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2.
Reproduction ; 132(6): 949-58, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17127755

ABSTRACT

Persistent organochlorine pollutants (POPs) are suspected to interfere with hormone activity and the normal homeostasis of spermatogenesis. We investigated the relationships between sperm DNA fragmentation, apoptotic markers identified on ejaculated spermatozoa and POP levels in the blood of 652 adult males (200 Inuits from Greenland, 166 Swedish, 134 Polish and 152 Ukrainian). Serum levels of 2, 2', 4, 4', 5, 5'-hexachlorobiphenyl (CB-153), as a proxy of the total POP burden, and of 1,1-dichloro-2,2-bis(p-chlorophenyl)-ethylene (p,p'-DDE), as a proxy of the total DDT exposure were determined. Sperm DNA fragmentation was measured by using the TUNEL assay, whereas immunofluorescence methods were utilized for detecting pro-apoptotic (Fas) and anti-apoptotic (Bcl-xL) markers. Both TUNEL assay and apoptotic markers were statistically differed across the four populations. No correlation between neither sperm DNA fragmentation nor apoptotic sperm parameters and the large variations in POPs exposure was observed for the separate study groups. However, considering the European populations taken together, we showed that both %TUNEL positivity and Bcl-xL were related to CB-153 serum levels, whereas our study failed to demonstrate any relations between DDE and %TUNEL positivity and apoptotic sperm biomarkers (Fas and Bcl-xL) in any region or overall regions. These results suggest that CB-153 and related chemicals might alter sperm DNA integrity and Bcl-xL levels in European adult males, but not in the highly exposed Inuit men. Additional issues (genetic background, lifestyle habits and characterization of total xeno-hormonal activities) need to be investigated in order to fully assess the population variations observed.


Subject(s)
Environmental Pollutants/toxicity , Inuit , Polychlorinated Biphenyls/toxicity , Spermatozoa/pathology , Adult , Apoptosis , Biomarkers/analysis , DNA Fragmentation , Dichlorodiphenyl Dichloroethylene/blood , Environmental Exposure , Environmental Pollutants/blood , Flow Cytometry , Greenland , Humans , In Situ Nick-End Labeling , Linear Models , Male , Poland , Polychlorinated Biphenyls/blood , Semen/chemistry , Sperm Count , Spermatozoa/drug effects , Sweden , Ukraine , White People , bcl-X Protein/analysis , fas Receptor/analysis
3.
Eat Weight Disord ; 10(2): 117-24, 2005 Jun.
Article in English | MEDLINE | ID: mdl-16114225

ABSTRACT

OBJECTIVE: Several theorists have hypothesized that stressful situations may trigger abnormal eating and even eating disorders in predisposed people. The purpose of this study was to assess whether a stressful situation would reveal an association between perfectionism and low self-esteem, and measures of eating disorder symptoms in male high school students. METHOD: A sample of 61 male high school students completed the Eating Disorder Inventory, the Multidimensional Perfectionism Scale, and the Self Liking and Competence Scale three times: on an average school day, on the day of an exam and on the day the subjects received the results of that exam. Linear regression analysis was carried out to verify whether the dimensions of perfectionism were associated with the measures of eating disorders. RESULTS: Interoceptive awareness was associated with 'Bulimia' only during the stressful situation and with 'Drive for thinness' both in stress and non stress situations. Other results were contradictory and difficult to interpret. DISCUSSION: The results suggest that in nonclinical male individuals stress might bring out a previously absent association between some psychological predisposing factors for eating disorders and an actual desire or plan for ED related thoughts and behaviours. Such a finding suggests that stress may stimulate behaviours related to eating disorders in a predisposed personality. A central role may be played by interoceptive awareness in male subjects.


Subject(s)
Feeding and Eating Disorders/psychology , Personality , Self Concept , Stress, Psychological , Adolescent , Adult , Causality , Humans , Italy , Linear Models , Male
4.
Biol Chem ; 382(12): 1697-705, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11843183

ABSTRACT

Studies of oxidative stress have classically been performed by analyzing specific, single antioxidants. In this study, susceptibility to oxidative stress in the human keratinocyte cell line NCTC2544 exposed to hydrogen peroxide (H2O2) was measured by the TOSC (total oxyradical scavenging capacity) assay, which discriminates between the antioxidant capacity toward peroxyl radicals and hydroxyl radical. The generation of H2O2-induced DNA damage, total antioxidant capacity and levels of antioxidant enzymes (catalase, superoxide dismutase, glutathione reductase, glutathione S-transferase, glutathione peroxidase) were studied. Exposure to H2O2-induced DNA damage that was gradually restored while a significant reduction in cellular TOSC values was obtained independently of stressor concentrations and the degree of DNA repair. Whereas TOSC values and cell resistance to H2O2 showed a good relationship, the extent of DNA damage is independent from cellular total antioxidant capacity. Indeed, maximum DNA damage and cell mortality were observed in the first 4 h, whereas TOSC remained persistently low until 48 h. Catalase levels were significantly lower in exposed cells after 24 and 48 h. Keratinocytes exposed after 48 h to a second H2O2 treatment exhibited massive cell death. A possible linkage was observed between TOSC values and NCTC2544 resistance to H2O2 challenge. The TOSC assay appears to be a useful tool for evaluating cellular resistance to oxidative stress.


Subject(s)
Antioxidants/metabolism , DNA Damage , Hydrogen Peroxide/toxicity , Keratinocytes/metabolism , Oxidative Stress/drug effects , Catalase/metabolism , Cell Survival/drug effects , Comet Assay , Free Radical Scavengers/metabolism , Glutathione Peroxidase/metabolism , Glutathione Reductase/metabolism , Glutathione Transferase/metabolism , Humans , Hydrogen Peroxide/metabolism , Hydroxyl Radical/metabolism , Keratinocytes/cytology , Keratinocytes/drug effects , Keratinocytes/enzymology , Microscopy, Electron , Peroxides/metabolism , Reactive Oxygen Species/metabolism , Superoxide Dismutase/metabolism
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