Calcium channel involvement in magnetic field inhibition of morphine-induced analgesia

Naunyn Schmiedebergs Arch Pharmacol. 1987 Sep;336(3):308-15. doi: 10.1007/BF00172683.

Abstract

An exposure for 60 min to a weak 0.5 Hz rotating magnetic field significantly reduced the day-time analgesic effects of morphine in male mice. The dihydropyridine (DHP) calcium channel antagonists diltiazem and nifedipine and the non-DHP antagonist verapamil, as well as the inorganic calcium channel blockers, La3+ and Co2+, differentially reduced, while the DHP calcium channel agonist, BAY K 8644, enhanced the inhibitory effects of the magnetic stimuli. In a similar manner, though to a lesser degree, the calcium channel antagonists and agonist, increased and decreased, respectively, the inhibitory effects of intracerebroventricular administrations of Ca2+ on morphine-induced analgesia. The calcium channel antagonists and agonists had no significant effects on naloxone-mediated reductions of morphine-induced analgesia. These results suggest that exposure to magnetic stimuli affects the functioning of calcium channels and the distribution of calcium ions, thereby, altering the effects of opiates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium Channel Agonists / pharmacology
  • Calcium Channel Blockers / pharmacology
  • Ion Channels / physiology*
  • Magnetics*
  • Mice
  • Morphine / pharmacology*
  • Pain / physiopathology*

Substances

  • Calcium Channel Agonists
  • Calcium Channel Blockers
  • Ion Channels
  • Morphine
  • Calcium