1.The role of G protein in the activation of phospholipase C from bovine brain.
Jung Hye KIM ; Dong Jin LEE ; Yeung Ju BYUN
Yeungnam University Journal of Medicine 1992;9(2):288-301
The objective of the present study was to identify the characteristics of phospholipase C (PLC) isozymes purified from bovine brain and to investigate their interrelationship with G protein. The purified PLC isozymes β, γ and δ were obtained and the characteristics of PLC activity on various concentrations of free Ca²⁺ were observed. The activity of PLC was increased with increasing Ca²⁺ concentration and the activity PLC δ was increased higher in the presence of phosphatidyl choline (PC) than in the absence of PC. For vesicle formation as the structure of cell membrane, cholic acid and deoxycholic acid as detergent on phosphatidylinositol bisphosphate (PIP₂) substrate containing PC were used, and then the activity of PLC isozymes were increased with increasing concentration of cholate, from 0.2% to 1% and were increased slightly in deoxycholate. In the PIP₂ containing phospholipid and glycolipid as brain extract, the activity of PLC isozymes were checked in 0.2-1% cholic acid. The activities of PLC isozymes were continuously increased up to 1% cholic acid. The quantitation of PLC isozymes from several bovine organs by radioimmunoassay was made. Brain was the most sufficient organ in terms of amount of PLC β and δ. A large amount of PLC δ was existed in adrenal gland. The binding capacity of GTPrS and G protein was observed and other observations of the binding effect of GTPrS-G protein and PLC monoclonal Ab-Protein A from tissue homogenate with PLC were made. From the observation the binding capacity was revealed the range of 0.11-1.49%. The effects of each type of G protein on the percent activity of purified PLC isozymes were observed. From the observation, activities of isozymes were increased in Goa & Gmix, and the activities of PLC β and δ were increased in Gβγ and Gia. Activities of PLC β and γ were decreased in Gta but PLC δ increased.
Adrenal Glands
;
Brain*
;
Cell Membrane
;
Cholates
;
Cholic Acid
;
Choline
;
Deoxycholic Acid
;
Detergents
;
GTP-Binding Proteins*
;
Isoenzymes
;
Phosphatidylinositols
;
Phospholipases*
;
Radioimmunoassay
;
Type C Phospholipases*
2.Driving of Motor Vehicles of the Epileptic Patients.
Yeung Ju BYUN ; Mee Young PARK ; Jung Sang HA
Yeungnam University Journal of Medicine 1994;11(1):16-29
No abstract available.
Humans
;
Motor Vehicles*
3.A clinical study of acute carbon monoxide intoxication.
Kyong Chan CHOI ; Mee Yeung PARK ; Jung Sang HAH ; Yeung Ju BYUN ; Choong Suh PARK
Yeungnam University Journal of Medicine 1991;8(1):86-97
To obtain the basic data of prognosis of acute carbon monoxide (CO) intoxication, one hundred and sixteen cases of CO intoxication defined by carboxyhemoglobin (COHb) and admitted via emergency room of Yeungnam University Hospital from Oct. '85 to April' 89 have been clinically analyzed and evaluated, including delayed postanoxic encephalopathy (DPE) and the following results were obtained. 1. The ratio of male to female was 1:1.5 and mental state was drowsy mostly (26.2% of 116 cases) 2. The more disturbed the mental state, the more decreased was the arterial pH and PaCO₂, which may be the result of metabolic acidosis. 3. The early laboratory findings in patients of CO intoxication were as follows: leukocytosis-65.5%, increase of hematocrit-23.3%, hyperglycemia-19.8%, increase of GPT-19.8% increase of creatinine-0.9% and glucosuria-12.1%. 4. The early findings of EKG were abnormal in 35.3%: change of rhythm-25.0%, abnormal ST segment 15.5% (change of rhythm and abnormal ST segment-5.2%) but the conduction disorder was not present. 5. The abnormal EEG above mild degree was 93.1%, of which moderate was most frequent (80.2%). 6. The incidence of DPE was 7.8% among all admitted CO patients. DPE cases had long duration of exposure time (8 hours), severe leukocytosis (20,000) and an abnormal EEG (MA).
Acidosis
;
Blood Gas Analysis
;
Brain Diseases
;
Carbon Monoxide*
;
Carbon*
;
Carboxyhemoglobin
;
Clinical Study*
;
Electrocardiography
;
Electroencephalography
;
Emergency Service, Hospital
;
Female
;
Humans
;
Hydrogen-Ion Concentration
;
Incidence
;
Leukocytosis
;
Male
;
Prognosis
4.Motor Driving of the Epileptic Patients.
Yeung Ju BYUN ; Yeung Ki LEE ; Se Jin LEE
Journal of the Korean Neurological Association 1995;13(4):843-853
Driving restrction for people with seizure disorder is intended to ensure the public's safety, but such resrictions may unduly harm the welfare of many people with seizures. There is a trend toward greater liberalization of driving standards for people with seizure disorder. The present survey indicates the current driving status of 194 male patients which were managed at the Yeungnam University Hospital from Jan. 1994 to JarL 1995. The result was as follows: 33% of the epileptic patients held traffic licences, 21% actually driving, 5% holding the licences and driving the truck and bus commercially; 72% of the patients took licences after onset of the disease, 29% disclosed by traffic authorities due to their military services; Over the half of the patients had complex partial seizure, 68% was seizure-free over one year, 91 % had no history of trabbic accident. Our traffic road regulations prohibited driving cars by epileptic patients, but practically the authorities permitted epileptic patients to drive cars case by case according to the medical certifications which were issued by the physician. In conclusion, we insist that new traffic road regulation, medical standards for permission and regulation, medico-legal- administrative committee, and thorough detection and regular follow-up of the patients were essential for safety of patients and other peoples.
Certification
;
Epilepsy
;
Follow-Up Studies
;
Humans
;
Male
;
Military Personnel
;
Motor Vehicles
;
Seizures
;
Social Control, Formal
5.A Case of Wilson's Disease Associated with Somatomotor Status Epileticus.
Cheoul JUNG ; Mee Yeong PARK ; Yeung Ju BYUN ; Choong Suh PARK
Journal of the Korean Neurological Association 1991;9(3):362-366
Wilson's disease is a genetically transmitted autosomal recessive disorder of copper metabolism which affects the liver. Brain and other organs. The seizure in Wilson's disease is not infrequent but. It's report is very rare in Korea. The frequency of seizure is about 10 times more than that of general population The statistical proportions of types of seizure associated with Wilson's disease do not differ significantly from that seen in the general population. And the most common seizure type is focal motor form. The issue of the mechanisms producing seizure in Wilson's disease has attracted controversy, but the cause of seizure seems to be related with copper itself. Although the seizure is well controlled by anticonvulsants, the prognosis of seizure depends on the treatment of Wilson`s disease. We report a case of Wilson's disease associated with somatomotor status epilepticus.
Anticonvulsants
;
Brain
;
Copper
;
Hepatolenticular Degeneration*
;
Korea
;
Liver
;
Metabolism
;
Prognosis
;
Seizures
;
Status Epilepticus
6.A Case of Primary Malignant Leptomeningeal Melanomatosis.
Yeung Ki LEE ; Yeung Ju BYUN ; Choong Seo PARK ; Won Hee CHOI
Journal of the Korean Neurological Association 1991;9(3):357-361
Primary malignant melaomatosis of leptomeninges is uncommon, not reported in the Korea to this time. Primary melanomatosis of leptomeninges are not associated with any specific clinical or radiological symptoms. The diagnosis was made by ultrastructural demonstration of malignant melanoma cells from CSF. The patient is 23 years male, who has had meningeal irritating symptoms such as intermittent headache. Nausea, vomiting and disturbed consciousness. Brain CT and MRI showed no mass lesion but cytology of cerebrospinal fluid revealed malignant melanoma cells. There was no evidence of extracerebral melanoma.
Brain
;
Cerebrospinal Fluid
;
Consciousness
;
Diagnosis
;
Headache
;
Humans
;
Korea
;
Magnetic Resonance Imaging
;
Male
;
Melanoma
;
Nausea
;
Vomiting
7.A Case of Idiopathic Hypoparathyroidism with Albright's Hereditary Osteodystrophy.
Jin Kook KIM ; Yeung Ju BYUN ; Choong Seo PARK
Journal of the Korean Neurological Association 1991;9(3):349-356
A 27 years old female patient who had some features of idiopathic hypoparathryoid manifestation such as hypocalcemica, hyperphosphatemia. Chronic tetany, no evidence of osteomalacia, rickets and renal insufficiency, also was found to have certain characteristic skeletal and developmental abnormalities :rounded face, short neck, thick-set stocky body habitus, brachymetatarsia and mental retardation, which are attributable to Albright's Hereditary Osteodystrophy. On the basis of a circulating immunoreative Parathormone level, this case could be considered as idiopathic hypoparathyrodism rather than psuedohypoparathyroidism, despite of Albright's Hereditary Osteodystrophy because the patient's circulating parathormone level is normal range in C-terminal radioimmunoassay system. Presumably, the suggested explanation about the patients normal range of immunoreative parathormone is that the hypoparathyroid state is not a deficiency of circulating parathormone but an ineffectiveness of acitve parathormone because of a defect in conversion of secreted proparatbyroid hormone into an active form as proposed by Nusynowitz et al.(l973) The similar concentrations in immunoreactive parathormone levels of patient's family in same radioimmunoassay systems support this hypothesis. We concluded this case as idiopathic hypoparathyroidism with Albright's Hereditary Osteodystrophy.
Adult
;
Female
;
Humans
;
Hyperphosphatemia
;
Hypoparathyroidism*
;
Intellectual Disability
;
Neck
;
Osteomalacia
;
Parathyroid Hormone
;
Radioimmunoassay
;
Reference Values
;
Renal Insufficiency
;
Rickets
;
Tetany
8.A Case of One and A Half Syndrome.
Khyoung Yhun O ; Jung Sang HAH ; Yeung Ju BYUN ; Choong Suh PARK
Yeungnam University Journal of Medicine 1988;5(1):167-172
One and a half syndrome is an ipsilateral gaze paresis or palsy combined with and internuclear ophthalmoplegia on contralateral gaze. The lesion site is at the paramedian pontine reticular formation and the adjacent MLF. The common causes are unilateral pontine infarction and multiple sclerosis. We experienced a case of one and a half syndrome which has a suspected small pontine infarct.
Infarction
;
Multiple Sclerosis
;
Ocular Motility Disorders
;
Paralysis
;
Paresis
;
Pontine Tegmentum
9.A Case of Musicogenic Epilepsy.
Yeung Ju BYUN ; Jeung Sang HAH ; Choong Seo PARK
Journal of the Korean Neurological Association 1989;7(1):123-130
In Patients subject to convulsions the attacks occur sporadically, and the factors reponsible for precipitation of a seizure at any given time are usually unknown. In a small number of patients certain sensory stimuli may consistently initiate an attack. The sensory modality involved varies in different patients: however, the entire group has been referred to by the term 'reflex epilepsy.' In certain rare instances, listening to music produces seizures and this subdivision of reflex epilepsy has been called "musicogenic epilepsy". By the Critchley, in 1937, several particular types of musical stimuli were reported, but frequency of such stmuli was much rare and there has been no report yet in Korea. This 40 years old fernale patient revealed a ternporal lobe seizure, which appeared whenever listened to old korean popular songs. The etiology was not known and the response to anti-epileptic drugs was good.
Adult
;
Epilepsy, Reflex*
;
Humans
;
Korea
;
Music
;
Seizures
10.A Case of Gelastic Epilepsy, probable Orbito-frontal Origin.
Yeung Ju BYUN ; Jung Sang HAH ; Choong Suh PARK
Journal of the Korean Neurological Association 1988;6(2):300-305
Laughter as an epileptic phenomenon is very uncommon. The introduction of the term gelastic epilepsy by Daly and Mulder (1957) may have resulted in less precision in diagnosis. Laughter does not necessarily include Mirth (gelos). Smiling may be volumtary or barely perceptible, whereas the laryngeal and respiratory components of laughter are more likely to be involuntary and are definite. To this time the loction of this epilepsy is said to be related with temporal lobe and hypothalamus. This case which we present with reviewing of the literature has paroxysmally a burst of loud, high-pitched laughter without any emotional expression. It suggests that at the production of this laughter some fasciorespiratory pathways might be involved, and that the start of this epileptic discharge is probably from a lesion of the orbito-frontal area.
Diagnosis
;
Epilepsies, Partial*
;
Epilepsy
;
Hypothalamus
;
Laughter
;
Smiling
;
Temporal Lobe