2011
DOI: 10.1007/s00429-011-0317-x
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Glutamatergic and cholinergic pedunculopontine neurons innervate the thalamic parafascicular nucleus in rats: changes following experimental parkinsonism

Abstract: The tegmental pedunculopontine nucleus (PPN) is a basal ganglia-related structure that has recently gained renewed interest as a potential surgical target for the treatment of several aspects of Parkinson's disease. However, the underlying anatomical substrates sustaining the choice of the PPN nucleus as a surgical candidate remain poorly understood. Here, we characterized the chemical phenotypes of different subtypes of PPN efferent neurons innervating the rat parafascicular (PF) nucleus. Emphasis was placed … Show more

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Cited by 21 publications
(17 citation statements)
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“…Although our data show no Egr-1 expression in cholinergic neurons, suggesting that they may not be affected in this animal model, we cannot rule out the existence of false negatives. The difference in the expression between the ascending and descending pathways may reflect a selective excitatory drive of STN-projecting neurons and a potential increased inhibition of GiN-projecting neurons (not detectable by the basal level of IEGs expression), in agreement with the data from other groups proposing an increased excitation (Breit et al 2001; Orieux et al 2000; Barroso-Chinea et al 2011) or an increased inhibition (Nandi et al 2002) in the Parkinsonian PPN. In this way, an imbalanced output between the two motor pathways may underlie the gait disturbances associated with PD.…”
Section: Discussionsupporting
confidence: 87%
“…Although our data show no Egr-1 expression in cholinergic neurons, suggesting that they may not be affected in this animal model, we cannot rule out the existence of false negatives. The difference in the expression between the ascending and descending pathways may reflect a selective excitatory drive of STN-projecting neurons and a potential increased inhibition of GiN-projecting neurons (not detectable by the basal level of IEGs expression), in agreement with the data from other groups proposing an increased excitation (Breit et al 2001; Orieux et al 2000; Barroso-Chinea et al 2011) or an increased inhibition (Nandi et al 2002) in the Parkinsonian PPN. In this way, an imbalanced output between the two motor pathways may underlie the gait disturbances associated with PD.…”
Section: Discussionsupporting
confidence: 87%
“…The CM/Pf complex also receives significant afferents from various subcortical sources, including the superior colliculus (Grunwerg et al, 1992; Redgrave et al, 2010), the pedunculopontine tegmental nucleus (Pare et al, 1988; Parent et al, 1988; Barroso-Chinea et al, 2011), the cerebellum (Royce et al, 1991; Ichinohe et al, 2000), the raphe nuclei, the locus coeruleus (Lavoie and Parent, 1991; Royce et al, 1991; Vertes et al, 2010), and from the mesencephalic, pontine and medullary reticular formation (Comans and Snow, 1981; Steriade and Glenn, 1982; Hallanger et al, 1987; Cornwall and Phillipson, 1988; Vertes and Martin, 1988; Royce et al, 1991; Newman and Ginsberg, 1994). …”
Section: Afferent Connections Of Center Median/parafascicular (Cm/pf)mentioning
confidence: 99%
“…Electrical stimulation of the PPTg induces a burst firing of dopaminergic neurons (Lokwan et al, 1999; Floresco et al, 2003), and induces the release of dopamine in the striatum (Chapman et al, 1997; Forster and Blaha, 2003; Miller and Blaha, 2004). The PPTg also controls activity of the striatum through its bilateral projection to the caudal intralaminar nuclei (Erro et al, 1999; Barroso-Chinea et al, 2011). …”
Section: Pptg As a Part Of Basal Gangliamentioning
confidence: 99%