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小鼠和大鼠红细胞生成的数学模型。第3部分:红细胞生成受抑制

A mathematical model of erythropoiesis in mice and rats. Part 3: Suppressed erythropoiesis.

作者信息

Wulff H, Wichmann H E, Pantel K, Loeffler M

机构信息

Medizinische Universitätsklinik I, Köln, FRG.

出版信息

Cell Tissue Kinet. 1989 Jan;22(1):51-61. doi: 10.1111/j.1365-2184.1989.tb00200.x.

Abstract

A mathematical model of erythropoietic cell production and its regulation process has been proposed in a preceding paper. It is primarily based on the assumption that the number of cell divisions taking place in the CFU-E and erythropoietic precursor stages can be regulated depending on the oxygen supply to the tissue. Here we provide evidence that this model adequately describes situations of suppressed erythropoiesis. In detail this implies a quantitative description of the following processes: (1) changes in tissue oxygen tension (Pto2) due to increase in red cell numbers (red cell transfusion, posthypoxia), decrease in plasma volume (dehydration) or increase in atmospheric oxygen pressure (hyperoxia), (2) Pto2 dependent reduction of erythropoietin (EPO) production, (3) dose-response of reduced EPO-levels on erythropoietic amplification (omission of three to five mitoses). Model simulations are compared to experimental data obtained from red cell transfusion, posthypoxia, hyperoxia and dehydration. A satisfactory agreement suggests that the model adequately describes and correlates different ways to suppress erythropoiesis. It quantifies the role and relative contribution of the haematocrit, haemoglobin concentration, atmospheric oxygen pressure, tissue oxygen pressure and plasma volume as triggers in erythropoietic suppression under various conditions. In conjunction with the preceding two papers it could be shown that one unique set of model parameters is sufficient to describe erythropoiesis in steady state, stimulation and suppression. Limitations of the model are discussed and experiments for a more detailed investigation of the feedback mechanisms are proposed.

摘要

在前一篇论文中提出了红细胞生成细胞产生及其调节过程的数学模型。它主要基于这样一种假设,即在CFU - E和红细胞生成前体阶段发生的细胞分裂数量可以根据组织的氧气供应进行调节。在这里,我们提供证据表明该模型能够充分描述红细胞生成受抑制的情况。详细来说,这意味着对以下过程的定量描述:(1) 由于红细胞数量增加(红细胞输血、缺氧后)、血浆量减少(脱水)或大气氧分压增加(高氧)导致的组织氧张力(Pto2)变化;(2) Pto2依赖性促红细胞生成素(EPO)产生的减少;(3) 降低的EPO水平对红细胞生成扩增的剂量反应(省略三到五次有丝分裂)。将模型模拟结果与从红细胞输血、缺氧后、高氧和脱水实验中获得的数据进行比较。令人满意的一致性表明该模型能够充分描述并关联抑制红细胞生成的不同方式。它量化了血细胞比容、血红蛋白浓度、大气氧分压、组织氧压力和血浆量在各种条件下作为红细胞生成抑制触发因素的作用和相对贡献。结合前两篇论文可以表明,一组独特的模型参数足以描述稳态、刺激和抑制状态下的红细胞生成。讨论了该模型的局限性,并提出了用于更详细研究反馈机制的实验。

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