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果蝇遗传毒性试验中咖啡的研究。

Investigation of coffee in Drosophila genotoxicity tests.

作者信息

Graf U, Würgler F E

出版信息

Food Chem Toxicol. 1986 Aug;24(8):835-42. doi: 10.1016/0278-6915(86)90073-6.

Abstract

Two preparations of coffee (instant coffee and freeze-dried home-brew coffee) were tested in different mutagenicity assays in germ cells as well as in somatic cells of Drosophila melanogaster. The three end-points assayed in germ cells were sex-linked recessive lethals (mainly gene mutations and small chromosome aberrations), dominant lethals (cytotoxic effects as well as genotoxic effects) and sex-chromosome losses (chromosome breakage and non-disjunction). The aqueous coffee solutions were fed either to adult male flies for 3 days or to growing larvae during the whole larval development. Treated males were crossed with appropriately marked females, and the different genetic end-points were analysed in the F1 or F2 generation. The test concentrations (instant coffee 4% (w/v), home-brew coffee 3%) were acutely toxic in adult males (killing approximately 75 and 90% of the exposed flies, respectively). No increase in deaths was caused in larvae by the same concentrations. Only cytotoxic effects were observed in the test for dominant lethals. No conclusive genotoxic effects could be detected in any of the three germ cell assays. The coffee preparations were also tested for induction of mutation and mitotic recombination in somatic cells of the wing imaginal disc. Larvae trans-heterozygous for two recessive wing hair markers were fed high concentrations of the coffees for varying periods of time. Wings of surviving adult flies were analysed for mosaic spots. Twin spots exhibiting both mutant phenotypes are produced by mitotic recombination; single spots showing one or the other phenotype are the result of somatic mutation, such as gene mutation or deletion, or of mitotic recombination. Both coffees had weak effects on normal (repair-proficient) cells as well as on excision repair-defective cells in this assay. Additional experiments with pure caffeine and decaffeinated coffee show that these weak effects in somatic cells were most probably caused by the caffeine present in the two coffees.

摘要

对两种咖啡制剂(速溶咖啡和冻干自制咖啡)进行了测试,采用不同的致突变性试验,检测其对黑腹果蝇生殖细胞和体细胞的影响。在生殖细胞中检测的三个终点指标分别为性连锁隐性致死(主要是基因突变和小染色体畸变)、显性致死(细胞毒性效应以及遗传毒性效应)和性染色体丢失(染色体断裂和不分离)。将咖啡水溶液喂给成年雄蝇3天,或在整个幼虫发育期间喂给正在生长的幼虫。将处理过的雄蝇与适当标记的雌蝇杂交,并在F1或F2代中分析不同的遗传终点指标。测试浓度(速溶咖啡4%(w/v),自制咖啡3%)对成年雄蝇具有急性毒性(分别杀死约75%和90%的暴露果蝇)。相同浓度对幼虫未造成死亡增加。在显性致死试验中仅观察到细胞毒性效应。在三种生殖细胞试验中的任何一种中均未检测到确凿的遗传毒性效应。还对咖啡制剂进行了测试,检测其对翅成虫盘体细胞中突变和有丝分裂重组的诱导作用。将两个隐性翅毛标记的转杂合幼虫在不同时间段内喂食高浓度的咖啡。对存活成年果蝇的翅膀进行镶嵌斑分析。表现出两种突变表型的双斑是由有丝分裂重组产生的;显示一种或另一种表型的单斑是体细胞突变的结果,如基因突变或缺失,或有丝分裂重组的结果。在该试验中,两种咖啡对正常(修复 proficient)细胞以及切除修复缺陷细胞均有微弱影响。用纯咖啡因和脱咖啡因咖啡进行的额外实验表明,体细胞中的这些微弱影响很可能是由两种咖啡中存在的咖啡因引起的。

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