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3H-metaraminol releasing action of mescaline from rat hypothalamus in vitro

Om D. Gulati, Nandkumar S. Shah

European Journal of Pharmacology November 15, 1977 DOI: 10.1016/0014-2999(77)90249-7 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics In vitro experiment Peer reviewed
Population Rat isolated hypothalamus
Interventions Mescaline Cocaine Tetrodotoxin Lidocaine Tyramine
Dose 4 x 10(-4) M mescaline, 3 x 10(-5) M cocaine, 3 x 10(-7) M tetrodotoxin, 6 x 10(-5) M lidocaine, 3 x 10(-4) M tyramine, 6 x 10(-2) M KCl
Duration 50 min of efflux
Topics Mescaline
Key findings Mescaline releases 3H-metaraminol from rat hypothalamus via both calcium-independent (tyramine-like) and calcium-dependent (lidocaine-sensitive) mechanisms.

Abstract

The amine releasing action of mescaline was investigated in rat isolated hypothalamus labeled with 3H-metaraminol. Mescaline had no effect on the uptake of 3H-metaraminol but produced its release in a concentration-related manner. 4 x 10(-4) M mescaline, which produced submaximal effects was used for subsequent experiments. 3 x 10(-5) M cocaine had no effect on the 3H-metaraminol releasing action of mescaline. Mescaline was fully effective in Ca2+-free medium while 6 x 10(-2) M KCl was ineffective. 3 x 10(-7) M tetrodotoxin or 6 x 10(-5) M lidocaine partially blocked mescaline-induced release but substantially or completely blocked 3 x 10(-2) M KCl-induced release. Prior exposure of hypothalamus to 3 x 10(-4) M tyramine reduced the releasing action of mescaline. Thus, mescaline appears to release 3H-metaraminol both by Ca2+-independent (tyramine-like) and Ca2+-dependent (lidocaine-sensitive) mechanisms. 3 x 10(-4) M tyramine and 6 x 10(-2) M KCl released 14C from control hypothalamus labelled with 14C-mescaline, but not from reserpinized hypothalamus. The amounts of 14C recovered in 14C-mescaline labeled control and reserpinized hypothalamus at the end of 50 min of efflux were similar suggesting a poor retention of 14C-mescaline by storage particles.

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