The action of several ligands on the low- (LVA,T) and high-threshold (HVA,L and N) Ca channels of adult rat sensory neurons and human neuroblastoma IMR32 cells has been investigated. In both cell types, 40 microM Cd2+ and 6.4 microM /omega-Conotoxin (omega-CgTx) selectively blocked the HVA channels, sparing the majority of LVA channels that were antagonized by amiloride and Ni2+. In 50% of the cells, however, /omega-CgTx spared also a 15% of HVA channels that proved to be sensitive to BAY K 8644. The agonistic action of BAY K 8644 on [omega-CgTx-resistant HVA channels caused a large Ba current increase, prolonged current deactivation and acceleration of HVA channels inactivation that was particularly evident in adult rat DRG.

Action of Ca2+ agonists/antagonists in mammalian peripheral neurons / E. Carbone, F. Clementi, A. Formenti, A. Pollo, E. Sher. - In: CELL BIOLOGY INTERNATIONAL REPORTS. - ISSN 0309-1651. - 13:12(1989 Dec), pp. 1155-1164.

Action of Ca2+ agonists/antagonists in mammalian peripheral neurons

A. Formenti;
1989

Abstract

The action of several ligands on the low- (LVA,T) and high-threshold (HVA,L and N) Ca channels of adult rat sensory neurons and human neuroblastoma IMR32 cells has been investigated. In both cell types, 40 microM Cd2+ and 6.4 microM /omega-Conotoxin (omega-CgTx) selectively blocked the HVA channels, sparing the majority of LVA channels that were antagonized by amiloride and Ni2+. In 50% of the cells, however, /omega-CgTx spared also a 15% of HVA channels that proved to be sensitive to BAY K 8644. The agonistic action of BAY K 8644 on [omega-CgTx-resistant HVA channels caused a large Ba current increase, prolonged current deactivation and acceleration of HVA channels inactivation that was particularly evident in adult rat DRG.
Peripheral Nerves; Calcium Channels; Animals; Tumor Cells, Cultured; Membrane Potentials; Calcium Channel Blockers; Neurons, Afferent; Neuroblastoma
Settore BIO/09 - Fisiologia
dic-1989
http://journals.ohiolink.edu/ejc/article.cgi?issn=03091651&issue=v13i0012&article=1155_aocaimpn
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/212530
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