1.The distribution of inositol 1,4,5-trisphosphate 3-kinase in rat cerebellum.
Hae Kyoung LEE ; Jae Pil KO ; Seung Jun HWANG ; Young Suk SUH
Korean Journal of Anatomy 1993;26(1):94-102
No abstract available.
Animals
;
Cerebellum*
;
Inositol 1,4,5-Trisphosphate*
;
Inositol*
;
Rats*
2.Clinical application of laparoscopy in gynecology.
Cheol Ho LEE ; Ann Su YI ; Kyoung Do PRK ; Hong Pil KIM ; Il Kyun CHUNG ; Ki Sung CHUNG
Korean Journal of Obstetrics and Gynecology 1993;36(7):1744-1752
No abstract available.
Gynecology*
;
Laparoscopy*
3.The effect of Zirconium Nitride coating on shear bond strength with denture base resin in Co-Cr alloy and titanium alloy.
Chan PARK ; Kyoung Hun LEE ; Hyun Pil LIM
Journal of Dental Rehabilitation and Applied Science 2016;32(3):194-201
PURPOSE: The purpose of this study was to evaluate of Zirconium Nitride (ZrN) coating on shear bond strength with denture base resin in Co-Cr and Ti-6Al-4V alloy. MATERIALS AND METHODS: Co-Cr and Ti-6Al-4V alloy disks (10 mm in diameter, 2.5 mm in thickness; each other: n = 14) were prepared and divided with 2 groups each other by ZrN coating. After primer was applied to disks surface, denture base resin with diameter 6 mm, height 5 mm was bonded on metal disk surface. After surface roughness was measured by Profiler, shear bond strength was determined with Universal testing machine and analyzed with two-way ANOVA. The specimen surfaces and failure mode were examined using a scanning electron microscope. RESULTS: ZrN coated groups showed significantly higher rough surface than non-coated groups (P < 0.05). Irrespective of alloy materials, shear bond strength of ZrN coated groups were lower than non-coated groups (P < 0.001). The scanning electron microscope (SEM) of ZrN coated groups showed mixed and adhesive fractures. CONCLUSION: ZrN coating weakened bonding strength between denture base resin and Co-Cr, Ti-6Al-4V alloy.
Adhesives
;
Alloys*
;
Denture Bases*
;
Dentures*
;
Titanium*
;
Zirconium*
4.A Case of Primary Hypomagnesemia.
Kyoung A CHUN ; Sung Pil JANG ; Young Dae HAM ; Jin Hwa JEONG ; Jeong Ho LEE
Journal of the Korean Pediatric Society 2000;43(8):1153-1156
Primary hypomagnesemia is a rare inherited disorder and it is considered to be due to either a defect in the intestinal transport of magnesium or a defect in renal tubular transport. It is important to measure the urinary excretion of magnesium to differentiate the causes of magnesium deficiency. We report here an one-month-old female infant of primary hypomagnesemia who presented generalized tonic-clonic seizures. She had hypomagnesemia(<1.5mg/dL) and several seizure attacks but normal magnesium creatinine ratio in random urine and normal magnesium excretion in 24-hour urine. Continuous oral magnesium supplementation was necessary to avoid the recurrence of symptoms and maintain serum rnagnesium levels.
Creatinine
;
Female
;
Humans
;
Infant
;
Magnesium
;
Magnesium Deficiency
;
Recurrence
;
Seizures
5.A Case of Acute Renal Failure due to Bilateral Acute Pyelonephritis.
Kyoung Soo KIM ; Kyu Beck LEE ; Hee Moo LEE ; Kwon CHOI ; Bum Soo KIM ; Hyang KIM ; Sang Jong LEE ; Chan Pil PARK ; Moon Hyang PARK
Korean Journal of Nephrology 1998;17(6):988-993
Although urinary tract infections are common in adults, pyelonephritis is rarely considered in the differential diagnosis of acute renal failure. Acute pyelonephritis without urinary tract obstruction, previous renal diseases or septic shock is a rare cause of acute renal failure. Despite appropriate antibiotic therapy, recovery of renal function could be slow and incomplete. We experienced a 45 year-old woman with diabetes who developed bilateral acute pyelonephritis followed by acute renal failure. The renal biopsy revealed diffuse edematous and focal fibrotic inters- titium with infiltration of lymphocytes compatible with interstitial nephritis. Although her renal function improved gradually with antimicrobial treatment, the process was incomplete and renal dysfunction persisted at about 10-month follow-up, suggesting permanent renal damage. Therefore, we report this case with brief review of related literature.
Acute Kidney Injury*
;
Adult
;
Biopsy
;
Diagnosis, Differential
;
Female
;
Follow-Up Studies
;
Humans
;
Lymphocytes
;
Middle Aged
;
Nephritis, Interstitial
;
Pyelonephritis*
;
Shock, Septic
;
Urinary Tract
;
Urinary Tract Infections
6.Effects of exercise on hematological and serum biochemical parameters in riding ponies
Jeong-Ja KO ; Young-Woo LEE ; Jong-Pil SEO ; Kyoung-Kap LEE
Korean Journal of Veterinary Research 2020;60(1):33-37
The purpose of the present study was to investigate changes in hematological and serum biochemical parameters in ponies exercising 3 times a day. The study included 10 healthy 4- to 5-year-old Jeju crossbred ponies used in riding lessons at an equestrian riding school. Hematology and serum chemistry samples were obtained before the initial lesson and after the last lesson of the day. The post-exercise results showed that packed cell volume, white blood cell, red blood cell, hemoglobin, and total protein levels increased significantly (p < 0.05). Serum Na + also increased significantly (p < 0.01), but serum Ca ++ decreased significantly p < 0.01).Creatinine kinase, aspartate amino transferase, gamma glutamyl transferase, blood urea nitrogen, creatinine, and bilirubin levels increased significantly (p < 0.05), but the glucose level decreased significantly (p < 0.05). Furthermore, the serum cortisol hormone level increased significantly (p < 0.01). The results suggest that participating in riding lessons three times a day may result in various physiological changes, indicating the presence of exercise-related stress in riding ponies.
7.A Case of DiGeorge Syndrome With Ocular Manifestation.
Kyoung Min KIM ; Ji Woong LEE ; Bo Young CHUN ; Jae Pil SHIN ; Si Yeol KIM
Journal of the Korean Ophthalmological Society 2009;50(12):1909-1912
PURPOSE: DiGeorge syndrome (chromosome 22q11.2 deletion syndrome) is a syndrome of multiple congenital anomalies characterized by hypoplasia or aplasia of the thymus and parathyroid, cardiovascular malformation, immune deficiency, cleft palate, characteristic facial features, and hypocalcemia. Ocular findings of DiGeorge syndrome are posterior embryotoxon, retinal vascular tortuosity, strabismus, ptosis, amblyopia and tilted optic disc. The authors present a case of DiGeorge syndrome with ocular manifestation not reported previously in Korea. Case summary: A six-year old female diagnosed with DiGeorge syndrome was referred to the authors' department within the hospital. The chief complaint was blurring vision in both eyes. Best corrected visual acuity of the right eye was 0.5 and of the left eye was 0.63. Cycloplegic refraction revealed high hyperopia and astigmatism in both eyes (OD: +7.25 Dsph; -2.5 Dcyl axis 180degrees, OS: +6.25 Dsph; -3.75 Dcyl axis 180degrees). In addition, hypertelorism, ptosis and tortuous retinal vessels during fundus examination were noted. CONCLUSIONS: Upon the initial diagnosis of DiGeorge syndrome in children, a comprehensive ocular examination is necessary because other ocular conditions may exist which can affect the visual development of the patient.
Amblyopia
;
Astigmatism
;
Axis, Cervical Vertebra
;
Child
;
Cleft Palate
;
DiGeorge Syndrome
;
Eye
;
Female
;
Humans
;
Hyperopia
;
Hypertelorism
;
Hypocalcemia
;
Korea
;
Retinal Vessels
;
Retinaldehyde
;
Strabismus
;
Thymus Gland
;
Vision, Ocular
;
Visual Acuity
8.Action and Signaling of Lysophosphatidylethanolamine in MDA-MB-231 Breast Cancer Cells.
Soo Jin PARK ; Kyoung Pil LEE ; Dong Soon IM
Biomolecules & Therapeutics 2014;22(2):129-135
Previously, we reported that lysophosphatidylethanolamine (LPE), a lyso-type metabolite of phosphatidylethanolamine, can increase intracellular Ca2+ ([Ca2+]i) via type 1 lysophosphatidic acid (LPA) receptor (LPA1) and CD97, an adhesion G-protein-coupled receptor (GPCR), in MDA-MB-231 breast cancer cells. Furthermore, LPE signaling was suggested as like LPA1/CD97-Gi/o proteins-phospholipase C-IP3-Ca2+ increase in these cells. In the present study, we further investigated actions of LPE not only in the [Ca2+]i increasing effect but also in cell proliferation and migration in MDA-MB-231 breast cancer cells. We utilized chemically different LPEs and a specific inhibitor of LPA1, AM-095 in comparison with responses in SK-OV3 ovarian cancer cells. It was found that LPE-induced Ca2+ response in MDA-MB-231 cells was evoked in a different manner to that in SK-OV3 cells in terms of structural requirements. AM-095 inhibited LPE-induced Ca2+ response and cell proliferation in MDA-MB-231 cells, but not in SK-OV3 cells, supporting LPA1 involvement only in MDA-MB-231 cells. LPA had significant effects on cell proliferation and migration in MDA-MB-231 cells, whereas LPE had less or no significant effect. However, LPE modulations of MAPKs (ERK1/2, JNK and p38 MAPK) was not different to those by LPA in the cells. These data support the involvement of LPA1 in LPE-induced Ca2+ response and cell proliferation in breast MDA-MB-231 cells but unknown GPCRs (not LPA1) in LPE-induced responses in SK-OV3 cells. Furthermore, although LPE and LPA utilized LPA1, LPA utilized more signaling cascades than LPE, resulting in stronger responses by LPA in proliferation and migration than LPE in MDA-MB-231 cells.
Breast
;
Breast Neoplasms*
;
Cell Proliferation
;
Ovarian Neoplasms
9.Two Cases of Single Ventricle.
Pil Rae CHUNG ; Kyoung Gyun SHIN ; Chong Soo KIM ; Seung Kyu LEE ; Sung Soon KIM ; Hong Do CHA
Journal of the Korean Pediatric Society 1977;20(3):222-225
Two cases of single ventricle were diagnosed in a 2 year and 5 months old female baby an. a 8 year old boy according to cardiac catheterization with selective cineangiogram. We report these cases with review of a little literature.
Cardiac Catheterization
;
Cardiac Catheters
;
Child
;
Female
;
Humans
;
Infant
;
Male
10.Surgical Treatment for Descending Necrotizing Mediastinitis.
Kyoung Min RYU ; Pil Won SEO ; Seongsik PARK ; Seok Kon KIM ; Jae Woong LEE ; Jae Wook RYU
The Korean Journal of Thoracic and Cardiovascular Surgery 2008;41(1):82-88
BACKGROUND: Descending necrotizing mediastinitis (DNM) is a serious disease originating in odontogenic or oropharyngeal infection with high mortality despite adequate antibiotics and aggressive surgery. We analyzed results of treatment for DNM. MATERIAL AND METHOD: We studied 8 cases diagnosed as DNM from 1998 to 2007. All patients received emergent surgical drainage and debridement with broad spectrum antibiotics just after diagnosis. Antibiotics were changed after bacterial susceptibility testing. The surgical approach included 2 cases of cervicotomy, 6 cases of cervicotomy, and a thoracotomy. RESULT: The interval between symptom onset and hospitalization was 4.6+/-1.8 days (1~9 day). DNM originated in 4 cases of odontogenic infection (50%), 2 cases of oropharyngeal infection (25%), and 2 cases of unknown origin (25%). Causative organisms were found in 6 cases; Streptococcus in 4 cases, Staphylococcus in 1 case, and Klebsiella in 1 case. The Endo DNM classification was type I (2 cases), IIA (3 cases), and IIB (3 cases). The incidence of thoracotomy was 75%. The surgical mortality rate was 25% (2/8). The cause of death was multiple organ failure caused by septic shock. All mortality cases received only cervicotomy and aggravated infections after initial drainage. CONCLUSION: Early diagnosis, immediate surgical drainage, and adequate antibiotics, including covered anaerobes, are required. Thoracotomy should be performed with cervicotomy even for localized DNM.
Anti-Bacterial Agents
;
Cause of Death
;
Debridement
;
Drainage
;
Early Diagnosis
;
Hospitalization
;
Humans
;
Incidence
;
Klebsiella
;
Mediastinitis
;
Multiple Organ Failure
;
Necrosis
;
Shock, Septic
;
Staphylococcus
;
Streptococcus
;
Thoracotomy