Artículo

Gut Permeability and Glucose Absorption Are Affected at Early Stages of Graft Rejection in a Small Bowel Transplant Rat Model

Stringa, Pablo Luis Icon; Romanin, David Emmanuel Icon; Lausada, Natalia Raquel ; Papa Gobbi, Rodrigo Icon; Zanuzzi, Carolina Natalia Icon; Martín, Pedro Icon; Abate, Juan Cruz ; Cabanne, Ana Icon; Arnal, Nathalie Icon; Vecchio Dezillio, Leandro Emmanuel ; Milesi, Verónica Icon; Portiansky, Enrique Leo Icon; Gondolesi, Gabriel Eduardo Icon; Rumbo, Martín Icon

Otros responsables

Fecha

11/2017

Editorial

Lippincott Williams & Wilkins

Revista

Transplantation Direct

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

2373-8731

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

BACKGROUND: intestinal transplantation (ITx) faces many challenges due to the complexity of surgery and to the multiple immunological reactions that leads to the necessity of rigorous follow-up for early detection of acute cellular rejection (ACR). Our aim was to determine the kinetics of ACR using an experimental ITx model, with emphasis in the characterization of the process using different approaches, including the use of functional assays of absorptive and barrier function. METHODS: ITx in rats conducting serial sampling was performed. Clinical monitoring, graft histology, proinflammatory gene expression and nitrosative stress determination were performed. Also, glucose absorption, barrier function using ovalbumin translocation and contractile function were analyzed. RESULTS: the model used reproduced the different stages of ACR. Allogeneic ITx recipients showed signs of rejection from post-operative day (POD) 5, with increasing severity until 12 POD. Histological evaluation showed mild rejection in early sampling and severe rejection at late stages, with alterations in all graft layers. IL-6, CXCL 10, IFNg and nitrite plasmas levelsshowed behaviour coincident with histopathology. Remarkably, allogeneic grafts showed a marked alteration of glucose absorptive capacity from POD 5 that was sustained until endpoint. Coincidently, barrier function alteration was evidenced by luminal OVA translocation to serum. Contractile function was progressively impaired along ACR. CONCLUSIONS: glucose absorption and barrier function are altered at early stages of ACR, when histological alterations or gene expression changes were much subtle. This observation may provide simple evaluation tools that could be eventually translated to the clinics to contribute to early ACR diagnosis.

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