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奎纳克林对小肠缺血再灌注后血浆丙二醛的影响。

Influence of quinacrine on plasma malondialdehyde after small intestinal ischemia and reperfusion.

作者信息

Otamiri T A

机构信息

Department of Surgery, University Hospital, Linköping, Sweden.

出版信息

Circ Shock. 1988;24(1):63-9.

PMID:2830996
Abstract

The influence of quinacrine on malondialdehyde (MDA) as an index of lipid peroxidation, activities of phospholipase A2 (PLA2), and myeloperoxidase (MPO)--a neutrophil granulocyte maker in plasma--was examined in rats following ischemia and reperfusion. In the absence of quinacrine, ischemia and reperfusion caused increased MDA content and increased activities of PLA2 and myeloperoxidase in the plasma. All these effects were efficiently inhibited by the PLA2 inhibitor quinacrine. The finding indicates that the occurrence of an increased level of MDA following intestinal ischemia may be used for diagnostic purposes and points to the possibility that high plasma MDA might indicate a need for PLA2 inhibitor treatment.

摘要

研究了在大鼠缺血再灌注后,将奎纳克林作为脂质过氧化指标的丙二醛(MDA)、磷脂酶A2(PLA2)的活性以及髓过氧化物酶(MPO)——血浆中的一种中性粒细胞标志物——的影响。在没有奎纳克林的情况下,缺血再灌注导致血浆中MDA含量增加以及PLA2和髓过氧化物酶活性增加。PLA2抑制剂奎纳克林有效抑制了所有这些作用。该发现表明,肠道缺血后MDA水平升高的情况可用于诊断目的,并指出血浆中高MDA水平可能表明需要进行PLA2抑制剂治疗的可能性。

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