• 대한핵의학회지
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• 제26권1호
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• pp.127-132
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• 1992

Colloidal $^{32}P$ chromic phosphate is used to prevent hepatic metastasis from colorectal cancer. It is speculated that the intravenous injection of colloidal $^{32}P$ chromic phosphate can cause genotoxicity. To evaluate the genotoxicity of intravenously injected colloidal $^{32}P$ chromic phosphate, authors performed a micronuclei test in mice bone marrow. Mice (ICR strain, $25\sim30g$) were divided to 4 groups: control, group 1 (19.166 KBq/g, usual therapeutic dose in human), group 2 (191.66 KBq/g), and group 3 (1916.6 KBq/g). Five mice of each group were sacrificed at days 1, 2, 3, 5, 7 and 14. Bone marrow were smeared and stained with Wright-Giemsa method. One thousand polychromatic erythrocytes (PCE) and normochromatic erythrocytes (NCE) were counted under the light microscope, and the number of micronucleated PCEs and NCEs were recorded. The frequency of micronuclei in PCE and NCE in the control group was $0.3{\pm}0.06%\;and\;0.45{\pm}0.10%$, respectively. At group 1, frequency of micronuclei is not different from the control. However, frequencies of micronuclei in PCE at groups 2 and 3 were significantly increased from day 1 and persisted to day 14. The frequency of micronuclei in NCE was increased only at group 3. In conclusion, the frequency of micronuclei increases as the dose of colloidal $^{32}P$chromic phosphate increases, while micronuclei was not induced at the usual therapeutic dose. And the frequency of micronuclei persistently elevated for 14 days in the cases of higer doses.

• 한국환경보건학회지
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• 제37권6호
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• pp.429-439
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• 2011

Objectives: Ethylene oxide (EtO) is classified as a human carcinogen, but EtO is still widely used to sterilize heat-sensitive materials in hospitals. Employees working around sterilizers are exposed to EtO after sterilization. The aim of the present study was to assess the exposure of EtO level, coupled with occupationally induced micronuclei from hospital workers. The influence of genetic polymorphisms of detoxifying genes (GSTT1 and GSTM1) and DNA repair genes (XRCC1 and XRCC3) on the frequencies of micronuclei in relation to exposure of EtO was also investigated. Methods: The study population was composed of 35 occupationally exposed workers to EtO, 18 student controls and 44 unexposed hospital controls in Korea. Exposure to EtO is measured by passive personal samplers. We analyzed the frequencies of micronuclei by performing cytokinesis-block micronucleus assay (CBMN assay) and GSTM1, GSTT1, XRCC1, and XRCC3 were also genotyped by performing polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Results: The frequencies of micronuclei in EtO exposure group, student controls and hospital controls were $18.00{\pm}7.73$, $10.47{\pm}7.96$ and $13.86{\pm}6.35$ respectively and their differences were statistically significant, but no significant differences according to the level of EtO were observed. There was a dose-response relationship between the frequencies of micronuclei and cumulative dose of EtO, but no significantly differences were observed. We also investigated the influence of genetic polymorphisms (GSTM1, GSTT1, XRCC1, and XRCC3) on the frequencies of micronuclei, but there were no differences in the frequencies of micronuclei by genetic polymorphisms. Conclusions: The frequencies of micronuclei in EtO exposure group was significantly higher than control groups. A dose-response relationship was found between the level of EtO exposure and the frequencies of micronuclei, but no statistically differences were observed. We also found that the frequencies of micronuclei were increased according to cumulative EtO level. There was no association of the genetic GSTM1, GSTT1, XRCC1, and XRCC3 state with the frequency of micronuclei induced by EtO exposure.

• Toxicological Research
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• 제6권1호
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• pp.29-40
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• 1990

Cytotoxic effects of cytosine arabinoside and vinblastine on cultured fibroblasts were determined by colorimetric assays of neutral red (NR) and tetrazolium MTT, and by mutagenicity tests . Cytosine arabinoside and vinblastine were highly toxic by showing that concentrations of NR-50 and MTT-50 of two drugs were lower than 100 ${\mu}$M. At mid-point cytotoxicityvalue of two drugs, frequencies of micronuclei and SCEs were very high and chromosome showed structural abnormalities. The sizes of micronuclei formed by vinblastine were larger than those induced by cytosine arabinoside. These results suggest that cytosine arabinoside and vinblastine have highy mutagenic and severe cytotoxic effects on the cultured mouse fibroblasts.

• 한국독성학회:학술대회논문집
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• 한국독성학회 2002년도 Current Trends in Toxicological Sciences
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• pp.124-124
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• 2002

In order to determine the effect of the DNA repair inhibitors, cytosine arabinoside(Ara C)and 3-aminobenzamide(3AB) on the frequenceis of chromosomal aberrations and micronuclei induced by radiation. After in vitro exposure of human lymphocytes to x-ray(1-3Gy) DNA repair inhibitors, Ara C and 3AB were treated and the frequencies of micronuclei, translocation and dicentric chromosomes were analysed using FISH technique with DNA probe for chromosome 4.(omitted)

• Archives of Pharmacal Research
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• 제28권9호
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• pp.1079-1085
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• 2005

The purpose of this study was to investigate the safety of chitosan oligosaccharide and the effects of chitosan oligosaccharide on mercury induced genotoxicity in mice using the micronuclei and chromosome aberration. The micronuclei test was performed by microscopic examination $(\times1,000,\;stained\;using\;a\;May-Grunwald\;solution)$ after administering 0.01, 0.1, and $1\%(10\;mg/mL)$ chitosan oligosaccharide for 7, 60, and 180 days ad libitum in mice. Total micronuclei of 1,000 polychromatic erythrocytes were recorded for each group. There was no difference between the untreated and experimental groups. The intake periods and concentrations of chitosan oligosaccharide did not affect the occurrence of micronuclei in bone marrow cells (P>0.05). The chromosomal aberration test was performed by microscopic examination $({\times}1,000,\;stained\;using\;a\;4\%\;Giemsa\;solution)$ after administering the same concentration of chitosan oligosaccharide to mice, in $F_1,\;F_2,\;F_3$ generations and parents. The frequency of chromosomal aberrations was defined as [Ydr=(D+R)/total number of counted lymphocytes]. Similar to the micronuclei test, there was no difference between the untreated and treated groups. These results showed that the intake periods and concentrations of chitosan oligosaccharide did not affect chromosomal aberrations in bone marrow cells (P>0.05). To investigate the effect of chitosan oligosaccharide on mercury-induced chromosome aberration, mice in each condition were supplied with $^{203}HgCl_2$ and chitosan oligosaccharide ad libitum. Chitosan oligosaccharide significantly inhibited $^{203}HgCl_2-induced$ chromosome aberration in mice. Based on the results of this study, it may be concluded that the chitosan oligosaccharide is a nontoxic material that could be used as a suppressor of heavy metal-induced genotoxicity.

• 대한핵의학회지
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• 제34권1호
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• pp.74-81
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• 2000

목적: 마우스를 전신조사한 다음 골수세포를 추출하여 중기염색체 분석법과 미소핵 검사법으로 방사선량별 염색체 이상의 빈도를 관찰하고 이를 통하여 표준선량반응곡선을 얻어내어 방사선이 인체 골수세포에 미치는 영향을 추정하기 위해 이 연구를 시행하였다. 대상 및 방법: ICR계 마우스를 대상으로 각각 0, 1, 2, 3, 4, 5, 10 Gy를 조사하고 대퇴골의 골수를 추출하여 중기염색체 분석법을 시행하였고, 0, 1, 2, 3, 4, Gy를 조사한 후 미소핵 분석법을 시행하였다. 각각의 조사량에 따라 중기염색체에서 이중 중심체형 염색체와 반지형 염색체를 계수하였고, 다염성적혈구에서 관찰된 미소핵을 계수하였다. 결과: 중기염색체에서 이중 중심체형 염색체와 반지형 염색체의 빈도를 나타내는 Ydr 값은 0, 1, 2, 3, 4, 5, 10 Gy에서 각각 0.002, 0.107, 0.33, 0.625, 1.055, 1.662, 5.843이었고 선량-반응관계를 선형회귀분석한 결과 방사선량(D)과 염색체이상 빈도(YDR)와의 관계는 YDR=0.0176+0.0324D+0.0567$D^2$ (r=1.0, p<0.001)으로 나타났다. 다염성적혈구에서 관찰된 미소핵은 0, 1, 2, 3, 4, Gy에서 각각 0.001, 0.062, 0.218, 0.478, 0.841로 방사선량(D)과 미소핵의 빈도(mn)와의 관계는 F(mn)=0.0019+0.0073D+0.00506$D^2$ (r=1.0, p<0.001)로 나타나 선량에 따른 염색체이상의 빈도는 이차함수식으로 증가함을 알 수 있었다. 두 가지의 검사방법간에는 매우 강한 상관관계를 나타내었다(r=0.99, p<0.01). 결과: 마우스의 골수세포에서 중기염색체 분석법과 미소핵 검사법은 생체 내의 피폭선량을 평가하는데 매우 유용하였고, 이 두 가지 검사법 중 어느 방법을 사용하여도 방사선에 의한 생물학적 효과를 평가할 수 있을 것으로 사료되었다.

• Journal of Radiation Protection and Research
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• 제29권1호
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• pp.9-15
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• 2004

방사선에 의해 유도되는 사람 말초혈액 림프구 미소핵 관찰빈도를 높이면서 생물학적 선량평가법으로서 활용 가능성을 확인하고자 본 연구를 수행하였다. 우선 5명의 건강한 사람으로부터 혈액을 제공 받아 선량영역을 0에서 800cGy로 하여 감마선$(^{137}Cs)$을 조사 한 후 김사와 아크리딘 오렌지 형광 염색하고 미소핵 출현빈도를 비교하였다. 아크리딘 오렌지 염색법을 이용하여 미소핵을 관찰하였을 때, 김사 염색법에 비교하여 적갈색의 비특이성 과립과 녹황색의 DNA가 붉은색의 세포질을 배경으로 명확히 구별되었을 뿐만 아니라 선량이 증가하면서 검출율도 높았다. 아울러, 말초혈액 T와 B-림프구에 대하여 선량영역을 0에서 50cGy로 하여 방사선을 조사한 후 미소핵 출현빈도를 아크리딘 오렌지 염색하여 김사염색과 비교한 바, B-림프구에서 선량이 증가하면서 적어도 2배 이상 높게 관찰되었다. 본 실험 결과, 사람 말초 혈액 B-림프구를 대상으로 한 아크리딘 오렌지 형광염색 미소핵 분석법은 저선량 방사선 인체영향 평가나 과피폭 선량추정시 활용이 가능 할 것으로 생각된다.

• 한국환경성돌연변이발암원학회지
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• 제18권2호
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• pp.93-97
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• 1998

The results of chromosome aberration test in mammalian cells in culture (Chinese hamster lung fibroblast cells) showed no induction of structural and numerical aberrations by antifungal agents of YH1715 series regardless of metabolic activation. While positive control group (mitomycin C and benzo(a)pyrene) showed structural chromosome aberrations of 37% and 23%, respectively. The in vivo induction of micronuclei was measured in polychromatic erythrocytes in bone marrow of male ddY mouse given YH1715R and YH1729R at 1, 0.5, 0.25 g/kg by p.o. once. After 24 hours, animals were sacrificed and evaluated 40 the incidence of micronucleated polychromatic erythrocytes in whole erythrocytes. Although a positive response for induction of micronuclei in animals treated with mitomycin C demonstrated the sensitivity of the test system for detection of a chemical clastogen, YH1715R did not induce micronuclei in bone marrow of ddY male mice but induced cytotoxicity to bone marrow cells at the highest concentration (1 g/kg, p〈0.05), and YH1729R induced micronuclei in bone marrow of ddY male mice dose dependently (p<0.05) but did not induce cytotoxicity to bone marrow cells.

• 한국환경성돌연변이발암원학회지
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• 제22권4호
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• pp.289-295
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• 2002

This study was conducted to quantify of micronucleus frequencies in human umbilical cord blood by supravital staining method with acridine orange, and to find some factors that affected on micronucleus frequncies in humans. In this study, we used umbilical cord blood of new born infants that have sufficient reticulocytes compared with adult peripheral blood. The cord bloods were taken after childbirth from 60 normal infants in industrial and coastal region in Korea. The total of 3 ${mu}ell$ cord blood was applied to slide coated with acridine orange, and micronuclei were observed under fluorescent microscopy. Demographic factors and independent variables were collected from mothers by questionnaire. The frequencies of micronuclei in umbilical cord blood of new born infants were 0-5 per 2,000 reticulocytes by supravital staining method, and mean value and standard deviation were 1.75$\pm$0.97. There were no significant difference by the regions, smoking habits of father or mother. However, age of mother showed significant positive correlation with frequencies of micronuclei (p<0.05). Smoking at home by fathers also was found as a significant variable by muliple regression analysis. Therefore, further studies would be needed for genotoxicological evaluation of new born infants by microneuli test using supravital staining method.

• 약학회지
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• 제37권3호
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• pp.278-285
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• 1993

The anticlastogenic effect of N-acetylcysteine was tested in vivo in mouse bone-marrow micronucleus assay. The frequencies of micronuclei induced by adriamycin (5 mg/kg i.p.) in bonemarrow cells were decreased by the oral administration of N-acetylcysteine at 12 h before adriamycin injection. The observed suppressing effect was not a reflection of a delay in the formation of micronuclei by the cytotoxic effect of N-acetylcysteine. The anticlastogenic effects of SH compound including N-acetylcysteine, cysteine, cystine, S-carboxy methylcysteine and glutathione were also investigated by the multiple pretreatment. Each SH compound was administered orally every day for 5 days and adriamycin (5 mg/kg i.p.) was injected at 24h after the last dose of test compound. N-acetylcysteine and glutathione showed significantly the suppressive effect at dose of 10 and 25 mg/kg for N-acetylcysteine and at the dose of 25 mg/kg for glutathione. Our study suggests that N-acetylcysteine is capable of protecting the chromosomal damages in the normal cells during cancer chemotherapy by adriamycin, and may act as an anticlastogen against induction of micronuclei by superoxide generating agent such as adriamycin.