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1.
Aquat Toxicol ; 167: 257-64, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26382854

ABSTRACT

The metabolic effects induced by feed contaminated with a lower or a higher concentration of -nonylpnenol (NP), 4-tert-octylphenol (t-OP) or bisphenol A (BPA), three environmental endocrine disruptors, were assessed in juvenile sea bream liver. Histological analysis demonstrated that all these three xenobiotics induced hepatic lipid accumulation and steatosis. These findings prompted analysis of the expression of the major molecules involved in lipid metabolism: peroxisome proliferator activated receptors (which is encoded by ppars), fatty acid synthase (encoded by fas), lipoprotein lipase (encoded by lpl) and hormone-sensitive lipase (encoded by hsl). The enzymes encoded by ppars and fas are in fact responsible for lipid accumulation, whereas lpl- and hsl- encoded proteins play a pivotal role in fat mobilization. The three xenobiotics modulated ppar mRNA expression: pparα mRNA expression was induced by the higher dose of each contaminant; pparß mRNA expression was upregulated by the lower doses and in BPA2 fish ppary mRNA overexpression was induced by all pollutants. These data agreed with the lipid accumulation profiles documented by histology. Fas mRNA levels were modulated by the two NP doses and the higher BPA concentration. Lpl mRNA was significantly upregulated in all experimental groups except for BPA1 fish while hsl mRNA was significantly downregulated in all groups except for t-OP2 and BPA1 fish. The plasma concentrations of cortisol, the primary stress biomarker, were correlated with the levels of pepck mRNA level. This gene encodes phosphoenolpyruvate carboxykinase which is one of the key enzymes of gluconeogenesis. Pepck mRNA was significantly overexpressed in fish exposed to NP2 and both t-OP doses. Finally, the genes encoding cyclooxygenase 2 (cox2) and 5-lipoxygenase (5 lox), the products of which are involved in the inflammatory response, transcriptions were significantly upregulated in NP and BPA fish, whereas they were unchanged in t-OP specimens. The present findings suggest that dietary xenobiotic contamination can give rise to metabolic disorders also in fish and highlight the potential for their vertical transfer through the trophic levels and ultimately to humans.


Subject(s)
Diet , Lipid Metabolism/drug effects , Liver/drug effects , Sea Bream/physiology , Water Pollutants, Chemical/toxicity , Xenobiotics/toxicity , Animals , Fatty Liver/chemically induced , Fish Proteins/genetics , Gene Expression Regulation/drug effects , Sea Bream/metabolism
2.
G Chir ; 23(11-12): 450-2, 2002.
Article in Italian | MEDLINE | ID: mdl-12652923

ABSTRACT

The Authors report the results of a short term follow-up in 28 patients treated for sialolithiasis. Extracorporeal lithotripsy is safe, effective and minimally invasive therapeutical option. Open surgery is reserved to cases of failure of noninvasive procedure.


Subject(s)
Lithotripsy , Parotid Diseases/therapy , Salivary Gland Calculi/therapy , Submandibular Gland Diseases/therapy , Adult , Female , Follow-Up Studies , Humans , Male , Time Factors
3.
J Chromatogr B Biomed Sci Appl ; 746(2): 325-9, 2000 Sep 15.
Article in English | MEDLINE | ID: mdl-11076087

ABSTRACT

Remacemide hydrochloride, a novel anticonvulsant agent, and its major active metabolite, desglycinylremacemide, were measured simultaneously in brain tissue by high-performance liquid chromatography with UV detection. Intra- and inter-assay variations for remacemide (1, 5, 10 microg/ml) were 5.1, 10.5 and 3.1% and 3.1, 4.0 and 1.3%, respectively. Intra- and inter-assay variations for desglycinylremacemide (1, 5, 10 microg/ml) were 4.2, 3.8 and 8.4% and 7.9, 8.8 and 3.1%, respectively. Limits of detection and quantification for both analytes were 4 and 31 ng/ml, respectively, with recovery consistently > or =85%. This reliable assay has applications in the pre-clinical neuropharmacokinetic and neuropharmacodynamic investigation of remacemide hydrochloride.


Subject(s)
Acetamides/metabolism , Brain/metabolism , Chromatography, High Pressure Liquid/methods , Phenethylamines/metabolism , Animals , Male , Mice , Mice, Inbred ICR , Reproducibility of Results , Sensitivity and Specificity , Spectrophotometry, Ultraviolet
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