The Journal of Neuroscience, December 15, 1998, 18(24):10680-10687
Psychostimulant-Induced Fos Protein Expression in the Thalamic
Paraventricular Nucleus
Ariel Y.
Deutch,
Michael
Bubser, and
Cheryl D.
Young
Departments of Psychiatry and Pharmacology, and Center for
Molecular Neuroscience, Vanderbilt University School of Medicine,
Nashville, Tennessee 37212
Lesions of glutamatergic afferents to the nucleus accumbens have
been reported to block psychostimulant-induced behavioral sensitization. However, thalamic glutamatergic projections to the
nucleus accumbens have received little attention in the context of
psychostimulant actions. We examined the effects of acute amphetamine and cocaine administration on expression of Fos protein in the thalamic
paraventricular nucleus (PVT), which provides glutamatergic inputs to
the nucleus accumbens and also receives dopaminergic afferents.
Immunoblot and immunohistochemical studies revealed that both
psychostimulants dose-dependently increased PVT Fos expression. PVT
neurons retrogradely labeled from the nucleus accumbens were among the
PVT cells that showed a Fos response to amphetamine. D2
family dopamine agonists, including low doses of the
D3-preferring agonist 7-OH-DPAT, increased the
numbers of Fos-like-immunoreactive neurons in the PVT. Conversely, the effects of cocaine and amphetamine on PVT Fos expression were blocked
by pretreatment with the dopamine D2/3 antagonist
raclopride. Because PVT neurons express D3 but not other
dopamine receptor transcripts, it appears that psychostimulants induce
Fos in PVT neurons through a D3 dopamine receptor. We
suggest that the PVT may be an important part of an extended circuit
subserving both the arousing properties and reinforcing aspects of psychostimulants.
Key words:
amphetamine; cocaine; dopamine; D3 dopamine receptor; Fos; nucleus accumbens; thalamic paraventricular nucleus
Copyright © 1998 Society for Neuroscience 0270-6474/98/182410680-08$05.00/0