2.Anatomical Study of Musculus Pyramidalis in Korean Adults.
Ho Suck KANG ; Young Chul YANG ; Byung Pil CHO ; Jeong Sik KO
Korean Journal of Physical Anthropology 1990;3(1):13-21
The report of the M. pyramidalis was studied in 51 cadavers of Korean adults (male 33, female 18). Origin, insertion and number of this muscle were observed, and the length and breadth were also measured. The results were as follows : 1. The right pyramidal muscle was absent in one male cadaver, and the left pyramidal muscle was absent in two male cadavers. 2. In one male cadaver, pyramidal muscles of both sides had bifurcated origin. 3. In Korean adults, the average length of this muscle was 6.72cm in right, 7.05cm in left, and the breadth was about 2.0cm in both sides. The morphological index was 31.10 in right, and 29.55 in left. 4. In Korean male, the average length of this muscle was 1.93cm in right, 7.42cm in left, and the breadth was 1.93cm in right and 1.92cm in left. The morphological index was 28.70 in right and 26.58 in left. 5. In Korean female, the average length was 6.26cm in right, 6.38cm in left. and the breadth was 2.13cm in right and 2.12cm in left. The morphological index was 35.57 in right and 34.63 in left. 6. Compared with other human races, the pyramidal muscle was less frequently wanting in Asians (3.9%), including the Korean adults, than wanting in European (19.9%), American Whites (20.4%) and Negroes (15.1%). 7. The morphological index of this muscle was little differences existing in male of the human races, but this index was higher in Korean female (35.0) than in Japanese female (24.4) and in American female Whites (25.8). The morphological index was 32.3 in American female Negroes.
Adult*
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African Continental Ancestry Group
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Asian Continental Ancestry Group
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Cadaver
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Continental Population Groups
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Female
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Humans
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Male
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Muscles
4.Reactive Plasticity of Neuroglial Cells on Brain Lesion.
E Tay AHN ; Jeong Sik KO ; Kyung Ho PARK
Korean Journal of Anatomy 1998;31(5):711-725
Neuroglial cells are actively participate in the pathogenesis or in the recovery procedures following brain lesions. The study was performed to evaluate the plasticity of glial cells following different degree of brain lesions. Neurosurgical operations were made on the rats fixed on the stereotaxic apparatus. Tissue column of 3 mm-diameter was isolated in the caudatoputamen with concomitant severe bleeding in the first group. In the second group, the sensorimotor cortex was suctioned out with moderate bleeding. In the third group, the mammillary body was electrically coagulated with minimal bleeding. Caudatoputamens, as a lesioned tissue or as a target tissue of lesioned area, were studied light and electron microscopically. Observations on reactivities and plasticities of neuroglial cells on the different situations, the following results were obtained : 1. Astrocytes were swollen within an hour following brain lesions. 2. In case of smaller lesion, astroglia alone remove altered structures. 3. Microglia are increased in number, if the lesion is large with severe bleeding. The microglia might come from blood monocyte via transformation to pericyte. 4. In large lesion, astroglia were greatly hypertropied, and microglia might be moving and functioning effeciently within the hypertropied cytoplasm of astroglia. 5. In the stabilizing stage, astroglia produce glial fibers and fix the exhausted microglia. Fixed microglia are proceed into apoptotic process in the cytoplasm of astroglia and removed by them. All these procedures might be controlled by various receptors and secretions of astroglia. It means that astroglia is not only the basic supporting element of nervous tissue, but also an actively functioning element for the most effective homeostatic functioning of the neuropil.
Animals
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Apoptosis
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Astrocytes
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Brain*
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Cytoplasm
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Hemorrhage
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Mamillary Bodies
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Microglia
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Monocytes
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Neuroglia*
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Neuropil
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Pericytes
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Plastics*
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Rats
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Suction
5.Electron microscopic study on the motor control system of the brain of the head-irradiated rats II. ultrastructural study on the pineal gland of the head-irradiated rats.
Tae Seung CHO ; Nam Gil YANG ; E Tay AHN ; Jeong Sik KO
Korean Journal of Anatomy 1991;24(1):36-53
No abstract available.
Animals
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Brain*
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Pineal Gland*
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Rats*
7.Effects of Adriamycin or CP -2 on the Spleen of Mouse Implanted with Ehrlich Carcinoma Cells: An Autoradiographic Study.
Jeong Sik KO ; E Tay AHN ; Kyung Ho PARK ; Jin Gook KIM
Korean Journal of Physical Anthropology 2002;15(3):185-195
In this experiment, side effects of two anticancer drugs (adriamycin and CP -2) on the structure of spleen were histologically studied. Each of ICR mice was inoculated with 1 x10 7 Ehrlich carcinoma cells subcutaneously in the inguinal area. From next day, 0.2 ml of saline solution, adriamycin (2 mg/kg) or CP -2 (30 mg/kg) were injected subcutaneously every other day. The day following the 7th injection of adriamycin or CP -2, each mouse was injected with a single dose of 0.7 micro Ci/gm of methyl -3 H -thymidine (25 Ci/mmol, Amersham Lab., England) through tail vein. Seventy minutes after the thymidine injection, animals were sacrificed, and splenic tissues were collected and fixed in 10% neutral formalin. Deparaffinized sections were coated with autoradiographic emulsion EM -1 (Amersham Lab., England) in the dark room and dried, and were kept in a light -tight box. The sections were exposured for 5 weeks in the dark room, and were developed in D -19 developer. The number of the labeled cells in the areas of the white pulp, the red pulp and the marginal zone (mean number of labeled cells per 0.21 mm 2 ) were observed and calculated. In the spleen of adriamycin treated group, vacuoles containing pyknotic nuclei were observed frequently. Whereas in the CP -2 treated group, morphological changes of the spleen were not observed. The number of the labeled cells of normal control, experimental control, CP -2 treated and adriamycin treated groups were 240.3 +/-53.28, 252.3+/- 58.24, 216.7 +/-55.17 and 45.4 +/-15.46, respectively, and most of the labeled cells were located near the marginal zone of the spleen. In the adriamycin treated group, labeled cells containing a few silver grains of 3 H -thymidine were observed more frequently than in those of the normal and experimental control groups. From the above results, adriamycin and CP -2 may suppress the DNA synthesis of the splenic tissues. Especially, CP -2 does not results any histological defect on the splenic tissues. These result suggest that CP -2 is expected as one of effective anticancer drugs.
Animals
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Edible Grain
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DNA
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Doxorubicin*
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Formaldehyde
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Mice*
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Mice, Inbred ICR
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Silver
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Sodium Chloride
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Spleen*
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Thymidine
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Vacuoles
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Veins
8.Morphometric Analysis of the Skull by Moire Contourography.
Duk Soo KIM ; Jeong Sik KO ; Kyung Ho PARK ; Dae Kyoon PARK
Korean Journal of Physical Anthropology 2014;27(3):165-171
The non-metric analysis of the skulls is very useful for estimating sex and determination of ancestry, the accuracy tends to depend on the amount of experiences of the observers, and so inter-observer errors might be happened. Many researchers are trying to find out more objective methods for determination of ancestry. The purpose of this presentation is to show the usefulness of moire contourography for analyzing the skull. The master screen that is similar to the gratings was made by steel rods, which were arranged as equally spaced parallel lines. Halogen light source was illuminated by lantern slide projector. The skeletal materials were documented crania, composed of 87 male and 47 female, from William M. Bass Donated Skeletal Collection housed at the Department of Anthropology, University of Tennessee. The skulls were placed just behind the master screen as anatomical position using cubic craniophore. The angle between the light source and camera was 65degrees, the distance between camera and the master screen was 1.2 m. Frontal view, left lateral and right lateral view were taken. From the frontal view, fringe patterns were analyzed for first five contour lines which were mainly located around the Glabella. The results were as followed; Type I for male was 53% and female was 4%; Type II for male was 29% and female was 2%; Type III for male was 2% and female was 15%; Type IV for male was 6% and female was 55%. From the lateral view, fringe patterns were analyzed for first four contour lines. However, first and second contour lines were critical to determine the shape and the results were as followed; Type I for male was 52% and female was 22%; Type II for male was 38% and female was 26%; Type III for male was 8% and female was 17%; Type IV for male was 2% and female was 35%. According to this study, different fringe patterns might be dependent on the degree of development of bone marker such as Glabella, Supercillary arch, Euryon and Mastoid process. For example, Supercillary arches were very well developed and slope of forehead above the Glabella was declined, fringe pattern showed reverse triangle shape. If Supercillary arches were poorly developed and slope of forehead above the Glabella was flat, fringe pattern showed home plate shape. The present research shows that moire contourography might be used as more objective methods for estimating sex. And it would be helpful to determine the ancestry when the lateral aspects were analyzed. In the future, continuing study need to be performed with same master screen for different ancestry.
Anthropology
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Bass
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Female
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Forehead
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Humans
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Male
;
Mastoid
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Skull*
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Steel
;
Tennessee
10.Morphological Study on the Mouse Spleen following the Administration of Mercuric Chloride or Potassium Dichromate.
Jeong Sik KO ; E Tay AHN ; Kyung Ho PARK ; Jin Gook KIM
Korean Journal of Anatomy 2001;34(4):353-366
This experiment was performed to study the morphological changes of the spleen of mice following injection of sodium dichromate (K2Cr2O7) or mercuric chloride (HgCl2). Male mice were divided into normal and experimental groups. The mice were subcutaneously injected with mercuric chloride (5 mg or 10 mg/kg) or sodium dichromate (10 mg or 20 mg/kg). Animals were sacrificed on 6 hours, 1 day, 3 days, 1 week and 2 weeks after injections. Pieces of splenic tissue were taken from each mouse, and fixed in 10% neutral formalin for light microscopy. The paraffin sections were stained with hematoxylin-eosin, Masson-trichrome, Bielschowsky's silver impregnation or aldehyde-fuchsin stain. For electron microscopy, the tissues were fixed in 2.5% glutaraldehyde-1.5% paraformalde-hyde, and post-fixed in 1% osmium tetroxide. Dehydrated blocks were embedded in araldite mixture. The ultrathin sections stained with uranyl acetate and lead citrate were observed with JEM 100CX-II electron microscope. On histological study, in the early stage (6 hours) of experimental groups, splenic white pulp exhibited numerous vacuoles containing pyknotic nuclei were observed as compared with those of normal control group. But after 3 days(sodium dichromate, 10 mg/kg or 20 mg/kg; mercuric chloride, 5 mg/kg) and 1 week (mercuric chloride, 10mg/kg), the morphology was recovered to normal one. In the experimental groups, positive reactions to Bielschowsky's silver impregnation, Masson-trichrome or aldehyde-fuchsin stain were similar to those of normal control group. On the ultrastructural study, in white pulps of experimental groups, nuclear bodies were observed frequently in the nuclei of the lymphocytes and the reticular cells, and myelin figures were observed in the nucleus or in the cytoplasm of the lymphocytes and the reticular cells. The plasma cells showed many irregularly distended cisternae of granular endoplasmic reticula and the macrophages containing phagosomes, were observed frequently. From the above results, it was concluded that potassium dichromate or mercuric chloride could disturb the normal differentiation or maturation of the lymphocytes and the reticular cells of the spleen, especially in the early stage of treatment. But histological changes occurred in the spleen following injection of the potassium dichromate or mercuric chloride were recovered to normal appearance in 3 days (potassium dichromate) or 1 week (mercuric chloride). Mercuric chloride was more harmful than potassium dichromate on the spleen.
Animals
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Citric Acid
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Cytoplasm
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Formaldehyde
;
Humans
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Lymphocytes
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Macrophages
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Male
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Mercuric Chloride*
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Mice*
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Microscopy
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Microscopy, Electron
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Myelin Sheath
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Osmium Tetroxide
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Paraffin
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Phagosomes
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Plasma Cells
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Potassium Dichromate*
;
Potassium*
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Silver
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Sodium
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Spleen*
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Vacuoles