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1.
Transplant Proc ; 44(8): 2313-6, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23026582

RESUMO

To study whether treatment with the beta-blocker atenolol (AT) attenuates intestinal dysfunction caused by ischemia (I) and reperfusion (R), rats were treated with AT (1.5 mg · kg(-1), intravenously) or saline solution (SS) prior to I (60 minutes), which was produced by occlusion of the superior mesenteric artery, and/or R (120 minutes). After I or I/R, 2-cm jejunal segments were mounted in an organ bath to study neurogenic contractions stimulated by electrical pulses or KCl using a digital recording system. Thin jejunal slices were stained with hematoxylin and eosin for optical microscopy analysis. Compared to the sham group, jejunal contractions were similar in the I + AT and the I/R + AT groups, but reduced in the I + SS and the I/R + SS groups. The jejunal enteric nerves were damaged in the I + SS and the I/R + SS groups, but not in the I + AT and the I/R + AT. These results suggest that AT may attenuate intestinal dysfunction caused by I and I/R.


Assuntos
Antagonistas de Receptores Adrenérgicos beta 1/farmacologia , Atenolol/farmacologia , Fármacos Gastrointestinais/farmacologia , Jejuno/irrigação sanguínea , Jejuno/efeitos dos fármacos , Traumatismo por Reperfusão/prevenção & controle , Animais , Citoproteção , Modelos Animais de Doenças , Estimulação Elétrica , Sistema Nervoso Entérico/efeitos dos fármacos , Sistema Nervoso Entérico/fisiopatologia , Motilidade Gastrointestinal/efeitos dos fármacos , Jejuno/inervação , Jejuno/patologia , Jejuno/fisiopatologia , Masculino , Cloreto de Potássio/farmacologia , Ratos , Ratos Wistar , Traumatismo por Reperfusão/patologia , Traumatismo por Reperfusão/fisiopatologia
2.
Transplant Proc ; 42(2): 457-60, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20304164

RESUMO

To study whether treatment with L-nitro-arginine methyl ester (L-NAME), an inhibitor of nitric oxide biosynthesis, attenuates intestinal dysfunction caused by ischemia (I) and/or reperfusion (R), rabbits were treated with L-NAME (15 mgxkg(-1), intervenously) or saline olution (SS) prior to I (60 minutes) induced by occlusion of superior mesenteric artery and/or R (120 minutes). After I or I/R, isolated jejunal segments (2 cm) were mounted in an organ bath to study nerve-mediated contractions stimulated by electrical pulses or KCI using a digital recording system. Thin jejunal slices were stained (hematoxylin and eosin) for analysis by optical microscopy. Compared with a sham group, the jejunal contractions were similar in the I/R + L-NAME, but reduced in I + SS, I/R + SS, and I + L-NAME groups. The jejunal enteric nerves were damaged in the I + SS, I/R + SS, and I + L-NAME cohorts, but not among the I/R + L-NAME cohort. These results suggested that L-NAME attenuated intestinal dysfunction caused by R but not by I.


Assuntos
Motilidade Gastrointestinal/efeitos dos fármacos , Enteropatias/prevenção & controle , NG-Nitroarginina Metil Éster/farmacologia , Traumatismo por Reperfusão/prevenção & controle , Traumatismo por Reperfusão/fisiopatologia , Animais , Estimulação Elétrica , Isquemia/fisiopatologia , Jejuno/efeitos dos fármacos , Jejuno/inervação , Jejuno/fisiologia , Masculino , Contração Muscular/efeitos dos fármacos , Contração Muscular/fisiologia , Coelhos , Cloreto de Sódio/farmacologia
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