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司托巴定可保护大鼠肾脏免受缺血/再灌注损伤。

Stobadine protects rat kidney against ischaemia/reperfusion injury.

作者信息

Guz Galip, Demirogullari Billur, Ulusu Nuray N, Dogu Cihangir, Demirtola Arzu, Kavutcu Mustafa, Omeroglu Suna, Stefek Milan, Karasu Cimen

机构信息

Department of Nephrology, Gazi University Faculty of Medicine, Ankara, Turkey.

出版信息

Clin Exp Pharmacol Physiol. 2007 Mar;34(3):210-6. doi: 10.1111/j.1440-1681.2007.04574.x.

DOI:10.1111/j.1440-1681.2007.04574.x
PMID:17250641
Abstract
  1. Ischaemia-reperfusion (I/R) injury, one of the main causes of acute renal failure, still needs satisfactory treatment for routine clinical application. Stobadine, a novel synthetic pyridoindole anti-oxidant, has the ability to reduce tissue injury induced by mechanisms involving reactive oxygen species during I/R. The aim of the present study was to determine the effects of stobadine on renal I/R injury. 2. Forty male Wistar rats were randomly divided into four groups as follows: sham, I/R, stobadine treated and I/R + stobadine treated. Stobadine (2 mg/kg, i.v.) was given intravenously to two groups of rats. The stobadine-treated group was treated with stobadine following sham operation before the abdominal wall was closed, whereas the I/R + stobadine group received stobadine at the beginning of reperfusion. Renal I/R was achieved by occluding the renal arteries bilaterally for 40 min, followed by 6 h reperfusion. Immediately thereafter, blood was drawn and tissue samples were harvested to assess: (i) serum levels of blood urea nitrogen and creatinine; (ii) serum and/or tissue levels of malondialdehyde (MDA), glutathione (GSH), glucose 6-phosphate dehydrogenase (G-6PD), 6-phosphogluconate dehydrogenase (6-PGD), glutathione reductase (GR) and glutathione peroxidase (GPx); (iii) renal morphology; and (iv) immunohistochemical staining for P-selectin. 3. Stobadine was able to significantly attenuate the renal dysfunction as a result of renal I/R injury. Ischaemia-reperfusion resulted in a significant increase in serum and kidney MDA levels and a decrease in serum and kidney GSH. Stobadine treatment at the beginning of reperfusion attenuated both the increased MDA levels and decreased GSH secondary to I/R injury. In addition, the decreased G-6PD activity observed after I/R was significantly attenuated by stobadine treatment. Stobadine did not alter 6-PGD activity after I/R. Neither GR nor GPx activity was significantly changed in the I/R alone or the I/R + stobadine groups compared with the sham group. In addition, stobadine decreased the morphological deterioration and high P-selectin immunoreactivity secondary to renal I/R injury. 4. A pyridoindole anti-oxidant, stobadine exerts a renal protective effect in renal I/R injury, which is probably due to its radical-scavenging and anti-oxidant activities.
摘要
  1. 缺血再灌注(I/R)损伤是急性肾衰竭的主要病因之一,其常规临床应用的治疗效果仍不尽人意。司他定是一种新型合成的吡啶吲哚抗氧化剂,具有减轻I/R期间由活性氧介导机制所导致的组织损伤的能力。本研究旨在确定司他定对肾I/R损伤的影响。2. 40只雄性Wistar大鼠被随机分为以下四组:假手术组、I/R组、司他定治疗组和I/R +司他定治疗组。两组大鼠均静脉注射司他定(2 mg/kg)。司他定治疗组在腹壁缝合前的假手术后给予司他定,而I/R +司他定组在再灌注开始时给予司他定。通过双侧阻断肾动脉40分钟,随后再灌注6小时来实现肾I/R。此后立即采血并采集组织样本,以评估:(i)血清尿素氮和肌酐水平;(ii)血清和/或组织中丙二醛(MDA)、谷胱甘肽(GSH)、葡萄糖6-磷酸脱氢酶(G-6PD)、6-磷酸葡萄糖酸脱氢酶(6-PGD)、谷胱甘肽还原酶(GR)和谷胱甘肽过氧化物酶(GPx)的水平;(iii)肾脏形态;以及(iv)P-选择素的免疫组织化学染色。3. 司他定能够显著减轻肾I/R损伤所致的肾功能障碍。缺血再灌注导致血清和肾脏MDA水平显著升高,血清和肾脏GSH水平降低。再灌注开始时给予司他定治疗可减轻I/R损伤继发的MDA水平升高和GSH降低。此外,司他定治疗可显著减轻I/R后观察到的G-6PD活性降低。司他定未改变I/R后的6-PGD活性。与假手术组相比,单独I/R组或I/R +司他定组的GR和GPx活性均无显著变化。此外,司他定减轻了肾I/R损伤继发的形态学恶化和高P-选择素免疫反应性。4. 作为一种吡啶吲哚抗氧化剂,司他定在肾I/R损伤中发挥肾保护作用,这可能归因于其自由基清除和抗氧化活性。

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