Evolution of the basal ganglia: new perspectives through a comparative approach

The basal ganglia (BG) have received much attention during the last 3 decades mainly because of their clinical relevance. Our understanding of their structure, organisation and function in terms of chemoarchitecture, compartmentalisation, connections and receptor localisation has increased equally. Most of the research has been focused on the mammalian BG, but a considerable number of studies have been carried out in nonmammalian vertebrates, in particular reptiles and birds. The BG of the latter 2 classes of vertebrates, which together with mammals constitute the amniotic vertebrates, have been thoroughly studied by means of tract‐tracing and immunohistochemical techniques. The terminology used for amniotic BG structures has frequently been adopted to indicate putative corresponding structures in the brain of anamniotes, i.e. amphibians and fishes, but data for such a comparison were, until recently, almost totally lacking. It has been proposed several times that the occurrence of well developed BG structures probably constitutes a landmark in the anamniote‐amniote transition. However, our recent studies of connections, chemoarchitecture and development of the basal forebrain of amphibians have revealed that tetrapod vertebrates share a common pattern of BG organisation. This pattern includes the existence of dorsal and ventral striatopallidal systems, reciprocal connections between the striatopallidal complex and the diencephalic and mesencephalic basal plate (striatonigral and nigrostriatal projections), and descending pathways from the striatopallidal system to the midbrain tectum and reticular formation. The connectional similarities are paralleled by similarities in the distribution of chemical markers of striatal and pallidal structures such as dopamine, substance P and enkephalin, as well as by similarities in development and expression of homeobox genes. On the other hand, a major evolutionary trend is the progressive involvement of the cortex in the processing of the thalamic sensory information relayed to the BG of tetrapods. By using the comparative approach, new insights have been gained with respect to certain features of the BG of vertebrates in general, such as the segmental organisation of the midbrain dopaminergic cell groups, the occurrence of large numbers of dopaminergic cell bodies within the telencephalon itself and the variability in, among others, connectivity and chemoarchitecture. However, the intriguing question whether the basal forebrain organisation of nontetrapods differs essentially from that observed in tetrapods still needs to be answered.

[1]  R. Faull,et al.  The cells of origin of nigrotectal, nigrothalamic and nigrostriatal projections in the rat , 1978, Neuroscience.

[2]  D. Reis,et al.  Light‐microscopic immunocytochemical localization of tyrosine hydroxylase in prenatal rat brain. I. Early ontogeny , 1981, The Journal of comparative neurology.

[3]  D. Reis,et al.  Light‐microscopic immunocytochemical localization of tyrosine hydroxylase in prenatal rat brain. II. Late ontogeny , 1981, The Journal of comparative neurology.

[4]  S. Haber,et al.  The distribution of enkephalin immunoreactive fibers and terminals in the monkey central nervous system: An immunohistochemical study , 1982, Neuroscience.

[5]  I. Goodman,et al.  Dopaminergic nature of feeding-induced behavioral stereotypies in stressed pigeons , 1983, Pharmacology Biochemistry and Behavior.

[6]  André Parent,et al.  Comparative neurobiology of the basal ganglia , 1986 .

[7]  P. Greengard,et al.  DARPP-32, a dopamine- and adenosine 3':5'-monophosphate-regulated phosphoprotein: regional, tissue, and phylogenetic distribution , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  A. Lohman,et al.  On the Basal Ganglia of a Reptile: The Lizard Gekko Gecko , 1987 .

[9]  C. Saper,et al.  Pedunculopontine tegmental nucleus of the rat: Cytoarchitecture, cytochemistry, and some extrapyramidal connections of the mesopontine tegmentum , 1987, The Journal of comparative neurology.

[10]  Richard F. Martin,et al.  Primate neostriatal neurons containing tyrosine hydroxylase: Immunohistochemical evidence , 1987, Neuroscience Letters.

[11]  W. Smeets,et al.  Immunocytochemical analysis of the dopamine system in the forebrain and midbrain of Raja radiata: Evidence for a substantia nigra and ventral tegmental area in cartilaginous fish , 1987, The Journal of comparative neurology.

[12]  P. Reiner,et al.  The immunohistochemical localization of choline acetyltransferase in the cat brain , 1987, Brain Research Bulletin.

[13]  W. Smeets,et al.  Histochemical identification of pallidal and striatal structures in the lizard Gekko gecko: Evidence for compartmentalization , 1987, The Journal of comparative neurology.

[14]  E. Font,et al.  The Reptilian Striatum Revisited: Studies on Anolis Lizards1 , 1988 .

[15]  T. Hattori,et al.  Tyrosine hydroxylase-like immunoreactive neurons in the striatum of the rat , 1989, Neuroscience Letters.

[16]  W. Smeets,et al.  Distribution of noradrenaline immunoreactivity in the forebrain and midbrain of the lizard Gekko gecko , 1989, The Journal of comparative neurology.

[17]  S. Haber,et al.  Interrelationship of the distribution of neuropeptides and tyrosine hydroxylase immunoreactivity in the human substantia nigra , 1989, The Journal of comparative neurology.

[18]  J. Penney,et al.  The functional anatomy of basal ganglia disorders , 1989, Trends in Neurosciences.

[19]  Y. Smith,et al.  The output neurones and the dopaminergic neurones of the substantia nigra receive a GABA‐Containing input from the globus pallidus in the rat , 1990, The Journal of comparative neurology.

[20]  A. Reiner,et al.  Extensive co‐occurrence of substance P and dynorphin in striatal projection neurons: An evolutionarily conserved feature of basal ganglia organization , 1990, The Journal of comparative neurology.

[21]  P. Hoogland,et al.  Distribution of choline acetyltransferase immunoreactivity in the telencephalon of the lizard Gekko gecko. , 1990, Brain, behavior and evolution.

[22]  A. Lohman,et al.  Afferent connections of the striatum and the nucleus accumbens in the lizard Gekko gecko. , 1990, Brain, Behavior and Evolution.

[23]  M. Delong,et al.  Primate models of movement disorders of basal ganglia origin , 1990, Trends in Neurosciences.

[24]  G. E. Alexander,et al.  Functional architecture of basal ganglia circuits: neural substrates of parallel processing , 1990, Trends in Neurosciences.

[25]  A. Graybiel Neurotransmitters and neuromodulators in the basal ganglia , 1990, Trends in Neurosciences.

[26]  A. Reiner,et al.  The patterns of neurotransmitter and neuropeptide co-occurrence among striatal projection neurons: conclusions based on recent findings , 1990, Brain Research Reviews.

[27]  W. Smeets Comparative aspects of the distribution of substance P and dopamine immunoreactivity in the substantia nigra of amniotes. , 1991, Brain, behavior and evolution.

[28]  Y. Smith,et al.  Convergence of synaptic inputs from the striatum and the globus pallidus onto identified nigrocollicular cells in the rat: A double anterograde labelling study , 1991, Neuroscience.

[29]  W. Smeets,et al.  Comparative analysis of dopamine and tyrosine hydroxylase immunoreactivities in the brain of two amphibians, the anuran Rana ridibunda and the urodele Pleurodeles waltlii , 1991, The Journal of comparative neurology.

[30]  W. Smeets,et al.  Comparative aspects of the basal ganglia‐tectal pathways in reptiles , 1991, The Journal of comparative neurology.

[31]  J. C. Stoof,et al.  Differences in the regulation of acetylcholine release upon D2 dopamine and N-methyl-d-aspartate receptor activation between the striatal complex of reptiles and the neostriatum of rats , 1991, Brain Research.

[32]  Nancy J. Woolf,et al.  Cholinergic systems in mammalian brain and spinal cord , 1991, Progress in Neurobiology.

[33]  A. Reiner,et al.  Immunohistochemical localization of DARPP-32 in striatal projection neurons and striatal interneurons: implications for the localization of D1-like dopamine receptors on different types of striatal neurons , 1991, Brain Research.

[34]  A. Lohman,et al.  The Dorsal Ventricular Ridge and Cortex of Reptiles in Historical and Phylogenetic Perspective , 1991 .

[35]  Helmut Wicht,et al.  The Forebrain of the Pacific Hagfish: A Cladistic Reconstruction of the Ancestral Craniate Forebrain; pp. 45–54 , 1992 .

[36]  A. Reiner,et al.  Biotinylated dextran amine as an anterograde tracer for single- and double-labeling studies , 1992, Journal of Neuroscience Methods.

[37]  P. Dean,et al.  Topographical organization of the nigrotectal projection in rat: Evidence for segregated channels , 1992, Neuroscience.

[38]  S. Haber,et al.  Organization of the output of the ventral striatopallidal system in the rat: Ventral pallidal efferents , 1993, Neuroscience.

[39]  W. Smeets,et al.  Noradrenaline in the brain of the south african clawed frog Xenopus laevis: A study with antibodies against noradrenaline and dopamine‐β‐hydroxylase , 1993, The Journal of comparative neurology.

[40]  R. J. McDonald,et al.  A triple dissociation of memory systems: hippocampus, amygdala, and dorsal striatum. , 1993, Behavioral neuroscience.

[41]  W. Smeets,et al.  Distribution of choline acetyltransferase immunoreactivity in the brain of the lizard Gallotia galloti , 1993, The Journal of comparative neurology.

[42]  Bernd Fritzsch Fast axonal diffusion of 3000 molecular weight dextran amines , 1993, Journal of Neuroscience Methods.

[43]  Luis Puelles,et al.  Expression patterns of homeobox and other putative regulatory genes in the embryonic mouse forebrain suggest a neuromeric organization , 1993, Trends in Neurosciences.

[44]  Mark D. Johnson,et al.  Localization of NADPH diaphorase activity in monoaminergic neurons of the rat brain , 1993, The Journal of comparative neurology.

[45]  A. Reiner,et al.  Distribution of choline acetyltransferase immunoreactivity in the pigeon brain , 1994, The Journal of comparative neurology.

[46]  W. Smeets,et al.  Phylogeny and development of catecholamine systems in the CNS of vertebrates , 1994 .

[47]  A. Butler,et al.  The evolution of the dorsal pallium in the telencephalon of amniotes: Cladistic analysis and a new hypothesis , 1994, Brain Research Reviews.

[48]  H. Groenewegen,et al.  The specificity of the ‘nonspecific’ midline and intralaminar thalamic nuclei , 1994, Trends in Neurosciences.

[49]  C. Marsden,et al.  The functions of the basal ganglia and the paradox of stereotaxic surgery in Parkinson's disease. , 1994, Brain : a journal of neurology.

[50]  Charles J. Wilson,et al.  Striatal interneurones: chemical, physiological and morphological characterization , 1995, Trends in Neurosciences.

[51]  A. Parent,et al.  Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop , 1995, Brain Research Reviews.

[52]  P. Winn,et al.  The pedunculopontine tegmental nucleus: Where the striatum meets the reticular formation , 1995, Progress in Neurobiology.

[53]  A. Reiner,et al.  Neurotransmitter organization and connectivity of the basal ganglia in vertebrates: implications for the evolution of basal ganglia. , 1995, Brain, behavior and evolution.

[54]  André Parent,et al.  Chemical anatomy of primate basal ganglia , 1995, Progress in Neurobiology.

[55]  A. Parent,et al.  Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidium in basal ganglia circuitry , 1995, Brain Research Reviews.

[56]  O. Marín,et al.  Nitric oxide synthase in the brain of a urodele amphibian (Pleurodeles waltl) and its relation to catecholaminergic neuronal structures , 1996, Brain Research.

[57]  G. Sancesario,et al.  Colocalization of somatostatin, neuropeptide Y, neuronal nitric oxide synthase and NADPH-diaphorase in striatal interneurons in rats , 1996, Brain Research.

[58]  S. T. Kitai,et al.  Cholinergic and noncholinergic tegmental pedunculopontine projection neurons in rats revealed by intracellular labeling , 1996, The Journal of comparative neurology.

[59]  G. Panzica,et al.  Coexistence of NADPH-diaphorase and tyrosine hydroxylase in the mesencephalic catecholaminergic system of the Japanese quail , 1996, Journal of Chemical Neuroanatomy.

[60]  A. Reiner,et al.  Calretinin is largely localized to a unique population of striatal interneurons in rats , 1996, Brain Research.

[61]  R. Turner,et al.  Dopaminergic Neurons Intrinsic to the Primate Striatum , 1997, The Journal of Neuroscience.

[62]  A. Reiner,et al.  Avian homologues of mammalian intralaminar, mediodorsal and midline thalamic nuclei: immunohistochemical and hodological evidence. , 1997, Brain, behavior and evolution.

[63]  G. Striedter The telencephalon of tetrapods in evolution. , 1997, Brain, behavior and evolution.

[64]  W. Smeets,et al.  Basal ganglia organization in amphibians: Afferent connections to the striatum and the nucleus accumbens , 1997, The Journal of comparative neurology.

[65]  A. Reiner,et al.  The efferent projections of the dorsal and ventral pallidal parts of the pigeon basal ganglia, studied with biotinylated dextran amine , 1997, Neuroscience.

[66]  W. Smeets,et al.  Distribution of NADPH‐diaphorase and nitric oxide synthase in relation to catecholaminergic neuronal structures in the brain of the lizard Gekko gecko , 1997, The Journal of comparative neurology.

[67]  W. Smeets,et al.  Basal ganglia organization in amphibians: efferent connections of the striatum and the nucleus accumbens. , 1997, The Journal of comparative neurology.

[68]  Ewert Jp,et al.  Neural correlates of key stimulus and releasing mechanism : a case study and two concepts , 1997 .

[69]  W. Smeets,et al.  Basal ganglia organization in amphibians: development of striatal and nucleus accumbens connections with emphasis on the catecholaminergic inputs , 1997, The Journal of comparative neurology.

[70]  S. Anderson,et al.  Mutations of the Homeobox Genes Dlx-1 and Dlx-2 Disrupt the Striatal Subventricular Zone and Differentiation of Late Born Striatal Neurons , 1997, Neuron.

[71]  W. Smeets,et al.  Distribution of choline acetyltransferase immunoreactivity in the brain of anuran (Rana perezi, Xenopus laevis) and urodele (Pleurodeles waltl) amphibians , 1997, The Journal of comparative neurology.

[72]  W. Smeets,et al.  Anatomical Substrate of Amphibian Basal Ganglia Involvement in Visuomotor Behaviour , 1997, The European journal of neuroscience.

[73]  Sten Grillner,et al.  Afferents of the lamprey striatum with special reference to the dopaminergic system: A combined tracing and immunohistochemical study , 1997, The Journal of comparative neurology.

[74]  T. Maeda,et al.  A dopamine-synthesizing cell group demonstrated in the human basal forebrain by dual labeling immunohistochemical technique of tyrosine hydroxylase and aromatic l-amino acid decarboxylase , 1998, Neuroscience Letters.

[75]  A. Reiner,et al.  Structural and functional evolution of the basal ganglia in vertebrates , 1998, Brain Research Reviews.

[76]  R. Nieuwenhuys,et al.  Holosteans and Teleosts , 1998 .

[77]  W. Smeets,et al.  Basal ganglia organization in amphibians: Chemoarchitecture , 1998, The Journal of comparative neurology.

[78]  Angus C Nairn,et al.  The DARPP-32/protein phosphatase-1 cascade: a model for signal integration 1 Published on the World Wide Web on 22 January 1998. 1 , 1998, Brain Research Reviews.

[79]  W. Smeets,et al.  Basal ganglia organization in amphibians: evidence for a common pattern in tetrapods , 1998, Progress in Neurobiology.

[80]  Garrett E. Alexander Basal ganglia , 1998 .

[81]  W. Smeets,et al.  Evolution of the basal ganglia in tetrapods: a new perspective based on recent studies in amphibians , 1998, Trends in Neurosciences.

[82]  Y. Smith,et al.  Microcircuitry of the direct and indirect pathways of the basal ganglia. , 1998, Neuroscience.

[83]  J. Rubenstein,et al.  Comparison of the mammalian and avian telencephalon from the perspective of gene expression data. , 1999, European journal of morphology.

[84]  S. Haber,et al.  The distribution of dynorphinergic terminals in striatal target regions in comparison to the distribution of substance P-containing and enkephalinergic terminals in monkeys and humans , 1999, Neuroscience.

[85]  P. Redgrave,et al.  The basal ganglia: a vertebrate solution to the selection problem? , 1999, Neuroscience.

[86]  W. Smeets,et al.  Cholinergic and catecholaminergic neurons relay striatal information to the optic tectum in amphibians. , 1999, European journal of morphology.