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1.
J Laryngol Otol ; 105(5): 349-52, 1991 May.
Article in English | MEDLINE | ID: mdl-2040836

ABSTRACT

The study has been carried out on biopsies taken from four patients affected by squamous cell carcinoma and four patients affected by undifferentiated carcinoma of nasopharyngeal type (UCNT). Three healthy volunteers have served as controls. All the specimens have been studied by SEM. The neoplastic conditions cause obvious alterations both in the mucosal surface and in the morphology of the cellular apex.


Subject(s)
Carcinoma/ultrastructure , Nasopharyngeal Neoplasms/ultrastructure , Aged , Carcinoma, Squamous Cell/ultrastructure , Humans , Male , Microscopy, Electron, Scanning , Microvilli/ultrastructure , Middle Aged , Nasal Mucosa/ultrastructure
2.
Alcohol Alcohol ; 24(2): 121-8, 1989.
Article in English | MEDLINE | ID: mdl-2719769

ABSTRACT

It has been suggested that lipid peroxidation plays a role in the pathogenesis of chronic alcoholic liver disease (CALD). However, whether or not CALD differs from chronic non alcoholic liver disease (CLD) in lipid peroxidation, is still questionable. Thirty-eight patients affected by CALD and CLD who were matched for age, sex, nutrition and liver function tests (LFTs) and 17 controls (C) took part in this study. The following tests were performed: serum and liver malondialdehyde (MDA) determination by the TBA test, liver total glutathione (GSH) estimate, mitochondrial (ALDH2) and cytosolic (ALDH1) aldehyde dehydrogenase activity determinations. Patients who showed signs of malnutrition were excluded from this study. Serum and hepatic TBA-reactive substances resulted in a slight increase in chronic liver patients compared to controls but did not show any difference between CALD and CLD groups. Liver total glutathione did not show any change. Hepatic ALDH2 activity was significantly (P less than 0.01) higher in CALD than in CLD and control patients whereas ALDH1 did not show any difference. These results suggest that the increased lipid peroxidation in CALD and in CLD is probably secondary to liver damage rather than being the pathogenic factor.


Subject(s)
Aldehyde Dehydrogenase/blood , Lipid Peroxidation , Liver Diseases, Alcoholic/enzymology , Liver/enzymology , Adult , Cytosol/enzymology , Female , Glutathione/metabolism , Humans , Isoenzymes/blood , Liver Function Tests , Male , Malondialdehyde/blood , Middle Aged , Mitochondria, Liver/enzymology
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