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Diabetes Care, Vol 21, Issue 8 1310-1316, Copyright © 1998 by American Diabetes Association
Insufficient glycemic control increases nuclear factor-kappa B binding activity in peripheral blood mononuclear cells isolated from patients with type 1 diabetes
MA Hofmann, S Schiekofer, M Kanitz, MS Klevesath, M Joswig, V Lee, M Morcos, H Tritschler, R Ziegler, P Wahl, A Bierhaus and PP Nawroth
Department of Medicine, University of Heidelberg, Germany.
OBJECTIVE: The redox-sensitive transcription factor nuclear factor-kappa B
(NF-kappa B) is believed to contribute to late diabetic complications. It
is unknown whether NF-kappa B is influenced by glycemic control. RESEARCH
DESIGN AND METHODS: To determine whether NF-kappa B is activated in
patients with insufficient glycemic control (HbA1c > 10%), we developed
a tissue culture-independent electrophoretic mobility shift assay
(EMSA)-based semiquantitative detection system that allowed us to determine
NF-kappa B activation in ex vivo-isolated peripheral blood mononuclear
cells (PBMCs). We included 43 patients with type 1 diabetes in this
cross-sectional study. 10 of those received the antioxidant thioctic acid
(600 mg/day p.o.) for 2 weeks. RESULTS: Monocytes of patients with HbA1c
levels > 10% demonstrated significantly higher NF-kappa B binding
activity in an EMSA and a stronger NF-kappa B staining in
immunohistochemistry than monocytes of patients with HbA1c levels of 6-8%.
The increase in NF-kappa B activation correlated with an increase in
plasmatic markers of lipid peroxidation. Treatment with the antioxidant
thioctic acid decreased NF-kappa B binding activity. CONCLUSIONS:
Hyperglycemia induces activation of the transcription factor NF-kappa B in
ex vivo-isolated PBMCs of patients with type 1 diabetes. NF-kappa B
activation is at least partially dependent on oxidative stress, since the
antioxidant thioctic acid significantly lowered the extent of NF-kappa B
binding activity.

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Copyright © 1998 by the American Diabetes Association.
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