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Ischemic preconditioning and atenolol on lung injury after intestinal ischemia and reperfusion in rats

机译:缺血预处理和阿替洛尔对大鼠肠缺血再灌注后肺损伤的影响

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The aim of this study was evaluate the beta blocker atenolol (AT) and ischemic preconditioning (IPC) strategies for tissue protection against systemic effects of intestinal ischemia (I) and reperfusion (R) injury. Forty-two rats were pretreated with AT (1.5 mg · kg-1), 0.9% saline solution (SS; 0.1 mL), or IPC and then subjected to prolonged occlusion of the superior mesenteric artery for 60 minutes leading to I followed or not by 120 minutes of R, according to the group. For IPC, 5 minutes of I prior to 10 minutes of R were established. After this process of I or I-R, the right lung of each animal was adequately prepared for staining with hematoxylin and eosin and subsequent histologic analysis for quantification of inflammatory infiltrate was done. The left lung was frozen and prepared for assessment of oxidative stress by the quantification of thiobarbituric acid-reactivity substances (TBARS). Histologic analysis showed an important inflammatory infiltrate in the I-R + SS (I-R + SS = 4.5), which was significantly (P .05) reduced by IPC (I-R + IPC = 3.0) or AT (I-R + AT = 3.0). Likewise, the TBARS levels were decreased by both strategies (I-R + SS = 0.63; I-R + IPC = 0.23; I-R + AT = 0.38; P .05). Our results showed that AT and IPC attenuate pulmonary lesions caused by intestinal I and R process.
机译:这项研究的目的是评估β受体阻滞剂阿替洛尔(AT)和缺血预处理(IPC)策略,以保护组织免受肠道局部缺血(I)和再灌注(R)损伤的全身影响。 42只大鼠用AT(1.5 mg·kg-1),0.9%盐溶液(SS; 0.1 mL)或IPC进行预处理,然后长时间肠系膜上动脉闭塞60分钟,导致是否进行I根据该小组,R的变化为120分钟。对于IPC,先建立5分钟的I,再建立10分钟的R。经过I或I-R的这个过程后,每只动物的右肺已准备就绪,可用苏木精和曙红染色,并随后进行了组织学分析以定量炎性浸润。冷冻左肺,并准备通过定量硫代巴比妥酸反应性物质(TBARS)评估氧化应激。组织学分析显示I-R + SS有重要的炎性浸润(I-R + SS = 4.5),IPC(I-R + IPC = 3.0)或AT(I-R + AT = 3.0)显着降低(P <.05)。同样,两种策略均降低了TBARS水平(IR + SS = 0.63; IR + IPC = 0.23; IR + AT = 0.38; P <.05)。我们的结果表明,AT和IPC可减轻由肠I和R过程引起的肺部病变。

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