVtk cDNA (LtkSN) was constructed. Cultured primary rat smooth muscle cells (SMCs) infected with this vector (SMC/LtkSN) were transplanted to the balloon injured rat right carotid artery. One week after transplantation, HSVtk gene therapy group was administered a 2-week treatment of ganciclovir (30 mg/kg/d). Three weeks after balloon injury and SMC/LtkSN transplantation, carotid arteriography was performed and carotid arteries were perfusion-fixed for histologic examination. RESULTS: Carotid arteriographic evaluation comparing with the uninjured left carotid artery showed that the mean luminal diameter of HSVtk gene therapy group (n=5, 85+/-3%) was significantly larger than that of balloon injury only group (n=5, 65+/-5%). The neointimal mass of HSVtk gene therapy group was less than that of balloon injury only group. SMC/LtkSN transplantation without ganciclovir treatment group (n=3) showed asymmetric intimal proliferation probably because of gravitational pooling of seeding. There were inflammatory cell infiltrations at the gravity dependent portion of HSVtk gene therapy group. CONCLUSION: Retrovirus-mediated HSVtk gene therapy following balloon injury of the rat carotid artery reduced neointimal expansion and arteriographic stenosis.
Angiography
;
Animals
;
Carotid Arteries*
;
Carotid Artery Injuries*
;
Cell Death
;
Constriction, Pathologic*
;
DNA
;
DNA, Complementary
;
Ganciclovir
;
Genetic Therapy*
;
Gravitation
;
Herpes Simplex*
;
Hyperplasia
;
Myocytes, Smooth Muscle
;
Phenobarbital
;
Phosphotransferases*
;
Rats*
;
Simplexvirus*
;
Thymidine Kinase
;
Zidovudine
2.Clinical observations on group A streptococcal bacteremia.
Dong Woon JUN ; Joon Myung KIM ; Eung KIM ; Kil Jin CHANG ; Chun Soo HONG
Korean Journal of Infectious Diseases 1993;25(3):195-201
No abstract available.
Bacteremia*
3.Effects of Brain Death on the Myocardium in Canine Brain Death Models.
Myeong Chan CHO ; Gi Byoung NAM ; Dong Woon KIM ; Seong Sook KIM
Korean Circulation Journal 1996;26(1):100-111
BACKGROUND: Clinical and experimental studies have suggested that brain death may cause hemodynamic, electrocardiographic, functional or histopathologic changes of the heart. METHODS: Brain death was induced by increasing intracranial pressure(ICP) abruptly by intermittent bolus injection of saline(model ) or gradually by continuous infusion of saline(model ) to the epidural catheter in 5 mongrel dogs, respectively. Hemodynamic and biochemical changes during the process of brain death and histopathologic changes of the myocardium were analyzed and compared in two brain death models, and the association of apoptosis was also evaluated. RESULTS: 1) Two predominant subsets of acute contraction band lesion were produced in both brain death models : paradiscal and holocystic contraction band lesions. Both contraction band lesions were more prevalent in brain death model . 2) The frequency of both contraction band lesions was lowest in the epicardial layer and highest in the endocardial layer in both models, but no correlation was observed between the degree of contraction band lesions and ICP, LV maximum +dp/dt or catecholamine levels. There was no statistical difference between any of the LV circumferential blocks and either type of contraction band lesion, and transaxial distribution was not also different in both models. 3) There was no remarkable histopathologic changes in the analysis of major epicardial coronary arteries. Apoptotic cells were suggested in the scattered myocytes in the light microscopy and apoptosis was detected by in situ nick end labeling method. Electron microscopy revealed a condensation of nuclear chromatin and convolution of nuclear membrane in those myocytes. CONCLUSIONS: Myocardial changes due to brain were observed frequently, and few apoptotic cells were found in the brain death heart. Studies on the treatment strategy to minimize damages of myocardial structure and function caused by brain death should be followed in the near future.
Animals
;
Apoptosis
;
Brain Death*
;
Brain*
;
Catheters
;
Chromatin
;
Coronary Vessels
;
Dogs
;
Electrocardiography
;
Heart
;
Hemodynamics
;
In Situ Nick-End Labeling
;
Microscopy
;
Microscopy, Electron
;
Muscle Cells
;
Myocardium*
;
Nuclear Envelope
4.Correlation between Visual Analogue Scale (VAS) and Verbal Rating Scale (VRS) in Measurement of Pruritus Intensity.
Young Woon PARK ; Dong Young KIM ; Hyoseung SHIN ; Kyu Han KIM
Korean Journal of Dermatology 2014;52(7):514-515
No abstract available.
Pruritus*
5.The Effects of Electrical Nerve Stimulation on Glycogen Content of the Slow and Fast Twitch Muscles in Rats
Duk Seop SHIN ; Sae Dong KIM ; Joo Chul IHN ; Yong Woon KIM ; Suck Kang LEE
The Journal of the Korean Orthopaedic Association 1989;24(2):613-618
This study observed the changes of the glycogen content in extensor digitorum and soleus by electrical stimulation on the sciatic nerve with various frequencies, and the result were compared with those of treadmill running exercise. The results are summarized as follows ; The glycogen content of extensor digitorum longus was greater than that of the soleus in the normal group, and the reducing amount of glycogen content of extensor digitorum longus was greater than that of the soleus by overnight fasting. As the frepuency of electrical stimulation was increased by 2, 5 and 10Hz., the glycogen content of the extensor digitorum longus was slightly reduced or changed minimally. As the loading period of clectrical stimulation was increased to 30 and 90minutes, the glycogen content of extensor digitorum longus was much reduced from early stage, and that of the soleus was the same tendency as the frepuency increased. The glycogen content of the extensor digitorum longus was proportionally reduced by treadmill running excercise, and that of the soleus was much reduced from the early stage. In summary, based on the experimental evidence of this investigation, it showed the different physio-chemical responses of th fast and slow twitch muscle fibers by electrical stimulation, and also not the equal responses of muscle fibers by electrical stimulation and treadmill running exercise.
Animals
;
Electric Stimulation
;
Fasting
;
Glycogen
;
Muscles
;
Rats
;
Running
;
Sciatic Nerve
6.Electron Microscopic Study of the Renal Proximal and Distal Convuluted Tubular Epithelial and Distal Convoluted Tubular Epithelial Cells after Administration of Aspirin.
Sung Gum HONG ; Cheul Woon BACK ; Im Ju KANG ; Byung Heon KIM ; Dong Koo LEE
Journal of the Korean Pediatric Society 1983;26(6):564-572
No abstract available.
Aspirin*
;
Epithelial Cells*
7.Hypercarbia Due to Mistaken Supply of Carbon Dioxide Originating from Nitrous Oxide Gas Tank: A case report.
Mi Woon KIM ; Dong Hoon CHOO ; Hyun Sul LIM
Korean Journal of Anesthesiology 1999;36(3):524-528
A 49 year-old male was scheduled for a cholecystectomy, thereafter a 37 year-old female scheduled for removal of a epidural hematoma in the same operating room. Both of them had no specific medical problems and past medical histories for anesthesia. For those reasons, anesthesia was induced with thiopental sodium and succinylcholine with endotracheal intubation. After induction, vital signs including body temperatures were stable. But moisture dew in the unidirectional valves and corrugated tubes, and color changes of soda lime were discovered. At that time, severe hypercarbia was recognized by arterial blood gas analysis in both cases. In both cases, there were no malfunctions in unidirectional valves, expiratory valves, corrugation tubes, soda lime, ventilators and there connection parts in the anesthetic machines. Also there were no abnormalities of blood pressures, electrocardiograms, pulse oxymeters, temperatures and the pulse in the patient monitoring systems except capnography. At first, we thought that medical signs revealed malignant hyperthermias. But vital signs, air way pressures and functions of all kinds of anesthetic machine components including ventilators were normal. After discontinuing N2O gas deliveries in the operation room, hypercarbias disappeared. Thus, anesthetic gas delivery systems via central piping systems were checked and it was discovered that CO2 gas was in the N2O gas tank instead of N2O.
Adult
;
Anesthesia
;
Blood Gas Analysis
;
Body Temperature
;
Capnography
;
Carbon Dioxide*
;
Carbon*
;
Cholecystectomy
;
Electrocardiography
;
Female
;
Hematoma
;
Humans
;
Intubation, Intratracheal
;
Male
;
Malignant Hyperthermia
;
Middle Aged
;
Monitoring, Physiologic
;
Nitrous Oxide*
;
Operating Rooms
;
Succinylcholine
;
Thiopental
;
Ventilators, Mechanical
;
Vital Signs
8.Serum Indeces Protein Fibrils Expression in Candida albicans.
Choon Myung KOH ; Kyoung Ho LEE ; Woon Seob SHIN ; Dong Hwa KIM
Journal of the Korean Society for Microbiology 1999;34(3):277-283
The fibrillar coat of Candida albicans is of interest as its significance in antigenicity, antiphagocytosis, and adherence to host tissues. The partial biochemical properties and ultrastructure of fibrillar coat induced by rabbit sera were examined. The induced fibrillar layer was destroyed by treatments of lyticase, proteinase K and dithiothreitol. The total protein concentration of fibrillar cell wall lysate was higher than that of non-fibrillar cell wall lysate, but the total sugar concentration was similar. On SDS-PAGE analysis, the protein profiles between in fibrillar cells and in non-fibrillar cells were shown to be different. In fibrillar cells, the major bands of cell wall lysate were 83, 66, 54, 47, 33, and 26 kDa in dithiothreitol-treated lysate. The proteins of 26 and 19 kDa were predominant in lyticase-treated lysate. Although the fibrillar thickness and protein amount of cell wall lysate were increased in according to the incubation time, the protein profiles did not changed. These results suggest that the proteins of 83, 66, 54, 47, 33, 26, and 19 kDa may be major constituents of fibrillar coat in C. albicans.
Candida albicans*
;
Candida*
;
Cell Wall
;
Dithiothreitol
;
Electrophoresis, Polyacrylamide Gel
;
Endopeptidase K
9.Antibacterial Activity of an Antibiotic (K-681) from Streptomyces sp. 681 against Staphylococcus aureus.
Choon Myung KOH ; Woon Seob SHIN ; Jung Bae KIM ; Dong Heui YI
Journal of the Korean Society for Microbiology 1998;33(1):69-75
The antimicrobial agents reduced infectious diseases significantly. However, antibiotic resistance has followed for almost every antimicrobial agent. Especially, Staphylococcus aureus was one of the most notorious for the multidrug resistance. Streptomyces sp. 681 has been selected for antibiotic-producing strain against methicillin-resistant Staphylococcus aureus (MRSA) from 1,000 strains of Actinomycetales which had been isolated from soil. In antimicrobial susceptibility test, all of the test strains were susceptible to vancomycin. However, most strains of Staphylococcus aureus were found to be resistant to methicillin. Ninety eight (75%) strains out of 129 strains showed multiple resistance pattern to more than 5 antimicrobial agents. The MIC values of the purified antibiotic (K-681) were 1-32 ug/ml against Gram-positive bacteria compared to >128 ug/ml against Grarn-negative bacteria or fungi. The MIC was 8 ug/ml for 90% of the 129 clinical isolates of S. aureus. The antibiotic showed no cytotoxicity against P 388, HeLa, and S180 at the concentration of 500 ug/ml.
Actinomycetales
;
Anti-Infective Agents
;
Bacteria
;
Communicable Diseases
;
Drug Resistance, Microbial
;
Drug Resistance, Multiple
;
Fungi
;
Gram-Positive Bacteria
;
Methicillin
;
Methicillin-Resistant Staphylococcus aureus
;
Soil
;
Staphylococcus aureus*
;
Staphylococcus*
;
Streptomyces*
;
Vancomycin
10.Identification of Mycobacterium tuberculosis in Pleural Effusion by Polymerase Chain Reaction(PCR).
Sun Taec KIM ; Chang Woon GANG
Tuberculosis and Respiratory Diseases 1995;42(5):695-702
BACKGROUND: Since polymerase chain reaction(PCR) was devised by Saiki in 1985, it has been used extensively in various fields of molecular biology. Clinically, PCR is especially useful in situation when microbiological or serological diagnosis is limited by scanty amount of causative agents. Thus, PCR can provide rapid and sensitive way of detecting M. tuberculosis in tuberculosis pleurisy which is diagnosed in only about 60% of cases by conventional method. METHOD: To evaluate the diagnostic usefulness of PCR in tuberculosis pleurisy, The results of PCR was compared with those of conventional method, including pleural biopsy. The pleural effusion fluid was collected from 7 proven patients, 7 clinically suspected patients and control group(7 patients with malignant effusion). We extracted DNA from pleural fluid by modified method of Eisennach method(1991). The amplification target for PCR was 123 base pair DNA, a part of IS6110. RESULT: 1) Sensitivity of PCR: We detected upto 50fg DNA. 2) In patients with pleural effusion of proven tuberculosis, the positive rate of PCR was 85.7% (6/7). In patients with pleural effusion of clinically suspected tuberculosis, the positive rate was 71.5% (5/7). In control group, positive rate was 0% (0/7). CONCLUSION: We concluded that PCR methd could be a very rapid, sensitive and specific one for diagnosis of M tuberculosis in pleural effusion. Further studies should be followed for the development of easier method.
Base Pairing
;
Biopsy
;
Diagnosis
;
DNA
;
Humans
;
Molecular Biology
;
Mycobacterium tuberculosis*
;
Mycobacterium*
;
Pleural Effusion*
;
Pleurisy
;
Polymerase Chain Reaction
;
Tuberculosis