1.Apoptosis and Expression of Nitric Oxide Synthase in Hypoxic Ischemic Cerebral Injury of Rats.
Hye Kyeung LIM ; Young Hun CHUNG ; Keon Su LEE ; Kyu Sang SONG
Journal of the Korean Child Neurology Society 2003;11(1):37-46
PURPOSE: Recently, it was reported that apoptosis in hypoxic ischemic cerebral injury is involved in neuronal injury while nitric oxide synthase(NOS) is involved in neuronal apoptosis. The aim of the present study is to investigate the relationship between the expression pattern of NOS and the apoptosis in hypoxic ischemic cerebral injury of rats. METHODS: To investigate the expression pattern of nitric oxide synthase and the relationship between apoptosis and activity of NOS, immunoelectron microscopic examination and in situ apoptosis detection(TUNEL) were performed in male Sprague Dawley rats. Ischemic injury was induced by permanent ligation of left common carotid artery and hypoxic injury by exposure of a mixture of 10% oxygen+90% nitrogen gas. Unicryl embedding method was used for immunoelectron microscopy and Apoptag kit for apoptosis. RESULTS: The number of apoptotic cells reached the highest at 24 hr, decreased after 72 hr and maintained the expression level until 168 hr. nNOS was expressed in neurons of the cortex, peaked at 24 hr and decreased after 72 hr. However, nNOS was not detected in the hippocampus. eNOS was expressed at 12 hr and at 24 hr in the hippocampus and the cortex, respectively, and persisted at each time point. iNOS was expressed after 72 hr in the cerebral cortex and the hippocampus. CONCLUSION: The expression of three isoforms of NOS in hypoxic ischemic cerebral injury was different in time. nNOS seems to be involved in cortical damage in the early phase of hypoxic ischemic cerebral injury and iNOS is related to apoptotic cell deaths in the late phase, but further study on their mechanisms will be needed.
Animals
;
Anoxia
;
Apoptosis*
;
Carotid Artery, Common
;
Cell Death
;
Cerebral Cortex
;
Hippocampus
;
Humans
;
Ischemia
;
Ligation
;
Male
;
Microscopy, Immunoelectron
;
Neurons
;
Nitric Oxide Synthase*
;
Nitric Oxide*
;
Nitrogen
;
Protein Isoforms
;
Rats*
;
Rats, Sprague-Dawley
2.Apoptosis and Expression of Nitric Oxide Synthase in Hypoxic Ischemic Cerebral Injury of Rats.
Hye Kyeung LIM ; Young Hun CHUNG ; Keon Su LEE ; Kyu Sang SONG
Journal of the Korean Child Neurology Society 2003;11(1):37-46
PURPOSE: Recently, it was reported that apoptosis in hypoxic ischemic cerebral injury is involved in neuronal injury while nitric oxide synthase(NOS) is involved in neuronal apoptosis. The aim of the present study is to investigate the relationship between the expression pattern of NOS and the apoptosis in hypoxic ischemic cerebral injury of rats. METHODS: To investigate the expression pattern of nitric oxide synthase and the relationship between apoptosis and activity of NOS, immunoelectron microscopic examination and in situ apoptosis detection(TUNEL) were performed in male Sprague Dawley rats. Ischemic injury was induced by permanent ligation of left common carotid artery and hypoxic injury by exposure of a mixture of 10% oxygen+90% nitrogen gas. Unicryl embedding method was used for immunoelectron microscopy and Apoptag kit for apoptosis. RESULTS: The number of apoptotic cells reached the highest at 24 hr, decreased after 72 hr and maintained the expression level until 168 hr. nNOS was expressed in neurons of the cortex, peaked at 24 hr and decreased after 72 hr. However, nNOS was not detected in the hippocampus. eNOS was expressed at 12 hr and at 24 hr in the hippocampus and the cortex, respectively, and persisted at each time point. iNOS was expressed after 72 hr in the cerebral cortex and the hippocampus. CONCLUSION: The expression of three isoforms of NOS in hypoxic ischemic cerebral injury was different in time. nNOS seems to be involved in cortical damage in the early phase of hypoxic ischemic cerebral injury and iNOS is related to apoptotic cell deaths in the late phase, but further study on their mechanisms will be needed.
Animals
;
Anoxia
;
Apoptosis*
;
Carotid Artery, Common
;
Cell Death
;
Cerebral Cortex
;
Hippocampus
;
Humans
;
Ischemia
;
Ligation
;
Male
;
Microscopy, Immunoelectron
;
Neurons
;
Nitric Oxide Synthase*
;
Nitric Oxide*
;
Nitrogen
;
Protein Isoforms
;
Rats*
;
Rats, Sprague-Dawley
3.ABO*Ael03/O Genotype with ABO Discrepancy: The First Case in Korea.
Bo Kyeung JUNG ; Gye Ryung CHOI ; Jung Hee CHANG ; Hye Nan CHO ; Jong Jin HYUN ; Myung Hyun NAM ; Chaeseung LIM ; Ji Seon CHOI
Annals of Laboratory Medicine 2015;35(1):137-140
The Ael subgroup expresses the least amount of A antigens and could only be detected by performing the adsorption-elution test. The frequency of the Ael subgroup is about 0.001% in Koreans, and the Ael02 allele, which originates from A102, is the most frequently identified allele in the Korean population. We report a Korean family with the Ael03 allele identified by molecular genetic analysis. To the best of our knowledge, this is the first such report in Korea to date.
ABO Blood-Group System/*genetics
;
Alleles
;
Base Sequence
;
DNA Mutational Analysis
;
Exons
;
Frameshift Mutation
;
Humans
;
Male
;
Middle Aged
;
Pedigree
;
Phenotype
;
Polymerase Chain Reaction
;
Republic of Korea