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1.
Braz J Med Biol Res ; 51(7): e7372, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29846410

RESUMEN

The effect of bisacodyl on the treatment of rats with slow transit constipation (STC) was studied. Forty-five female Wister rats were divided into control group, STC group, and STC bisacodyl group. The immunohistochemical method was used to determine interstitial cells of Cajal (ICC) and the expression of c-Kit protein. Body mass and the number of defecations were significantly decreased in the STC group compared with the control group on the 100th day after diphenoxylate administration, while dry weight of feces was significantly increased and the intestinal transit time was prolonged. There were significant differences in the number of defecations, dry weight of feces, and intestinal transit time among the three groups. The number of defecations was higher, dry weight of feces was lower, and intestinal transit time was shorter in the STC bisacodyl group compared to the STC group. In addition, ICC basement membrane dissolution occurred in the colon wall of the STC group. The connection between ICC and surrounding cells was destroyed, and the nucleus shrunken to different degrees. Moreover, c-Kit expression in the STC group was significantly lower than the control group. The connection between ICC and surrounding cells in the STC bisacodyl group was significantly stronger than the STC group, and the number of ICC and the expression of c-Kit were increased. Bisacodyl could reduce the severity of STC in rats by increasing the number of ICC and the expression of c-Kit.


Asunto(s)
Bisacodilo/uso terapéutico , Catárticos/uso terapéutico , Colon/metabolismo , Estreñimiento/tratamiento farmacológico , Tránsito Gastrointestinal/efectos de los fármacos , Células Intersticiales de Cajal/efectos de los fármacos , Proteínas Proto-Oncogénicas c-kit/metabolismo , Animales , Colon/efectos de los fármacos , Colon/patología , Estreñimiento/metabolismo , Estreñimiento/fisiopatología , Femenino , Tránsito Gastrointestinal/fisiología , Inmunohistoquímica , Células Intersticiales de Cajal/metabolismo , Células Intersticiales de Cajal/patología , Ratas , Ratas Wistar
2.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;51(7): e7372, 2018. tab, graf
Artículo en Inglés | LILACS | ID: biblio-951733

RESUMEN

The effect of bisacodyl on the treatment of rats with slow transit constipation (STC) was studied. Forty-five female Wister rats were divided into control group, STC group, and STC bisacodyl group. The immunohistochemical method was used to determine interstitial cells of Cajal (ICC) and the expression of c-Kit protein. Body mass and the number of defecations were significantly decreased in the STC group compared with the control group on the 100th day after diphenoxylate administration, while dry weight of feces was significantly increased and the intestinal transit time was prolonged. There were significant differences in the number of defecations, dry weight of feces, and intestinal transit time among the three groups. The number of defecations was higher, dry weight of feces was lower, and intestinal transit time was shorter in the STC bisacodyl group compared to the STC group. In addition, ICC basement membrane dissolution occurred in the colon wall of the STC group. The connection between ICC and surrounding cells was destroyed, and the nucleus shrunken to different degrees. Moreover, c-Kit expression in the STC group was significantly lower than the control group. The connection between ICC and surrounding cells in the STC bisacodyl group was significantly stronger than the STC group, and the number of ICC and the expression of c-Kit were increased. Bisacodyl could reduce the severity of STC in rats by increasing the number of ICC and the expression of c-Kit.


Asunto(s)
Animales , Femenino , Ratas , Bisacodilo/uso terapéutico , Tránsito Gastrointestinal/efectos de los fármacos , Catárticos/uso terapéutico , Colon/metabolismo , Proteínas Proto-Oncogénicas c-kit/metabolismo , Estreñimiento/tratamiento farmacológico , Células Intersticiales de Cajal/efectos de los fármacos , Tránsito Gastrointestinal/fisiología , Inmunohistoquímica , Ratas Wistar , Colon/efectos de los fármacos , Colon/patología , Estreñimiento/fisiopatología , Estreñimiento/metabolismo , Células Intersticiales de Cajal/metabolismo , Células Intersticiales de Cajal/patología
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