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大鼠缺血再灌注后的肾功能及皮质(Na⁺+K⁺)-ATP酶活性、丰度和分布

Renal function and cortical (Na(+)+K(+))-ATPase activity, abundance and distribution after ischaemia-reperfusion in rats.

作者信息

Coux Gabriela, Trumper Laura, Elías M Mónica

机构信息

Farmacología, Departamento de Ciencias Fisiológicas, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, CONICET, Suipacha 531, Rosario, Argentina.

出版信息

Biochim Biophys Acta. 2002 Jan 2;1586(1):71-80. doi: 10.1016/s0925-4439(01)00087-4.

Abstract

The effects of ischaemic injury and reperfusion on renal function, cortical ATP content, alkaline phosphatase activity and (Na(+)+K(+))-ATPase activity and abundance in cortical homogenates and isolated basolateral and apical membranes were examined. Rats were submitted to 5 or 40 min of right renal artery occlusion and 60 min of reperfusion. Renal function of the ischaemic-reperfused kidney was studied by conventional clearance techniques. Our results show that 1 h of reperfusion after a short period of renal ischaemia (5 min) allows the complete restoration of the biochemical features of cortical cells and functional properties of the injured kidney. A longer period of ischaemia, such as 40 min, followed by 1 h of reperfusion showed functional and biochemical alterations. ATP recovered from 26% after 40 min of ischaemia to 50% of control values after 1 h reperfusion. However, renal function was strongly impaired. Brush border integrity was compromised, as suggested by AP excretion and actin appearance in urine. Although total cortical (Na(+)+K(+))-ATPase activity was not different from controls, its distribution in isolated apical and basolateral membranes was abnormal. Remarkably, we detected an increase in alpha-subunit protein abundance that may suggest that (Na(+)+K(+))-ATPase synthesis is promoted by ischaemia-reperfusion. This increase may play an important role in the pathophysiology of ischaemic acute renal failure.

摘要

研究了缺血性损伤和再灌注对肾功能、皮质ATP含量、碱性磷酸酶活性以及皮质匀浆、分离的基底外侧膜和顶端膜中(Na⁺+K⁺)-ATP酶活性及丰度的影响。将大鼠右肾动脉阻断5或40分钟,然后再灌注60分钟。采用传统的清除技术研究缺血再灌注肾的肾功能。我们的结果表明,短时间肾缺血(5分钟)后1小时的再灌注可使皮质细胞的生化特征和受损肾脏的功能特性完全恢复。较长时间的缺血,如40分钟,随后1小时的再灌注则显示出功能和生化改变。ATP从缺血40分钟后的26%恢复到再灌注1小时后的对照值的50%。然而,肾功能严重受损。如碱性磷酸酶排泄和尿中肌动蛋白出现所示,刷状缘完整性受到损害。尽管总的皮质(Na⁺+K⁺)-ATP酶活性与对照无差异,但其在分离的顶端膜和基底外侧膜中的分布异常。值得注意的是,我们检测到α亚基蛋白丰度增加,这可能表明缺血再灌注促进了(Na⁺+K⁺)-ATP酶的合成。这种增加可能在缺血性急性肾衰竭的病理生理学中起重要作用。

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