Literature DB >> 17183537

Collateralization of the tectonigral projection with other major output pathways of superior colliculus in the rat.

Véronique Coizet1, Paul G Overton, Peter Redgrave.   

Abstract

Dopaminergic (DA) neurons exhibit a short-latency, phasic response to unexpected, biologically salient stimuli. The superior colliculus (SC) is also sensitive to such stimuli and sends a projection directly to DA-containing regions of the ventral midbrain. Recent evidence suggests that the SC is a critical relay for transmitting short-latency <span class="Disease">visual information to DA neurons. An important question is whether the ventral midbrain is an exclusive target of tectonigral neurons, or whether the tectonigral projection is a collateral branch of other tectofugal pathways. Double-label retrograde anatomical tracing techniques were used to address this issue. Injections of either Diamidino Yellow or Fluorogold into substantia nigra pars compacta (SNc) were combined with larger injections of True Blue into one of the following efferent projections of the SC: 1) target regions of the ipsilateral ascending projection to the thalamus; 2) the crossed descending tecto-reticulo-spinal pathway; 3) target structures of the ipsilateral descending projection; and 4) the contralateral superior colliculus. Moderate numbers of double-labeled neurons were observed following combined injections into substantia nigra and individual nuclei in the thalamus (ventromedial nucleus, 21.3%; central lateral, 18.4%; parafasicular nucleus 6.0%). Much less double-labeling was associated with injections into either of the descending projections (crossed, 1.0-3.2%; uncrossed, 0.2-2.7%) or the contralateral SC (0.7-1.9%). These results suggest: i) the SC may provide a coordinated input concerning the occurrence of unpredicted sensory events to both the substantia nigra and striatum (via the thalamus); and ii) few gaze-related motor signals are simultaneously relayed to DA-containing regions of the ventral midbrain.

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Year:  2007        PMID: 17183537      PMCID: PMC3124759          DOI: 10.1002/cne.21202

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


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