20 research outputs found
Effectiveness of conceptual inquiry instruction on the inquiry skills achievement of high school students in the biology class
ํ์๋
ผ๋ฌธ(๋ฐ์ฌ)--์์ธๅคงๅญธๆ ก ๅคงๅญธ้ข :็งๅญธๆ่ฒ็ง ็็ฉๅฐๆป,1996.Docto
(A) genetic study on the dimension of dental arches in twins
์ํ๊ณผ/์์ฌ[ํ๊ธ]
A Genetic study on the dimension of dental arches in twins.
Nam Il Kim, D.D.S.
Department of Medical Science, Graduate School, Yonsei University
The purpose of this study is to evaluate the influence of genetics of the
dimensions of dental arches in twins.
Thirty-four pairs of Korean twins, of which twenty-three were monozygotic and
eleven dizygotic, participated in the study.
The twins ranged in age from 6 years to 12 years with mixed dentition.
The results were as follows:
1) No significant differences were observed between male and female in mean
interpair differences of monozygotic twins.
2) Mean interpair differences of monozygotic twins were lesser than those of
dizygotic twins.
3) Highly significiant zygotic differences were observed in the mean interpair
differences of the width of upper and lower dental arch. This suggest that there is
a significant component of hereditary variability.
[์๋ฌธ]
The purpose of this study is to evaluate the influence of genetics of the dimensions of dental arches in twins.
Thirty-four pairs of Korean twins, of which twenty-three were monozygotic and eleven dizygotic, participated in the study.
The twins ranged in age from 6 years to 12 years with mixed dentition.
The results were as follows:
1) No significant differences were observed between male and female in mean interpair differences of monozygotic twins.
2) Mean interpair differences of monozygotic twins were lesser than those of dizygotic twins.
3) Highly significiant zygotic differences were observed in the mean interpair differences of the width of upper and lower dental arch. This suggest that there is a significant component of hereditary variability.restrictio
(A) study on experimental infection of Korean chipmunks (Eutamias sibiricus asiaticus) by candida albicans
์ํ๊ณผ/๋ฐ์ฌ[ํ๊ธ]
1751๋
John Hill์ ์ํ์ฌ Candids๊ฐ ์ต์ด๋ก ๊ด์ฐฐ๋์์ผ๋ฉฐ Berkhout(1923)์ ์ํ์ฌ C
andida๋ผ ์ฌ๋ช
๋ช
๋ ์ด๋ ํ์ฌ๊น์ง 100์ฌ์ข
์ด ๋ณด๊ณ ๋์ด ์๋ค. ์ด์คCandida albicans๋ง์ด
๋ณ์์ฑ์ ๋ํ๋ธ๋ค๊ณ ์๋ ค์ ธ ์์ผ๋ ๊ทผ๋์ ์์ ํCandida์ข
๋ค๋ ์ง๋ณ์ ์ผ๊ธฐํ ์ ์๋ค
๋ ๋ณด๊ณ ๊ฐ ์์ผ๋ฉฐ ๊ฐ์ข
์ง๊ท ์ฆ์ ๊ฐ์ผ ์ฆ๊ฐ์ถ์ธ์ ๋๋ถ์ด ์บ๋๋ค์ฆ ์ญ์ ์ฆ๊ฐํ๋ ํ์์
๋ํ๋ด๊ณ ์๋ค. ์ด๋ฌํ ์ง๊ท ์ฆ์ ์ฆ๊ฐ์ถ์ธ๋ ํญ์์ ์ ๋จ์ฉ, ๋ฉด์ญ์ต์ ์ ์ ์ฌ์ฉ, ๊ฐ์ข
์ข
์ ๋ฐ ๋ฉด์ญ๊ฒฐํ์ฑ ์งํ ๋ฑ ์ฌ๋ฌ๊ฐ์ง ์์ธ์ ์ํ๋ค๊ณ ๋ณด๊ณ ๋์ด ์๋ค.
ํ์ฌ๊น์ง ๊ฐ์ข
์ง๊ท ์ฆ์ ์์ธ๊ท ์ ๋ํ ์ ๋นํ๊ณ ์ฐ์ํ ์คํ๋๋ฌผ์ด๋ Candida species
์ ๋ํ ์คํ๋๋ฌผ์ ๊ดํ ์ฐ๊ตฌ๋ ๋ณ๋ก ์ฐพ์๋ณผ ์ ์์ผ๋ฉฐ ํ์๋ค ๊ฐ์๋ ์๋ก ๋ค๋ฅธ ์๊ฒฌ๋ค
์ด ์๋ ์ค์ ์ด๋ค.
๋ฐ๋ผ์ ๋ณธ ์ฐ๊ตฌ์์๋ ์ฐ์ธ์๋ ๋ฏธ์๋ฌผํ๊ต์ค์์ ์ฐ๊ตฌ ๊ฐ๋ฐํ์ฌ ํ์ฌ๊น์ง ํญ์ฐ๊ตฐ์ฆ์
๋ํ์ฌ ์ข์ ์คํ๋๋ฌผ๋ก์ ๋ณด๊ณ ๋ ํ๊ตญ์ฐ ๋ค๋์ (Eutamias sibiricus asiaticus)๋ฅผ ์ฌ์ฉ
ํ์ฌ ์ธ๊ณ์ ์ผ๋ก ๋๋ฆฌ ๋ถํฌ๋์ด ์์ผ๋ฉฐ ์ฌ์ฌ์ฑ ์ง๊ท ์ฆ์ ์ผ๊ธฐํ๋ ์ง๊ท ์ ์ผ์ข
์ธ Candida
albicans์ ๋ํ ๊ฐ์์ฑ ์ฌ๋ถ๋ฅผ ๊ท๋ช
ํ๊ณ ์คํ๋๋ฌผ๋ก์์ ์ด์ฉ๊ฐ๋ฅ์ฑ ์ฌ๋ถ๋ฅผ ๊ท๋ช
ํ ๋ชฉ
์ ์ผ๋ก ์คํ์ ์ฐฉ์ํ์ฌ ๋ค์๊ณผ ๊ฐ์ ๊ฒฐ๊ณผ๋ฅผ ์ป์๋ค.
1. ์ ๋งฅ์ ํตํ์ฌ ๋ค๋์ฅ์ Candida albicans๋ฅผ ๊ฐ์ผ์์ผฐ์ ๊ฒฝ์ฐ LD^^50 ๋ 1ml๋น 5.7
ร10**4 cell ์ด์์ผ๋ฉฐ ๋ค๋์ฅ์์ 100% ์ฌ๋ง์จ์ ๋ํ๋ธ 1ml๋น 3.2ร10**5 cell์์์
๋ง์ฐ์ค์ฌ๋ง์จ์ 20%์ด์๋ค.
2. ์ ๋งฅ๋ด๋ก ์ฃผ์ฌํ ๋ค๋์ฅ์ ์ง์ ๋๋ง๊ฒ๊ฒฝ ๋ฐ ๋ฐฐ์์ฑ์ ์์๋ ๊ท ์ ์ข
4์ผ ํ๋ถํฐ๋ ์
์ฅ์์๋ง ๊ท ๊ฒ์ถ์ด ๊ฐ๋ฅํ์๋ค.
3. ๊ฐ ์ฅ๊ธฐ์์์ ์๊ท ์์ธก์ ๊ฒฐ๊ณผ๋ ์ ์ฅ์ ์ ์ธํ๊ณ ๋ ๊ท ์ ์ข
1์ผ๋ด์ง 2์ผ ์ด๋ด์ ์ต
๊ณ ์ ๋ฌํ์๋ค๊ฐ ๊ธ์ํ ๊ฐ์ํ์์ผ๋ ์ ์ฅ์์๋ 31์ผ๊น์ง๋ ๊ท ์ ๊ด์ฐฐ์ด ๊ฐ๋ฅํ์๋ค.
4. ํ์กํ์ ๊ฒ์ฌ์ฑ์ ์ ์์ด์ ๋ฐฑํ๊ตฌ์ ์๋ ๊ท ์ ์ข
์ ์ ๋นํ์ฌ ๊ท ์ ์ฆ 4์ผ์ 4๋ฐฐ์
์ค๊ฐ๋ฅผ ๋ณด์๋ค.
5. ๋ณ๋ฆฌ์กฐ์งํ์ ์๊ฒฌ์ ๋ณด๋ฉด ์ ์ข
์ด๊ธฐ์๋ ๊ฐ ์ฅ๊ธฐ์์ ์กฐ์ง ๋ณํ์์ด ๊ตฐ์ฒด์ ๊ด์ฐฐ์ด
๊ฐ๋ฅํ์์ผ๋ ๊ท ์ ์ข
31์ผ์์๋ ์ ์ฅ์์ ์ฌํ ๋ค๋ฐ์ฑ๊ตญ์ ๋์ ๋ฐ ๊ดด์ ๋ฅผ ์ด๋ํ ํ์
์ ๊ด์ฐฐํจ๊ณผ ๋์์ ๋ง์ ๊ท ์ฌ์ฒด๊ฐ ๋ฐ๊ฒฌ๋์๋ค.
์ด์์ ์คํ๊ฒฐ๊ณผ๋ฅผ ์ข
ํฉํ์ฌ ๋ณผ ๋ ํ๊ตญ์ฐ ๋ค๋์ฅ๋ Candida albicans์ ๋ํ์ฌ ๊ฐ์์ฑ
์ ๊ฐ์ง๊ณ ์๋ ๋์์ ์คํ๋๋ฌผ๋ก์์ ๊ฐ๋ฅ์ฑ์ ๋ดํฌํ๊ณ ์๋ค๊ณ ์ฌ๋ฃ๋๋ค.
[์๋ฌธ]
Introduction
In 1751, John Hill observed yeast-like organisms harvested from rotting
vegetation, which he named Monilia. But, the genus Monilia was erected by Persoon
in 1797 to encompass certain species of fungi isolated from rotting fruit. In 1923,
Berkhout reclassified the genus Candida and this name was accepted as a "nomen
conservandum'by the 8th Botanical Congress at Paris in 1954.
It is generally recognized that Candida albicans is the only species of Candida
known to be pathogenic to man and to a number of laboratory animals, but recently
it has been found that all of the Candida species may be involved in any from of
candidiasis. Presently, Candida albicans is one of the normal flora of the
alimentary tract, mucous membrane, oral cavity and skin of many mammals. The
incidence of human disease caused by this organism has increased steadily in recent
years due to the wider use of immuno-suppressive drugs and broad spectrum
antibiotics. The variety of predisposing factors, the range of the clinical
disease, and the poor antibiotic chemotherapy now avilable have made candidasis a
serious clinical problem. The need to understand the immunity, host-parasite
relationship and pathogenesis involved in human diseases due to Candida albicans
has made it desirable animal model for candidasis that mimics the systemic disease
seen in human.
Several animal models from disseminated candidiasis have been described. Baine et
al. (1974) used the rabbit to study systemic candidiasis and estab1ished that the
infection is of a chronic nature. Hurley and Winner (1963) described the
histological picture of experimental Candida albicans infection in the tissue of
mice. But up untill now, a properly susceptible and sensitive animal model for
experimental systemic candidiasis has not been found.
For this reason, the author has also studied the course of an experimental
Candida albicans infection in the Korean chipmunks (Eutamias sibiricus asiaticus)
in order to establish whether this animal can be used as an experimental animal
model.
Materials and Methods
A. Materials
1. Experimental organism: Candida albicans ATCC 7491 was obtained from H.
Miyazaki (Juntendo University, Tokyo, Japan). It was maintained in our laboratory
by transfers on Sabouraud's glucose agar slant.
The morphological and biochemical characteristics of Candida albicans were
verified by microscopic observation and sugar fermentation reactions.
2. Animals: Wild chipmunks were obtained. They were maintained on a nutritional
diet and their adaptability to caged life was observed for 2 months prior to
inoculation with fungal suspension. Also, white ICR-mice were obtained from the
Institute of Leprosy, Japan and were used in all of the control studies.
B. Methods
1. Challenge Procedure: Aliquots of the stored Candida albicans suspension
diluted in saline were prepared to obtain the proper dose of administration. 0.2 ml
of the appropriate suspension were injected into the tail vein. Otherwise, 0.5 ml
of the suspension were injected intraperitoneally.
2. Enumeration of the Candida albicans Viab1e Unit: Chimmunks were sacrificed,
under aseptic condition. The appropriate organs were removed and weighed and placed
in tissue homogenizers. Sterile saline was added. Each organ was homogenized and
then number of Candida albicans viable units in the homogenate was determined by
the pour plate dilution method, using Sabouraud's glucose agar. Colony forming
units (CFU) were determined by counting the colonies used as a source of the
organisms.
3. Histopathological Study: Experimental animals Were sacrificed at 24 hours, 48
hours and 31 days after intarvenous inoculation of approximately 3.2ร10**3
cell/ml. Sections of brain, lung, heart, liver, spleen and kidney were studied
after staining with hematoxylin eosin and Periodic acid-Schiff's reagent.
4. Hematological Study: Experimental chipmunks were infected with 3.2ร10**3
cell/ml, and 0.5ml of whole blood were obtained daily for 5 days by cutting tail
vein. Blood was placed in tubes containing 0.3% sodium citrate solution, and white
blood cell(WBC), red blood cell (RBC) and hematocrit counts were determined with
Hema-Count TM System Model MK-3 type.
Results and Conclusions
1. Mortality Rate and Histopathological Study: In an attempt to produce a
disseminated infection, up to 3.2ร10**5 cell/ml of Candida albicans were given
intravenously. With this inoculum, death of all animals was observed within 24
hours. The LD^^50 was determined as 5.7ร10**4 cell/ml. Between the inocula of
2.0ร10**4 cell/ml and 7.2ร10**4 cell/ml mortality rose sharply, increasing from
10% to 90%.
Autopsies of animals given lethal and sublethal doses of Candida albicans
intravenous revealed disseminated microabscesses or inflammatory cell infiltrations
throughout the kidney, heart, lung, liver and spleen. Also, Candida albicans could
be cultured from these organs in the early stage of infection and cells in the
mycelial phase were demonstrated histopathologically in the renal and myocardial
abscesses after 31 days.
2. Course of Infection: For the study of the course of infection over time, a
sublethal dose of Candida albicans was given (3.2ร10**4 cel1/ml) and animals were
autopsied at 24, 48, 72, 96, 120 hours and 31 days after injection, spleen, liver,
lung, heart and kidney were cultured. Over the next 5 days, colony counts revealed
a decreasing number of viable organisms in all tissues except the kidney. Between
24 hours and 48 hours the decline was rapid: between 96 hours and 120 hours all
nonrenal organs became sterile.
Although the initial renal colony counts was similar to colony counts in other
organs, there was gradual increase in renal colony count over the first 2 days of
infection, with maximal counts of viable organism of 7.0ร10**5 CFU/gm tissue at 3
days. Subsequently, there was a gradual decline in colony count. By day 31, the
colony counts was 4.8ร10**3 CFU/gm tissue.
3. Hematological Study: Paralleling the inefection, leukocytosis was observed 24
hours after injection and continued to rise until 4 days, when the total count of
(18.05ยฑ4.26)ร10**3 WBC/cmm was seen. Blood cultures were positive for the
infecting organism for the entire 5 days period of the blood collection.
4. In summary of the above results, the chipmunk appears to be one of the most
susceptible to Candida albicans among all the experimental animals known to date.
Therefore this animal can be adopted as an expermental animal model for candidiasis
.restrictio
้ๅฎๅธธ ๆฒณๅทๆฐด่ณช ่ฑซๆธฌ์ ์ํ GUI ์์คํ ์ ้็ผ
ํ์๋
ผ๋ฌธ(์์ฌ)--์์ธ๋ํ๊ต ๋ํ์ :ํ ๋ชฉ๊ณตํ๊ณผ ํ ๋ชฉ๊ณตํ์ ๊ณต,1995.Maste