1. Whole-cell currents were recorded from cultures of dissociated neocortical neurones of the rat. Rat alpha-calcitonin gene-related peptide (CGRP; 1 nM-1 microM) caused significant dose-dependent decreases in the voltage-activated transient (A-current) and delayed rectifier K+ currents. Forskolin (10 nM-20 microM) mimicked this effect. Peak K+ currents were gradually decreased after loading neurones with cyclic AMP (100 microM) through patch pipettes. CGRP was ineffective in neurones loaded with cyclic AMP. 2. CGRP (0.5-2 microM) increased cytosolic cyclic AMP concentration and this effect was mimicked by forskolin (5-40 microM). 3. CGRP (0.1-1 microM) reduced high-threshold Ca2+ currents; as did forskolin (5-20 microM) and cyclic AMP loaded into the neurones. In contrast, low-threshold Ca2+ currents were not affected by any of these agents. 4. Voltage-activated Na+ currents were significantly reduced by both CGRP (0.1-1 microM) and forskolin (5-20 microM). A similar effect was observed when cells were loaded with cyclic AMP. 5. We conclude that, in neocortical neurones, CGRP attenuates voltage-activated currents by stimulating the intracellular cyclic AMP signalling system.

Zona, C., Farini, D., Palma, E., Eusebi, F. (1991). Modulation of voltage-activated channels by calcitonin gene-related peptide in cultured rat neurones. THE JOURNAL OF PHYSIOLOGY, 433, 631-643.

Modulation of voltage-activated channels by calcitonin gene-related peptide in cultured rat neurones

ZONA, CRISTINA;FARINI, DONATELLA;
1991-02-01

Abstract

1. Whole-cell currents were recorded from cultures of dissociated neocortical neurones of the rat. Rat alpha-calcitonin gene-related peptide (CGRP; 1 nM-1 microM) caused significant dose-dependent decreases in the voltage-activated transient (A-current) and delayed rectifier K+ currents. Forskolin (10 nM-20 microM) mimicked this effect. Peak K+ currents were gradually decreased after loading neurones with cyclic AMP (100 microM) through patch pipettes. CGRP was ineffective in neurones loaded with cyclic AMP. 2. CGRP (0.5-2 microM) increased cytosolic cyclic AMP concentration and this effect was mimicked by forskolin (5-40 microM). 3. CGRP (0.1-1 microM) reduced high-threshold Ca2+ currents; as did forskolin (5-20 microM) and cyclic AMP loaded into the neurones. In contrast, low-threshold Ca2+ currents were not affected by any of these agents. 4. Voltage-activated Na+ currents were significantly reduced by both CGRP (0.1-1 microM) and forskolin (5-20 microM). A similar effect was observed when cells were loaded with cyclic AMP. 5. We conclude that, in neocortical neurones, CGRP attenuates voltage-activated currents by stimulating the intracellular cyclic AMP signalling system.
feb-1991
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore BIO/09 - FISIOLOGIA
English
Con Impact Factor ISI
Animals; Second Messenger Systems; Calcium; Cyclic AMP; Ion Channels; Potassium; Electrophysiology; Sodium; Calcitonin Gene-Related Peptide; Cerebral Cortex; Rats; Cells, Cultured; Neurons; Cytosol; Forskolin
Zona, C., Farini, D., Palma, E., Eusebi, F. (1991). Modulation of voltage-activated channels by calcitonin gene-related peptide in cultured rat neurones. THE JOURNAL OF PHYSIOLOGY, 433, 631-643.
Zona, C; Farini, D; Palma, E; Eusebi, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/65237
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