Korean J Anat.  2006 Apr;39(2):91-102.

Screening of Low Molecular Metabolite, FS390 as an Inhibitor of Neurotransmitter Release from PC12 Cells

Affiliations
  • 1Department of Biology, College of Natural Science, Chonbuk National University, Jeonju 561-756, Korea.
  • 2Department of Anatomy, College of Medicine, Wonkwang University, Iksan 570-749, Korea.
  • 3Department of Infection Biology, College of Medicine, Wonkwang University, Iksan 570-749, Korea. yusikmj@gmail.com

Abstract

We established an in vitro experimental system using the following procedure. We first introduced tritium-labeled norepinephrine ([3H]-NE) into PC12 cells. The [3H]-NE incorporated-PC12 cells were stimulated by a high concentration (60 mM) of K+ buffer during 12 minutes. Then, we collected 100 microliter supernatant and counted the amount of [3H]-NE release from PC12 cells with a scintillation counter. After screening fungal, Streptomyces spp. or bacterial product using this experimental sytem, we obtained FS390 from Streptomyces spp. which inhibited [3H]-NE release from PC12 cells. FS390 also inhibits the release of ATP as a neurotransmitter of PC12 cells and rat cortical neurons. The inhibitory effect was seen even when the PC12 cells were treated with low K+ buffer containing ionomycin (1 micrometer) as an ionopore. This result suggests that the inhibitory action of FS390 on neurotransmitter release appeared after the influx of Ca2+.

Keyword

PC12 cells; Neurotransmitter release; Exocytosis; Streptomyces spp.; Inhibitor

MeSH Terms

Adenosine Triphosphate
Animals
Exocytosis
Ionomycin
Mass Screening*
Neurons
Neurotransmitter Agents*
Norepinephrine
PC12 Cells*
Rats
Scintillation Counting
Streptomyces
Adenosine Triphosphate
Ionomycin
Neurotransmitter Agents
Norepinephrine
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