Alpha-lipoic acid modifies circulating angiogenic factors in patients with type 2 diabetes mellitus

被引:24
作者
Dworacka, Marzena [1 ]
Iskakova, Saule [2 ]
Krzyzagorska, Ewa [3 ]
Wesolowska, Anna [1 ]
Kurmambayev, Yergen [2 ]
Dworacki, Grzegorz [4 ]
机构
[1] Poznan Univ Med Sci, Dept Pharmacol, PL-60805 Poznan, Poland
[2] West Kazakhstan State Med Univ, Dept Pharmacol, Aktobe, Kazakhstan
[3] Poznan Specialist Ctr Med Care, Diabetol Out Patient Clin, Poznan, Poland
[4] Poznan Univ Med Sci, Dept Clin Immunol, PL-60805 Poznan, Poland
关键词
Alpha-lipoic acid; Type; 2; diabetes; VEGF; bFGF; MCP-1; IL-10; OXIDATIVE STRESS; GLUCOSE-UPTAKE; GROWTH-FACTOR; NEUROPATHY; ATHEROSCLEROSIS; EXPRESSION; RATS; POLYNEUROPATHY; ARTERIOGENESIS; HYPERGLYCEMIA;
D O I
10.1016/j.diabres.2014.11.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: In recent years interest has been focused on angiogenesis as a process involved in coronary artery disease (CAD) and diabetic distal sensorimotor polyneuropathy (DSPN). Recent studies have demonstrated the possible angiogenesis-modulating potential of alphalipoic acid (ALA) for DSPN and CAD. The aim of our study was to investigate the influence of ALA on serum angiogenic factors in patients with DM-2 (type 2 diabetes) with CAD and DSPN. Methods: Sixty patients with type 2 DM (T2DM) and CAD and 25 non-diabetic subjects were studied. Thirty patients with T2DM, CAD and DSPN were given 600 mg of ALA a day for 90 days. VEGF, bFGF, MCP-1, angiogenin, IL-12 and IL-10 concentrations in the sera were measured by flow cytometry. Results: ALA significantly increased VEGF, bFGF and IL-10 and decreased MCP-1 serum concentrations in patients with T2DM and CAD and DSPN. VEGF and IL-10 serum levels, both before and after ALA-treatment, were higher in this group than in T2DM and CAD patients, while circulating bFGF was higher and MCP-1 serum level lower in patients with T2DM and CAD and DSPN only in the post-ALA-treatment, compared to the T2DM and CAD group. Conclusions: ALA may influence angiogenesis in type 2 diabetic patients through an effect on some circulating factors including VEGF, bFGF, MCP-1 and IL-10. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:273 / 279
页数:7
相关论文
共 45 条
[1]   Role of insulin resistance and hyperglycemia in the development of atherosclerosis [J].
Bansilal, Sameer ;
Farkouh, Michael E. ;
Fuster, Valentin .
AMERICAN JOURNAL OF CARDIOLOGY, 2007, 99 (4A) :6B-14B
[2]   Commentary - Glucose, VEGF-A, and diabetic complications [J].
Benjamin, LE .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (04) :1181-1184
[3]   Vascular endothelial growth factor and its receptor, Flt-l, in the plasma of patients with coronary or peripheral atherosclerosis, or type II diabetes [J].
Blann, AD ;
Belgore, FM ;
McCollum, CN ;
Silverman, S ;
Lip, PL ;
Lip, GYH .
CLINICAL SCIENCE, 2002, 102 (02) :187-194
[4]   Whither pathogenetic treatments for diabetic polyneuropathy? [J].
Boulton, Andrew J. M. ;
Kempler, Peter ;
Ametov, Alexander ;
Ziegler, Dan .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2013, 29 (05) :327-333
[5]   Plaque angiogenesis versus compensatory arteriogenesis in atherosclerosis [J].
Chen, Chu-Huang ;
Walterscheid, Jeffrey P. .
CIRCULATION RESEARCH, 2006, 99 (08) :787-789
[6]   COMPARISON OF MICRO-ENZYMATIC AND HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC METHODS FOR THE ASSAY OF SERUM 1,5-ANHYDROGLUCITOL [J].
CHUSNEY, GD ;
PHILIPPA, M ;
PICKUP, JC .
CLINICA CHIMICA ACTA, 1995, 235 (01) :91-99
[7]   Neovascularization in diabetes and its complications. Unraveling the angiogenic paradox [J].
Costa, Paulo Zoe ;
Soares, Raquel .
LIFE SCIENCES, 2013, 92 (22) :1037-1045
[8]  
Da Ros R, 2005, CURR DRUG TARGETS, V6, P503
[9]   Serum VEGF increases in diabetic polyneuropathy, particularly in the neurologically active symptomatic stage [J].
Deguchi, T. ;
Hashiguchi, T. ;
Horinouchi, S. ;
Uto, T. ;
Oku, H. ;
Kimura, K. ;
Makisumi, K. ;
Arimura, K. .
DIABETIC MEDICINE, 2009, 26 (03) :247-252
[10]   Interleukin-12: Biological properties and clinical application [J].
Del Vecchio, Michele ;
Bajetta, Emilio ;
Canova, Stefania ;
Lotze, Michael T. ;
Wesa, Amy ;
Parmiani, Giorgio ;
Anichini, Andrea .
CLINICAL CANCER RESEARCH, 2007, 13 (16) :4677-4685