G. Seghieri et al., PLASMA AND PLATELET ASCORBATE POOLS AND LIPID-PEROXIDATION IN INSULIN-DEPENDENT DIABETES-MELLITUS, European journal of clinical investigation, 28(8), 1998, pp. 659-663
Citations number
41
Categorie Soggetti
Medicine, Research & Experimental","Medicine, General & Internal
Background As diabetes mellitus represents a situation in which produc
tion of peroxides is increased, the aim of this study was to investiga
te the relationship between plasma and platelet levels of ascorbic aci
d (AA)/dehydroascorbic acid (DHA) and those of malonyldialdehyde (MDA)
, an indirect marker of lipoperoxides, both assayed using high-perform
ance liquid chromatography (HPLC), in 59 patients with insulin-depende
nt diabetes mellitus (IDDM) compared with 51 healthy control subjects
matched for sex, age, smoking habits, as well as for dietary intake of
energy, alcohol and vitamin C. Results Mean plasma and platelet MDA w
ere significantly higher in the patients affected with IDDM than in co
ntrol subjects. Moreover, the diabetic group was characterized by a hu
ge decrease in plasma AA [8.45 +/- 5.5 mu mol L-1 (SD) vs. 33.4 +/- 7.
6 mu mol L-1, P = 0.0001], mirrored by a significant increase in plasm
a DHA (11.9 +/- 3.9 mu mol L-1 vs. 3.9 +/- 2.5 mu mol L-1, P = 0.0001)
. No detectable DHA was observed in the platelets from both diabetic a
nd control subjects, whereas AA was significantly increased in platele
ts from diabetic patients compared with control subjects (42.6 +/- 7.4
vs. 34.8 +/- 5.1 nmol 10(-9) platelets, P = 0.0001). Platelet AA in t
he diabetic group was significantly inversely correlated with glycated
haemoglobin (r = -034; P = 0.04) and directly with plasma AA (r = 0.3
9; P = 0.02), the sum of plasma AA+ DHA (r = 0.44; P = 0.009) and with
platelet MDA (r = 0.38; P = 0.02). Conclusion (a) The ratio plasma AA
/DHA is significantly lowered in IDDM in association with an increase
in MDA levels; (b) only AA is detected in platelets, being augmented i
n the diabetic group; (c) plasma ascorbate depletion does not reflect
platelet levels of AA; and, finally, (d) metabolic control, as well as
intracellular lipoperoxides, modulates platelet AA in IDDM.