Abstract |
Non- NMDA receptor antagonists CNQX, DNQX, and NBQX (10-40 mg/kg IP) were tested against pentylenetetrazol-induced (100 mg/kg SC) seizures in 7 to 90-day-old rats. All three drugs significantly decreased the incidence of tonic hindlimb component of tonic-clonic pentylenetetrazol seizures, often in favor of increased incidence of forelimb tonus throughout development. In addition, in 7 to 25-day-old rats, DNQX and NBQX decreased the severity of seizures due to a decrease in total incidence of the tonic component of tonic-clonic seizures compared to age-matched controls. However, neither drug was able to consistently suppress the incidence or increase latency to onset of clonic and tonic-clonic pentylenetetrazol seizures. The data suggest that, during development, non- NMDA receptor transmission may play a role in the generation of the tonic component, but not in the generation of other components of pentylenetetrazol-induced seizures.
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Authors | L Velísek, H Kubová, P Mares, D Vachová |
Journal | Pharmacology, biochemistry, and behavior
(Pharmacol Biochem Behav)
Vol. 51
Issue 1
Pg. 153-8
(May 1995)
ISSN: 0091-3057 [Print] United States |
PMID | 7617727
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anticonvulsants
- Quinoxalines
- Receptors, AMPA
- Receptors, Kainic Acid
- 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
- FG 9041
- 6-Cyano-7-nitroquinoxaline-2,3-dione
- Pentylenetetrazole
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Topics |
- 6-Cyano-7-nitroquinoxaline-2,3-dione
(pharmacology)
- Aging
(physiology)
- Animals
- Anticonvulsants
(pharmacology)
- Behavior, Animal
(drug effects)
- Epilepsy, Tonic-Clonic
(chemically induced, prevention & control)
- Hindlimb
(drug effects, physiology)
- Male
- Muscle Tonus
(drug effects)
- Pentylenetetrazole
- Quinoxalines
(pharmacology)
- Rats
- Rats, Wistar
- Receptors, AMPA
(antagonists & inhibitors)
- Receptors, Kainic Acid
(antagonists & inhibitors)
- Seizures
(chemically induced, prevention & control)
- Synaptic Transmission
(drug effects)
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