Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0002895 (sickle cell disease)
 11,747 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Adipocyte differentiation of mouse embryonic fibroblasts (MEFs) derived from c-Src wild-type or c-Src-deficient (abbreviated as MEF+/+ and MEF-/- hereafter) C57BL/6 mice was induced by ascorbic acid (A) and beta-glycerophosphate (G). TCDD clearly suppressed differentiation of MEF+/+, but not MEF-/-, as measured by increased accumulation of triglycerides associated with increased expression of adipocyte differentiation-specific genes such as peroxisome proliferators activated receptor (PPAR)gamma, stearoyl-CoA desaturase (SCD-1). Studies on inducibility of TCDD-activated genes such as cytochrome P450 (CYP)1A1 and CYP1B1 revealed a comparable dose response in both MEF+/+ and MEF-/-. Furthermore, the binding activity of AhR complexes to xenobiotic response elements (XREs) was similar in both cell lines. We further studied the effect of TCDD on CCAAT/enhancer binding proteins (C/EBP), which are known to be important regulators of cell differentiation. TCDD induced C/EBPbeta and C/EBPdelta mRNA expression and DNA binding activity in a time- and dose-dependent manner in MEF+/+ but not in MEF-/-. The levels of C/EBPbeta and C/EBPdelta were still elevated in differentiated MEF+/+ after 10 days of treatment with TCDD. In MEF-/-, C/EBPbeta and C/EBPdelta are highly expressed constitutively. In contrast to MEF+/+, TCDD does not cause any significant change of these transcription factors in MEF-/-. These data indicate that suppression of differentiation by TCDD in MEF requires a functional c-Src activity and induced levels of C/EBPbeta and C/EBPdelta, including their maintenance at high levels by TCDD, rather than ultimate high levels of these C/EBP isoforms.
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PMID:Interaction of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) with induced adipocyte differentiation in mouse embryonic fibroblasts (MEFs) involves tyrosine kinase c-Src. 1450 2

Vanillin is useful as anti-sickle cell anemia, anti-mutagen and anti-bacteria agent. However, vanillin must be administered at high concentration and cannot be oxidized by the upper gastrointestinal track of patients to be medically effective. In this study, we assessed the toxic effect of vanillin when administered in an un-oxidized form at high concentrations (150 and 300 mg/kg) via oral and intra-peritoneal injection. It was found that 300 mg/kg vanillin injection caused the rats to be unconscious without exerting any toxic effect on blood cells, kidney and liver. Besides, it showed blood protective property. Further analysis with GenomeLab GeXP genetic system on brain tissues showed that the expression of most xenobiotic metabolism, cell progression, tumor suppressor, DNA damage and inflammation genes were maintained at normal level. However, the expression of a few xenobiotic metabolism, cell cycle arrest and apoptosis genes were up-regulated by 5% ethanol injection. Nevertheless, when 5% ethanol was injected with the presence of vanillin, the expression was back to normal level. It is postulated that vanillin might have neuro-protective property. In conclusion, vanillin is not toxic at high concentration in both oral and intra-peritoneal injection and could provide blood and brain protective properties.
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PMID:Toxicology study of vanillin on rats via oral and intra-peritoneal administration. 2080 60