Blood levels of pro-inflammatory and anti-inflammatory cytokines during an oral glucose tolerance test in patients with symptoms suggesting reactive hypoglycemia

被引:16
|
作者
Eik Filho, W. [1 ,2 ]
Marcon, S. S. [2 ,3 ]
Krupek, T. [4 ]
Previdelli, I. T. S. [5 ,6 ]
Pereira, O. C. N. [5 ,6 ]
Silva, M. A. R. C. P. [4 ]
Bazotte, R. B. [4 ]
机构
[1] Univ Estadual Maringa, Dept Med, Disciplina Endocrinol, Maringa, Parana, Brazil
[2] Univ Estadual Maringa, Ctr Ciencias Saude, Programa Pos Grad Ciencias Saude, Maringa, Parana, Brazil
[3] Univ Estadual Maringa, Dept Enfermagem, Maringa, Parana, Brazil
[4] Univ Estadual Maringa, Dept Farmacol & Terapeut, Maringa, Parana, Brazil
[5] Univ Estadual Maringa, Dept Estat, Maringa, Parana, Brazil
[6] Univ Estadual Maringa, Programa Pos Grad Bioestat, Maringa, Parana, Brazil
关键词
Pro-inflammatory cytokines; Anti-inflammatory cytokines; Glucose tolerance test; Inflammation; Postprandial glycemia; TYPE-2; DIABETIC-PATIENTS; STRESS; BIOMARKERS; CHEMOKINES; PLASMA;
D O I
10.1590/1414-431X20165195
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We evaluated the impact of postprandial glycemia on blood levels of pro-inflammatory and anti-inflammatory cytokines during an oral glucose tolerance test in non-diabetic patients with symptoms suggesting reactive hypoglycemia. Eleven patients with clinical symptoms suggesting reactive hypoglycemia received an oral glucose solution (75 g). Blood was collected at 0 (baseline), 30, 60, 120 and 180 min after glucose ingestion and the plasma concentrations of interferon-alpha (IFN-alpha), interferon-gamma (IFN-gamma), interleukin-1 receptor antagonist (IL-1RA), interleukin 2 (IL-2), interleukin-2 receptor (IL-2R), interleukin 4 (IL-4), interleukin 6 (IL-6), interleukin 8 (IL-8), interleukin 10 (IL-10), interleukin-12 (IL-12), interleukin 13 (IL-13), interleukin 15 (IL-15), interleukin 17 (IL-17), IFN-gamma inducible protein 10 (IP-10), monocyte chemotactic protein 1 (MCP1), monokine induced by IFN-gamma (MIG), macrophage inflammatory protein-1 alpha (MIP-1 alpha), interleukin-1 beta (IL-1 beta), colony stimulating factor (G-CSF), granulocyte-macrophage CSF (GM-CSF), basic fibroblast growth factor (FGF-basic), eotaxin, tumor necrosis factor alpha (TNF alpha), epidermal growth factor (EGF), hepatocyte growth factor (HGF), vascular endothelial growth factor (VEGF), macrophage inflammatory protein-1 alpha (MIP-1 alpha), and 1 beta (MIP-1 beta) were evaluated. Overall, glycemic levels increased, reached its maximum at 30 min (phase 1), returned to baseline levels at 120 min (phase 2), followed by a mild hypoglycemia at 180 min (phase 3). During phase 1, cytokine blood levels were maintained. However, we observed a synchronous fall (P<0.05) in the concentrations of pro-inflammatory (IL-15, IL-17, MCP-1) and anti-inflammatory cytokines (FGF-basic, IL-13, IL-1RA) during phase 2. Furthermore, a simultaneous rise (P<0.05) of pro-inflammatory (IL-2, IL-5, IL-17) and anti-inflammatory cytokines (IL-4, IL-1RA, IL-2R, IL-13, FGF-basic) occurred during phase 3. Thus, mild acute hypoglycemia but not a physiological increase of glycemia was associated with increased blood levels of anti-inflammatory and pro-inflammatory cytokines.
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页数:5
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