TY - JOUR
T1 - Effects of Picrotoxin Treatment on GABAA Receptor Supramolecular Complexes in Rat Brain
AU - Ito, Yoshihisa
AU - Lim, Dong Koo
AU - Nabeshima, Toshitaka
AU - Ho, Ing K.
PY - 1989/4
Y1 - 1989/4
N2 - Abstract The effects of acute and chronic administration of a subconvulsive dose of picrotoxin on t‐[35S]butylbieyclophosphorothionate ([35S]TBPS), [3H]muscimol, and [3H]flunitrazepam binding characteristics in various regions and on the convulsant potency of picrotoxin in Sprague‐Dawley rats were examined. Acute administration of a sub‐convulsive dose of picrotoxin (3 mg/kg, i. p.) significantly increased [35S]TBPS and [3H]muscimol binding in cerebellum (CB) with no change in frontal cortex (FC). In rats treated chronically with picrotoxin (3 mg/kg, i.p., daily for 10 days), the Bmax of [35S]TBPS binding site was significantly decreased in the FC., striatum (ST), and CB with no change in KD values. Neither [3H]muscimol binding in the FC and CB nor [3H]fiunitrazepam binding in the FC was affected in these rats. In addition, the potency of pentobarbital to inhibit [35S]TBPS binding in vitro was not altered following acute or chronic treatment of picrotoxin. Chronic administration of picrotoxin did not affect convulsive ED50 or LD50 of picrotoxin; however, it delayed the onset of convulsions and increased the time to death. These results suggest that treatment with picrotoxin at a subconvulsive dose for 10 days causes down‐regulation of [35S]TBPS binding sites and that this down‐regulation might be related, at least in part, to the decreased extent of convulsant potency of picrotoxin. In addition, the results indicate possible interaction between convulsant binding sites and GABAA receptor sites in the CB following picrotoxin treatment.
AB - Abstract The effects of acute and chronic administration of a subconvulsive dose of picrotoxin on t‐[35S]butylbieyclophosphorothionate ([35S]TBPS), [3H]muscimol, and [3H]flunitrazepam binding characteristics in various regions and on the convulsant potency of picrotoxin in Sprague‐Dawley rats were examined. Acute administration of a sub‐convulsive dose of picrotoxin (3 mg/kg, i. p.) significantly increased [35S]TBPS and [3H]muscimol binding in cerebellum (CB) with no change in frontal cortex (FC). In rats treated chronically with picrotoxin (3 mg/kg, i.p., daily for 10 days), the Bmax of [35S]TBPS binding site was significantly decreased in the FC., striatum (ST), and CB with no change in KD values. Neither [3H]muscimol binding in the FC and CB nor [3H]fiunitrazepam binding in the FC was affected in these rats. In addition, the potency of pentobarbital to inhibit [35S]TBPS binding in vitro was not altered following acute or chronic treatment of picrotoxin. Chronic administration of picrotoxin did not affect convulsive ED50 or LD50 of picrotoxin; however, it delayed the onset of convulsions and increased the time to death. These results suggest that treatment with picrotoxin at a subconvulsive dose for 10 days causes down‐regulation of [35S]TBPS binding sites and that this down‐regulation might be related, at least in part, to the decreased extent of convulsant potency of picrotoxin. In addition, the results indicate possible interaction between convulsant binding sites and GABAA receptor sites in the CB following picrotoxin treatment.
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U2 - 10.1111/j.1471-4159.1989.tb01848.x
DO - 10.1111/j.1471-4159.1989.tb01848.x
M3 - Article
C2 - 2538560
AN - SCOPUS:0024594211
SN - 0022-3042
VL - 52
SP - 1064
EP - 1070
JO - Journal of neurochemistry
JF - Journal of neurochemistry
IS - 4
ER -