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重症疟疾中的氧化应激与流变学

Oxidative stress and rheology in severe malaria.

作者信息

Dondorp A M, Omodeo-Salè F, Chotivanich K, Taramelli D, White N J

机构信息

Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

出版信息

Redox Rep. 2003;8(5):292-4. doi: 10.1179/135100003225002934.

Abstract

There is mounting evidence that the release of haemozoin (beta-haematin), which is produced in large amounts during malaria infection and is released into the circulation during schizont rupture, is associated with damage to cell membranes through an oxidative mechanism. The red blood cell membrane is thus oxidised, causing rigidity of the cell. This can contribute to the pathophysiology of severe malaria, since red blood cells will have to deform considerably in order to squeeze through the microcirculation, the patency of which is disturbed by sequestered red blood cells containing the mature forms of the parasite. Rigidity of red blood cells forms a new target for intervention. Since this seems to be caused by oxidative damage to the red blood cell membrane, the anti-oxidant N-acetylcysteine is a promising candidate for adjunctive treatment in severe malaria, which still has a mortality rate as high as 20%.

摘要

越来越多的证据表明,疟色素(β-血红素)的释放与细胞膜损伤有关,这种损伤是通过氧化机制造成的。疟色素在疟疾感染期间大量产生,并在裂殖体破裂时释放到循环系统中。红细胞膜因此被氧化,导致细胞僵硬。这可能会导致严重疟疾的病理生理过程,因为红细胞必须大幅变形才能挤过微循环,而含有成熟寄生虫形式的被隔离红细胞会干扰微循环的通畅。红细胞的僵硬形成了一个新的干预靶点。由于这似乎是由红细胞膜的氧化损伤引起的,抗氧化剂N-乙酰半胱氨酸有望成为严重疟疾辅助治疗的候选药物,严重疟疾的死亡率仍然高达20%。

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