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Pirfenidone attenuates ischaemia-reperfusion injury in the rat small intestine.

机译:吡非尼酮减轻大鼠小肠缺血再灌注损伤。

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摘要

1. Pirfenidone, an antifibrotic compound with anti-inflammatory effects, has been investigated in a rat model of acute experimental ischaemia-reperfusion injury of the small intestine. 2. Occlusion of the superior mesenteric artery in young adult female rats for 30 min followed by reperfusion for 120 min induced significant local and systemic effects, including tissue haemorrhage with oedema, elevated serum concentrations of tumour necrosis factor (TNF)-alpha, neutropenia, hypotension and bradycardia. 3. Administration of pirfenidone (200 mg/kg, p.o., i.v. or i.p.) 30 min before occlusion completely inhibited the increase in serum TNF-alpha concentrations. Pirfenidone inhibited, but did not completely prevent, tissue damage in the small intestine, as well as hypotension and oedema, but neutropenia and bradycardia were not significantly changed by treatment. 4. Thus, pirfenidone effectively moderates both local and some systemic effects of ischaemia-reperfusion injury in the rat small intestine model.
机译:1.吡非尼酮是一种具有抗炎作用的抗纤维化化合物,已在小肠急性实验性缺血再灌注损伤的大鼠模型中进行了研究。 2.将成年雌性大鼠的肠系膜上动脉闭塞30分钟,然后再灌注120分钟,引起明显的局部和全身性影响,包括组织水肿和水肿,血清肿瘤坏死因子(TNF)-α浓度升高,中性粒细胞减少,低血压和心动过缓。 3.在闭塞前30分钟施用吡非尼酮(200mg / kg,口服,静脉内或腹膜内)完全抑制血清TNF-α浓度的增加。吡非尼酮可抑制但不能完全预防小肠组织损伤以及低血压和水肿,但中性粒细胞减少和心动过缓并未因治疗而明显改变。 4.因此,吡非尼酮可有效减轻大鼠小肠模型局部缺血再灌注损伤的局部和全身作用。

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