Effect of des-tyrosine-gamma-endorphin on neocortical spike-and-wave spindling in DBA/2J mice.
A Capasso, L Sorrentino, A Di Giannuario, S Pieretti, A Loizzo
Index: Eur. J. Pharmacol. 261(1-2) , 209-12, (1994)
Full Text: HTML
Abstract
The effect of a beta-endorphin cleavage product devoid of opioid effects, des-tyrosine-gamma-endorphin (DT gamma E) on the neocortical spike-and-wave spindling episodes in the electrocorticogram (ECoG) of DBA/2J mice was studied. DT gamma E (0.01-1.0 mg/kg, i.p.) dose dependently reduced the spike-and-wave bursts duration. However, the low dose did not induce consistent modifications of the spike-and-wave bursts number while the dose of 0.1 and 1.0 mg/kg induced a progressive diminution. Furthermore, at all doses DT gamma E did not induce any alterations of the spike-and-wave bursts amplitude, frequency, and desynchronized activity when compared to the pre-drug period. These results indicate that this beta-endorphin fragment may affect brain excitability.
Related Compounds
Related Articles:
1985-01-01
[Immunogenetics 22(4) , 309-14, (1985)]
1993-01-01
[Gen. Pharmacol. 24(1) , 83-8, (1993)]
1983-12-01
[Psychiatry Res. 10(4) , 243-52, (1983)]
1994-02-01
[J. Pharmacol. Exp. Ther. 268(2) , 1040-50, (1994)]
1988-09-01
[Br. J. Psychiatry 153 , 354-8, (1988)]