Aj. Perales et al., EFFECTS OF MAGNESIUM-SULFATE ON THE NORADRENALINE-INDUCED CEREBRAL VASOCONSTRICTOR AND PRESSOR-RESPONSES IN THE GOAT, British journal of obstetrics and gynaecology, 104(8), 1997, pp. 898-903
Objective To examine the ability of magnesium sulphate to counteract t
he noradrenaline-induced cerebral vasoconstrictor and presser response
s in goats by using both in vivo and in vitro techniques. Design Cereb
ral blood flow was measured in vivo by means of an electromagnetic flo
w probe around the internal maxillary artery. Isometric tension was re
corded in vitro from rings of goat middle cerebral artery maintained i
n an organ bath. Results 1. In vivo. Continuous infusion of noradrenal
ine (10 mu g/min) directly into the cerebral arterial supply elicited
sustained decrease in cerebral blood flow (61% [SEM 3] of control valu
es) and increase in cerebral vascular resistance (178% [SEM 9] of cont
rol values). Magnesium sulphate, injected directly into the cerebral a
rterial supply (10-300 mg) or infused intravenously (0.3 g and 3 g dur
ing 15 min) at the noradrenaline-induced steady state, increased cereb
ral blood flow by decreasing cerebral vascular resistance in a dose-de
pendent manner. A similar result was obtained when intravenous magnesi
um sulphate (3 g/15 min) was tested against the cerebral vasoconstrict
or and presser responses induced by intravenous infusion of noradrenal
ine (30 mu g/min). 2. In vitro. When compared with the response obtain
ed in a control medium (1 mmol/L Mg2+), 10 mmol/L Mg2+ significantly i
nhibited the maximum contraction elicited by noradrenaline (10(-8) to
3 x 10(-3) mol/L) from 45% [SEM 4] to 26% [SEM 4]. Conclusions Magnesi
um sulphate reverses the noradrenaline-induced cerebral vasoconstricto
r and presser responses by a direct inhibitory action of Mg2+ on the a
ctions of noradrenaline in the cerebral and peripheral vascular beds,
which leads to a decrease in vascular resistance. These results could
explain, at least in part, the beneficial effects of magnesium sulphat
e in the management of preeclampsia and eclampsia.