Keywords
striatum, substantia nigra, Parkinson disease, Huntington disease, ventral tegmental area
Chapter Outline
The Basal Ganglia Include Five Major Nuclei, 124
Basal Ganglia Circuitry Involves Multiple Parallel Loops That Modulate Cortical Output, 125
Interconnections of the Basal Ganglia Determine the Pattern of Their Outputs, 127
The Cerebral Cortex, Substantia Nigra, and Thalamus Project to the Striatum, 127
The Internal Segment of the Globus Pallidus and the Reticular Part of the Substantia Nigra Provide the Output From the Basal Ganglia, 127
The Subthalamic Nucleus Is Part of an Indirect Pathway Through the Basal Ganglia, 127
Perforating Branches From the Circle of Willis Supply the Basal Ganglia, 127
Many Basal Ganglia Disorders Result in Abnormalities of Movement, 128
Historically, the basal ganglia have been considered as major components of the motor system. In fact, they have a much broader role than that and are probably involved to some extent in most forebrain functions. However, their relationship to movement is their best understood aspect, and that is what shows up clinically in disorders like Parkinson disease and Huntington disease. The interrelationships of the basal ganglia and motor areas of the cerebral cortex are emphasized in this chapter, but you should keep in mind that the basal ganglia have extensive connections, similar in principle and parallel in detail, with most other areas of the cerebral cortex.
The Basal Ganglia Include Five Major Nuclei
The striatum and globus pallidus are the major forebrain components of the basal ganglia.
The substantia nigra and subthalamic nucleus are interconnected with the striatum and globus pallidus.
The terms strio – and – striate are used to refer to fibers coming from or going to the striatum; for example, corticostriate fibers start in the cerebral cortex and end in the caudate nucleus or putamen. Similarly, the terms pallido – and – pallidal , nigro – and – nigral , and subthalamo – and – subthalamic are used to refer to fibers coming from or going to the globus pallidus, the substantia nigra, or the subthalamic nucleus.
The caudate nucleus parallels the lateral ventricle, having an enlarged head in the wall of the anterior horn, a smaller body adjacent to the body of the ventricle, and a still smaller tail adjacent to the inferior horn.
The caudate nucleus and putamen merge with each other anteriorly at the base of the septum pellucidum; the area of fusion is nucleus accumbens , recognized as a third division of the striatum.
The lenticular nucleus (putamen + globus pallidus) underlies the insula and is shaped like a wedge cut from a sphere. The globus pallidus is the more medial, tapering part of the wedge, extending toward the interventricular foramen and thalamus; it has two parts with distinctive connections, an external segment ( GPe ) adjacent to the putamen and an internal segment ( GPi ) closer to the thalamus.
The substantia nigra is mostly located in the rostral midbrain, between the cerebral peduncle and the red nucleus; part of it extends rostrally just into the diencephalon. The substantia nigra is another two-part structure. The compact part ( SNc ), closer to the red nucleus, contains the pigmented, dopaminergic neurons for which the substantia nigra was named; the reticular part ( SNr ), adjacent to the cerebral peduncle, is in effect a displaced piece of GPi.
The subthalamic nucleus, as its name implies, is located inferior to the thalamus, just above the most rostral part of the substantia nigra.
Basal Ganglia Circuitry Involves Multiple Parallel Loops That Modulate Cortical Output
Afferents from the cortex reach the striatum and subthalamic nucleus; efferents leave from the globus pallidus and substantia nigra.
The striatum is, in a sense, the major input part of the basal ganglia, collecting excitatory (glutamate) inputs from large cortical areas (different areas for different parts of the striatum). GPi and SNr are the principal output structures, sending inhibitory (gamma-aminobutyric acid [GABA]) projections to the thalamus, which in turn projects back to a restricted portion of this large cortical area ( Fig. 19.3 ). Because thalamocortical projections are excitatory, the globus pallidus is in a position to suppress or facilitate cortical activity by way of varying patterns of inhibition in the thalamus; the balance of excitatory and inhibitory connections interposed between the striatum and GPi/SNr helps determine the pattern. For example, inhibiting an inhibitory GPi neuron could have the same net effect on the thalamus as increasing excitatory inputs to the same part of the thalamus ( Fig. 19.4 ).