V. Coiro et al., DOPAMINERGIC AND CHOLINERGIC CONTROL OF ARGININE-VASOPRESSIN SECRETION IN TYPE-I DIABETIC MEN, European journal of clinical investigation, 25(6), 1995, pp. 412-417
Citations number
24
Categorie Soggetti
Medicine, Research & Experimental","Medicine, General & Internal
Enhanced cholinergic and dopaminergic controls of anterior pituitary f
unction have been described in insulin-dependent diabetes mellitus (ID
DM). In order to verify whether similar neurotransmitter alterations a
lso affect the regulation of posterior pituitary hormone secretion, th
e arginine-vasopressin (AVP) responses to the dopaminergic agonist apo
morphine and in a different occasion to physostigmine, an acetylcholin
esterase inhibitor, were evaluated in normal (n=10) and type I diabeti
cs (n=16). In addition, a control test with normal saline was performe
d in all subjects. None of the diabetic patients were affected by neur
opathy or other diabetic complications. They were divided into two gro
ups according to the duration of their disease (less than 10 years: gr
oup 1, n = 8; more than 10 years: group 2, n=8). Physostigmine (12.5 m
u g kg(-1)) was infused intravenously over 10 min; apomorphine (60 mu
g kg(-1)) was injected subcutaneously. Basal AVP concentrations were s
imilar in all groups and remained constant during the control test. In
contrast, both drugs induced significant increments in plasma AVP lev
els in the normal controls and diabetic subjects. However, physostigmi
ne- and apomorphine-induced AVP increments were twofold higher in diab
etics than in control subjects. No significant differences were observ
ed between diabetics of groups 1 and 2. No significant correlations be
tween duration of diabetes and peak AVP responses to physostigmine or
apomorphine were found within each group or when all diabetic subjects
were considered together. These data indicate enhancement of both dop
aminergic and cholinergic stimulatory regulations of AVP secretion in
patients with uncomplicated IDDM, regardless of the duration of diabet
es.