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1.
J Dev Orig Health Dis ; 10(4): 479-487, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-30626462

RESUMO

Environmental factors during perinatal life can lead to changes in the mammary gland, making it susceptible to cancer in adulthood. Breastfeeding has a special importance since it takes place at a critical period of growth and development of the newborn. We aimed to analyze if an appropriate lactation protects the offspring against mammary carcinogenesis during adult life and explore the mechanisms involved in the protective effect. One-day-old Sprague-Dawley female rats were randomly distributed in litters of three (L3), eight (L8) or 12 (L12) pups per dam, to induce a differential consumption of breast milk. At 55 days of age, the animals were treated with a single dose of dimethylbenzanthracene to study tumor latency, incidence and progression. Histological, immunohistochemical and Western blot studies were performed. We observed lower incidence and higher latency in L3 compared to the other groups. The mitotic index and expression of proliferating cell nuclear antigen (PCNA) was significantly augmented in tumors of L12 rats compared to L3 and L8, while the apoptotic index was augmented in tumors of L3 v. L12. Cleaved caspase 8 was significantly higher in tumors from L3 compared to L12. Tumors developed in L3 have a greater number of apoptotic bodies and a greater expression of caspase 8. These results demonstrate that the animals that maintained a higher intake of maternal milk (L3) presented lower incidence and greater tumor latency. Lower consumption of breast milk (L12) would increase tumor mitosis and the expression of PCNA, explaining the higher tumor incidence observed in this group.


Assuntos
Aleitamento Materno/estatística & dados numéricos , Neoplasias Mamárias Animais/prevenção & controle , Leite/química , Envelhecimento , Animais , Apoptose , Feminino , Incidência , Lactação , Neoplasias Mamárias Animais/epidemiologia , Leite/estatística & dados numéricos , Mitose , Gravidez , Ratos , Ratos Sprague-Dawley
2.
Histochem Cell Biol ; 147(6): 759-769, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28191619

RESUMO

Experimental hypothyroidism retards mammary carcinogenesis promoting apoptosis of tumor cells. ß-catenin plays a critical role in cell adhesion and intracellular signaling pathways conditioning the prognosis of breast cancer. However, the mechanistic connections associated with the expression of ß-catenin in thyroid status and breast cancer are not known. Therefore, we studied the relationship between the expression and localization of ß-catenin and apoptosis in mammary tumors induced by 7,12-dimethylbenz(a)anthracene (DMBA) in hypothyroid (Hypot) and euthyroid (EUT) rats. Female Sprague Dawley rats were treated with a dose of DMBA (15 mg/rat) at 55 days of age and were then divided into two groups: HypoT (0.01% 6-N-propyl-2-thiouracil in drinking water, n = 54) and EUT (untreated control, n = 43). Latency, incidence and progression of tumors were determined. At sacrifice, tumors were obtained for immunohistological studies and Western Blot. The latency was longer (p < 0.05), the incidence was lower (p < 0.0001) and tumor growth was slower (p < 0.01) in HypoT rats compared to EUT. The expression of Bax, cleaved caspase-9 and caspase-3 was significantly higher in tumors of HypoT than in EUT (p < 0.05) indicating the activation of the intrinsic pathway. In this group, ß-catenin was expressed in the plasma membrane and with less intensity, while its expression was nuclear and with greater intensity in the EUT (p < 0.05). Moreover, the expression of survivin was reduced in tumors of HypoT rats (p < 0.05). In conclusion, decreased expression of ß-catenin and its normal location in membrane of mammary tumors are associated with augmented apoptosis via activation of the intrinsic pathway in HypoT rats.


Assuntos
Apoptose , Progressão da Doença , Hipotireoidismo/metabolismo , Neoplasias Mamárias Animais/metabolismo , beta Catenina/metabolismo , Animais , Feminino , Hipotireoidismo/induzido quimicamente , Propiltiouracila , Ratos , Ratos Sprague-Dawley
3.
Vet Microbiol ; 156(3-4): 336-42, 2012 May 04.
Artigo em Inglês | MEDLINE | ID: mdl-22119188

RESUMO

Pets can be reservoirs of Shiga toxin-producing Escherichia coli (STEC) strains. The aim of this study was to examine nine strains belonging to several serotypes (O91:H21, O91:H16, O178:H19, O8:H19, O22:H8, O22:HNT, ONT:H8), previously recovered from cats or dogs. To this end, we assessed a set of additional virulence genes (stx(2) subtype, subAB, ehxA, eae and saa), cytotoxic activity, and genetic relationships with strains isolated from cattle, meat and humans using pulsed-field gel electrophoresis (PFGE). Most of the isolates carried the stx(2) and/or stx(2vh-b) sequences, while only the O91:H21 isolate presented the mucus-activatable stx(2d) variant, as confirmed by sequencing the genes of subunits A and B. All the strains showed cytotoxic activity in cultured cells. One of the two O178:H19, selected for its high level of cytotoxicity in Vero cells, showed the ability to cause functional alterations in the human colon mucosa in vitro. None of the strains possessed the subAB, eae or saa genes and only the strains belonging to serotype O8:H19 carried the ehxA gene. The isolates shared 90-100% similarity by PFGE to epidemiologically unrelated strains of the corresponding serotypes recovered from cattle, meat or humans. Our results demonstrate that dogs and cats may have a role in the infection of humans by STEC, probably serving as a vehicle for bovine strains in the cycle of human infection, and thus emphasize the health risks for owners and their families.


Assuntos
Gatos/microbiologia , Cães/microbiologia , Escherichia coli Shiga Toxigênica/classificação , Sequência de Aminoácidos , Animais , Argentina , Bovinos/microbiologia , Chlorocebus aethiops , Eletroforese em Gel de Campo Pulsado , Proteínas de Escherichia coli/genética , Fezes/microbiologia , Humanos , Carne/microbiologia , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Sorotipagem , Escherichia coli Shiga Toxigênica/patogenicidade , Células Vero , Fatores de Virulência/genética
4.
Rev Argent Microbiol ; 37(3): 117-21, 2005.
Artigo em Espanhol | MEDLINE | ID: mdl-16323657

RESUMO

Shiga toxin-producing E. coli (STEC) is one of the most important emergent pathogen in foods, being its main reservoir bovine cattle. STEC can cause diarrhea, hemorrhagic colitis and hemolytic-uremic syndrome. The present work have studied the cytotoxic action in human colon of cultures of two STEC strains isolated from faeces of calves with bloody diarrhea. Colonic mucosa was mounted as a diaphragm in a Ussing chamber and incubated with the cultures of pathogenic strains. Net water flow (Jw) decreased and the short-circuit current (Isc) increased significantly (p < 0.01) compared to negative control. Tissues showed an erosion of the mucose, epithelial exfoliation, and presence of pseudo-membranes in the lumen. Mild circulatory lesions were observed in the lamina propia. A moderate neutrophils infiltration was observed in the lumen and into the epithelial cells. Colonic crypts were not disrupted. Both experimental strains caused a similar lesion on colon tissues. This is the first study that shows that cultures of STEC strains isolated from bovine cattle produce cytotoxic effects in vitro in human colon.


Assuntos
Doenças dos Bovinos/microbiologia , Colo/microbiologia , Diarreia/veterinária , Infecções por Escherichia coli/veterinária , Escherichia coli O157/patogenicidade , Mucosa Intestinal/microbiologia , Animais , Transporte Biológico , Água Corporal/metabolismo , Bovinos , Colo/metabolismo , Colo/patologia , Diarreia/microbiologia , Células Epiteliais/metabolismo , Células Epiteliais/microbiologia , Células Epiteliais/patologia , Infecções por Escherichia coli/microbiologia , Escherichia coli O157/isolamento & purificação , Escherichia coli O157/fisiologia , Humanos , Técnicas In Vitro , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patologia , Neutrófilos/patologia , Especificidade da Espécie , Virulência
5.
Rev. argent. microbiol ; Rev. argent. microbiol;37(3): 117-121, jul.-sep. 2005. ilus
Artigo em Espanhol | LILACS | ID: lil-634493

RESUMO

Escherichia coli productor de toxina Shiga (STEC) es el patógeno emergente en alimentos de mayor impacto, siendo su principal reservorio el ganado bovino. STEC puede causar diarrea, colitis hemorrágica y síndrome urémico hemolítico. El presente trabajo estudió la acción citotóxica de dos cepas de STEC aisladas de heces de terneros diarreicos en colon humano in vitro. Los fragmentos se montaron como un diafragma en una cámara de Ussing y se incubaron con las cepas patógenas. El flujo neto absortivo de agua (Jw) disminuyó y la corriente de cortocircuito (Isc) aumentó significativamente (P < 0,01) con respecto al control negativo. Los tejidos presentaron erosión de la mucosa, exfoliación del epitelio, y presencia de pseudomembranas en el lumen. A nivel de la lámina propia se observaron lesiones circulatorias leves. Una moderada infiltración de neutrófilos se observó en el lumen y en las células epiteliales. Las criptas colónicas no se vieron afectadas. El grado de lesión fue similar en ambas cepas experimentales. Este es el primer estudio que demuestra que cultivos de cepas de STEC aisladas de ganado bovino producen efectos citotóxicos en colon humano in vitro.


Shiga toxin-producing E. coli (STEC) is one of the most important emergent pathogen in foods, being its main reservoir bovine cattle. STEC can cause diarrhea, hemorrhagic colitis and hemolytic-uremic syndrome. The present work have studied the cytotoxic action in human colon of cultures of two STEC strains isolated from faeces of calves with bloody diarrhea. Colonic mucosa was mounted as a diaphragm in a Ussing chamber and incubated with the cultures of pathogenic strains. Net water flow (Jw) decreased and the short-circuit current (Isc) increased significantly (p < 0,01) compared to negative control. Tissues showed an erosion of the mucose, epithelial exfoliation, and presence of pseudo-membranes in the lumen. Mild circulatory lesions were observed in the lamina propia. A moderate neutrophils infiltration was observed in the lumen and into the epithelial cells. Colonic crypts were not disrupted. Both experimental strains caused a similar lesion on colon tissues. This is the first study that shows that cultures of STEC strains isolated from bovine cattle produce cytotoxic effects in vitro in human colon.


Assuntos
Animais , Bovinos , Humanos , Doenças dos Bovinos/microbiologia , Colo/microbiologia , Diarreia/veterinária , Infecções por Escherichia coli/veterinária , /patogenicidade , Técnicas In Vitro , Mucosa Intestinal/microbiologia , Transporte Biológico , Água Corporal/metabolismo , Colo/metabolismo , Colo/patologia , Diarreia/microbiologia , Células Epiteliais/metabolismo , Células Epiteliais/microbiologia , Células Epiteliais/patologia , Infecções por Escherichia coli/microbiologia , /isolamento & purificação , /fisiologia , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patologia , Neutrófilos/patologia , Especificidade da Espécie , Virulência
6.
Rev. argent. microbiol ; Rev. argent. microbiol;37(3): 117-21, 2005 Jul-Sep.
Artigo em Espanhol | BINACIS | ID: bin-38290

RESUMO

Shiga toxin-producing E. coli (STEC) is one of the most important emergent pathogen in foods, being its main reservoir bovine cattle. STEC can cause diarrhea, hemorrhagic colitis and hemolytic-uremic syndrome. The present work have studied the cytotoxic action in human colon of cultures of two STEC strains isolated from faeces of calves with bloody diarrhea. Colonic mucosa was mounted as a diaphragm in a Ussing chamber and incubated with the cultures of pathogenic strains. Net water flow (Jw) decreased and the short-circuit current (Isc) increased significantly (p < 0.01) compared to negative control. Tissues showed an erosion of the mucose, epithelial exfoliation, and presence of pseudo-membranes in the lumen. Mild circulatory lesions were observed in the lamina propia. A moderate neutrophils infiltration was observed in the lumen and into the epithelial cells. Colonic crypts were not disrupted. Both experimental strains caused a similar lesion on colon tissues. This is the first study that shows that cultures of STEC strains isolated from bovine cattle produce cytotoxic effects in vitro in human colon.

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