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胰岛素治疗对2型糖尿病患者趋化因子受体CCR5表达及所选炎症标志物的影响

Influence of insulin therapy on expression of chemokine receptor CCR5 and selected inflammatory markers in patients with type 2 diabetes mellitus.

作者信息

Bogdanski P, Pupek-Musialik D, Dytfeld J, Jagodzinski P P, Jablecka A, Kujawa A, Musialik K

机构信息

Department of Internal Medicine, Metabolic Disorders and Hypertension, Karol Marcinkowski University of Medical Sciences, Szamarzewskiego 84, 61-847 Poznan, Poland.

出版信息

Int J Clin Pharmacol Ther. 2007 Oct;45(10):563-7. doi: 10.5414/cpp45563.

Abstract

OBJECTIVE

Leukocyte migration to the subendothelial space is considered crucial in the initiation of atherosclerosis. There is increasing evidence that overexpression of chemokine receptors contribute to this process. CCR5 is one of the receptors present on peripheral T lymphocytes, monocytes and macrophages. We decided to evaluate the expression of CCR5 on monocytes and macrophages in peripheral blood and selected inflammatory markers in patients with type 2 diabetes mellitus before and after the initiation of insulin therapy.

MATERIAL AND METHODS

A total of 10 patients with newly diagnosed type 2 diabetes and 6 healthy control subjects were studied. Assessment of CCR5 expression on the surface of monocytes and macrophages in peripheral blood was performed using flow cytometry before the initiation of insulin therapy and after 5-week treatment. Serum concentrations of RANTES, TNF-alpha, IL-6 and hsCRP were assessed.

RESULTS

When compared to control subjects, we observed higher densities of CCR5 on the surface of peripheral blood monocytes and macrophages and higher concentrations of RANTES, TNF-alpha, IL-6 and hsCRP before insulin therapy. After 5-week insulin therapy, there was a significant decrease in the expression of CCR5 on the surface of these cells and a significant fall in serum levels of RANTES, IL-6, TNF-alpha and hsCRP.

CONCLUSIONS

Type 2 diabetes leads to an increase in the inflammatory process, and insulin therapy inhibits the early stages of this process.

摘要

目的

白细胞迁移至内皮下间隙被认为在动脉粥样硬化的起始过程中至关重要。越来越多的证据表明趋化因子受体的过表达促成了这一过程。CCR5是外周T淋巴细胞、单核细胞和巨噬细胞上存在的受体之一。我们决定评估2型糖尿病患者在开始胰岛素治疗前后外周血单核细胞和巨噬细胞上CCR5的表达以及选定的炎症标志物。

材料与方法

共研究了10例新诊断的2型糖尿病患者和6名健康对照者。在开始胰岛素治疗前及治疗5周后,使用流式细胞术对外周血单核细胞和巨噬细胞表面的CCR5表达进行评估。评估血清中RANTES、TNF-α、IL-6和hsCRP的浓度。

结果

与对照者相比,我们观察到胰岛素治疗前外周血单核细胞和巨噬细胞表面CCR5密度更高,RANTES、TNF-α、IL-6和hsCRP浓度更高。5周胰岛素治疗后,这些细胞表面CCR5的表达显著降低,血清中RANTES、IL-6、TNF-α和hsCRP水平显著下降。

结论

2型糖尿病导致炎症过程增加,胰岛素治疗抑制该过程的早期阶段。

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