We performed this study to investigate whether α- and β-adrenergic agonists are able to regulate intracellular free magnesium concentrations [Mg2+]i in platelets from healthy and obese individuals. Twenty-six informed consent men (14 healthy and 12 obese) were enrolled in the study. We measured fasting plasma glucose, insulin, epinephrine and norepinephrine. Platelet [Mg2+]i at the baseline and after stimulation with clonidine or isoproterenol was measured by fluorescent probe mag-fura-2. In platelets from healthy subjects, α-adrenergic stimulation by clonidine led to a dose dependent decrease in [Mg2+]i (basal: 245 ± 39 μM: clonidine 5 pg/mL: 109 ± 27 μM, p < 0.05; clonidine 10 pg/mL: 77 ± 26 μM, p < 0.01). while no significant change in platelet [Mg2+]i was detected in obese men. Furthermore, the co-incubation with clonidine (10 pg/mL) and yohimbine (50-100 pg/mL) completely abated the effect of clonidine on [Mg2+]i in platelets from healthy individuals. Analysis of the time course for platelet magnesium showed that the intracellular magnesium loss induced by clonidine (10 pg/mL) was time-dependent. Conversely, the β-adrenergic agonist isoproterenol was able to produce a significant rise in [Mg2+]i, in platelets from healthy individuals (basal: 234 ± 40 μM: isoproterenol 2.5 pg/mL: 594 ± 44 μM, p < 0.05; isoproterenol 5 pg/mL: 681 ± 56 μM, p < 0.01), while no such finding was detectable in platelets from obese patients. When platelets from healthy subjects were co-stimulated with isoproterenol (5 pg/mL) and propranolol (10-20 pg/mL), the ionophoric effect of the β-adrenergic agonist was completely reverted. The time course of isoproterenol (5 pg/mL) effect on platelet [Mg2+]i showed that the ionophoric effect of isoproterenol was time-dependent. In conclusion, (1) the stimulation of α-adrenergic receptor by clonidine is able to induce a significant dose- and time-dependent fall in platelet [Mg2+]i; (2) the stimulation of β-adrenoceptors by isoproterenol lead to a signifcant time- and dose-dependent rise in platelet (Mg2+]i; (3) the ionic effect of α- and β-adrenergic stimulation is not detectable in obese subjects, in whom is probably present a reduced sensitivity to the ionic effect of adrenergic agonists.
Effects of α- And β-adrenergic stimulation on free magnesium concentrations in platelets from healthy and obese individuals
Corsonello, A.;
2001-01-01
Abstract
We performed this study to investigate whether α- and β-adrenergic agonists are able to regulate intracellular free magnesium concentrations [Mg2+]i in platelets from healthy and obese individuals. Twenty-six informed consent men (14 healthy and 12 obese) were enrolled in the study. We measured fasting plasma glucose, insulin, epinephrine and norepinephrine. Platelet [Mg2+]i at the baseline and after stimulation with clonidine or isoproterenol was measured by fluorescent probe mag-fura-2. In platelets from healthy subjects, α-adrenergic stimulation by clonidine led to a dose dependent decrease in [Mg2+]i (basal: 245 ± 39 μM: clonidine 5 pg/mL: 109 ± 27 μM, p < 0.05; clonidine 10 pg/mL: 77 ± 26 μM, p < 0.01). while no significant change in platelet [Mg2+]i was detected in obese men. Furthermore, the co-incubation with clonidine (10 pg/mL) and yohimbine (50-100 pg/mL) completely abated the effect of clonidine on [Mg2+]i in platelets from healthy individuals. Analysis of the time course for platelet magnesium showed that the intracellular magnesium loss induced by clonidine (10 pg/mL) was time-dependent. Conversely, the β-adrenergic agonist isoproterenol was able to produce a significant rise in [Mg2+]i, in platelets from healthy individuals (basal: 234 ± 40 μM: isoproterenol 2.5 pg/mL: 594 ± 44 μM, p < 0.05; isoproterenol 5 pg/mL: 681 ± 56 μM, p < 0.01), while no such finding was detectable in platelets from obese patients. When platelets from healthy subjects were co-stimulated with isoproterenol (5 pg/mL) and propranolol (10-20 pg/mL), the ionophoric effect of the β-adrenergic agonist was completely reverted. The time course of isoproterenol (5 pg/mL) effect on platelet [Mg2+]i showed that the ionophoric effect of isoproterenol was time-dependent. In conclusion, (1) the stimulation of α-adrenergic receptor by clonidine is able to induce a significant dose- and time-dependent fall in platelet [Mg2+]i; (2) the stimulation of β-adrenoceptors by isoproterenol lead to a signifcant time- and dose-dependent rise in platelet (Mg2+]i; (3) the ionic effect of α- and β-adrenergic stimulation is not detectable in obese subjects, in whom is probably present a reduced sensitivity to the ionic effect of adrenergic agonists.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
