Electrophysiological characteristic of ATP-activated currents of trigeminal ganglion neurons with different diameter in rat.
- Author:
Yu-Qin ZHANG
1
;
Jia-Lie LUO
;
Hui NIE
;
Fan ZHU
;
Zhi-Wang LI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Cells, Cultured; Membrane Potentials; Neurons; physiology; Patch-Clamp Techniques; Rats; Rats, Sprague-Dawley; Receptors, Purinergic P2; metabolism; Trigeminal Ganglion; physiology
- From: Chinese Journal of Applied Physiology 2007;23(3):319-323
- CountryChina
- Language:Chinese
-
Abstract:
AIMTo explore the characteristic of ATP-activated current in trigeminal ganglion (TG) neurons of rat.
METHODSWhole-cell patch-clamp was performed.
RESULTS(1) The majority (92.1%) of TG neurons responded to ATP applied externally with inward currents. We recorded three distinct ATP-activated currents: fast, slow and intermediate, which were concentration-dependent. (2) In general, the fast ATP-activated currents were distributed mainly in small-diameter TG neurons, the slow ATP-activated currents were distributed mainly in large-diameter TG neurons, and the intermediate ATP-activated currents were distributed mainly in intermediate-diameter TG neurons. (3) The time course of rising phase from 10% to 90% of the three distinct ATP-activated currents were as follows: fast: (33.6 +/- 4.5) ms; intermediate: (62.2 +/- 9.9) ms; slow: (302.1 +/- 62.0) ms, and that of desensitizing phase were (399.4 +/- 58.2) ms (fast), and > 500 ms (slow) respectively. (4) From the current-voltage relationship curves, it can be seen that the reversal potential values of the three distinct ATP-activated currents were the same, all being 0-5mV. And they all were characterized by inward rectification. (5) The dose-response curve for fast ATP-activated current shifted downwards as compared with the intermediate ATP-activated current, and that for the slow ATP-activated current shifted upwards.
CONCLUSIONThe EC50s of the three curves tended to be identical. The results suggested that three kinds of distinct ATP-activated currents could be mediated by various subtypes of P2X receptors assembled by different subunits, and the subtypes existed in TG neurons of different diameters and transmit different information.