• 동아시아식생활학회지
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• 제11권1호
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• pp.19-25
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• 2001

This study was performed to examine the antimutagenic and cytotoxic effects of potato vinegar and commercial vinegars(cider, brown rice, persimmon vinegars) on Salmonella typhimurium TA98, TA100 and cancer cell lines using Ames test and cytotoxicity assay, respectively. In Ames test, all vinegars did notexhibit any mutagenicity , but showed substantial inhibitory effects against N- methyl - N -nitro - N- nitrosog -uanidine(MNNG) , 4-nitroquinoline-1-oxide(4NQO), 3-amino-1,4-dimethyl-5H-pyrido(4,3-b)indol(Trp-P-1)and benzo( $\alpha$ )pyrene(B( $\alpha$ )P). The number of revertants per plate decreased significantly when these vinegars(80 ug/plate) were added to the assay system using TA100 strain. Especially, potato vinegar(80 ug/plate) showed high inhibition rate of 69.9% against mutagenicity of B( $\alpha$ )P on TA100 strain. In the cytotoxicity assay, these vinegars also showed prominent cytotoxic activity against human cancer cell lines. Potato vinegar(10 ug/well) showed the strongest cytotoxic effect against HT1080 (fibrosacoma cell) andK562 ( myelogenous leukemia) at the same concentration when compared with other vinegars.

• 동아시아식생활학회지
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• 제11권6호
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• pp.466-471
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• 2001

염색체 이상유발물질인 benzo($\alpha$)yrene(B($\alpha$)P) 을 마우스에 50, 100, 그리고 150 mg/kg으로 투여한 경우의 소핵생성은 각각 6.6$\pm$0.6, 9.2$\pm$0.6 그리고 10.4$\pm$0.9로서 농도증가에 비례적으로 증가하였으며, 대조군에서는 1.4$\pm$0.4의 소핵생성을 나타내었다. B($\alpha$ )P을 150 mg/kg과 참취뿌리 에탄올 추출물을 각각 50. 100, 150 그리고 200 mg/kg으로 동시에 투여한 경우 각각 24.50, 22.55, 59.80 그리고 79.41%의 소핵생성 억제효과를 나타내었다. 참취뿌리 용매분획물 실험에서는 헥산, 클로로포름, 에틸아세테이트, 부탄올 및 물분획물이 시료농도인 10 mg/kg의 투여군에서 양성대조군에 비해 각각 3.9, 35.3, 40.2, 11.8 및 49.0%의 소핵생성 억제율을 나타내었다. 시료농도 80 mg/kg의 투여군에서는 양성대조군에 비해 각각 78.4. 65.7. 75.5, 68.6 그리고 77.5%의 소핵생성 억제율을 나타내었다. 참취뿌리 에탄올추출물의 용매분획물은 80 mg/kg의 투여농도에서 비교적 높게 소핵생성 억제율이 나타났다.

• 한국식품과학회지
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• 제41권1호
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• pp.21-26
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• 2009

본 연구는 인도산, 중국산, 국내산 참깨를 열풍 건조 후 착유기를 통해 제조한 참기름에서의 PAHs 함량변화와 대형 마트에서 판매되고 있는 참기름에서의 PAHs 함량을 분석하기 위하여 실시하였다. 분석표준물질은 돌연변이원성과 발암성이 있는 것으로 알려진 8가지 PAHs를 선정하여 HPLC/FLD를 이용하여 정성 정량분석을 하였고, 색차계를 이용하여 명도(L), 적색도(a), 황색도(b)를 측정하였다. 분석결과 원산지 별 볶은 후 착유한 참기름에서 PAHs 함량은 볶지 않았을 때보다 유의적으로 증가하였다. 볶지 않은 참기름인 경우 PAHs 함량은 인도산, 중국산, 국내산 순이었다. 인도산 참깨에서 0.95 ${\mu}g$/kg의 PAHs 가 검출되었는데 이는 환경으로부터 PAHs가 생성될 수 있다는 점을 추측할 수 있었다. $250^{\circ}C$에서 25분간 볶은 참기름인 경우 중국산, 국내산, 인도산 순으로 PAHs가 검출되었다. 중국산 참깨에서 PAHs 함량은 3.97 ${\mu}g$/kg으로 볶지 않았을 때보다 약 4배 이상 증가하였다. 중국산 참깨는 다른 원산지 참깨에 비해 볶는 온도와 시간에 영향을 많이 받는 것으로 사료된다. 국내에서 판매되고 있는 참기름 중 PAHs 함량 분석한 결과, PAHs 총 함량은 0.79-2.15 ${\mu}g$/kg으로 검출 되었다. 국내 기준 규격으로 설정되어 있는 Benzo[${\alpha}$]pyrene 함량은 0-0.19 ${\mu}g$/kg으로 기준치인 2 ${\mu}g$/kg 이하로 검출되었다. 이는 제조회사에서 PAHs 저감화를 위해 제조과정을 변화시킨 결과로 추측할 수 있다. 원산지 별 참기름과 시중에 판매되는 참기름과의 색도를 비교해 본 결과 $250^{\circ}C$에서 25분 볶은 후 착유한 인도산, 중국산, 국내산 참기름의 명도(L)는 43.31, 41.15, 41.64이었고, 적색도(a)는 13.11, 13.12, 12.48이었고, 황색도(b)는 15.24, 11.87, 11.95이었다. 이는 시중에 판매되는 4종의 참기름과 유사한 색도를 나타내었다. 또한 참기름의 품질평가는 수율, 색도, 향미성분, 지방산 조성 변화를 통해 이뤄지고 있는데, 연구결과를 종합해보면 원산지 별로 큰 차이를 보이지 않았다. 이에 따라 PAHs 생성량이 적은 국내산과 인도산의 참깨가 참기름원료로 적당하며, PAHs의 생성량이 많은 중국산 참깨에 대한 보다 많은 모니터링 연구가 필요할 것으로 생각된다.

• 한국응용과학기술학회지
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• 제31권3호
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• pp.534-540
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• 2014

가공조건 차이에 따른 한방차의 성분변화를 분석한 결과, 팽화공정 처리한 것은 볶음공정을 한 것보다 조회분, 수분, 조단백질, 고형분 용출율이 증가하였으며 조지방은 소폭 감소하였다. 벤조피렌[$B({\alpha})P$]함량은 0.35 ppb에서 0.18 ppb로 크게 감소하였다. 전체적으로 심한 열처리 과정이 없는데도 불구하고 $B({\alpha})P$이 검출된 이유는 식품 중 $B({\alpha})P$는 주로 음식을 조리, 가공할 때 식품의 주성분인 탄수화물, 단백질, 지방 등이 열분해 되어 생성되기 때문이다. 한방차에서 맛, 향, 색상 모두 큰 차이를 보이지 않으나 다소 텁텁한 느낌이 강하고, 시큼한 맛이 강하여 선호도를 떨어뜨리는 것으로 나타났다.

• Preventive Nutrition and Food Science
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• 제2권3호
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• pp.232-235
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• 1997

This study was investigated to determine antimutagenic effects of enzymatic browning reaction products (PEBRPs) obtained by reaction of polyphenol compouns with oxidase extracted from potato. Catechol (Ca) PEBRPs showed the strongeest inhibitor effects with 90% inhibition on benzo-($\alpha$)-pyrene(B($\alpha$)P) induced mutagenesis in Salmonella typhimurium TA98, but he least with40% inhibition on the 2-aminofluorene (2-AF) induced mutagenesis in TA98. The strong antimutagenic activities with 80% inhibition were observed in the presence of 100$\mu\textrm{g}$/plate of hydroquinone(HQ)-PEBRP on the B($\alpha$)P or 3-amino-1,4-dimethyl-5H-pyrido[4,3-b]indole(Trp-P-1) induced mutagenesis in TA98, whereas HQ-PEBRP showed the least antimutagenic effect on 2-AF-induced mutagenesis. The addition of 100$\mu\textrm{g}$ hydroxyhydroquinone(HHQ)-PEBRP to the plate led to approximately 82% inhibitory effects on 2-AF or Trp-P-1 induced mutagenesis in TA98, whereas the least antimutagenicity was obsrved in the4-nitroquinoline-1-oxide(4-NQO) induced mutagenesis in the presence of 100$\mu\textrm{g}$/plate of HHQ-PEBRP. More than 80% inhibiton were observed in the presence of 200$\mu\textrm{g}$/plate of Pyrogalol(Py)-PEBRP on the B($\alpha$)P or Trp-P-1 induced mutagenesis in TA98, but the least with 38% inhibition on 4-NQO induced mutagenesis in TA98. The results indicate that enzymatic browing reaction products of potato have a strong modulatory effect on mutagen induced mutagenesis in TA98.

• 한국발생생물학회지:발생과생식
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• 제16권4호
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• pp.289-294
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• 2012

Gene expressions of cytochrome P4501A (CYP1A), aryl hydrocarbon receptor (AhR) and vitellogenin (Vg) by endocrine disruptors, benzo[${\alpha}$]pyrene (B[a]P) and tributyltin (TBT) were examined in cultured eel hepatocytes which were isolated from eels treated previously with B[a]P (10 mg/kg) or estradiol-$17{\beta}$ (20 mg/kg) in vivo, and the relationship between CYP1A, AhR and Vg genes were studied. When the cultured eel hepatocytes were treated with B[a]P ($10^{-6}-10^{-5}M$) the gene expressions of CYP1A and AhR were enhanced in a concentration-dependent manner. However, when treated with TBT ($10^{-9}-10^{-5}M$) the gene expressions of CYP1A and AhR were suppressed at high concentrations ($10^{-6}-10^{-5}M$), while having no effects at low concentrations ($10^{-9}-10^{-7}M$). Gene expression of Vg was also suppressed by TBT in a concentration-dependent manner in cultured eel hepatocytes which was previously treated in vivo with estradiol-$17{\beta}$.

• 한국식품영양과학회지
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• 제23권4호
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• pp.698-703
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• 1994

In spore rec-assay using B. subtillus H17(rec) and M 45(rec) , the ethanol extract of buckwheat leaves showed antimutagenicity in condition of low concentrations, but its did comutagenicity in condition of high concentrations. In Ames test, the ethanol extract of buckwheat leaves reduced the mtabenicity of N-methyl-N' -nitro-N-nitrosoguaidine (MNNG), benzo (a) pyrene(B($\alpha$)P), 2-amino-fluorene(2AF), and 3-amino -1, 4-dime-thyl-5-H-pyrido(4, 3-b) indol(Trp-P-1) in Salmonella typhimurium TA98 and TA100. The ethanol extract was fractionated by hexane, ethylacetate, butanol and water. Among Them hexane fraction showed the highest inhibition rate on the mutagenicity of B($\alpha$)P, and so did chloroform fraction on the mutagenicity of MNNG in S. typhimurium Ta98 and TA100. To elucidate the antimutagenic mechanism of the ethanol extract, it was mixed and co-incubated with various metagens, S9 mix, and the bacteria with different experimental orders and different reaction times. The ethanol extract did not affect reversion rate of pre-mutated. S.typhimurium. However, when the ethanol extract was added to the mutagens before their interaction with S.typhimurium , it reduced the mutation rate to 152$\pm$12-273$\pm$18 colonies/plates in case of MNNG, and 135$\pm$13-195$\pm$10 colonies/ plates in case of B($\alpha$)P), showing strong desmutagenic activity.

• 대한약리학회지
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• 제28권2호
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• pp.213-222
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• 1992

Benzopyrene (BP), 7,12-dimehyl benzanthracene (DMBA), nitrosomethyl urea (NUMU) 및 nicotine과 같은 발암성 화학물질들이 바이러스 감염된 vero 세포의 단층 세포 배양에서 I형 단순성포진 바이러스 (HSV-1)의 복제, 세포융해, DNA합성 및 단백질 합성에 미치는 효과를 관찰하였다. 1. BP와 DMBA는 HSV-1의 복제와 세포융해작용을 유의성있게 억제하였으나 nicotine과 NMU는 별로 억제하지 않았다. 2. 모든 발암성 화학물질은 바이러스의 DNA합성을 억제하지 못하였지만 새로 합성되는 후손바이러스 DNA로 부터 표현되는 gamma 단백질의 표현은 BP와 DMBA에 의해서 현저하게 억제되었다. 그러나 모든 발암성 화학물질은 바이러스의 alpha 및 beta 단백질의 합성은 억제하지 못하였다. 이상의 결과로 보아 발암성화학물질이 존재하고 있는 배지내에서 새로 합성되는 바이러스의 DNA로 부터 표현되는 gamma 단백질의 결함이 있음을 알 수가 있었으며 이같은 개념은 발암화학물질의 존재하에서 바이러스의 DNA와 단백질이 거의 정상적으로 합성됨에도 불구하고 바이러스의 복제가 일어나지 않는다는 사실이 뒷받침해주고 있다.

• Journal of Microbiology and Biotechnology
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• 제14권2호
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• pp.268-275
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• 2004

To investigate the potential application of the single-cell gel electrophoresis (SCGE) assay to carp as an aquatic pollution monitoring technique, gill, liver, and blood cells were isolated from carp exposed to a direct-acting mutagen, N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), or indirect mutagen, $benzo[\alpha]pyrene$ $(B[\alpha]P)$, then the DNA strand breakage was analyzed using the assay. Based on testing 5 different cell isolation methods and 6 electrophoretic conditions, the optimized assay conditions were found to be cell isolation by filter pressing and electrophoresis at a lower voltage and longer running time (at 0.4 V/cm for 40 min). In preliminary experiments, gill and liver cells isolated from carp exposed to MNNG in vitro exhibited DNA damage signals even with 0.5 ppb exposure, which is a much higher dose than previously reported. In the gill cells isolated from carp exposed to 0.01-0.5 ppm MNNG in vivo, significant dose-and time-dependent increases were observed in the tail for 4 days. As such, the linear correlation between the relative damage index (RDI) values and time for each dose based on the initial 48-h exposure appeared to provide effective criteria for the genotoxicity monitoring of direct-acting mutagenic pollution. In contrast, the in vivo exposure of carp to 0.25-1.0 ppm of $B[\alpha]P$ for 7 days resulted in dose-and time-dependent responses in the liver cells, in which 24-h delayed responses for metabolizing activation and gradual repair after 48 h were also observed. Thus, the negative-sloped linear correlation between the RDI and time at each dose based on the initial 48 h appeared to provide more effective criteria for the genotoxicity monitoring of indirect mutagenic pollution.

• 동아시아식생활학회지
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• 제7권4호
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• pp.527-537
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• 1997

This study was performed to determine the effects of antimutagenicity of Porturaca oleracea L. in Korea. In Ames test, the ethanol extract of Poturaca oleracea L. inhibited mutagenic activity of N-methyl-N'-nitro-N-nitrosoguanidine(MNNG), , 4-nitroquinoline-1-oxide(4NQO), benzo($\alpha$)pyrene (B($\alpha$)P) and 3-amino-1,4-dimethyl-5H-pyrido-(4,3-b)indole (Trp-P-1) in Salmonella typhimurium TA98 and TA100. But hot-water extract Poturaca oleracea L. only Inhibited mutagenic activity of MNNG in Salmonella typhimurium TA100, On 4NQO, the ethanol extract 100-1,600$\mu\textrm{g}$/plate of Porturaca oleracea L. showed a slight inhibitory effect of 13-48%, 4-47% in TA98 and TA100, respectively, but on MNNG, it showed higher inhibitory effect of 6-86% in TA100, And the treatment of 1,600$\mu\textrm{g}$/plate of ethanol extract of Porturacea L. had strong antimutagenicity with 74-87% inhibition against TA98 and TA100 induced by B(a)P and with 85-93% inhibition against TA98 and TA100 induced by Trp-P-1. The ethanol extract was fractionated with ether. chloroform, ethylacetate, butanol and water. Among them, most of the fraction except water fraction showed strong antimutagenicity effects against mutation induced by 4-NQO, MNNG, B(a)P and Trp-P-1. Chloroform fraction had strong antimutagenicity with 91% inhibition against TA100 induced by MNNG, diethyl etherfraction had strong antimutagenicity with 92%, 98% inhibition against TA98 and TA100 induced by 4NQO, Chloroform fraction had strong antimutagenicity with 97% inhibition against TA100 induced by B (a)P and diethyl etherfraction had strong antimutagenicity with 98% inhibition against both strain Induced by Trp-P-1, respectively.