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

Naunyn-Schmiedeberg s Archives of PharmacologyPublished 1 September 1987
Martin Kavaliers, Klaus‐Peter Ossenkopp
Citations71
SJR quartileQ2
SJR score0.77
SNIP0.86

TL;DR

It is suggested that exposure to magnetic stimuli affects the functioning of calcium channels and the distribution of calcium ions, thereby, altering the effects of opiates.

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.

Keywords

NeuroscienceBiochemistry, Genetics and Molecular Biology