Chemical anatomy of pallidal afferents in primates

• Published in: Brain Structure and Function Vol. 221; no. 9; pp. 4291 - 4317
• Main Authors: Eid, Lara, Parent, Martin
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01-12-2016; Springer Nature B.V
• Subjects: Acetylcholine - metabolism; Afferent Pathways - chemistry; Afferent Pathways - cytology; Animals; Biomedical and Life Sciences; Biomedicine; Cell Biology; Cholinergic Neurons - chemistry; Cholinergic Neurons - cytology; Dopamine; Dopamine - metabolism; Dopaminergic Neurons - chemistry; Dopaminergic Neurons - cytology; Globus Pallidus - chemistry; Globus Pallidus - cytology; Globus Pallidus - ultrastructure; Humans; Macaca fascicularis; Macaca nemestrina; Mice; Neurology; Neurons; Neurons - chemistry; Neurons - cytology; Neurons - ultrastructure; Neurosciences; Primates; Rats; Review; Saimiri; Serotonergic Neurons - chemistry; Serotonergic Neurons - cytology; Serotonin; Serotonin - metabolism; Synapses - ultrastructure; Globus pallidus; Basal ganglia; Acetylcholine; Dopamine; Serotonin; Monkey
• ISSN: 1863-2653; 1863-2661; 0340-2061
• DOI: 10.1007/s00429-016-1216-y

Neurons of the globus pallidus receive massive inputs from the striatum and the subthalamic nucleus, but their activity, as well as those of their striatal and subthalamic inputs, are modulated by brainstem afferents. These include serotonin (5-HT) projections from the dorsal raphe nucleus, cholinergic (ACh) inputs from the pedunculopontine tegmental nucleus, and dopamine (DA) afferents from the substantia nigra pars compacta. This review summarizes our recent findings on the distribution, quantitative and ultrastructural aspects of pallidal 5-HT, ACh and DA innervations. These results have led to the elaboration of a new model of the pallidal neuron based on a precise knowledge of the hierarchy and chemical features of the various synaptic inputs. The dense 5-HT, ACh and DA innervations disclosed in the associative and limbic pallidal territories suggest that these brainstem inputs contribute principally to the planification of motor behaviors and the regulation of attention and mood. Although 5-HT, ACh and DA inputs were found to modulate pallidal neurons and their afferents mainly through asynaptic (volume) transmission, genuine synaptic contacts occur between these chemospecific axon varicosities and pallidal dendrites, revealing that these brainstem projections have a direct access to pallidal neurons, in addition to their indirect input through the striatum and subthalamic nucleus. Altogether, these findings reveal that the brainstem 5-HT, ACh and DA pallidal afferents act in concert with the more robust GABAergic inhibitory striatopallidal and glutamatergic excitatory subthalamopallidal inputs. We hypothesize that a fragile equilibrium between forebrain and brainstem pallidal afferents plays a key role in the functional organization of the primate basal ganglia, in both health and disease.