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镰状细胞贫血中氧合血液的流变学异常。

Abnormal rheology of oxygenated blood in sickle cell anemia.

作者信息

Chien S, Usami S, Bertles J F

出版信息

J Clin Invest. 1970 Apr;49(4):623-34. doi: 10.1172/JCI106273.

Abstract

The viscosity of oxygenated blood from patients with sickle cell anemia (Hb SS disease) was found to be abnormally increased, a property which contrasts with the well recognized viscous aberration produced by deoxygenation of Hb SS blood. Experiments designed to explain this finding led to considerations of deformation and aggregation, primary determinants of the rheologic behavior of erythrocytes as they traverse the microcirculation. Deformability of erythrocytes is in turn dependent upon internal viscosity (i.e. the state and concentration of hemoglobin in solution) and membrane flexibility. Definition of the contribution made by each of these properties to the abnormal viscosity of oxygenated Hb SS blood was made possible by analysis of viscosity measurements, made over a wide range of shear rates and cell concentrations, on Hb SS erythrocytes and normal erythrocytes suspended in Ringer's solution (where aggregation does not occur) and in plasma. Similar measurements were made on the two cell types separated by ultracentrifugation of Hb SS erythrocytes: high density erythrocytes composed of 50 to 70% irreversibly "sickled" cells (ISC) and low density erythrocytes composed of over 95% non-ISC. Under all experimental conditions (hematocrit, shear rate, and suspending medium) the viscosity of ISC exceeds that of normal erythrocytes. The viscosity of non-ISC is elevated only in the absence of aggregation and over intermediate ranges of hematocrit. Analyses of the data reveal (a) an elevated internal viscosity of ISC: (b) a reduced membrane flexibility of both ISC and non-ISC, particularly at low shear rates; and (c) a reduced tendency for aggregation displayed by both cell types. The abnormal viscosity of oxygenated Hb SS blood can be attributed to the altered rheology of ISC and, to a lesser extent, of non-ISC. These studies assign a role to the abnormal rheology of Hb SS erythrocytes in the pathogenesis of sickle cell anemia, even under conditions of complete oxygenation.

摘要

研究发现,镰状细胞贫血(血红蛋白SS病)患者的氧合血液粘度异常增加,这一特性与血红蛋白SS血液脱氧所产生的广为人知的粘性异常形成对比。旨在解释这一发现的实验引发了对变形和聚集的思考,变形和聚集是红细胞在微循环中流动时流变行为的主要决定因素。红细胞的可变形性又取决于内部粘度(即溶液中血红蛋白的状态和浓度)和膜的柔韧性。通过对悬浮在林格氏溶液(不发生聚集)和血浆中的血红蛋白SS红细胞和正常红细胞在广泛的剪切速率和细胞浓度范围内进行粘度测量分析,得以确定这些特性各自对氧合血红蛋白SS血液异常粘度的贡献。对通过超速离心血红蛋白SS红细胞分离出的两种细胞类型进行了类似测量:由50%至70%不可逆“镰状”细胞(ISC)组成的高密度红细胞和由超过95%非ISC组成的低密度红细胞。在所有实验条件(血细胞比容、剪切速率和悬浮介质)下,ISC的粘度均超过正常红细胞。非ISC的粘度仅在无聚集且血细胞比容处于中等范围时升高。数据分析表明:(a)ISC的内部粘度升高;(b)ISC和非ISC的膜柔韧性均降低,尤其是在低剪切速率下;(c)两种细胞类型的聚集倾向均降低。氧合血红蛋白SS血液的异常粘度可归因于ISC流变学的改变,在较小程度上也归因于非ISC流变学的改变。这些研究表明,即使在完全氧合的情况下,血红蛋白SS红细胞的异常流变学在镰状细胞贫血的发病机制中也起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9db/322516/8760fd846ff1/jcinvest00220-0045-a.jpg

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