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猫的红细胞病理学及海因茨小体介导的溶血机制

Erythrocyte pathology and mechanisms of Heinz body-mediated hemolysis in cats.

作者信息

Christopher M M, White J G, Eaton J W

机构信息

Department of Veterinary Pathobiology, University of Minnesota, St. Paul.

出版信息

Vet Pathol. 1990 Sep;27(5):299-310. doi: 10.1177/030098589002700501.

Abstract

Despite the frequency of both oxidant drug-induced and spontaneous Heinz body formation in cats, the cellular and biochemical mechanisms by which Heinz bodies result in red blood cell (RBC) destruction and hemolytic anemia in this species remain unknown. Feline spleens are non-sinusoidal and inefficient at removing Heinz body-containing RBC from the circulation; therefore, alternative mechanisms must be involved in accelerated RBC destruction. Propylene glycol (PG) ingestion causes dose-dependent Heinz body formation and decreased RBC survival in cats. We investigated several aspects of Heinz body-containing RBC from three cats ingesting diets that provided 8.0 g PG/kg body weight for up to 3 weeks, in order to characterize cellular lesions that are associated with the presence of Heinz bodies and that might contribute to chronic, accelerated RBC destruction, as well as to gain insight into the mechanism by which PG induces Heinz body formation. Erythrocytes with PG-induced Heinz bodies had decreased levels of reduced glutathione and adenosine triphosphate and reduced deformability. There was no change in hemoglobin isoelectric focusing or membrane lipid peroxidation. Electrophoretic patterns of Heinz body-containing RBC membranes were significantly altered, and membrane surface charge distribution was disturbed. Progressively protruding Heinz bodies suggested that extrusion of Heinz bodies may be a means of cell healing and/or destruction in the absence of splenic pitting. When compared to results obtained using RBC from cats treated with the oxidant drug phenylhydrazine, significant differences were noted in packed cell volume, turbidity index, membrane heme, and morphologic appearance of Heinz bodies. Our results indicate that multiple cellular abnormalities develop in RBC with PG-induced Heinz bodies that do not cause acute hemolysis but that may shorten RBC survival. Propylene glycol-induced Heinz bodies provide an ideal model for studying the chronic effects of Heinz bodies on RBC structure and function and may be useful in understanding the mechanisms of formation and the consequences of endogenous Heinz bodies in cats.

摘要

尽管猫体内由氧化药物诱导和自发形成海因茨小体的情况很常见,但海因茨小体导致该物种红细胞(RBC)破坏和溶血性贫血的细胞及生化机制仍不清楚。猫的脾脏是非窦性的,从循环中清除含海因茨小体的红细胞的效率很低;因此,必然存在其他机制参与红细胞的加速破坏。摄入丙二醇(PG)会导致猫体内海因茨小体形成呈剂量依赖性,并降低红细胞存活率。我们研究了三只摄入含8.0 g PG/kg体重饮食长达3周的猫的含海因茨小体红细胞的几个方面,以确定与海因茨小体存在相关的、可能导致慢性、加速红细胞破坏的细胞损伤,并深入了解PG诱导海因茨小体形成的机制。含有PG诱导海因茨小体的红细胞中还原型谷胱甘肽和三磷酸腺苷水平降低,变形性降低。血红蛋白等电聚焦或膜脂质过氧化没有变化。含海因茨小体红细胞膜的电泳图谱发生了显著改变,膜表面电荷分布受到干扰。逐渐突出的海因茨小体表明,在没有脾脏去核作用的情况下,海因茨小体的挤出可能是细胞修复和/或破坏的一种方式。与用氧化药物苯肼处理的猫的红细胞结果相比,在血细胞比容、浊度指数、膜血红素和海因茨小体的形态外观方面发现了显著差异。我们的结果表明,含有PG诱导海因茨小体的红细胞会出现多种细胞异常,这些异常不会导致急性溶血,但可能会缩短红细胞存活时间。丙二醇诱导的海因茨小体为研究海因茨小体对红细胞结构和功能的慢性影响提供了一个理想模型,可能有助于理解猫体内内源性海因茨小体的形成机制及其后果。

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