Mutation Research Letters最新文献

筛选
英文 中文
Study on the antimutagenic effect of pine needle extract 松针提取物的抗诱变作用研究
Mutation Research Letters Pub Date : 1995-08-01 DOI: 10.1016/0165-7992(95)00026-7
Zhiming Kong , Zhengtao Liu , Bangyu Ding
{"title":"Study on the antimutagenic effect of pine needle extract","authors":"Zhiming Kong ,&nbsp;Zhengtao Liu ,&nbsp;Bangyu Ding","doi":"10.1016/0165-7992(95)00026-7","DOIUrl":"10.1016/0165-7992(95)00026-7","url":null,"abstract":"<div><p>The micronulceus test and sister-chromatic exchange (SCE) test were used to research the antimutagenic effect of pine needle extract. The results showed that the mutagenic effect of cyclosphamide (CP) was inhibited by the pine needle extract. The micronucleus frequencies (MNF) of mouse bone marrow and human lymphocytes from peripheral blood were decreased with the effect of the extract (the dose was 2000 mg/kg or 5 mg/ml); the frequency of SCE in human lymphocytes was also reduced significantly, which indicated that the MNF and the SCE frequencies were negatively correlated with the dose of pine needle extract (<em>r</em> = −0.9782, −0.9587, −.09765, respectively). This suggested that the pine needle extract was an effective antimutagen and it is important to choose the proper doses of pine needle extract for antitumor effect.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 3","pages":"Pages 101-104"},"PeriodicalIF":0.0,"publicationDate":"1995-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)00026-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18572452","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 29
A comparative study of TK6 human lymphoblastoid and L5178Y mouse lymphoma cell lines in the in vitro micronucleus test TK6人淋巴母细胞样细胞与L5178Y小鼠淋巴瘤细胞系体外微核试验的比较研究
Mutation Research Letters Pub Date : 1995-08-01 DOI: 10.1016/0165-7992(95)00027-5
Li-Shi Zhang , Masamitsu Honma, Makoto Hayahshi, Takayoshi Suzuki, Atsuko Matsuoka, Toshio Sofuni
{"title":"A comparative study of TK6 human lymphoblastoid and L5178Y mouse lymphoma cell lines in the in vitro micronucleus test","authors":"Li-Shi Zhang ,&nbsp;Masamitsu Honma,&nbsp;Makoto Hayahshi,&nbsp;Takayoshi Suzuki,&nbsp;Atsuko Matsuoka,&nbsp;Toshio Sofuni","doi":"10.1016/0165-7992(95)00027-5","DOIUrl":"10.1016/0165-7992(95)00027-5","url":null,"abstract":"<div><p>Micronucleus induction was compared in human lymphoblastoid TK6 and mouse lymphoma L5178Y cell lines treated with model clastogens and spindle poisons, i.e., X-rays, methyl methanesulfonate, ethyl methanesulfonate, mitomycin C, colcemid, and vincristine. The spontaneous micronucleated cell (MNC) frequency was stable and reproducible in both cell lines. All clastogens and spindle poisons studied here induced micronuclei in both cell lines. They increased MNC frequency at lower concentrations or caused a greater increase at the same concentration in TK6 cells. These clastogens and spindle poisons, however, were also more toxic to TK6 than to L5178Y cells and when comparison was based on cytotoxicity, they showed more efficient MNC induction in L5178Y cells. In conclusion, neither cell line was superior to the other, and both of them can be used as target cells in the in vitro micronucleus assay.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 3","pages":"Pages 105-115"},"PeriodicalIF":0.0,"publicationDate":"1995-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)00027-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18572453","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 52
Micronucleus assay in pulmonary alveolar macrophages, a simple model to detect genotoxicity of environmental agents entering through the inhalation route 肺泡巨噬细胞微核测定,一种检测环境物质经吸入途径进入的遗传毒性的简单模型
Mutation Research Letters Pub Date : 1995-07-01 DOI: 10.1016/0165-7992(95)90071-3
K. Sahu, R.K. Das
{"title":"Micronucleus assay in pulmonary alveolar macrophages, a simple model to detect genotoxicity of environmental agents entering through the inhalation route","authors":"K. Sahu,&nbsp;R.K. Das","doi":"10.1016/0165-7992(95)90071-3","DOIUrl":"10.1016/0165-7992(95)90071-3","url":null,"abstract":"<div><p>A simple and short-term micronucleus (MN) test in pulmonary alveolar macrophages (PAMs) of rats has been developed to assess potential genotoxic effects of gaseous environmental agents. The protocol has been tested in model experiments with indoor air pollutants like mosquito coil smoke (MCS) and mosquito mat vapour (MMV). Smears of pulmonary lavage fluid collected in hypotonic (0.56%) KC1 solution were fixed in absolute methanol and stained in Giemsa (10%). Characteristically the large size of the PAMs facilitates easy scoring of MN. An interval of 32 h post exposure seems to be suitable for MN preparation. A comparison of the concentration-response data on CAs (at 24 h post exposure) and MN (at 32 h post exposure) clearly reveals the validity of the MN assay in PAMs</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 2","pages":"Pages 61-65"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90071-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18655308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
The transmission of FISH-painted patterns derived from complex chromosome exchanges fish彩绘图案的传播源于复杂的染色体交换
Mutation Research Letters Pub Date : 1995-07-01 DOI: 10.1016/0165-7992(95)90075-6
John R.K. Savage
{"title":"The transmission of FISH-painted patterns derived from complex chromosome exchanges","authors":"John R.K. Savage","doi":"10.1016/0165-7992(95)90075-6","DOIUrl":"10.1016/0165-7992(95)90075-6","url":null,"abstract":"<div><p>The first 26 families of complex chromosome-type exchanges (from three breaks in two chromosomes to five breaks in five chromosomes) have been evaluated, and the 15 060 exchanges resulting from unrestricted restitution or rejoining of the break ends yields 203 distinctive patterns, if a single participating chromosome is FISH-painted.</p><p>If we assume that any exchange that produces an acentric fragment of any sort (compound-terminal or interstitial) will be ultimately eliminated in a continuously dividing cell population, then, irrespective of family origin, only 17 of these patterns (≈8%) will be transmitted, long-term.</p><p>The 17 are illustrated, and the implications briefly discussed.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 2","pages":"Pages 87-95"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90075-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18655923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 32
An investigation of the cytotoxic and mutagenic potential of low intensity laser irradiation in Friend erythroleukaemia cells 低强度激光照射对Friend红白血病细胞的细胞毒性和致突变潜能的研究
Mutation Research Letters Pub Date : 1995-07-01 DOI: 10.1016/0165-7992(95)90072-1
I.D. Logan , P.G. McKenna , Y.A. Barnett
{"title":"An investigation of the cytotoxic and mutagenic potential of low intensity laser irradiation in Friend erythroleukaemia cells","authors":"I.D. Logan ,&nbsp;P.G. McKenna ,&nbsp;Y.A. Barnett","doi":"10.1016/0165-7992(95)90072-1","DOIUrl":"10.1016/0165-7992(95)90072-1","url":null,"abstract":"<div><p>The purpose of this study was to investigate the cytotoxic and genotoxic potential of low intensity laser irradiation (660 nm, 12 mW, 5 kHz) on mammalian cells. Thymidine kinase (TK)-positive and TK-deficient Friend erythroleukaemia (FEL) cells, clone 707 and subclone 707BUF respectively, were used in this investigation. Following irradiation of exponentially growing cells in suspension at doses of 2 and 20 J/cm<sup>2</sup> a number of sensitive bioassays were used to facilitate the detection of laser-induced mutations, DNA damage and cell killing. Mutations were assessed by the examination of chromosome spreads, the determination of micronucleus frequency and by the determination of the mutant frequency at the <em>hypoxanthine-guanine phosphoribosyltransferase (hgprt)</em> locus. DNA damage was quantified using a sensitive ELISA. The cytotoxic effect of laser irradiation was assessed using a cloning assay. The results of this investigation did not show any significant increase in mutation frequency, DNA damage or cell survival in the laser-irradiated cells, compared to sham-irradiated controls. The lack of any demonstrable cytotoxic and genotoxic effects of low intensity laser irradiation on mammalian cells in culture would support it as being a safe modality for clinical use.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 2","pages":"Pages 67-71"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90072-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18655309","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
XPG protein has a structure-specific endonuclease activity XPG蛋白具有结构特异性内切酶活性
Mutation Research Letters Pub Date : 1995-07-01 DOI: 10.1016/0165-7992(95)90070-5
Kieran G. Cloud, Binghui Shen, Gary F. Strniste, Min S. Park
{"title":"XPG protein has a structure-specific endonuclease activity","authors":"Kieran G. Cloud,&nbsp;Binghui Shen,&nbsp;Gary F. Strniste,&nbsp;Min S. Park","doi":"10.1016/0165-7992(95)90070-5","DOIUrl":"10.1016/0165-7992(95)90070-5","url":null,"abstract":"<div><p>Biochemically active human DNA repair protein, xeroderma pigmentosum G (XPG), was overexpressed in insect cells by a recombinant baculovirus. The recombinant baculovirus produced XPG with a mobility of ∼ 185 kDa in a denaturing polyacrylamide gel. Indirect immunofluorescence studies demonstrated that the recombinant full-length XPG protein was expressed predominantly as a nuclear protein. The recombinant XPG protein was purified to apparent homogeneity using Q-sepharose, S-300 size exclusion, and Mono Q column chromatography. XPG protein showed a structure-specific DNA endonuclease activity, and a preferential affinity to single-stranded DNA and RNA compared to double-stranded DNA.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 2","pages":"Pages 55-60"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90070-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18655307","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 37
Sample size for the estimation of polychromatic to normochromatic erythrocyte ratio in the bone marrow micronucleus test 骨髓微核试验中估计多染红细胞与正染红细胞比例的样本量
Mutation Research Letters Pub Date : 1995-07-01 DOI: 10.1016/0165-7992(95)90076-4
B. Bhaskar Gollapudi, Lisa G. McFadden
{"title":"Sample size for the estimation of polychromatic to normochromatic erythrocyte ratio in the bone marrow micronucleus test","authors":"B. Bhaskar Gollapudi,&nbsp;Lisa G. McFadden","doi":"10.1016/0165-7992(95)90076-4","DOIUrl":"10.1016/0165-7992(95)90076-4","url":null,"abstract":"","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 2","pages":"Pages 97-99"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90076-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18655924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 78
The suitability of rat peripheral blood in suchronic studies for the micronucleus assay 大鼠外周血用于微核试验的适宜性
Mutation Research Letters Pub Date : 1995-07-01 DOI: 10.1016/0165-7992(95)90073-X
Shougo Asanami, Kazuyuki Shimono, Osamu Sawamoto, Kazunobu Kurisu, Motoo Uejima
{"title":"The suitability of rat peripheral blood in suchronic studies for the micronucleus assay","authors":"Shougo Asanami,&nbsp;Kazuyuki Shimono,&nbsp;Osamu Sawamoto,&nbsp;Kazunobu Kurisu,&nbsp;Motoo Uejima","doi":"10.1016/0165-7992(95)90073-X","DOIUrl":"https://doi.org/10.1016/0165-7992(95)90073-X","url":null,"abstract":"<div><p>To examine the suitability of using rat peripheral blood from animals used in subchronic toxicity studies for micronucleus analysis, we orally administered phenacetin or 6-mercaptopurine for 14 days to groups of six rats and compared their micronucleus frequencies to the bone marrow micronucleus frequencies of rats similarly treated for only 2 days. In the 14-day test, phenacetin significantly increased the frequency of micronucleated reticulocytes in peripheral blood at 500 mg/kg starting from day 9, and at 750 and 1500 mg/kg starting from day 6; 6-mercaptopurine topurine gave a positive response at 20 mg/kg starting from day 6. Positive responses in the bone marrow assay were obtained at the same dose levels. In the 2-day test, micronucleated polychromatic erythrocyte frequencies increased significantly at 1000 and 2000 mg/kg for phenacetin, and at 50, 100, and 200 mg/kg for 6-mercaptopurine. These results suggest that micronucleus assays using peripheral blood from rats in subchronic animal studies of phenacetin and 6-mercaptopurine are feasible and at least as sensitive for the assessment of micronuclei as an acute bone marrow micronucleus test.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 2","pages":"Pages 73-78"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90073-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72106908","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 29
Streptozotocin-induced genotoxic effects in Chinese hamster cells: The resistant phenotype of V79 cells 链脲佐菌素对中国仓鼠细胞的基因毒性作用:V79细胞的抗性表型
Mutation Research Letters Pub Date : 1995-07-01 DOI: 10.1016/0165-7992(95)90074-8
M.S. Capucci , M.E. Hoffmann , A.T. Natarajan
{"title":"Streptozotocin-induced genotoxic effects in Chinese hamster cells: The resistant phenotype of V79 cells","authors":"M.S. Capucci ,&nbsp;M.E. Hoffmann ,&nbsp;A.T. Natarajan","doi":"10.1016/0165-7992(95)90074-8","DOIUrl":"10.1016/0165-7992(95)90074-8","url":null,"abstract":"<div><p>The genotoxic effects of the methylating agent streptozotocin (STZ) on Chinese hamster cells CHO-9 and V79 were evaluated. The induction of cell killing, chromosomal aberrations, sister-chromatid exchanges (SCEs) and mutations was analyzed. Comparisons were made with the the STZ aglyconic analogue <em>N</em>-methyl-<em>N</em>-nitrosourea (MNU). V79 cells were found to be more resistant than CHO-9 cells to STZ and MNU killing effects, as well as to the induction of chromosomal aberrations and SCEs; however, V79 and CHO-9 cells appeared to be equally sensitive to the induction of 6-thioguanine resistant mutants by STZ. These results suggest that an error-free mechanisms that tolerates DNA methylation damage confers a resistant phenotype to V79 cells to the genotoxic effects of methylation damage.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 2","pages":"Pages 79-85"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90074-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18655311","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Clastogenicity of isoamylene oxide to rat lymphocytes in culture 氧化异丙烯对培养大鼠淋巴细胞的致裂性
Mutation Research Letters Pub Date : 1995-06-01 DOI: 10.1016/0165-7992(95)90025-X
B.Bhaskar Gollapudi , V.Ann Linscombe , J.W. Wilmer
{"title":"Clastogenicity of isoamylene oxide to rat lymphocytes in culture","authors":"B.Bhaskar Gollapudi ,&nbsp;V.Ann Linscombe ,&nbsp;J.W. Wilmer","doi":"10.1016/0165-7992(95)90025-X","DOIUrl":"10.1016/0165-7992(95)90025-X","url":null,"abstract":"<div><p>The mutagenic activity of the aliphatic epoxide isoamylene oxide (2-methyl-2,3-epoxybutane) is not readily detectable in the standard Ames test. In this study, the clastogenic potential of isoamylene oxide was evaluated using an in vitro mammalian cell culture system. Approximately 48 h after establishing primary cultures of rat lymphoocyte cultures, the cells were treated for 4 h with various concentrations of isoamylene oxide (50, 166.7, 500, 1666.7 and 5000 μg/ml in the initial assay and 500, 1000, 2000, 3000, 4000, and 5000 μg/ml in the confirmatory assay). The cultures were harvested 24 h after termination of the treatment. Based upon the mitotic indices, cultures treated with the three highest concentrations in both the initial and confirmatory assays were evaluated to estimate the chromosomal aberration frequencies. Isoamylene oxide demonstrated a strong clastogenic activity in this assay: up to 29% aberrant cells (without gaps) were observed at the highest concentration analyzed. The presence of an external metabolic activation system (S9) did not seem to influence the magnitude of the response at the dose levels analyzed.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"347 1","pages":"Pages 9-12"},"PeriodicalIF":0.0,"publicationDate":"1995-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90025-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18602924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信