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223 L-Arginine Modulate Intestinal Inflammation in Rats Submitted to Mesenteric Ischemia-Reperfusion Injury Ana Laura Aidar1, Leandro Ryuchi Iuamoto1, Eduardo Hiroshi Tikazawa1, Florense de Lucca Melo1, Karis de Campos1, Thais de Melo Alexandre e Silva1, Guilherme dos Santos Perez1, Fernando Lopes Carrara1, Jordan Bistafa Liu1, Jeferson Oliveira1, Hugo Pequeno Monteiro1, Djalma José Fagundes1,1, Murched Omar Taha1,1. 1Surgery Department, Sao Paulo Federal University, Sao Paulo, Brazil - email: [email protected] INTRODUCTION The ischemia (I) and reperfusion (R) promote intestinal lesions that alter the enteric motor function and compromise the prognosis of intestinal transplantation. Treatment with cytoprotective agents have been proposed to increase the success of intestinal transplants. L-arginine is an amino acid important precursor in the synthesis of nitric oxide and which is directly involved in oxidative stress resulting from ischemia and reperfusion injury. Thus interest is directed for the evaluation of the expression of genes that encode proteins involved in the oxidative stress and antioxidant defense. PURPOSE To study whether treatment with the L-arginine attenuates intestinal dysfunction caused by ischemia and reperfusion. MATERIALS AND METHODS Eighteen rats were used (n=6/group): Sham only submitted to surgery proceeding; IR group: submitted to IR proceeding and treated with saline solution (SS) and H+IR group: treated with Larg (100 mg/kg) injected into the femoral vein 5 minute before I, 5 minutes before R, and 55 minutes after R. In the end of experiment the animals were euthanized and the jejunal segments (2 cm) were removed and washed, and the Polymerase Chain Reaction in Real Time (real-time PCR) was performed. In summary the cDNA obtained in the previous stage was used as template in the PCR reaction in real time using the specific kits (Enteric Endothelial Cell Biology Biosciences - Qiagen, Co) for each sample was analyzed by real time PCR to 84 genes. RESULTS Compared with SG group, pro-apoptotic gene Bax and anti-apoptotic gene (Bcl2I2) were up-regulated. AVG ΔCt (Ct(GOI) - Ave Ct (HKG)) Fold Change Test Sample Control Sample Bax -0.32 +1.94 Test Sample / p-value Control Sample +4.78 0.000104 Blc2l2 -0.70 +2.81 +11.85 Symbol T-TEST 0.000026 Table 1: Expression of two genes related to enteric endothelial call biology from rats of Sham ischemia and reperfusion (SS+IR) and ischemic and reperfusion plus L-Arginina (Larg+IR) groups. Significant values of fold up (+) or down(-) regulation was marked in bold [2^(-Delta Ct)] CONCLUSIONS The pretreatment with L-arginine in mesenteric ischemia-reperfusion injury was demonstrated in rodents that could be related with ability of this drug to increase the expression of pro-apoptotic gene Bax and anti-apoptotic gene (Bcl2I2).