Striatum
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The striatum is a subcortical part of the telencephalon. It is a major part of the basal ganglia system : its input station.
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[edit] History
In the seventeenth and eighteenth centuries, the term "corpus striatum" was used to designate many distinct, deep, infracortical elements of the hemisphere (i.e. Vieussens, 1685). The Vogts (Cécile and Oskar, 1941) simplified the nomenclature by proposing the term striatum for all elements built with striatal elements (see Primate basal ganglia system): the caudate, the putamen and the fundus striati, that ventral part linking the two precedings together ventrally to the inferior part of the internal capsule.
The term neostriatum was forged by comparative anatomists comparing the subcortical structures between vertebrates.
[edit] Structure
The striatum forms a continuous and large mass, topographically separated by the internal capsule into the caudate nucleus medially, the putamen laterally and the fundus below, linking the two preceding ventrally; but a single entity. The striatum is homogeneous in term of neuronal components. It is built up of 4 neuronal types:[1]
- spiny neurons relatively close from the pyramidal neurons of the cortex due to the presence of spines with spine apparatus (acanthodendritic neurons), and make up 96% of the striatum.
- Leptodendritic (Deiter's) neurons(2%) with large, poorly bifurcated, arborisations looking like pallidonigral neurons.
- Spidery cholinergic interneurons(1%) morphologically entirely different from those observed in rodents (which must lead to very careful interspecific correlations).In primates they are the tonically Active Neurons (TANs). These briefly stop firing in concomitance to behaviourally salient situations and reward-related events.
- GABAergic parvalbumin expressing interneurons, which are fast-spiking, and express dopamine receptors
- GABAergic calretinin expressing interneurons
- GABAergic somatostatin expressing interneurons, which are low threshold spiking and express dopamine receptors
[edit] Organization
The striatum is spatially organized according to several levels.
[edit] Anatomical subdivisions and territories
The striatum is a single entity closed and continuous with a toric topology. The observable anatomical subdivisions (caudate, putamen, fundus) essentially induced by the internal capsule do not completely overlap with now accepted anatomo-functional subdivisions. The selective distribution of the axonal terminal arborisations of cortical sources differentiate the sensorimotor striatum, mainly putaminal but located in its dorsal part and in the lateroinferior part of the caudate. A great part of the remaining of the volume (essentially caudate) receiving from axonal endings from the frontal, parietal, temporal cortex forms the associative striatum. The separation between these two territories is rather clearcut and observable using calbindin immunochemistry. A third entity, the most inferomedial, raises more problems as there is no general agreement about its border with the associative striatum. The so-called limbic or ventral striatum is clearly delineated only by tracing the subicular territory. This corresponds to the so-called "accumbens nucleus" (meaning laying close to...the septum in this case, "accumbens septi"). This is not a nucleus and simply a striatal part made up of the same striatal elements. It forms thus the accumbens striatum. This is divided into two parts one ventromedian the shell and one dosolateral the core. They have a small topographical extent in primates.
[edit] "Compartments"
Immunochemical characteristics particularly acetyl cholinesterase differentiated "compartments" called 'striosomes' and matrix in which 'matrisomes'are sometimes differentiated.
[edit] Afferences
The most important afference in terms of quantity of axons is the corticostriatal connection. Almost all parts of the cortex, except for the primary visual and auditory cortex participate in the connection that counts hundreds of thousand axons. The cortical pyramidal neurons projecting to the striatum are located in the lamina V. They end mainly on the spines of the spiny neurons. They are (glutamatergic), exciting striatal neurons. Another well known afference is the nigrostriatal connection arising from the neurons of the pars compacta. While cortical axons synapse mainly on spine heads of spiny neurons, nigral axons synapse mainly on spine shafts. The thalamostriatal afference essentially comes in primates from the central region (centre median parafascicular complex see primate basal ganglia system).This is glutamatergic. The participation of truly intralaminar neurons is much more limited. The striatum receives afferences from other elements of the basal ganglia such as the subthalamic nucleus (glutamatergic) or the lateral pallidum (GABAergic).
[edit] Targets
The main efferent target of the striatum is the pallidonigral set.The basal ganglia core is made up of the striatum and its direct targets through the striato-pallidonigral bundle. The striato-pallidonigral bundle is a very dense bundle of fewly myelinated axons giving the whitish aspect to the set. This comprises successively the lateral pallidum (GPe), the medial pallidum (GPi), the pars lateralis of the substantia nigra (SNl)and the pars reticulat (SNr).This set is made up of the same genus of neurons. Its neurons are inhibited by GABAergic synapses from the striatum. Among these targets, one does not send axons outside the system (the lateral pallidum, thus a regulator). Another sends axons to the superior colliculus (pars lateralis of the nigra). Two others are the bases of basal ganglia system output to the thalamus forming two separate channels: one through the medial pallidum to VO and from there to the cortical SMA and another through the nigra reticulata to VA and from there to the frontal and the oculomotor cortex .
[edit] Function
Metabotropic dopamine receptors are present both on spiny neurons and on cortical axon terminals. Second messenger cascades triggered by activation of these dopamine receptors can modulate pre- and postsynaptic function, both in the short term and in the long term. The striatum is best known for its role in the planning and modulation of movement pathways but is also involved in a variety of other cognitive processes involving executive function. In humans the striatum is activated by stimuli associated with reward, but also by aversive, novel, unexpected or intense stimuli, and cues associated with such events. Recent fMRI evidence[citation needed] suggests that the common property linking these stimuli, to which the striatum is reacting, is saliency under the conditions of presentation. A number of other brain areas and circuits are also related to reward such as frontal areas.
[edit] Pathology
Parkinson's disease results in loss of dopaminergic innervation to the striatum (and other basal ganglia) and to the cascade of subsequent consequences. The lesion of the striatum is also involved in the Huntington disease, choreas, choreoathetosis and dyskinesias. It is also thought that addiction involves plasticity at striatal synapses.
[edit] References
- Aosaki T, Kiuchi K & Kawaguchi Y (1998) Dopamine D1-like receptor activation excites rat striatal large aspiny neurons in vitro. J Neurosci 15, 5180–90
- Apicella P (2002) Tonically active neurons in the primate striatum and their role in the processing of information about motivationally relevant events. Eur J Neurosci 16, 2017–26
- Cossette, M., Lecomte, F. and Partent, A. (2005) Morphology and distribution of dopaminergic intrinsic to human striatum. J. Chem. Neuroanat. 29: 1-11
- Holt DJ, Graybiel AM & Saper CB (1997) Neurochemical architecture of the human striatum. J Comp Neurol 21, 1–25
- Morris G, Arkadir D, Nevet A, Vaadia E & Bergman H (2004) Coincident but distinct messages of midbrain dopamine and striatal tonically active neurons. Neuron 8, 133–43
- Tepper JM & Bolam JP (2004) Functional diversity and specificity of neostriatal interneurons. Curr Opin Neurobiol 14, 685–92
- Yamada H, Matsumoto N & Kimura M (2004) Tonically active neurons in the primate caudate nucleus and putamen differentially encode instructed motivational outcomes of action. J Neurosci 7, 3500–10
- Yelnik, J., François, C., Percheron, G., Tandé, D. (1991) Morphological taxonomy of the neurons of the primate striatum. J. Comp. Neurol. 313:273-294
- Zink, CF, Pagnoni G, Martin-Skurski ME, Chappelow JC, & Berns GS (2004). Human striatal responses to monetary reward depend on saliency. Neuron 42, 509-17
