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1.
Egyptian Journal of Hospital Medicine [The]. 2015; 59 (April): 217-226
in English | IMEMR | ID: emr-173943

ABSTRACT

Aim of the work: bisphenol A [BPA] is a synthetic monomer that is polymerized to manufacture polycarbonate plastic products and resins, including those used in food packaging and dental sealants. It is used in the manufacture of a great variety of products including: compact disks, food can linings, plastic windows, car parts, adhesives, protective coatings and powder paints. This work aimed to study the effect of prenatal exposure to BPA on the endometrium of female rats


Materials and methods: thirty adult female albino rats were divided into three groups: rats in group 1 served as a control [G1] and received an equal amount of sesame oil to those of the treated groups; those in group 2 [G2] were administered by gavage 5.0 microg BPA/kg/day [low-dose group]; the third group [G3] received 50 microg BPA/kg/day [high-dose group]. The female offspring of each group were weaned at day 21 and maintained until 3 months old. The uteri were dissected for the histological and immuno-histochemical examination


Results: low-dose group showed degeneration of the epithelial lining of the endometrium with focal patches of increased epithelial cell layers. The high dose group revealed cytoplasmic hydropic degeneration and pyknotic nuclei of the epithelial cells. Estrogen receptors showed a significant decrease of positive cells in low dose treated group and this decrease markedly accentuated in the high dose one. Positive nuclei for Ki-67 were markedly increased with increasing doses of BPA


Conclusion: BPA showed obvious endometrial degenerative and proliferative histological changes. Therefore, the use of this substance in food packaging materials and in the manufacture of substances liable to come into contact with food and drink should be phased out


Subject(s)
Animals, Laboratory , Phenols , Endometrium/drug effects , Rats , Immunohistochemistry
2.
Egyptian Journal of Hospital Medicine [The]. 2014; 57 (October): 580-597
in English | IMEMR | ID: emr-160255

ABSTRACT

Exposure to crowding stress is associated with increased respiratory system morbidity, However, the underlying mechanisms are unclear. Thus, there is a need for more study of this harmful effect. Sulpiride had been shown to have a protective role against crowding stress on other systems but this role was not studied well on the respiratory and cardiovascular systems. Investigating the possible harmful effects of crowding on adult albino rats' lung and heart and the possible protective role of combined sulpiride treatment. The present study was carried out on 24 adult albino rats of local strain weighing 120 +/- 3 g which were randomly divided equally into Group 1[C, untreated negative control], Group 2 [Cr, crowding exposed or positive control] where rats were exposed to crowding in a cage [20x20x20 cm- 6 rats /cage] for 1 month, Group 3[D, sulpiride-treated] where the rats were exposed to sulpiride "0.028 mg/B.W./day" and Group 4 [Cr+D, crowding + sulpiride-treated]. Paraffin sections were prepared for histological, histochemical and morphometric studies. The data were statistically analysed. The rats exposed to crowding only or sulpiride only showed highly significant damaging changes on lung such as thickening in the interalveolar septa and obliteration of the alveoli, inflammatory cells infiltration within the pulmonary interstitium, peribronchiolar infiltration and fibrosis, thickening of the pulmonary blood vessels walls, interstitial collagen fibres deposition and apoptotic cellular changes. On the level of heart, significant decrease in the diameters of the myocardial muscle fibres with focal areas of necrosis, apoptotic changes and increased collagen fibres deposition was marked in sulpiride group. When crowding and sulpiride treatments were combined, the damaging effects were maximized on the lung and heart. These results provided evidence that crowding stress causes obvious lung and heart tissue damages. No protective role for sulpiride was proofed. This is because using sulpiride alone or in combination with crowding showed marked damaging effects on the lung and heart tissues


Subject(s)
Male , Animals, Laboratory , Stress, Physiological/physiology , Lung/physiology , Heart/physiology , Sulpiride , Protective Agents , Rats
3.
Indian J Med Microbiol ; 2007 Oct; 25(4): 323-9
Article in English | IMSEAR | ID: sea-53511

ABSTRACT

PURPOSE: This study was conducted to investigate the presence of bcl-2 protein in the serum of patients with viral hepatitis and to find out if there is any correlation between bcl-2 protein levels and cellular oxidative stress in the pathogenesis of viral hepatitis. METHODS: This study was carried out on 130 patients with viral hepatitis, 70 with chronic hepatitis, 30 with liver cirrhosis and 30 with hepatocellular carcinoma (HCC) in addition to 20 healthy persons as the control. Serum bcl-2 protein was estimated by enzyme-linked immunosorbent assay, serum malondialdehyde (MDA), nitric oxide (NO) and antioxidant enzymes (GSH, GSH-px, GR and SOD) were measured using spectrophotometric analysis. RESULTS: bcl-2 protein level was significantly elevated in the serum of HCC, cirrhosis and chronic hepatitis groups as compared to control group. There were significant positive correlations between higher bcl-2 protein level and viral hepatitis markers (HBsAg, anti-HCV antibodies) in HCC and cirrhotic patients as compared to chronic hepatitis group. An increase in oxidative stress markers (MDA, NO) and a decrease in antioxidant enzyme activities (SOD, GSH and GSH-px) were observed. However, there was a negative correlation between bcl-2 levels and GR in all studied patient groups. CONCLUSIONS: The release of oxidative free radicals, deficiency in antioxidant enzymes and the expression of bcl-2 protein might play a role in the pathogenesis of viral hepatitis. The ability to measure bcl-2 protein in the serum could be useful as a prognostic marker of cancer patients.


Subject(s)
Adolescent , Adult , Aged , Biomarkers , Carcinoma, Hepatocellular/physiopathology , Enzyme-Linked Immunosorbent Assay , Enzymes/blood , Female , Hepatitis B Surface Antigens/blood , Hepatitis C Antibodies/blood , Hepatitis, Chronic/physiopathology , Hepatitis, Viral, Human/physiopathology , Humans , Liver Cirrhosis/physiopathology , Male , Malondialdehyde/blood , Middle Aged , Nitric Oxide/blood , Oxidative Stress , Proto-Oncogene Proteins c-bcl-2/blood , Serum/chemistry , Spectrophotometry
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