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Diabetes, Vol 37, Issue 6 832-837, Copyright © 1988 by American Diabetes Association
Increased superoxide production by mononuclear cells of patients with hypertriglyceridemia and diabetes
K Hiramatsu and S Arimori
Department of Internal Medicine, Tokai University School of Medicine, Kanagawa, Japan.
Diabetic patients with hypertriglyceridemia frequently develop
atherosclerosis. Because superoxide (O2-) is suspected to play an important
role in the initiation of atherosclerosis, we investigated whether an
abnormal amount of O2- was produced by circulating mononuclear cells of
patients with both diabetes mellitus and hypertriglyceridemia. The rate of
production of superoxide dismutase-inhibitable O2- was measured when cells
were stimulated by either 4 beta-phorbol 12 beta-myristate 13 alpha-acetate
(PMA) or by opsonized zymosan (OZ). In addition, the rates of O2-
production by mononuclear cells drawn from three other groups (normal,
solely diabetic, and solely hypertriglyceridemic) were determined. We found
that the rate of O2- production by mononuclear cells from the diabetic
hypertriglyceridemic group was significantly higher than that from normal,
diabetic, and hypertriglyceridemic groups. When the rates of O2- production
by mononuclear cells were plotted against the levels of plasma triglyceride
for all individuals tested, they correlated positively (r = .73 in PMA
stimulation and r = .79 in OZ stimulation, P less than .01). However, the
rate of O2- production did not relate to other parameters, i.e., plasma
cholesterol level, hemoglobin A1 level in erythrocytes, and the molar ratio
of free cholesterol to phospholipid in mononuclear cells. Thus, we
concluded that the observed elevated rate of O2- production in the diabetic
hypertriglyceridemic mononuclear cells was a reflection of a
hypertriglyceridemic condition and was not unique to the diabetic
hypertriglyceridemic condition. Also, O2- may be involved in the
pathogenesis of atherosclerosis in diabetic hypertriglyceridemic patients
when atherogenic factors specific to diabetes are concomitantly present.

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Copyright © 1988 by the American Diabetes Association.
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