1. Melatonin reduces bacterial translocation after intestinal ischemia-reperfusion injury
- Author
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Pierpaolo Sileri, Domenico Benavoli, Marco Venza, Jarzembowski Tm, A.L. Gaspari, Paolo Gentileschi, Antonio Manzelli, G.S. Sica, Sileri, P, Sica, G, Gentileschi, P, Venza, M, Benavoli, D, Jarzembowski, T, Manzelli, A, and Gaspari, Al
- Subjects
Male ,medicine.medical_specialty ,Pathology ,Ileum ,Biology ,Gastroenterology ,Melatonin ,Cecum ,Peritoneal cavity ,medicine.artery ,Internal medicine ,medicine ,Animals ,Mesenteric lymph nodes ,Superior mesenteric artery ,Lung ,Transplantation ,Animal ,medicine.disease ,Rats, Inbred ACI ,Rats ,Intestines ,Disease Models, Animal ,Settore MED/18 - Chirurgia Generale ,medicine.anatomical_structure ,Liver ,Bacterial Translocation ,Reperfusion Injury ,Disease Models ,Lymph Nodes ,Peritoneum ,Spleen ,Surgery ,Inbred ACI ,Reperfusion injury ,medicine.drug - Abstract
Melatonin, the primary pineal hormone, has been reported to protect from oxidative injury after ischemia-reperfusion (IR). The aim of this study was to evaluate the effects of exogenous melatonin on intestinal integrity, ileal colonization, and bacterial translocation 45-minute after mesenteric IR. Sixteen male ACI rats randomly divided into two groups underwent 45-minutes intestinal ischemia by clamping the superior mesenteric artery. One hour prior to ischemia, study animals (n=8, group A) were treated with melatonin (10 mg/kg IP) while control animals (n=8, group B) received the same volume of saline solution. An additional six animals underwent laparotomy and served as a sham-operated group. Animals were sacrificed 24 hours after reperfusion; peritoneal swabs and biopsies of liver, spleen, lung, mesenteric lymph nodes, cecum, and terminal ileum were obtained for microbiology. The ileum samples were also processed for histopathological evaluation of IR-induced injury. Twenty-four hours after reperfusion bacterial translocation to the peritoneal cavity present in all group B animals was reduced to 37.5% among those that were melatonin-treated (group A; P
- Published
- 2004
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