A Study on the Role of Protein Kinase C upon the Acetylcholine Release in the Rat Hippocampus.
- Author:
Jong Sung KIM
1
;
Sung Don KANG
;
Jong Moon KIM
;
Bong Kyu CHOI
Author Information
1. Department of Neurosurgery, Wonkwang University, School of Medicine, Iri, Korea.
- Publication Type:Original Article
- Keywords:
Acetylcholine;
4 beta-phorbol 12,13-dibutyrate;
Polymyxin B;
Protein kinase C;
Tetrodotoxin
- MeSH:
Acetylcholine*;
Adenosine;
Animals;
Hippocampus*;
Polymyxin B;
Polymyxins;
Protein Kinase C*;
Protein Kinases*;
Rats*;
Tetrodotoxin
- From:Journal of Korean Neurosurgical Society
1995;24(2):115-122
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
The effects and interactions of 4 beta-phorbol 12,13-dibutyrate(PDB) and polymyxin B(PMB) with adenosine on the electrically-evoked acetylcholine(ACh) release were studied in rat hippocampus. Slices from rat hippocampus were equilibrated with 3H-choline and the release of the labeled product, 3H-ACh, which was evoked by electrical stimulation(3Hz, 2ms, 5Vcm-1, rectangular pulses) was measured. PDB(0.3-10 micorM), a selective protein kinase C(PKC) activator, increased the evoked ACh release in a dose related fashion with an increase in the basal rate of release. The effects of 1(M PDB were significantly inhibited by 0.3 micorM tetrodotoxin(TTX) pretreatment or Ca++-free medium. PMB(0.03-1mg), a selective PKC inhibitor, decreased the ACh release in a dose dependent manner with an increase in the basal rate of release. Adenosine(1-10 micorM) decreased the ACh release without changing the basal rate or release, and this effect was significantly inhibited by 8-cyclopentyl-1,3-dipropylxanthine(2 micorM), a selective A1-receptor antagonist treatment. However, adenosine effects were not affected by PDB and PMB. These results indicate that the PKC play a role in the ACh release in the rat hippocampus but is not involved in the post-receptor mechanism of the A1-adenosine receptor.
