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Diabetes Care, Vol 21, Issue 4 487-493, Copyright © 1998 by American Diabetes Association
Normalization of plasma lipid peroxides, monocyte adhesion, and tumor necrosis factor-alpha production in NIDDM patients after gliclazide treatment
AC Desfaits, O Serri and G Renier
Metabolic Unit, CHUM Research Center, Montreal, Quebec, Canada.
OBJECTIVE: To evaluate the effect of gliclazide administration to NIDDM
patients on 1) monocyte adhesion to cultured endothelial cells, 2) plasma
cytokine and lipid peroxide levels, and 3) monocyte cytokine production.
RESEARCH DESIGN AND METHODS: Poorly controlled glyburide-treated diabetic
patients (n = 8) and healthy control subjects (n = 8) were recruited. At
the beginning of the study, glyburide was replaced by an equivalent
hypoglycemic dose of gliclazide. Serum and monocytes were isolated from
blood obtained from control and diabetic subjects before and after 3 months
of treatment with gliclazide. RESULTS: Plasma lipid peroxide levels and
monocyte adhesion to endothelial cells are enhanced in NIDDM patients, and
gliclazide administration totally reverses these abnormalities. Before
gliclazide treatment, serum levels of cytokines did not differ in the
control and the diabetic groups, with the exception of an enhancement of
tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL)-6 in NIDDM
subjects. Basal and lipopolysaccharide (LPS)-stimulated monocyte production
of interleukin-1 beta, IL-6, and IL-8 did not differ between the two
groups. Furthermore, basal monocyte production of TNF-alpha was similar in
the control and the diabetic groups, whereas a marked increase in the
LPS-stimulated monocyte production of TNF-alpha was observed in the NIDDM
group. Gliclazide treatment lowered LPS-stimulated TNF-alpha production by
diabetic monocytes to levels similar to those observed in control subjects.
CONCLUSIONS: Gliclazide administration to NIDDM patients inhibits the
increased adhesiveness of diabetic monocytes to endothelial cells and
reduces the production of TNF-alpha by these cells. These results suggest
that treatment of NIDDM subjects with gliclazide may be beneficial in the
prevention of atherosclerosis associated with NIDDM.

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Copyright © 1998 by the American Diabetes Association.
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