Intracellular glutathione deficiency is associated with enhanced nuclear Factor-κB activation in older noninsulin dependent diabetic patients

被引:18
作者
Arnalich, F [1 ]
Hernanz, A
López-Maderuelo, D
De La Fuente, M
Arnalicha, FM
Andrés-Mateos, E
Fernández-Capitán, C
Montiel, C
机构
[1] Autonomous Univ Madrid, Sch Med, Hosp La Paz, Dept Med, E-28049 Madrid, Spain
[2] Autonomous Univ Madrid, Sch Med, Hosp La Paz, Dept Clin Biochem, E-28049 Madrid, Spain
[3] Univ Complutense Madrid, Dept Anim Physiol, Fac Biol Sci, Madrid, Spain
[4] Autonomous Univ Madrid, Sch Med, Dept Pharmacol, E-28049 Madrid, Spain
[5] Hosp Maternal La Paz, Med Interna Serv, Madrid 28046, Spain
关键词
glutathione; thiol compounds; lipid peroxides (TBARS); oxidative stress; nuclear factor kappa B; peripheral blood mononuclear cells; non-insulin-dependent diabetes mellitus; aging;
D O I
10.1080/10715760100301371
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetes mellitus may be associated with intracellular glutathione (GSH) deficiency. Since in vivo studies have shown that plasma intracellular GSH plays a key role in regulating the activation of nuclear factor kappaB (NF-kappaB), we have investigated the relationship between intracellular thiols (GSH, homocysteine, cysteine and cysteinyglycine) and NF-kappaB activity in the peripheral blood mononuclear cells (PBMC) of 63 elderly non-insulin dependent diabetes mellitus (NIDDM) patients (28 microalbuminurics and 35 normoalbuminurics) and 30 healthy age- and sex-matched subjects. In addition, we have measured plasma concentrations of these thiol compounds, serum concentrations of interleukin-6 (IL-6) and vascular cell adhesion molecule-1 (sVCAM-1), that are partly dependent on the NF-kappaB activation, as well as the serum levels of thiobarbituric acid reacting substances (TBARS), as index of lipid peroxidation. Diabetic patients with microalbuminuria (MAB) and normoalbuminuria had NF-kappaB activity 2.1- and 1.5-fold greater, respectively, than the control group. As compared to normoalbuminuric patients, patients with MAB had significantly higher levels of glycemia, plasma homocysteine, and serum concentrations of TBARS, IL-6 and sVCAM-1 (in all cases, p < 0.01), and significantly lower GSH content in the PBMC (p < 0.05). The intracellular GSH in PBMC correlated with NF-kappaB activation (r = - 0.82; p < 0.0001), serum TBARS (r = -0.60; p < 0.001), and with fasting glycemia (r = -0.56; p < 0.001) in patients with MAB, whereas a weaker association between GSH levels in PBMC and NF-kappaB activation (r = -0.504, p < 0.001) was seen in patients without MAB. These results suggest that the decrease of intracellular GSH content in elderly NIDDM patients with MAB is strongly associated with enhanced NF-kappaB activation, which could contribute to the development of increased glomerular capillary permeability and its rapid progression.
引用
收藏
页码:873 / 884
页数:12
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