E. Bello et al., Impairment of renal vasodilation with L-arginine is related to more severedisease in untreated hypertensive patients, HYPERTENSIO, 38(4), 2001, pp. 907-912
Citations number
35
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Data remain insufficient to place the decreased response to L-arginine in h
ypertensive patients within a consistent pathophysiological sequence. The a
im of the present study in patients with essential hypertension was to asse
ss the relationships between the response to L-arginine and a set of releva
nt clinical and laboratory parameters. In this prospective, interventional
study, we administered L-arginine to untreated hypertensive individuals and
healthy control subjects and measured the clearance of inulin and of para-
aminohippurate and a set of biochemical and clinical variables. L-Arginine
infusion revealed major differences between control subjects and 1 subgroup
(group B) of hypertensive individuals. Group B hypertensives (n = 18) had
no increase in inulin clearance and no decrease in renal vascular resistanc
e with L-arginine; however, in another subset of hypertensive patients (gro
up A, n = 27), the insulin clearance increased and renal vascular resistanc
e decreased similar to the control group (group C, n = 11). The ambulatory
blood pressure monitoring in group B showed both an increased mean diastoli
c pressure and a "nondipper" pattern in the nocturnal regulation of arteria
l pressure. These findings in group B were accompanied by significant alter
ations in optic fundus and left ventricle hypertrophy and increased microal
buminuria (all, P<0.05). Furthermore, group B individuals had significantly
lower values of HDL cholesterol and a higher baseline atherogenic index, p
lasma insulin level, and glucose/insulin index. We disclose a previously un
described relationship between end organ repercussion and decreased renal h
emodynamic response to L-arginine. Our results may help to understand the m
echanisms that lead to target organ damage in hypertension.