• 한국식품저장유통학회지
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• 제8권4호
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• pp.399-404
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• 2001

김치 첨가 해물만두의 생리기능성을 조사하고자 시판 만두, 해물만두 및 20% 김치첨가 해물만두 추출물에 대한 항돌연변이, 항산화 효과 및 아질산염 소기능에 대하여 조사하였다. 간접돌면변이원으로 알려진 aflatoxin B$_1$을 첨가한 Salmonella typhimurium TA 100 및 YG 1024에 만두 추출물을 5 mg/plate 농도로 처리한 후 항돌연변이 효과를 조사한 결과 20% 김치첨가 해물만두의 돌연변이 저해율이 47% 및 61%로 가장 높게 나타났으며, 수소공여능은 모두 50% 이상의 활성을 나타내었고, 시판만두, 해물만두 및 20% 김치첨가 해물만두의 순으로 높게 나타났으나, 모두 0.1%의 BHT 첨가군 보다는 낮았다. Linoleic acid에 대한 과산화물가는 저장기간이 지남에 따라 대조군의 과산화물가는 크게 증가한 반면 20% 김치첨가 해물만두 첨가군에서는 대조군에 비하여 매우 낮게 나타났으며, 시판 및 해물만두 추출물의 경우는 약간 낮게 나타났으나 0.1% BHT 첨가군보다는 모두 높았다. 횐쥐의 liver homogenate에 만두추출물을 처리한 후 TBA가를 조사한 결과 20% 김치첨가 해물만두 추출물 처리구가 가장 낮게 나타났다. 아질산염 소거능은 모두 50% 이상이었다.

• Molecules and Cells
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• 제19권1호
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• pp.114-123
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• 2005

Nitropyrene, the predominant nitropolycyclic hydrocarbon found in diesel exhaust, is a mutagenic and tumorigenic environmental pollutant that requires metabolic activation via nitroreduction and ring oxidation. In order to determine the role of ring oxidation in the mutagenicity of 1-nitropyrene, its oxidative metabolites, 1-nitropyrene 4,5-oxide and 1-nitropyrene 9,10-oxide, were synthesized and their mutation spectra were determined in the coding region of hprt gene of CHO cells by a PCR amplification of reverse-transcribed hprt mRNA, followed by a DNA sequence analysis. A comparison of the two metabolites for mutation frequencies showed that 1-nitropyrene 9,10-oxide was 2-times higher than 1-nitropyrene 4,5-oxide. The mutation spectrum for 1-nitropyrene 4,5-oxide was base substitutions (33/49), one base deletions (11/49) and exon deletions (5/49). In the case of 1-nitropyrene 9,10-oxide, base substitutions (27/50), one base deletions (15/50), and exon deletions (8/50) were observed. Base substitutions were distributed randomly throughout the hprt gene. The majority of the base substitutions in mutant from 1-nitropyrene 4,5-oxide treated cells were $A{\rightarrow}G$ transition (15/33) and $G{\rightarrow}A$ transition (8/33). The predominant base substitution, $A{\rightarrow}G$ transition (11/27) and $G{\rightarrow}A$ transition (8/27), were also observed in mutant from 1-nitropyrene 9,10-oxide treated cells. The mutation at the site of adenine and guanine was consistent with the previous results, where the sites of DNA adduct formed by these compounds were predominant at the sites of purines. A comparison of the mutational patterns between 1-nitropyrene 4,5-oxide and 1-nitropyrene 9,10-oxide showed that there were no significant differences in the overall mutational spectrum. These results indicate that each oxidative metabolite exhibits an equal contribution to the mutagenicity of 1-nitropyrene, and ring oxidation of 1-nitropyrene is an important metabolic pathway to the formation of significant lethal DNA lesions.

• 한국식품과학회지
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• 제28권6호
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• pp.1059-1064
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• 1996

키토산의 in vitro 돌연변이 억제활성을 Salmonella typhimurium reversion assay와 SOS chromotest 이용하여 살펴보았다. S. typhimurium에 의한 시험된 간접변이원 Trp-P-2에 대해서 0.1-1.0 mg/plate의 chitosan농도로 시험하였을 때, 24-65%의 돌연변이 억제활성을 나타내었다(p<0.01). Chitosan농도 0.1-0.5 mg/plate 범위에서는 용량-반응(dose-responese)관계를 나타내면서 저해효과를 나타내었으며, 0.5 mg/plate이상의 농도에서는 오히려 저해효과가 감소하는 경향이었다. 반면, 직접변이원인 SA 및 2-NF로 유도된 돌연변이에 대해서는 시험한 어느 농도에서는 chitosan에 의한 돌연변이 억제효과가 나타나지 않았다. Chitosan은 직접변이원인 4-NQO에 의한 SOS 유도에 대해 chitosan농도가 0.15 mg/assay 및 0.20 mg/assay일 때 4-NQO에 의해 유도된 유도지수(induction factor) 8.290을 4.226및 4.516으로 낮추어 46-49%의 저해활성을 나타내었다. 간접변이원인 Trp-P-2에 의한 SOS 유도에 대한 chitiosan의 억제효과는 시험한 chitosan의 농도범위에서 약 9-39%의 저해활성을 나타내었으며, chitosan농도가 0.1 mg/assay이 경우를 제외하고는 chitosan농도 증가에 따라 비례적으로 SOS유도 저해활성이 나타났다. Trp-P-2d 의해 DNA 손상을 유도한 다음 chitosan의 세포내 역제(bio-antimutagenicity) 활성을 살펴 본 결과, 저농도에서는 세포의 억제(desmutagenicity) 특성을, 0.75-1.0 mg/plate의 비교적 고농도에서는 세포내 억제특성을 나타내었다.

• 한국약용작물학회지
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• 제3권1호
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• pp.40-44
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• 1995

용담의 조직배양기술과 병행하여 기내변이주 유도와 배양체의 Gentiopicroside 함량을 비교분석한 결과 1. 정아는 $NaN_3$ $0.001M{\sim}0.003M$에서 $48{\sim}74%$의 생존율을 보였고, EMS 0.05M에서 36% 생존하였으나 생육치 못하고 고사하였으며 MNH 처리유래 식물체의 기내 생육은 양호하였다. 2. 측아는 $NaN_3$의 농도가 높아질수록 생존율이 감소되었고 EMS는 전부 고사하였으며 MNU에서는 $4{\sim}32%$생존하였다. 배양 60일경의 기내 생육은$NaN_3$와 MNU 모두 정아처리에 비하여 저조한 경향이었다. 3. 종자 처리후 발아율은 $NaN_3$는 0.001M에서 41.4%인 반면 농도가 높을수록 감소하였고, EMS는 저농도인 0.05에서만, 4.8% NMU도 1mM에만 2.8%를 보였다. 기내생육은 $NaN_3$는 무처리구와 비슷한 생육을 보였고 EMS와 MNU 처리구는 생육이 불균일한 변이 발생을 보였다. 4. 용담 조직배양체의 gentiopicroside 함량비교에서 Callus는 40일 배양한 것이 0.038%, 80일 배양한 것이 0.051% 함유하였고 shoot는 신장형이 0.426%, 위축형이 2.710%였다. 특히 뿌리에서는 신장형이 0.883%, 위축형은 1.383%로 조사되었다.

• 한국환경성돌연변이발암원학회지
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• 제21권1호
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• pp.1-8
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• 2001

We have synthesized $^{99m}$Tc-mercaptoacetyltriglycine (MAG3)-biocytin as a new imaging agent for hepatobiliary scintigraphy. The aim of this study was to evaluate the usefulness of $^{99m}$Tc-MAG3-biocytin scintigraphy in differentiating carbon tetrachloride ( $CCl_4$)-induced hepatotoxicity from $\alpha$-naphthylisothiocyanate (ANIT)-induced cholestasis in mice, which reflecting the differential diagnosis of neonatal jaundice caused by neonatal hepatitis from congenital biliary atresia in humans. Methods: Balb/c mice (female, 20 g, n=4-6) were pretreated with $CCl_4$(0.5 or $1.0m\ell$/kg) and ANIT ($150 or 300 m\ell$/kg) 18 h before scintigraphy. Biochemical and histopathological examinations showed a pattern of typical acute hepatitis (increase of transaminases and hepatocellular necnsis) in $CCl_4$-treated mice and cholestasis (increase of alkaline phosphatase and ${\gamma}$-glutamyltransferase, and biliary hyperplasia) in ANIT-treated mice, respectively, Mice were fasted at least 4 hr prior to the intravenous injection of $^{99m}$Tc-MAG3-biocytin (18.5 MBq/20$\mu\textrm{g}$) in 2% human serum albumin in saline. Scintigraphy was performed with a ${\gamma}$-camera equipped with a 1-mm diameter pin-hole collimator for 30 min and images were acquired every 15 s. We compared the values of physical parameters, such as peak liver/heart ratio ($${\gamma}$_{max}$) and peak ratio time ($t_{max}$) far $^{99m}$Tc-MAG3-biocytin scintigraphy. Results: Scintigraphic parameters of the $CCl_4$-pretreated (0.5 $m\ell$/kg) group showed a 81.9% decrease of r$_{max}$, and 42.2% decrease of $t_{max}$, whereas the ANIT-pretreated ( $150m\ell$/kg) group showed a 53% decrease of $r_{max}$, and 2.36-fold increase of $t_{max}$, (P<0.05). These results demonstrate that the decrease of $r_{max}$ and the shortening of $t_{max}$ are characteristic features for hepatotoxicity, in contrast to the increase of $t_{max}$ and decrease of $r_{max}$ for biliary hyperplasia. Conclusion: $^{99m}$Tc-MAG3-biocytin hepatobiliary scintigraphy can distinguish hepatitis from cholestasis in mice model and may be similarly useful in humans which differentiating the cause of neonatal jaundice in clinical study.cal study.cal study.cal study.

• 한국식품과학회지
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• 제30권3호
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• pp.688-692
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• 1998

천연생리활성물질의 개발과 미이용자원의 효율적 재이용방안을 모색하기 위하여 13여종의 한국산 야생 버섯류를 에탄올과 물로 추출하여 각 시료추출물의 항변이원성 물질 검색을 시도하였다. B(a)P과 MNNG의 돌연변이 유발성에 미치는 야생버섯류의 에탄올 추출물과 물추출물의 항돌연변이 효과의 검토는 Salmonella typhimurium TA98과 TA100을 이용한 Ames 실험계를 이용하였으며 B(a)P에 대해 꽃구멍장이버섯(Polyporus dispansus), 깔때기꾀꼬리버섯(Cantharellus infundibuliformis), 진갈색주름버섯(Agaricus subrutilescens), 테미로버섯(Daedalea dickinsii), 목장말똥버섯 (Panaeolus papilionaceus) 및 턱수염버섯(Hydnum repandum) 등의 에탄올추출물에서 비교적 강한 항변이 원성을 나타내었다. 물추출물의 경우는 B(a)P에 대해서 턱수염버섯(Hydnum repandum)이 TA100에서 가장 강한 저해효과를 나타내었고 대부분의 시료는 낮거나 저해활성이 보이지 않았다. 직접변이원인 MNNG에 대해서는 야생버섯류의 에탄올추출물중 5종만 항변이원성이 관찰되었고, 물추출물의 경우는 꽃구멍장이버섯(Polyporus dispansus)이 가장 강한 저해효과를 보였으나 대부분의 버섯류는 낮거나 저해 효과를 거의 나타내지 않았다. 그중 직, 간접 변이원에 대해 가장 강한 저해 효과를 나타낸 꽃구멍장이 버섯의 에탄올추출물은 농도가 높을수록 항변이원성 효과가 증가하는 경향을 보였다.

• 한국환경성돌연변이발암원학회지
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• 제24권4호
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• pp.198-205
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• 2004

Cytochrome P4501B1(CYP1B1) is known to be inducible by xenobiotic compounds such as policyclic aromatic hydrocarbon(PAH) and dioxins such as 2,3,7,8-tetrachloro-dibenzo-p-dioxin(TCDD). And these induction of CYP1B1 is also regulated by many categories of chemicals. In order to investigate the effects of several chemicals on CYP1B1 gene expression in Hepa-I and MCF-7 cells, 5' flanking DNA of human CYP1B1 was cloned into pGL3 basic vector containing luciferase gene, and then transfected into these cells. After treatment of chemicals, the luciferase activity was measured. CYP1B1 enzyme metabolize PAHs and estradiol. CYP1B1 metabolize estradiol to 4-hydrozyestradiol that is considered as carcinogenic metabolite. Recent industrialized industrialized society, human has been widely been exposed to widespread environmental contaminants such as PAHs(polycyclic aromatic hydrocarbon) that are originated from the imcomplete combustion of hydrocarbons. PAHs are known to be ligands of the AhR(aryl hydrocarbon receptor). Induction of cytochrome P4501B1(CYP1B1) in cell culture is widely used as a biomarker for PAHs. Therefore we have studied the effect of PAHs in the human breast cancer cells MCF-7 to evaluate bioactivity of PAHs. We have used the United State of America EPA selected 13 different PAHs, PAHs mixtures and extracts from environmental samples to evaluate the bioassay system. We examined effects of PAHs on the CYP1B1-luciferase reporter gene and CYP1B1 mRNA level. Benzo(k)fluoranthene and dibenzo(a, h)anthracene showed strong response to CYP1B1 promoter activity stimulation, and also CYP1B1 mRNAs increase in MCF-7 cells in a concentration-dependent manner. RT-PCR analysis indicated that PAHs significantly up-regulate the level of CYP1B1 mRNA. Some flavonoids such as genistein, daidzein, chrysin, naringenin and morin were also investigeted. These flavonoids decreased B(k)F infuced luciferase activity at low concentration. But, these flavonoids exhibited stimulatory effect at high concentration.

• 동아시아식생활학회지
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• 제18권5호
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• pp.746-752
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• 2008

본 연구에서는 오미자 에탄올 추출물의 항산화 활성과 총폴리페놀 함량 및 총 플라보노이드 함량을 측정하고, Salmonella typhimurium TA100을 이용하여 항돌연변이 활성을 분석하였다. 오미자 에탄올 추출물의 DPPH 라디칼 소거능은 $500{\mu}g$/assay의 농도에서 57%이었고, $IC_{50}$값이 $435\;{\mu}g$/assay으로 나타나 비교적 높은 항산화 활성을 가지고 있음을 보여주었다. 오미자 에탄올 추출물의 총 폴리페놀 함량과 총 플라보노이드 함량은 각각 9.53 mg/g과 3.97 mg/g으로 분석되었다. 또한 오미자 에탄올 추출물은 sodium azide(5 mg/plate) 와 4-NQO(1 mg/plate)에 대한 항돌연변이 활성이 각각 45%, 82%로 나타나 4-NQO에 대해 높은 돌연변이 억제 효과를 가지고 있는 것으로 나타났다. 본 연구를 통해 오미자 에탄올 추출물이 높은 항산화 활성과 항돌연변이 활성을 가진 것으로 나타나, 앞으로 천연 항산화제 및 항돌연변이 기능성 소재로 사용될 수 있는 가능성을 보여주었다.

• 한국환경성돌연변이발암원학회지
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• 제26권4호
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• pp.119-124
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• 2006

There are $10{\sim}30%$ polyphenol and $2{\sim}4%$ caffeine in green tea. Caffeine is a kind of alkaloid containing nitrogen which cause stimulation, impatience, headache, insomnia, low birth weight infant. Because of these negative effect, decaffeined beverage came out and decaffeined coffee already have a big market since 1970s. Having proving the physiologic functions of green tea, high consumption of coffee is shifting to green tea. Because of the carcinogenic effect of the organic solvents, decaffeine processing with supercritical carbon dioxide has industrialized and have an advantage in environment-friendly and minimized flavor loss. Decaffeined green tea using supercritical carbon dioxide is considered to be safe but there are not enough study. We investigated the chromosome aberration test with mammalian cell line, CHL. When the cells were treated with 5000, 2000, 1000 ${\mu}g/ml$ and compared with the negative controls, there were no significant(P>0.05) increased chromosome aberration. Same results was observed when adding S9 mixture or not. As a result, water extract of decaffeined green tea using supercritical carbon dioxide does not induce chromosome aberration.

• 한국환경성돌연변이발암원학회지
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• 제26권4호
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• pp.125-132
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• 2006

Previous studies showed that epigallocatechin gallate(EGCG) have substantial effects of suppressing the N-methyl-N'-nitro-N-nitrosoguanidine(MNNG)-initiated cell transformation process on the bases of foci formation frequency and loss of anchorage dependency. In this study we tried to clarify the molecular mechanism of suppressing the cell transformation process. Mouse cell line balb/c 3T3 A31-1-1 was exposed 2 days to MNNG followed by 15 days 12-O-tetradecanoylphorbol-13-acetate(TPA) treatment for our transformation process. EGCG was added after the time point of 24 hours exposure to TPA and incubated for 19 days. 2029 genes were selected in our transformation process that showed fold change value of 1.5 or more in the microarray gene expression analysis covering the mouse full genome. These genes were found to be involved mainly in the cell cycle pathway, focal adhesion, adherens junction, TGE-$\beta$ signaling, apoptosis, lysine degradation, insulin signaling, ECM-receptor interaction. Among the genes, we focused on the 631 genes(FC>0.5) reciprocally affected by EGCG treatment. Our study suggest that EGCG down-regulate the gene expressions of up stream signaling factors such as nemo like kinase with MAPK activity and PI3-Kinase, Ras GTPase and down stream factors such as cyclin D1, D2, H, T2, cdk6.