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1.
Article in English | IMSEAR | ID: sea-37553

ABSTRACT

The relation between Helicobacter pylori (Hp) eradication and prevention of stomach carcinoid development has hitherto remained unclear. We therefore examined this problem using an Hp-infected and Hp-eradicated Mongolian gerbil (MG) model. Enterochromaffin-like (ECL) lesions (hyperplasia/dysplasia and carcinoid) were histopathologically evaluated in the glandular stomachs of Hp-infected and Hp-eradicated MGs. In addition, serum gastrin levels were analyzed. Hp infection induced significant increase in the development of ECL lesions in the glandular stomach, as well as serum gastrin levels as compared with non-infected MGs, while Hp eradication was associated with significant alleviation. The development of ECL lesions in the glandular stomach strongly correlated with titers of anti-Hp antibodies and serum gastrin levels in MGs. In conclusion, Hp infection induces carcinoid development, and Hp eradication prevents its occurrence in the glandular MG stomach, this being strongly linked with reduction in serum gastrin levels.


Subject(s)
Animals , Anti-Bacterial Agents/pharmacology , Carcinoid Tumor/etiology , Enterochromaffin-like Cells/pathology , Gastrins/blood , Gerbillinae , Helicobacter Infections/complications , Helicobacter pylori/drug effects , Hyperplasia , Male , Stomach Neoplasms/etiology
2.
Article in English | IMSEAR | ID: sea-37393

ABSTRACT

Peroxidation products formed from polyunsaturated lipids have DNA damaging potential. 4-oxo-2-hexenal (4-OHE), generated by the oxidation of omega-3 fatty acids, has been demonstrated to be mutagenic in vitro as assessed in the Ames test. To examine the carcinogenic risk of 4-OHE in vivo, initiation activity was investigated in a five-week liver assay, established to be effective for screening of carcinogenic potential of mutagens. Seven-week-old male F344 rats underwent two-thirds partial hepatectomy (PH) and were administered 4-OHE intragastrically at doses of 128, 80, 64, 40, 32, 20, or 0 mg/kg body weight (b.w.) at 18 hours thereafter, then being fed on diet containing 0.015% 2-acetylaminofluorene from weeks 2 to 4. All rats were given with 0.8 ml/kg b.w. CCl4 at week 3. At week 5, all survivors were sacrificed and initiation activity was assessed with reference to induction of glutathione S-transferase placental form (GST-P) positive foci in the liver. Mortality was significantly increased to 72.7% in the 128 mg/kg b.w. dose group compared with 0.9% in the control group. However, the average number of GST-P positive foci in the "128" dose group was 3.26-/+1.66 foci/cm2, not significantly different from the control value (2.78?1.33). Areas of GST-P positive foci were also similar (1.11-/+0.5 and 1.53-/+1.33 mm2/cm2 in "128" and the control groups, respectively). These results showed 4-OHE to have no significant initiation activity in.


Subject(s)
Aldehydes/toxicity , Animals , Dose-Response Relationship, Drug , Fatty Acids, Omega-3 , Lipid Peroxidation , Liver/drug effects , Male , Rats , Rats, Inbred F344
3.
Article in English | IMSEAR | ID: sea-37990

ABSTRACT

AIMS: We have previously demonstrated the importance of gastric and intestinal phenotypic expression for the histogenesis of stomach cancer. However, the phenotypes of stomach cancers arising after Helicobacter pylori (Hp) eradication have hitherto remained unclear. We therefore examined a series of lesions occurring after Hp eradication in the Mongolian gerbil (MG) model. METHODS: Totals of 6 and 20 advanced glandular stomach cancers were evaluated in Hp-eradicated and Hp-infected MGs treated with N-methyl-N-nitrosourea (MNU-MGs), using several gastrointestinal epithelial phenotypic markers. The lesions were divided phenotypically into gastric (G type), gastric-and-intestinal mixed (GI type), intestinal (I type), and null (N type) phenotypes. RESULTS: All 4 differentiated type lesions in Hp-eradicated MNU-MGs were classified as G type, while both of the undifferentiated lesions exhibit the GI type. In Hp-infected MNU-MGs, the lesions were classified as 10 G, 8 GI, and 2 I types, with undifferentiated type lesions having more intestinal phenotypic expression than their differentiated counterparts (P< 0.01). CONCLUSIONS: Our data suggest that the differentiated stomach cancers exhibit the G type in Hp-eradicated MNU-MGs, suggesting that a kind of non-neoplastic G type gland may be precancerous. Intestinalization may still occur, especially in undifferentiated stomach cancers, even if Hp eradication is successful.


Subject(s)
Adenocarcinoma/genetics , Animals , Carcinogens , Disease Models, Animal , Gerbillinae , Helicobacter Infections/complications , Helicobacter pylori/isolation & purification , Methylnitrosourea/therapeutic use , Phenotype , Stomach Neoplasms/genetics
4.
Article in English | IMSEAR | ID: sea-37978

ABSTRACT

Helicobacter pylori (Hp) infection is an important factor in human gastric disorders, including chronic active gastritis, peptic ulcers, intestinal metaplasia and cancer. Since epidemiologic studies overwhelmingly agree on a protective influence of fruits and vegetables in reducing the risk of gastric neoplasia and processed foods made from Prunus mume Sieb. et Zucc. (Japanese apricot or "Ume" in Japanese) are traditionally known for their miscellaneous medical effects, in the present study we investigated the efficacy of a fruit-juice concentrate of Japanese apricot (CJA) in the glandular stomach of Hp-infected Mongolian gerbils. Hp-inoculated gerbils were given CJA in their drinking water at concentrations of 1 and 3% for 10 weeks. The microscopic scores for gastritis and mucosal hyperplasia in the CJA groups were significantly lower than in the Hp-inoculated control group, with dose-dependence. Real-time PCR was performed to quantitate Hp by demonstrating urease A gene amount using gerbils glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene as an internal control. Average relative urease A gene dosage in the glandular stomach in the 1 and 3% CJA and Hp-inoculated control groups was 26.6 +/- 11.6% (average +/- SE), 30.3 +/- 10.5%, 100 +/- 40.9%, respectively, the fruit-juice concentrate causing significant lowering (P<0.01 and P<0.05, respectively, with 1 and 3%). These findings suggest that suppressive effects on gastric cancer development might also be expected as a result of decreased numbers of Hp and improvement of Hp-induced chronic active gastritis on administration of CJA.


Subject(s)
Administration, Oral , Animals , Beverages , Gastritis/microbiology , Gerbillinae , Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+)/genetics , Helicobacter Infections/complications , Helicobacter pylori/pathogenicity , Inflammation , Male , Plant Extracts/pharmacology , Polymerase Chain Reaction , Prunus/chemistry , Stomach Neoplasms/microbiology
5.
Acta cir. bras ; 9(4): 157-62, out.-dez. 1994. tab
Article in English | LILACS | ID: lil-143509

ABSTRACT

The evolution and phenotypic expression of mucosal lesions of the gastric stump were investigated in male rats submitted to gastric resection with reconstruction by the Bilroth II technique (biliopancreatic reflux - BPR) and by the Roux-en-Y procedure (without BPR). The animals were studied at 24, 36, 54 and 64 weeks after surgery. the phenotypic expression of the lesions was analyzed by immunohistochemical staining for pepsinogen isoenzyme 1 and by histochemical procedures for mucins. BPR was found to be responsible for the formation of adenomatous hyperplasia (AH) whose incidence and size increased with time. AH mainly consisted of gastric cells and always occurred in the transition of the gastrojejunal junction, and this site offers special conditions for the promoting effect of BPR to occur in full. In 101 rats submitted to BII procedures, 6 mucinous adenocarcinomas were diagnosed and this neoplasia expressed the phenotype of cells of the small intestine. The roux-en-Y procedure protects the gastric stump aginst the lesions observed in BII reconstruction


Subject(s)
Rats , Animals , Male , Gastrectomy/adverse effects , Stomach Neoplasms/etiology , Anastomosis, Roux-en-Y , Bile Reflux/complications , Gastrointestinal Transit , Hyperplasia/etiology , Immunohistochemistry , Gastric Mucosa/pathology , Stomach Neoplasms/pathology , Rats, Wistar , Time Factors
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