Blockade of the Subthalamo-nigral Pathway Prevents the Motor Component of Pilocarpine Induced Generalized Convulsive Seizure in Rats.
- Author:
Jae Young CHOI
1
;
Hye Sik KIM
;
Yeong In KIM
;
Seong Min PARK
;
Kwang Soo LEE
;
Beum Saeng KIM
Author Information
1. Department of Neurology, Catholic University Medical College.
- Publication Type:Original Article
- Keywords:
Subthalamus;
Substantia nigra;
Seizure;
Muscimol;
MK-801;
Pilocarpine Manuscript received October 13
- MeSH:
Animals;
Butyric Acid;
Cell Count;
D-Aspartic Acid;
Dizocilpine Maleate;
Epilepsy;
GABA Agonists;
Injections, Intraperitoneal;
Muscimol;
Pilocarpine*;
Rats*;
Rats, Sprague-Dawley;
Seizures*;
Status Epilepticus;
Substantia Nigra;
Subthalamic Nucleus;
Subthalamus
- From:Journal of the Korean Neurological Association
2000;18(2):192-198
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: The substantia nigra pars reticulata is a critical site for the control of epileptic seizures. The potentiation of the inhibitory gamma-amino butyric acid (GABA) ergic input from the striatum to the substantia nigra pars reticulata suppresses primary or secondary generalized seizures in rats. Recent data suggests that the projection from the subthala-mus to the substantia nigra pars reticulata plays a critical role in the control of some forms of epileptic seizures. METHODS: We examined the possible involvement of the excitatory glutamatergic input from the subthalamic nucleus (STN) to the substantia nigra in pilocarpine-induced seizures by the direct injection of GABA receptor agonist (muscimol) and n-methyl- D-aspartate (NMDA) receptor antagonist (MK-801) into the substantia nigra pars reticularis (SNr) and the subthalamic nucleus respectively. Sprague-Dawley rats were classified into four groups depending on the pretreatment; the injection of saline (STN sham) or muscimol (STN) into the subthalamic nucleus, and the injection of saline (SNr sham) or MK-801 (SNr) into the substantia nigra. Seizure was induced by the intraperitoneal injection of pilocarpine (400 mg/kg). RESULTS: Mean seizure stages in the STN group (1.5 +/-0.5) and SNr group (1.3 +/-0.5) were significantly lower than STN sham group (4.8 +/-0.4) and SNr sham group (4.8 +/-0.4) (P <0.05). Electroencephlograms showed typical status epilepticus patterns in the sham operation group but only discrete ictal discharges with slowing and intermittent ictal spikes were shown in both STN and SNr group. Viable cell numbers in the CA1 and CA3 in STN and SNr groups were significantly higher than those of the sham group (P <0.05). CONCLUSIONS: These results provide evidence for the role of subthalamo-nigral projections in the modulation of pilocarpine-induced seizures.
