Hippocampal hypoglycaemia-activated K+ channels: single-channel analysis of glucose and voltage dependence

Détails

ID Serval
serval:BIB_A7AD2E77705A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Hippocampal hypoglycaemia-activated K+ channels: single-channel analysis of glucose and voltage dependence
Périodique
Pflügers Archiv : European Journal of Physiology
Auteur⸱e⸱s
Tromba  C., Salvaggio  A., Racagni  G., Volterra  A.
ISSN
0031-6768 (Print)
Statut éditorial
Publié
Date de publication
11/1994
Volume
429
Numéro
1
Pages
58-63
Résumé
The effect of glucose on kinetics and the voltage-dependent characteristics of glucose-sensitive channels in hippocampal neurons were examined with the cell-attached mode of the patch-clamp technique. Recordings of a 100-pS K+ channel in the presence or absence of glucose demonstrate that the increase in channel open state probability (Po) induced by glucose deprivation (40- to 400-times the control in high-glucose medium) was largely due to a decrease in the global amount of time spent by the channel in a long-lived closed state. The Po value of the same 100-pS channel was also found to increase (by approx. 80-times) following a depolarization of 40 mV from rest, the main factor responsible for this being a dramatic shortening of the long closed-times on depolarization. Another glucose-sensitive channel of smaller conductance (approx. 10 pS) showed a similar dependence of Po on glucose, but different dependence on voltage, with long openings at the same hyperpolarized potentials where the 100-pS channel was almost always closed. Our results indicate that the action of glucose on the kinetics of hippocampal channels closely resembles that of ATP-sensitive channels in pancreatic beta-cells. Furthermore, they indicate that the two types of glucose-sensitive channels found in hippocampal neurons, differing not only in their single-channel conductance but also in the dependence on voltage, could play different roles in the responses of these cells to modified energetic supply.
Mots-clé
Animals Cells, Cultured Electrophysiology Glucose/*pharmacology Hippocampus/drug effects/*metabolism Hypoglycemia/*metabolism Islets of Langerhans/drug effects/metabolism Kinetics Membrane Potentials/drug effects/physiology Patch-Clamp Techniques Potassium Channels/drug effects/*metabolism Rats
Pubmed
Web of science
Création de la notice
24/01/2008 15:37
Dernière modification de la notice
20/08/2019 16:12
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