Effects of cholecystokinin octapeptide on neuronal activities in the rat nucleus tractus solitarius.
- Author:
Hyewhon RHIM
1
;
Chan Woong PARK
Author Information
1. Biomedical Research Center, Korea Institute of Science and Technology, 39-1 Hawholgok-dong, Sungbuk-gu, Seoul, South Korea.
- Publication Type:Original Article
- MeSH:
Action Potentials;
Animals;
Anxiety;
Brain;
Brain Stem;
Central Nervous System;
Cholecystokinin*;
Feeding Behavior;
Fires;
Membranes;
Neurons*;
Nociception;
Rats*;
Receptors, Cholecystokinin;
Reflex;
Sincalide*;
Solitary Nucleus*
- From:The Korean Journal of Physiology and Pharmacology
2000;4(4):275-281
- CountryRepublic of Korea
- Language:English
-
Abstract:
Cholecystokinin (CCK) is a gastrointestinal hormone which plays an important role in satiety and gastric motility. It is also widely distributed throughout the central nervous system, where it appears to be involved in the central control of anxiety, feeding behavior and nociception. Two distinct CCK receptor types, CCKA and CCKB, have been found in the brain. Both CCK receptors coexist in the rat nucleus tractus solitarius (NTS), which is the primary center for the coordination of peripheral and central activities related to gastrointestinal, cardiovascular and respiratory functions. In order to study ionic actions of CCK on each type of receptor, we investigated the effects of CCK-8S on neurons located in the NTS of the rat using whole-cell patch-clamp recordings in brainstem slices. Application of CCK-8S, under current clamp, produced a membrane depolarization accompanied by action potential firing. This CCK-evoked excitation was dose-dependent (10 nM ~ 10 micrometer) and observed in more than 60% of NTS neurons. Under voltage clamp conditions, CCK-8S induced an inward current with a notably increased spontaneous excitatory synaptic activity. However, CCK-8S did not significantly change the amplitude of pharmacologically isolated and evoked EPSP(C)s. Using selective CCKA and CCKB receptor antagonists, we observed two different effects of CCK-8S, which suggest CCKA receptor-mediated inhibitory and CCKB receptor-mediated excitatory effects in the NTS. These results may help to explain the ability of CCK to modulate gastrointestinal and other reflex systems in the NTS.
