• Applied Microscopy
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• 제24권3호
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• pp.46-54
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• 1994

오돈토글로썸 윤문 바이러스(ORSV)에 감염된 한국 자생춘란(Cymbidium goeringii) 초박절편의 전자현미경 관찰에서 ORSV 입자들은 집적되거나 환형상 평면구조로 다양한 크기의 불규칙적인 응집된 다발상들이 관찰되었다. 바이러스 입자들은 원형질체에서 다수 존재하였고, 세포벽과 원형질막 사이에서도 존재하였으며, 이들은 주로 응집된 평행상과 불규칙적인 산재된 형태로 관찰되었다. X-체 및 paramural body는 원형질막 주변에 존재하였고 액포와 유사한 낭상 구조체에 싸여있었다. 바이러스에 감염된 조직의 세포벽은 확장되어 있었다. ORSV에 감염된 세포내 엽록체는 불규칙적인 모습을 보였다. 미토콘드리아, 핵, 액포, 소포 및 기타 세포내 소기관들내에서는 바이러스 입자를 볼 수 없었다. 원형질연락사(plasmodesmata)는 다소 확장되고, 바이러스 입자들이 이들 원형질연락사 주변에 존재하였다.

• Applied Microscopy
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• 제30권3호
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• pp.303-310
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• 2000

문치가자미의 피부 상피층은 지지세포, 선세포 그리고 부속세포들로 구성된다. 지지세포는 표면세포, 중간세포 및 기저세포로 구분된다. 지지세포들의 세포질은 공통적으로 피질부와 수질부로 나누어지는때, 수질부에는 세포 소기관의 발달이 현저하며, 피질부에는 미세섬유의 발달이 뚜렷하다. 선세포들은 상피의 표면층과 중간층에 존재한다. 점액세포의 세포질은 AB-PAS에 청색으로 반응하였다. 곤봉방세포는 세포질에 원형의 중심공포와 발달된 미세섬유들을 가진다. 과립세포는 주로 중간층과 기저층에 존재하고, 세포질의 대부분은 막을 가진 전자밀도가 높은 과립들이 차지한다. 염세포는 주로 표층에 위치하며, 세포질의 대부분은 잘 발달된 미토콘드리아들이 차지한다. 색소세포는 세포질에 존재하는 함유물의 전자밀도에 따라 세 종류로 구분할 수 있다.

• 한국어병학회지
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• 제15권3호
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• pp.105-110
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• 2002

한국산 어류에 감염된 포자충의 종류와 병해를 조사 할 목적으로 2001년 9월부터 2002년 8월까지 양식중인 정읍산 메기와 만경강 하구의 기수 구역에 서식하는 자연산 문절망둑을 조사하였다. 이 들 어류에서 지금까지 한국 미기록종인 포자충의 감염이 확인되었다. 즉 메기의 장 상피조직에서 Myxobolus miyairii Kudo, 1919가, 문절망둑의 피하 근육조직에서 Henneguya tridentigeri Ozaki & Ishizaki, 1941가 검출되었다. 메기에 기생 된 M. miyairii는 장 상피조직에 42-77 (56) $\mu{m}$ × 59-93(73) $\mu{m}$크기의 백색 영양체가 무수히 관찰되었고, 포자의 길이는 11.0-12.0(11.3) $\mu{m}$이었다. 어체 기생율은 86.7-90%이었으나, 감염어는 별다른 병변을 발견할 수 없었다.

• 한국식품과학회지
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• 제20권5호
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• pp.650-658
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• 1988

발아 중인 대두와 두채 자엽부에서의 단백지 유동 현상을 광학현미경(LM)과 주사 전자현미경(TEM)을 이용하여 epidermis, vascular tissue 그리고 storage parenchyma에서 비교 관찰하였다. 발아 초기의 자엽에는 직경이 $0.1-15{\mu}m$에 해당하는 다양한 크기의 단백질 체(protein bodies)로 채워져 있었으며 epidermis와 vascular tissue의 단백질체는 parenchyma 세포보다 훨씬 적은 크기의 $0.1-5{\mu}m$였다. 발아가 진행됨에 따라, 단백질의 분해현상은 epidermis와 vascular tissue에서 먼저 시작되었다. 그 분해 유형은 먼저 침투한 수분에 의해 팽창된 단백질체의 외막에는 손상이 없어 단백질 체 내부와 외부로부터 가수분해가 일어났으며, 단백질이 완전히 분해도기 전에 단백질체 끼리의 융합 또한 관찰 되어졌다. 단백질체 분해의 결과는 세포내에 중심액포를 만든다는 것이며, 두채 성장 말기에는 액포막의 파괴현상도 관찰되었다.

• Journal of Ginseng Research
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• 제14권3호
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• pp.357-363
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• 1990

When mice irradiated by neutron (Be) are fed with ginseng concentrate, ginseng powder, and adaptagen of which the major ingredient is ginseng alkaloid to neutron (Be source) irradiated mouse, the following results are obtained. 1. The 50% lethal dose (LD50) for the neutron irradiation were 4 days at 600 rad, 7 days at 500 rad, 16 days at 400 rad, 33 days at 375 rad, and 55 days at 350 rad. In thistest, the standard amollntofirradiation was set at 375 rad/8 min. 2. Some spots appeared in the tail of the neutron-irradiated mouse because of blood congestion, and some had its tip tails cut. But the group administered with adaptagen did not show any of these symptoms. 3. The neutron irradiated mouse showed darkening the color of their lung-chloasmas while none of the adaptagen group had this symptom. 4. The lung tissue of the neutron irradiated mouse showed an increase of the karyolysis and cytoplasmic vacuole. 5. When both neutron irradiation and the ginseng sllbstances were given to the mouse at the same day, the 50% lethal days were increased to 29-33 days for the group administered with ginseng extract. 67 days for the group given with the ginseng powder. and 80 days for the groilp arith the adaptagen. 6. The survival rate of those fed with adaptagen for 33 days before the neutron-irradiation was 100%, while the 50% lethal daysofthe group fed with ginsengextract were 39 days and that of the group fed with ginseng powder were 69 days. 7. The serum valued of ${\gamma}$-globulin, IgG, and albumin were returned to normal condition in the group fed with adaptagen for 33 days before the neutron-irradiation. But those of the group which were given the irradiation and the ginseng substances at the same day did not show such a recovery.

• 한방안이비인후피부과학회지
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• 제18권1호
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• pp.221-233
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• 2005

Background and Objectives : Despite of high prevalence, Tinnitus remains obscure because the cause and mechanism is poorly understood. In the absence of a suitable animal model, past investigations tool place in humans. Recently, the animal model with sodium salicylate ototoxicity is broadly used because of its reversibility. Balyangtongum-Tang had been used clinically to treat tinnitus and other hearing problems. We investigated the effects of Balyangtongum-Tang on cochlear morphologic change induced by sodium salicylate ototoxicity and were to find out its therapeutic effects on ototoxicity in rat model. Materials and Methods : Healthy ten Sprague-Dawley rats were divided into normal(2), control(4) and sample(4) groups. The sample group was given extract of Balyangtongum - Tang(1cc/100g) once a day for 4 days. After 3 hours when last medication were given, the sample and control groups were injected intraperitoneally with sodium salicylate(500mg/kg). We observed the cochlear morphologic changes of rats every 1, 2, 3 and 5 hours after injection. Results : The electron microscopic finding of outer hair cell shows some changes in the curticular plate and cytoplasm. Some vacuoles were found in the control and sample groups. Vacuolization in the curticular plate and cytoplasm of the sample group after 3, 5 hours were similar to the control group. But the curticular plate of the sample group after 1, 2 hours did not from vacuole. On the other hand the control group after 1, 2 hours formed vacuoles in the curticular plate. Light microscopic findings of cochlear duct in control and sample groups didn't find any difference. Conclusion : The results suggest that extract of Balyangtongum-Tang reduces the morphologic changes induced by sodium salicylate ototoxicity and the effects are remarkable in frist 2 hours. However the effective times are different with previous studies, it seems to due to the difference of tolerance and sensitivity of laboratory animals.

• 대한세포병리학회지
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• 제10권1호
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• pp.61-66
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• 1999

Angiosarcomas are rare tumors, seen most commonly in the skin and soft tissue of head and neck legion. But it has been described in numerous body sites including thyroid, breast, liver, spleen, bone, etc.. Their biological behaviors depend on the microscopic grade, site of origin, and multifocality. We report the unique cytological features of an angiosarcoma in pleural fluid. A 61-year-old woman presented with a 6 month history of dyspnea on exertion and chest pain. Chest computerized tomography(CT) revealed multiple subpleural small nodules in the right lung and widespread all space consolidation and pleural effusion in the left lung. CT of liver revealed multiple small low attenuated lesion. The smears obtained from pleural fluid showed hypocellularity with a hemorrhagic background. The tumor cells were highly pleomorphic oval or spindle in shape and presented singly, in loose groups, in knitted syncytial aggregates, and in acinar pattern. Their nuclei had vesicular chromatin with delineated, thick nuclear membranes and occasionally a large eosinophilic, prominent nucleolus. The cytoplasm was plump, thin or protected in spindly fashion. Almost ail tumor cells showed variable sized intracytoplasmic vacuoles and their nuclei were sometimes crescentic by a huge vacuole. Occasional binucleated tumor cells and mitotic figures were present. Cellular debris and streaky materials were identified. Needle biopsy specimen from the pleura revealed anastomosing slit-like spaces lined by pleomorphic tumor cells. The tumor cells showed a strong reactivity for CD31 and vimentin and focal weak reactivity for factor VIII-related antigen.

• 식물조직배양학회지
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• 제25권6호
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• pp.495-500
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• 1998

인삼(Panax ginseng C. A. Meyer) 캘러스로부터 분리한 원형질체를 배양하면서 배양시간에 따른 원형질체의 미세구조 변화와 원형질막 표면을 전자현미경으로 조사하였다. 3일 동안 배양된 원형질체에서는 조면소포체, 리보좀, 골기체, 미토콘드리아, 전색소체 등의 세포기관들의 수가 증가하였고 미소관도 관찰되었다. 골기체 주변에는 많은 골기소낭들이 형성되어 세포질 전반에 존재하였고, 이들 소낭들은 원형질막 바깥으로 돌출되어 돌기를 형성하기도 하였다. 소포체에서 유래된 액포속에는 액포의 함입에 의하여 골기소낭들이 들어 있는데, 이들 액포들은 융합에 의한 exocytosis로 원형질막 근처로 이동하여 원형질막과 융합한 다음, 세포벽 물질을 원형질막 바깥으로 방출하여 원형질막에 침적하였다. 전색소체는 많은 전분립을 함유하고 있었고, 미소관들은 원형질막 근처에서 막과 평형으로 배열하고 있었다. 배양된 원형질체의 표면에는 섬유소로 구성되어 있는 원섬유들이 서로 연결되어 있는 것이 관찰되었다.

• 대한수의학회지
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• 제29권4호
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• pp.531-540
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• 1989

A new sudden death in rabbits appeared in China and Korea in 1984 and 1985, respectively, and was recognized to be an acute infectious disease caused by a virus. The disease was reported as a "new viral disease," and thereafter, a tentative name of "viral hemorrhagic disease", "hemorrhagic pneumonia" or "viral hemorrhagic pneumonia" has been described in the case reports. But authors had called the viral disease "rabbit viral hepatitis" due to picornavirus infection, because the principal lesion of the disease was an acute hepatitis. The purpose of this report is to describe the electron microscopic findings on the livers in experimentally infected rabbits. All the livers of the affected rabbits were shown to have degenerative changes of a type that is characteristic of acute hepatitis. In the liver cells, there were dilation of rER and mitochondria, vacuole formation of various sizes, and appearances of many virus-like particles in the vicinity of rER, granular bodies and crystalline arrays of viral particles in the cytoplasm with necrotic changes of the nucleus. Clusters of virus-like particles and viral crystals appeared in the cytoplasm of sinusoid endothelial cells and Kupffer's cells with morphological changes of organelles. Also viral crystals were demonstrated in the cytoplasm of macrophages among the liver cells. On the whole, the liver cells had many virus-like particles and a few crystalline arrays of viral particles. Therefore, this implies that the liver cells are the main site of the viral replication in inducing the viremia. It was concluded that the liver was the primary target organ of this viral disease, and the pathological and the ultrastructural evidence suggest that the virus may be belong to genus enterovirus.

• 대한수의학회지
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• 제35권2호
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• pp.317-326
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• 1995

The purpose of this study was to establish a method for in vitro culture of C parvum isolated in Korea by determination of suitable cell model to complete development of this parasite. The result obtained were summerized as follows: 1. To determine the most suitable cell line, six types of cell line were examined by microscopy. All cell lines were infected with C parvum and showed the highest infection score in HmLu cells. 2. The staining methods including DMSO-modified acid-fast(A-F) stain, hematoxylin-eosin(H & E) stain and immunofluorescence antibody(IFA) stain were applied to examine the infection of C parvum in cell culture. These staining methods were possible to examine the infection of C parvum in cell culture. The most sensitive one was IFA staining technique. 3. Developmental stages of C parvum in HmLu cell were observed. After the initial 8 hour incubation period, some trophozoites were observed. The meronts and gametes were appeared at 24-48 hour post inoculation(PI), and oocysts were observed firstly at 48-72 hour PI. 4. In H & E stain, the parasite appeared as basophilic within parasitophorous vacuole membrane(PVM) and lying in cytoplasm at near the nucleus of the host cells. It was able to distinguish the type I, type II meronts and gametes. 5. In DMSO-modified acid-fast stain, specific stained parasites were appeared firstly after 48 hour PI. The parasites were showed with different degrees of staining bright red color within PVM. 6. The endogenous stages of parasites in HmLu cell recovered at 48, 96, 120 and 144 hour after inoculation were reacted with rabbit immunized serum in immunofluorescence antibody and avidin-biotin complex peroxidase staining technique.