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对用于诱变剂的哺乳动物测试系统的需求:一些还原剂的作用。

The need for a mammalian test system for mutagens: action of some reducing agents.

作者信息

Stich H F, Wei L, Lam P

出版信息

Cancer Lett. 1978 Oct;5(4):199-204. doi: 10.1016/s0304-3835(78)80039-1.

DOI:10.1016/s0304-3835(78)80039-1
PMID:356961
Abstract

Reducing agents and cysteine, cysteamine, glutathione, ascorbic acid and H2O2 with and without the addition of Cu2+ did not increase significantly the frequency of mutations in the Salmonella test at non-toxic concentrations but triggered a marked DNA repair synthesis and induced a relatively high frequency of chromosome aberrations in cultured mammalian cells. Both latter effects were reduced by the addition of catalase to solutions of the reducing agents plus Cu2+. To avoid 'False Negatives' in mutagenicity screening the use of several test subjects including mammalian cells seems to be required.

摘要

在无毒浓度下,还原剂与半胱氨酸、半胱胺、谷胱甘肽、抗坏血酸以及添加或未添加Cu2+的H2O2,均未显著增加沙门氏菌试验中的突变频率,但会引发显著的DNA修复合成,并在培养的哺乳动物细胞中诱导相对较高频率的染色体畸变。在还原剂加Cu2+的溶液中添加过氧化氢酶后,后两种效应均减弱。为避免在致突变性筛选中出现“假阴性”,似乎需要使用包括哺乳动物细胞在内的多种试验对象。

相似文献

1
The need for a mammalian test system for mutagens: action of some reducing agents.对用于诱变剂的哺乳动物测试系统的需求:一些还原剂的作用。
Cancer Lett. 1978 Oct;5(4):199-204. doi: 10.1016/s0304-3835(78)80039-1.
2
Mutagenicity of glutathione and cysteine in the Ames test.谷胱甘肽和半胱氨酸在艾姆斯试验中的致突变性。
Science. 1983 May 27;220(4600):961-3. doi: 10.1126/science.6342137.
3
Mutogenic action of ascorbic acid.
Nature. 1976 Apr 22;260(5553):722-4. doi: 10.1038/260722a0.
4
The use of short-term tests to measure the preventive action of reducing agents on formation and activation of carcinogenic nitroso compounds.使用短期试验来测量还原剂对致癌亚硝基化合物形成和激活的预防作用。
Mutat Res. 1978 Mar;57(1):57-67. doi: 10.1016/0027-5107(78)90234-8.
5
How do in vivo mammalian assays compare to in vitro assays in their ability to detect mutagens?在检测诱变剂的能力方面,体内哺乳动物试验与体外试验相比如何?
Mutat Res. 1986 May;167(3):189-201. doi: 10.1016/0165-1110(86)90029-1.
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Protection from toxic and mutagenic effects of H2O2 by catalase induction in Salmonella typhimurium.鼠伤寒沙门氏菌中过氧化氢酶诱导对H2O2毒性和诱变作用的防护
Mutat Res. 1984 Nov-Dec;141(3-4):145-7. doi: 10.1016/0165-7992(84)90087-3.
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Role of copper and ceruloplasmin in oxidative mutagenesis induced by the glutathione-gamma-glutamyl transpeptidase system and by other thiols.铜和铜蓝蛋白在谷胱甘肽-γ-谷氨酰转肽酶系统及其他硫醇诱导的氧化诱变中的作用
Environ Mol Mutagen. 1997;29(1):63-72.
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Effect of hydrogen sulfide on the mutagenicity of hydrogen peroxide in Salmonella typhimurium strain TA102.硫化氢对鼠伤寒沙门氏菌TA102菌株中过氧化氢致突变性的影响。
Mutat Res. 1986 Sep;175(1):5-9. doi: 10.1016/0165-7992(86)90137-5.
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Genotoxicity of apomorphine and various catecholamines in the Salmonella mutagenicity test (Ames test) and in tests for primary DNA damage using DNA repair-deficient B. subtilis strains (rec assay).阿扑吗啡和各种儿茶酚胺在沙门氏菌致突变试验(艾姆斯试验)以及使用DNA修复缺陷型枯草芽孢杆菌菌株的原发性DNA损伤试验(rec试验)中的遗传毒性。
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Inhibitory effect of reducing agents on N-acetoxy- and N-hydroxy-2-acetylaminofluorene-induced mutagenesis.还原剂对N-乙酰氧基-和N-羟基-2-乙酰氨基芴诱导的诱变的抑制作用。
Cancer Res. 1978 May;38(5):1307-10.

引用本文的文献

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Environ Health Perspect. 1982 Nov;45:35-40. doi: 10.1289/ehp.824535.
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Effects of ascorbic and dehydroascorbic acid on the multiplication of tumor ascites cells in vitro.抗坏血酸和脱氢抗坏血酸对肿瘤腹水细胞体外增殖的影响。
J Cancer Res Clin Oncol. 1984;108(2):230-2. doi: 10.1007/BF00402472.
3
Exogenous glutathione induces sister chromatid exchanges, clastogenicity and endoreduplication in V79-E Chinese hamster cells.外源性谷胱甘肽可诱导V79-E中国仓鼠细胞发生姐妹染色单体交换、染色体断裂及核内复制。
Cell Biol Toxicol. 1985 Jun;1(3):123-31. doi: 10.1007/BF00120159.
4
The mechanism of cytogenetic genotoxicity of exogenous glutathione in V-79 cells in vitro--implication of hydrogen peroxide and general traits of oxidative chromosome damage.外源性谷胱甘肽对体外培养的V-79细胞的细胞遗传基因毒性机制——过氧化氢的影响及氧化性染色体损伤的一般特征
Cell Biol Toxicol. 1988 Jun;4(2):241-57. doi: 10.1007/BF00119249.
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Comparative pharmacokinetics and subacute toxicity of di(2-ethylhexyl) phthalate (DEHP) in rats and marmosets: extrapolation of effects in rodents to man.邻苯二甲酸二(2-乙基己基)酯(DEHP)在大鼠和狨猴体内的比较药代动力学及亚急性毒性:从啮齿动物效应推断对人类的影响
Environ Health Perspect. 1986 Mar;65:299-307. doi: 10.1289/ehp.8665299.