Effects of 5′-Adenosine Triphosphate on Intestinal Ischemia-Reperfusion in Rabbits

Abstract To study whether treatment with 5′-adenosine triphosphate (ATP), an agonist of P2 purine receptors, attenuated intestinal dysfunction caused by ischemia (I) and/or reperfusion (R), rabbits were treated with ATP (15 mg · kg−1 , intravenously) or saline solution (SS) 60 minutes before I by oc...

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Veröffentlicht in:Transplantation proceedings 2010-03, Vol.42 (2), p.461-464
Hauptverfasser: Taha, M.O, Miranda-Ferreira, R, Fagundes, D.J, Simões, R.S, Monteiro, H.P, Oliveira, I.S, Soares, K.R.M, Martins, M.C.L, Balbino, A.T, Rodrigues, F.F, Arruda, T.B, Abrão, M.S, Jurkiewicz, A, Caricati-Neto, A
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Sprache:eng
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Zusammenfassung:Abstract To study whether treatment with 5′-adenosine triphosphate (ATP), an agonist of P2 purine receptors, attenuated intestinal dysfunction caused by ischemia (I) and/or reperfusion (R), rabbits were treated with ATP (15 mg · kg−1 , intravenously) or saline solution (SS) 60 minutes before I by occlusion of the superior mesenteric artery and/or R (120 minutes). After I or I/R isolated 2-cm jejunal segments were mounted in an organ bath to study nerve-mediated contractions stimulated by electrical pulses or KCl using a digital recording system. Thin jejunal slices were stained (hematoxylin and eosin) for optical microscopy. Compared to a sham group, the jejunal contractions were similar to sham hosts among I + ATP, but reduced in I + SS, I/R + SS, and I/R + ATP groups. The jejunal-enteric nerves were damaged in I + SS, I/R + SS, and I/R + ATP, but not the I + ATP group. These results suggested that ATP attenuated intestinal dysfunction produced by I, but not that caused by R.
ISSN:0041-1345
1873-2623
DOI:10.1016/j.transproceed.2010.01.036