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Melanostatin (NPY) inhibited electrical activity in frog melanotrophs through modulation of K+, Na+ and Ca2+ currents
J A Valentijn1, H Vaudry, W Kloas
1European Institute for Peptide Research, Laboratory of Molecular Endocrinology, CNRS URA 650, UA INSERM, University of Rouen, Mont-Saint-Aignan, France.
Abstract:
1. Melanostatin, a thirty-six amino acid peptide recently isolated from the frog brain due to its ability to inhibit alpha-melanocyte-stimulating hormone (alpha-MSH) release, is the amphibian counterpart of mammalian neuropeptide Y (NPY). The effect of synthetic melanostatin on the bioelectrical activity of cultured frog melanotrophs was studied in 124 cells by using the whole-cell patch-clamp technique. 2. In current-clamp experiments, melanostatin (1 microM) provoked a reversible hyperpolarization and a suppression of spontaneous action potentials. In some cells the hyperpolarizing response was absent, but an arrest of spike firing still occurred. 3. Melanostatin-induced hyperpolarization was associated with a decrease in membrane resistance. In voltage-clamp experiments, melanostatin induced an outward current at a constant command potential. This hyperpolarizing outward current appeared to be carried by potassium ions. 4. Cell dialysis with the non-hydrolysable GTP analogue guanosine-5'-O-(3-thiotriphosphate) (GTP gamma S) sustained the outward current produced by melanostatin. Dopamine (1 microM), which generates a similar hyperpolarizing outward current in frog melanotrophs, was not capable of increasing the current provoked by melanostatin and sustained by GTP gamma S. 5. Melanostatin also modulated voltage-operated currents. The amplitude of voltage-activated potassium current was increased by 30%. 6. Melanostatin reduced the fast sodium current. This inhibitory effect was rather persistent compared to the other modulated currents. 7. Melanostatin markedly scaled down high voltage-activated N- and L-like calcium currents. The activation kinetics of these two calcium currents were not altered by the peptide. 8. Pretreatment of melanotrophs with pertussis toxin (1 microgram ml-1) blocked melanostatin-induced inhibition of N- and L-like calcium currents. 9. It is concluded that the NPY-related peptide melanostatin generates a very complex pattern of electrical responses in frog melanotrophs, including hyperpolarization and modulation of voltage-activated currents underlying action potentials. G proteins appear to mediate at least part of these effects.
Insights
Melanostatin, a frog peptide, alters electrical activity in melanotrophs by causing hyperpolarization and modulating ion currents. These effects, mediated by G proteins, impact action potentials and hormone release.
Area of Science:
- Neuroendocrinology
- Cellular electrophysiology
Background:
- Melanostatin is an amphibian peptide homologous to mammalian neuropeptide Y (NPY).
- It inhibits alpha-melanocyte-stimulating hormone (alpha-MSH) release from frog melanotrophs.
Purpose of the Study:
- To investigate the effects of synthetic melanostatin on the bioelectrical activity of cultured frog melanotrophs.
- To elucidate the ion channels and signaling pathways involved in melanostatin's action.
Main Methods:
- Whole-cell patch-clamp technique on cultured frog melanotrophs.
- Current-clamp and voltage-clamp recordings.
- Application of synthetic melanostatin, guanosine-5'-O-(3-thiotriphosphate) (GTP gamma S), dopamine, and pertussis toxin.
Main Results:
- Melanostatin induced reversible hyperpolarization and suppressed spontaneous action potentials.
- A G protein-mediated outward potassium current was observed.
- Melanostatin increased voltage-activated potassium currents and decreased fast sodium currents.
- It reduced high voltage-activated N- and L-like calcium currents, an effect blocked by pertussis toxin.
Conclusions:
- Melanostatin exerts complex electrical effects on frog melanotrophs, including hyperpolarization and modulation of voltage-gated currents.
- G proteins mediate at least part of melanostatin's signaling pathway.
- These actions likely contribute to the regulation of alpha-MSH release.