Background. The authors thought it interesting to examine the interrelation
ship between nitric oxide and diabetes mellitus by the determination of the
nitrite plasma levels, stable end-products of nitric oxide, in various cli
nical patterns of diabetes mellitus,
Methods, Our series consisted of 161 female subjects (mean age 54+/-7 years
, disease duration 5+/-3 months) subdivided into: a) 13 patients suffering
from insulin-dependent diabetes (IDDM) without clinical and instrumental si
gns of micro- and macroangiopathy; b) 148 suffering from non insulin-depend
ent diabetes mellitus (NIDDM) of whom: 1) 52 without vascular complications
(28 normal weight, BMI <25, and 24 obese, BMI >30); 2) 40 with clinical an
d instrumental signs of non hypertensive coronary heart disease (CHD); 3) 2
5 with CHD and hypertension (arterial blood pressure over 160/95 mmHg); 4)
31 with hypercholesterolemia (values over 250 mg/dl), All patients were exa
mined in good glycometabolic conditions reached by oral hypoglycemiant (12
cases) or insulin (149 cases) treatment, As normal control 37 female subjec
ts (mean age 48+/-7) without internistic diseases were considered For each
sample we determined the plasma levels of nitrites by the Gutman and Hollyw
ood method,
Results. Almost similar nitrite plasma levels in IDDM (17+/-0.5 mumol/L) an
d normal controls (17+/-0.2 mumol/L) were found; in non complicated non obe
se NIDDM a not significantly elevated value (21+/-0.8 mumol/L) as compared
with the IDDM and control group was found; the obese NIDDM patients showed
a value (18+/-0.4 munol/L) not significantly different in comparison with t
he non obese NIDDM group, In the NIDDM group with non hypertensive CHD) the
nitrite value was almost similar (20+/-0.5 mumol/L) to the corresponding g
roup without vascular complications, In the patients with CHD and hypertens
ion the nitrite level was superimposable (20+/-0.7 mumol/L) on the one reco
rded in NIDDM patients without vascular complications and in those with CHD
without hypertension, In NIDDM patients with hypercholesterolemia the mean
nitrite value was sharply elevated (24+/-0.8 mumol/L); the difference betw
een this group and those of non hypercholesterolemic, non obese, obese and
CHD (with or without hypertension) patients was significant (p<0.05).
Conclusions. It is conceivable that diabetes mellitus per se causes a tende
ntial not significant increase of NO production in comparison with normal c
ontrols; some factors such as blood pressure, overweight, disease duration,
therapeutic treatment and coronary complications appear not to influence N
O production, In hypercholesterolemic diabetic patients the nitrite enhance
d level in plasma might mean a compensatory response to a continuous inacti
vation of NO involved in a protective competition towards damaging factors
and chiefly against oxidised LDL.