Abstract:The distribution of catecholamine (CA) in the inferior olivary complex (IO) of various vertebrate (from fish to monkey) was investigated by means of the histofluorescence technique. In addition, using rats, a further attempt was made to elucidate the origins of CA in the IO. The IO of the lower vertebrates (from fish to birds) was in general poorly innervated by the CA neuron system. IO in the lower mammals, such as insectivora and bats, contained only a few CA nerve terminals, while that in the higher mammals… Show more
“…In the rat, the VLO, known to be involved in compensatory eye movements, is targeted by dopaminergic projections from the mesodiencephalic junction (Toonen et al 1998). Again, this can differ between species: In the cat, dopaminergic nerve terminals are most prominent in the DAO (Maqbool et al 1993) whereas catecholaminergic fibers are mostly seen in the MAO and lateral lamella of the PO in the monkey (Sladek and Bowman 1975;Kamei et al 1981). Interestingly, the noradrenaline fibers in the IO are much more homogeneously distributed in humans than in rat, cat, and monkey (Powers et al 1990).…”
Section: Neurotransmitters and Receptorsmentioning
The inferior olive provides all climbing fibers to the Purkinje cells in the cerebellar cortex and thereby has a strong impact on cerebellar output. As a consequence, the integration of inputs to olivary neurons as well as their intrinsic properties are critical for cerebellar function. In this chapter, all issues that are relevant for their ultimate function are addressed. This chapter starts by reviewing developmental aspects such as the origin and migratory routes of inferior olivary neurons and a description of their axonal outgrowth into climbing fibers innervating Purkinje cells. Subsequently, a detailed description of the olivary subdivisions and the ultrastructure of their neuropil is provided. This is characterized by the presence of dendro-dendritic gap junctions located in glomeruli and by the consistently combined excitatory and inhibitory innervation of their coupled spines. Furthermore, the electrophysiological behavior of olivary neurons is described and discussed. Finally, these unique properties are integrated in cellular and system models. Both type of models show that the inferior olive is very well able to control both rate
“…In the rat, the VLO, known to be involved in compensatory eye movements, is targeted by dopaminergic projections from the mesodiencephalic junction (Toonen et al 1998). Again, this can differ between species: In the cat, dopaminergic nerve terminals are most prominent in the DAO (Maqbool et al 1993) whereas catecholaminergic fibers are mostly seen in the MAO and lateral lamella of the PO in the monkey (Sladek and Bowman 1975;Kamei et al 1981). Interestingly, the noradrenaline fibers in the IO are much more homogeneously distributed in humans than in rat, cat, and monkey (Powers et al 1990).…”
Section: Neurotransmitters and Receptorsmentioning
The inferior olive provides all climbing fibers to the Purkinje cells in the cerebellar cortex and thereby has a strong impact on cerebellar output. As a consequence, the integration of inputs to olivary neurons as well as their intrinsic properties are critical for cerebellar function. In this chapter, all issues that are relevant for their ultimate function are addressed. This chapter starts by reviewing developmental aspects such as the origin and migratory routes of inferior olivary neurons and a description of their axonal outgrowth into climbing fibers innervating Purkinje cells. Subsequently, a detailed description of the olivary subdivisions and the ultrastructure of their neuropil is provided. This is characterized by the presence of dendro-dendritic gap junctions located in glomeruli and by the consistently combined excitatory and inhibitory innervation of their coupled spines. Furthermore, the electrophysiological behavior of olivary neurons is described and discussed. Finally, these unique properties are integrated in cellular and system models. Both type of models show that the inferior olive is very well able to control both rate
“…The above studies show conserved projections of the LC among vertebrates. However, these projections have been mapped at the populational level by anterograde/retrograde dye tracing [ 32 , 37 , 41 , 44 , 45 , 59 , 60 , 61 ], or immunostaining [ 13 , 62 , 63 , 64 ]. Next, a single-cell level wiring diagram will be important.…”
The locus coeruleus (LC) is a vertebrate-specific nucleus and the primary source of norepinephrine (NE) in the brain. This nucleus has conserved properties across species: highly homogeneous cell types, a small number of cells but extensive axonal projections, and potent influence on brain states. Comparative studies on LC benefit greatly from its homogeneity in cell types and modularity in projection patterns, and thoroughly understanding the LC-NE system could shed new light on the organization principles of other more complex modulatory systems. Although studies on LC are mainly focused on mammals, many of the fundamental properties and functions of LC are readily observable in other vertebrate models and could inform mammalian studies. Here, we summarize anatomical and functional studies of LC in non-mammalian vertebrate classes, fish, amphibians, reptiles, and birds, on topics including axonal projections, gene expressions, homeostatic control, and modulation of sensorimotor transformation. Thus, this review complements mammalian studies on the role of LC in the brain.
“…In rat, the dopaminergic projections from the mesodiencephalic junction target the VLO, which is involved in vertical compensatory eye movements (Toonen et al 1998), whereas in cat, the dopaminergic nerve terminals are most prominent in the DAO, which may be involved in sensorimotor processing during locomotion (Horn et al 2010(Horn et al , 2013Maqbool et al 1993). And again, differently, in nonhuman primates, catecholaminergic fibers are mostly seen in the MAO and lateral lamella of the PO (Kamei et al 1981;Sladek and Bowman 1975), whereas in humans the noradrenergic fibers in the IO are much more homogeneously distributed than in rat, cat, and monkey (Powers et al 1990).…”
Section: Neurotransmitters and Receptorsmentioning
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