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The role of aldose reductase inhibition in diabetic neutrophil phagocytosis and killing.

机译:醛糖还原酶抑制作用在糖尿病性中性粒细胞吞噬和杀伤中的作用。

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摘要

This study examines whether an aldose reductase inhibitor (statil, ICI) can enhance neutrophil oxidative killing by diabetic neutrophils. We have examined a radiometric assay of phagocytosis and killing of Candida albicans by neutrophils from 20 controls and 20 subjects with insulin-dependent diabetes under various in vitro glucose concentrations. Glucose was present at 5, 10 and 20 mM in the presence and absence of statil (11 microM). Phagocytosis was unaffected by raised glucose levels in controls and in diabetic subjects. Killing by the diabetic cells was inhibited by increasing concentrations of glucose, killing was 18.9 +/- 2.0, 16.9 +/- 2.4 and 14.8 +/- 2.0% (mean +/- s.e.m.) at 5, 10 and 20 mM glucose, respectively (P less than 0.05). With the addition of statil under the same conditions killing improved to 19.3 +/- 2.0, 23.2 +/- 2.2 and 23.6 +/- 2.4 (P less than 0.01), these values were similar to the controls (P greater than 0.01). We conclude therefore that aldose reductase inhibition restores oxidative killing to normal.
机译:这项研究检查了醛糖还原酶抑制剂(statil,ICI)是否可以增强糖尿病性中性粒细胞对中性粒细胞的氧化杀伤作用。我们已经研究了在各种体外葡萄糖浓度下,来自20名对照和20名胰岛素依赖型糖尿病患者的嗜中性粒细胞的吞噬作用和白色念珠菌杀死的放射测定。在存在和不存在statil(11 microM)的情况下,葡萄糖的存在量分别为5、10和20 mM。吞噬作用不受对照组和糖尿病患者葡萄糖水平升高的影响。葡萄糖浓度的升高抑制了糖尿病细胞的杀伤,在5、10和20 mM葡萄糖下,杀伤分别为18.9 +/- 2.0、16.9 +/- 2.4和14.8 +/- 2.0%(平均+/- sem)。 (P小于0.05)。在相同条件下添加statil可以将杀灭率提高到19.3 +/- 2.0、23.2 +/- 2.2和23.6 +/- 2.4(P小于0.01),这些值与对照相似(P大于0.01)。因此,我们得出的结论是,醛糖还原酶抑制作用使氧化杀伤恢复正常。

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