Expressional Change of Endothelial Nitric Oxide Synthase in Rat Cerebral Cortex after Kainic Acid-Induced Seizure.
- Author:
In Seop KIM
1
;
Young Buhm HUH
;
Chan PARK
;
Min Jeong KANG
;
Jae Ryong LEE
;
Jung Hye KIM
;
Jin Hwa YOO
;
Hee Kyung AHN
Author Information
1. Department of Anatomy, College of Medicine, Kyung Hee University, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Seizure;
Cerebral cortex;
eNOS;
VIP;
NPY;
Expression
- MeSH:
Animals;
Astrocytes;
Auditory Cortex;
Blood Vessels;
Brain;
Cerebral Cortex*;
Dilatation;
Kainic Acid;
Microvessels;
Motor Cortex;
Neurons;
Neuropeptide Y;
Nitric Oxide;
Nitric Oxide Synthase;
Nitric Oxide Synthase Type III*;
Rabeprazole;
Rats*;
RNA, Messenger;
Seizures*;
Somatosensory Cortex;
Synaptic Transmission;
Vasoactive Intestinal Peptide;
Visual Cortex
- From:Korean Journal of Anatomy
2000;33(4):471-478
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Administration of kainic acid (KA) results in induction of epileptiform activity and motor seizures. Nitric oxide (NO) mediates the increase in cerebral blood flow during seizure activity. However, the production site of NO has not been clearly defined. Recent studies showed that constitutive nitric oxide synthase may be induced under certain conditions. Therefore, this study was aimed to investigate the change in endothelial nitric oxide synthase (eNOS), neuropeptide Y (NPY) and vasoactive intestinal polypeptide (VIP) since these are involved in cerebral blood flow. Rats were treated with KA and killed at 6 hours, 1, 3, 6 and 12 days after seizure. Expressional changes were assessed by immunohisto-chemistry and RT-PCR. eNOS was detected in the blood vessels of the cerebral cortex of the control group, but was not detected in neurons. eNOS-positive neurons were induced in the cerebral cortex at 1 and 3 days after seizure and found in specific cortical areas, such as primary motor cortex, secondary motor cortex, primary somatosensory cortex, secondary somatosensory cortex, insular cortex, ectorhinal cortex, parietal association cortex, temporal association cortex, auditory cortex and visual cortex. The levels of eNOS mRNA increased at 1 and 3 days after seizure compared to controls. The staining intensity of eNOS-positive microvessels was elevated in samples obtained 1, 3, and 6 days after seizure compared to the control group. However, NPY- and VIP-positive neurons, and glial fibrillary acidic protein-positive astrocytes were not induced in the cerebral cortex after seizure. Therefore, specific neuroactive substances may be induced in the cerebral cortex after seizure. Nitric oxide, a free radical synthesized in the brain by NOS, is a messenger molecule that mediates vascular dilatation and neural transmission. Therefore, neurons showing induced eNOS-positivity and upregulated eNOS-positive microvessels may affect the cerebral blood flow and neuronal activity in the cerebral cortex after seizure.
