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 12,436 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Previous publications on the National Toxicology Program (NTP)-sponsored mutagenicity testing program in Drosophila dealt with evaluations of chemicals following adult treatment (feed, injection). The current paper deals with a comparison between the laboratories at Brown University (BRU) and the University of Wisconsin at Madison (UWM) regarding the response of larvae to treatment with chemicals in the sex-linked recessive lethal (SLRL) test and, where appropriate, the reciprocal translocation test as well. Dimethylnitrosamine (DMN) and dimethylbenz(a)anthracene were used first as reference mutagens. Six coded compounds were then evaluated regarding their repeatability in the two laboratories; the compounds were benzo(a)pyrene, 3-methylcholanthrene, coumarin, quinoline, formaldehyde, and 9-aminoacridine. It was concluded that at this time it would be imprudent to forgo larval treatment in cases where compounds proved negative after adult feeding. Accordingly, testing a series of 20 compounds negative after adult treatment is in progress.
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PMID:Chemical mutagenesis testing in Drosophila. VI. Interlaboratory comparison of mutagenicity tests after treatment of larvae. 251 Oct 11

High temperature coal tar was used as raw materials, and was distilled to 280 degrees C for getting coal tar soft pitch. Then refined soft pitch was obtained by solvent extracting and subsequent settlement method. Its soft point was 32 degrees C; the group compositions consisted of 53.67% heptane soluble, 39.47% heptane insoluble but toluene soluble, 6.86% toluene insoluble and 0.06% quinoline insoluble. The relative average molecular weight was about 292. Its average molecular formula was C22.22 H16.32 N0.12 S0.06 O0.33; the total content of heteroatom was less than 1. IR analytic results showed that its heteroatom O existed in the R-O-R and Ar-O-R structure; its heteroatom N existed in the R-NH-R and -N=, with the latter being primary. Its average structure was obtained by improved Brown-Lander model: five-membered condensed rings. UV analysis indicated that the majority was linear arrangement, and the minority was surface arrangement; namely, the chemical structure of the samples was mainly the cata-condensed structure, while the minority was peri-condensation.
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PMID:[Compositions and structure characterizations of coal tar refined soft pitch]. 1983 28

The aim of this study was to test the selectivity, in-vivo effectiveness, and potential mechanism of action of a linomide analogue (N-phenyl-1,2-dihydro-4-hydroxyl-2-oxo-quinoline-3-carboxamide, Lin05) for inhibition of choroidal neovascularization. The selectivity of Lin05 was tested in cell proliferation assays with human umbilical vein endothelial cells (HUVEC) and a retinal pigmented epithelial cell line(ARPE-19). In-vivo anti-angiogenic effect of Lin05 was investigated utilizing an experimental laser-induced choroidal neovascularization (ECNV) model in adult Brown Norway rats. Western blot and/or reverse transcriptase-PCR was used to test the effect of Lin05 on potential targets. Our results indicate that Lin05 is at least an 8-fold more selective inhibitor of endothelial cell proliferation compared to RPE cells. Systemic administration of Lin05 in an ECNV model was associated with a significant decrease in both vascular leakage on fluorescein angiography and lesion size by histopathology (p = 0.02). No systemic toxicity was detected for Lin05 in major organs such as the liver, lung and kidneys. Lin05 did not inhibit VEGF-induced VEGFR2 (KDR) phosphorylation in HUVEC nor was associated with decreased VEGF gene expression. Also it did not inhibit insulin-like growth factor (IGF-1) and Epidermal Growth Factor (EGF) induced activation of p42/p44 MAPK activation. It inhibited both PDGF- and bFGF-induced p42/p44 MAPK phosphorylation. However, the effect on PDGF was variable in different HUVEC cells. In conclusion, Lin05 is a potential anti-angiogenic agent for the treatment of eye diseases associated with pathological neovascularization. The anti-angiogenic effect of Lin05 is likely through inhibition of bFGF but not through inhibition of the VEGF/KDR pathway.
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PMID:Investigation of the potential utility of a linomide analogue for treatment of choroidal neovascularization. 2105

Increasing attention has been recently paid to the toxicity of additives used in food. The European Parliament and the Council published the REGULATION (EC) No. 1333/2008 on food additives establishing that the toxicity of food additives evaluated before 20th January 2009 must be re-evaluated by European Food Safety Authority (EFSA). The aim of this review is to survey current knowledge specifically on the toxicity issues of synthetic food colorants using official reports published by the EFSA and other available studies published since the respective report. Synthetic colorants described are Tartrazine, Quinoline Yellow, Sunset Yellow, Azorubine, Ponceau 4R, Erythrosine, Allura Red, Patent Blue, Indigo Carmine, Brilliant Blue FCF, Green S, Brilliant Black and Brown HT. Moreover, a summary of evidence on possible detrimental effects of colorant mixes on children's behaviour is provided and future research directions are outlined.
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PMID:Health safety issues of synthetic food colorants. 2697 83