John Libbey Eurotext

Magnesium Research


The influence of magnesium on morphine-induced stimulation of the reward system Volume 23, issue 1, March 2010


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Department of Pharmacology, University of Medicine and Pharmacy “Gr. T. Popa” Iasi, Romania

The present study was designed to assess the influence of magnesium (Mg) as MgCl 2 (10 or 40 mg/kg b.wt/day i.p.) and of its interaction with morphine on the reward system (RS) in Wistar rats. For this purpose, we evaluated conditioning place preference on a 12 day experiment schedule. Our data show that MgCl 2 (10 mg/kg b.wt/day) has moderate but significant effects on stimulating RS (increasing the time spent in associated conditioned compartment) (327.75 ± 11 s in the Mg (10 mg/kg b.wt) group vs 295.2 ± 8 s in the control (saline) group, p < 0.05) but not at higher Mg doses (40 mg/kg b.wt/day). We tested the influence of MgCl 2 (10 mg/kg b.wt./day i.p.) upon naloxone (2 mg/kg b.wt/ i.p.)-induced place aversion. Administrated alone, naloxone has an aversive effect on place preference. MgCl 2 (10 mg/kg b.wt/day i.p.) has a significantly decreased aversive effect of naloxone (280.7 ± 37 s in naloxone + MgCl 2 (10 mg/kg b.wt) group vs 189 ± 21 s in naloxone group, p < 0.05). MgCl 2 at both tested doses, added to morphine (3 mg/kg b.wt/day i.p), decreased the acquisition of morphine-induced place preference (262.2 ± 17 s) in morphine + MgCl 2 (40 mg/kg b.wt) group vs 462.15 ± 28 s in morphine group, p < 0.05). MgCl 2, 10 mg/kg b.wt/day i.p. decreased both morphine-induced place preference and naloxone-induced place aversion.