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Pavinee
Vilaipun1, Piyarat Govitrapong1,
Banthit Chetsawang1, Naiphinich
Kotchabhakdi and M.Ebadi2
1Neuro-Behavioral
Biology Center, Institute of Science and
Technology for Research and Development,
Mahidol University, Salaya Campus,
Nakornpathom 73170, Thailand; 2Department
of Pharmacology, Physiology and
Therapeutics, University of North Dakota,
School of Medicine and Health Science, USA
Key words:
dopamine transporter, serotonin,
norepinephrine, pineal gland
The
mammalian pineal glands contain several
neurotransmitters and receptors for amino
acids, biogenic amines, and peptides. Some
of these, such as dopamine and D1 and D2
dopamine receptors, have been identified and
characterized in bovine pineal gland. This
leads us to hypothesize that this organ
possesses a high-affinity dopamine
transporter mechanism for dopamine
substrate. This study is an attempt to
investigate the existence of dopamine
transporter in the bovine pineal gland. The
radio-ligand used was [3H] GBR 12935 and the
drug to define non-specific binding was GBR
12909. The association rate of [3H] GBR
12935 binding to pineal gland membranes was
examined as a function of time. The binding
reached equilibrium within 60 min of
incubation at 25oC. Drugs that block the
uptake of dopamine (GBR 12909, GBR 12395)
were effectively in displacing [3H] GBR
12935 from bovine gland whereas drugs that
block the uptake of serotonin (gluoxetine,
fluvoxamine), norepinephrine (desipramine)
and mixed reuptake inhibitor affecting
serotonin and norepinephrine (imipramine,
amitriptyline) were ineffective. The
specific binding to bovine pineal membrane
was higher than in rat striatum. The result
of this study indicates that dopamine
transporters are present in the bovine
pineal gland.
Acknowledgement:
This study was
supported by National Institute of
Neurological Disorders and Stroke, USA, 1RO1
NS-40160-1 grant.
(Presented
at the 3rd
International Congress of the Asian Sleep
Research Society on the New Millennium of
Sleep Research in Asia, December 3-7, 2000,
Bangkok, Thailand, and published in the
Program and Abstracts page A174.) |