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Serotonergic treatment normalizes midbrain dopaminergic neuron increase after periaqueductal gray stimulation
Journal article   Open access   Peer reviewed

Serotonergic treatment normalizes midbrain dopaminergic neuron increase after periaqueductal gray stimulation

S.Z.K. Tan, Y. Temel, A.Y. Chan, A.T.C. Mok, J.A.U. Perucho, A. Blokland, L. Aquili, W.L. Lim and L.W. Lim
Brain Structure and Function, Vol.225, pp.1957-1966
2020
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CC BY-NC-ND V4.0 Open Access

Abstract

Electrical stimulation of the dorsolateral periaqueductal gray (dlPAG) in rats has been shown to elicit panic-like behaviour and can be a useful as an unconditioned stimulus for modelling anticipatory fear and agoraphobia in a contextual fear conditioning paradigm. In this study, we further analysed our previous data on the effects of escitalopram (a selective serotonin reuptake inhibitor, SSRI) and buspirone (a 5-HT1A receptor partial agonist) on dlPAG-induced anticipatory fear behaviour in a rat model using freezing as a measure. We then attempted to unravel some of the interactions with dopamine signalling using tyrosine hydroxylase (TH) immunohistochemistry to probe the effects on dopaminergic neurons. We showed that acute treatment of escitalopram, but not buspirone, was effective in reducing anticipatory freezing behaviour, while chronic administrations of both drugs were effective. We found that the dlPAG stimulation induced increase number of dopaminergic neurons in the ventral tegmental area (VTA) which was reversed in both chronic buspirone and escitalopram groups. We further found a strong positive correlation between the number of dopaminergic neurons and freezing in the VTA and showed positive correlations between dopaminergic neurons in the VTA and substantia nigra pars compacta (SNpc) in escitalopram and buspirone groups, respectively. Overall, we showed that chronic treatment with an SSRI and a 5-HT1A agonist reduced anticipatory freezing behaviour which seems to be associated, through correlative studies, with a reversal of dlPAG stimulation induced increase in number of dopaminergic neurons in the VTA and/or SNpc.

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.5 Neuroscience
1.5.338 Serotonin Receptors
Web Of Science research areas
Anatomy & Morphology
Neurosciences
ESI research areas
Neuroscience & Behavior
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