Immunocytochemical study on the distribution of NOS-immunoreactive neurons in the cerebral cortex of aged rats.
- Author:
Yoon Hee CHUNG
1
;
Chung Min SHIN
;
Wang Jae LEE
;
Douk Ho HWANG
;
Byung Lan LEE
;
Sa Sun CHO
;
Sang Ho BAIK
;
Choong Ik CHA
Author Information
1. Department of Anatomy, Seoul National University, College of Medicine, Korea.
- Publication Type:Original Article
- Keywords:
Nitric oxide (NO);
Nitric oxide synthase (NOS);
aged rat;
cerebral cortex;
immunocytochemistry
- MeSH:
Aging;
Alzheimer Disease;
Animals;
Brain;
Cerebral Cortex*;
Dendrites;
Dentate Gyrus;
Entorhinal Cortex;
Forelimb;
Gyrus Cinguli;
Hindlimb;
Hippocampus;
Immunohistochemistry;
In Situ Hybridization;
Learning;
Long-Term Potentiation;
Memory;
Neurodegenerative Diseases;
Neurons*;
Neurotransmitter Agents;
Nitric Oxide;
Plastics;
Rabeprazole;
Rats*;
Telescopes
- From:Korean Journal of Anatomy
1999;32(4):437-449
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Nitric oxide (NO) involvement has been demonstrated in mechanisms of synaptic plasticity, particularly in hippocampal long-term potentiation, a mechanism that underlies certain forms of learning and memory. Further, NO has been shown to regulate various neurotransmitters which play an important role in learning and memory. Several findings suggest that NO production may be decreased in the aged rat. Changes in the nNOS-containing neurons with aging were demonstrated by immunocytochemistry and in situ hybridization. NOS-immunoreactive cells in aged rats were present in all cortical areas and the hippocampus, and the pattern of distribution was similar to that of the control group. The number of NOS-immunoreactive cells in the cerebral cortex was significantly decreased in the aged rats, but the extent of changes was variable in each area, and ranged from mild decrease (<30%) to severe decrease (>50%). Severely decreased areas were the cingulate cortex, parietal cortex area 1, temporal cortex area 1, 2, 3, medial part of occipital cortex area 2, monocular and binocular part of occipital cortex area 1, entorhinal cortex, hippocampus proper, dentate gyrus and subiculum. Moderately decreased areas (30~50%) were frontal cortex area 1, 2, 3, parietal cortex area 2, forelimb, hindlimb, lateral part of occipital cortex area 2. Slightly decreased area was insular cortex. Morphologically, the number of dendritic branches seemed to be decreased in aged group and the length of dendrites of NOS-IR neurons showed a tendency to shorten. These results indicate the involvement of neuronal system containing NOS in the aging brain, and provide the first morphological evidence for the loss of NOS neurons in the cerebral cortex of the aged rats by immunocytochemistry. Further multidisciplinary investigations involving normal aging and neurodegenerative disease such as Alzheimer's disease are needed to clarify the importance of nitric oxide changes in the cerebral cortex with aging.
