Oxidative DNA damage and augmentation of poly(ADP-ribose) polymerase/nuclear factor-kappa B signaling in patients with Type 2 diabetes and microangiopathy

• Published in: The international journal of biochemistry & cell biology Vol. 39; no. 9; pp. 1673 - 1684
• Main Authors: Adaikalakoteswari, Antonysunil, Rema, Mohan, Mohan, Viswanathan, Balasubramanyam, Muthuswamy
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Ltd 2007
• Subjects: Case-Control Studies; Diabetes Mellitus, Type 2 - complications; Diabetes Mellitus, Type 2 - metabolism; Diabetic Angiopathies - complications; Diabetic Angiopathies - metabolism; DNA - metabolism; DNA Damage; DNA-Formamidopyrimidine Glycosylase - metabolism; Female; Gene Expression Regulation; Humans; Male; Microangiopathy; Middle Aged; NF-kappa B - metabolism; NFκB; Oxidative DNA damage; Oxidative Stress; PARP; Poly(ADP-ribose) Polymerases - genetics; Poly(ADP-ribose) Polymerases - metabolism; Protein Binding; RNA, Messenger - genetics; RNA, Messenger - metabolism; Signal Transduction; Type 2 diabetes; Type 2 diabetes; PARP; NFκB; Microangiopathy; Oxidative DNA damage
• ISSN: 1357-2725; 1878-5875
• DOI: 10.1016/j.biocel.2007.04.013

Although oxidative stress and the subsequent DNA damage is one of the obligatory signals for poly(ADP-ribose) polymerase (PARP) activation and nuclear factor-kappa B (NFκB) alterations, these molecular aspects have not been collectively examined in epidemiological and clinical settings. Therefore, this study attempts to assess the oxidative DNA damage and its downstream effector signals in peripheral blood lymphocytes from Type 2 diabetes subjects without and with microangiopathy along with age-matched non-diabetic subjects. The basal DNA damage, lipid peroxidation and protein carbonyl content were significantly (p<0.05) higher in patients with and without microangiopathy compared to control subjects. Formamido Pyrimidine Glycosylase (FPG)-sensitive DNA strand breaks which represents reliable indicator of oxidative DNA damage were also significantly (p<0.001) higher in diabetic patients with (19.41±2.5) and without microangiopathy (16.53±2.0) compared to control subjects (1.38±0.85). Oxidative DNA damage was significantly correlated to poor glycemic control. PARP mRNA expression and PARP activity were significantly (p<0.05) increased in cells from diabetic patients with (0.31±0.03 densitometry units; 0.22±0.02PARPunits/mgprotein, respectively) and without (0.35±0.02; 0.42±0.05) microangiopathy compared to control (0.19±0.02; 0.11±0.02) subjects. Diabetic subjects with and without microangiopathy exhibited a significantly (p<0.05) higher (80%) NFκB binding activity compared to control subjects. In diabetic patients, FPG-sensitive DNA strand breaks correlated positively with PARP gene expression, PARP activity and NFκB binding activity. This study provides a comprehensive molecular evidence for increased oxidative stress and genomic instability in Type 2 diabetic subjects even prior to vascular pathology and hence reveals a window of opportunity for early therapeutic intervention.