Magnesium and other bivalent cations influence upon sodium montelukast effect in experimental-induced thermoalgesia

Magnes Res. 2008 Mar;21(1):38-42.

Abstract

We tested the influence of magnesium, zinc and copper upon the montelukast (MK, antagonist of cysteinyl leukotriene receptor type 1) effect in experimentally-induced thermoalgesia. We worked on 5 groups of 10 adults, each Wistar rats, that received: group I-control; group II: MK (10 mg/kg) unique administration; group III: MgCl2 (1 mM/kg/day) i.p., 3 days and MK (10 mg/kg) unique administration on the 3rd day; group IV: ZnCl2, (0.1 mM/kg/day), i.p., 3 days and MK (10 mg/kg) unique administration on the 3rd day; group V: copper acetate (0.05 mM/kg/day), i.p., 3 days and MK (10 mg/kg) unique administration on the 3rd day. We determined the thermoalgesic sensitivity (TS) using a tail flick analgesia meter, initially, 3 days after daily cation administration and 3 hours after MK administration. Our data show that MK has a statistically significant reduction of TS vs control group (3.76 +/- 1.04 s vs 1.81 +/- 0.98 s, p < 0.05). Copper and magnesium administration do not significantly change the MK effect to decrease TS. The co-administration of zinc and MK statistically significantly increased the TS of the group that received only MK (2.51 +/- 0.21 s vs 3.76 +/- 1.04 s, p < 0.05). Animals that received only cations (in the above mentioned doses) did not significantly change TS.

MeSH terms

  • Acetates / administration & dosage
  • Acetates / pharmacology*
  • Animals
  • Cations / administration & dosage
  • Cations / blood
  • Cations / pharmacology*
  • Copper / administration & dosage
  • Copper / blood
  • Copper / pharmacology
  • Cyclopropanes
  • Hot Temperature
  • Hyperalgesia / physiopathology
  • Hyperalgesia / prevention & control*
  • Injections, Intraperitoneal
  • Leukotriene Antagonists / administration & dosage
  • Leukotriene Antagonists / pharmacology
  • Magnesium / administration & dosage
  • Magnesium / blood
  • Magnesium / pharmacology*
  • Male
  • Quinolines / administration & dosage
  • Quinolines / pharmacology*
  • Rats
  • Rats, Wistar
  • Sulfides
  • Zinc / administration & dosage
  • Zinc / blood
  • Zinc / pharmacology

Substances

  • Acetates
  • Cations
  • Cyclopropanes
  • Leukotriene Antagonists
  • Quinolines
  • Sulfides
  • Copper
  • Magnesium
  • Zinc
  • montelukast