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PubMed1976

A comparative neuroanatomic study of retinal projections in two fishes: Astyanax hubbsi (the blind cave fish), and Astyanax mexicanus.

Retinofugal projections in the blind cave fish A. hubbsi and in the highly visual A. mexicanus were studied with both reduced silver and autoradiographic methods. Contrary to what has been reported for other teleosts, ipsilateral, as well as the generally accepted contralateral, projections were found in A. mexicanus. Bilateral retinofugal projections were traced to the dorsolateral thalamic nucleus and area pretectalis. Contralateral projections were traced to the lateral geniculate nucleus, nucleus pretectalis, accessory optic nucleus, nucleus corticalis, nucleus opticus hypothalamicus and the superficial layers of the optic tectum (strata opticum, fibrosum and griseum superficiale, and the cellular zone of griseum centrale). Retinal efferents in the blindfish, A. hubbsi, are sparse and totally crossed. Areas receiving a retinal projection include nucleus opticus hypothalamicus, lateral geniculate and the superficial layers of the medial third of the optic tectum. Preliminary behavioral studies are described and discussed in relation to the possible visual potential of this teleost.

Animals↗
PubMed1978

The cerebellofugal projections in the brachium conjunctivum of the rat. II. The ipsilateral and contralateral descending pathways.

The cerebellofugal projections in the ipsilateral and contralateral descending pathways of the brachium conjunctivum (B.C.) in the rat have been investigated in 22 animals using the Fink-Heimer technique to demonstrate the axonal degeneration resulting from complete B.C. lesions (6), partial B.C. lesions (14) and control lesions dorsal to the B.C. (2). The incidental degeneration resulting from the concomitant involvement of the structures surrounding the B.C. is accounted for in terms of known fiber pathways and from the results in the control experiments. This study confirms Ramón y Cajal's ('03) original observation that cerebellofugal fibers in the B.C. project caudally throughout the length of the hindbrain via both ipsilateral and contralateral descending pathways. The fibers forming the ipsilateral descending pathway proceed ventrally from the B.C. at the level of the trigeminal motor nucleus, turn caudally and terminate within nucleus reticularis parvocellularis (Rpa). In particular, fibers within this pathway terminate densely in two cytoarchitecturally distinct Rpa subnuclei--nucleus "k" (Meessen and Olszewski, '49) and a caudal linear subnucleus--which project to the cerebellum (Faull, '77). The contralateral descending pathway (B.C.de) roceeds caudally from the decussation of the B.C. within the ventromedial region of the magnocellular nuclei of the reticular formation of the pons and medulla. Cerebellofugal fibers of the B.C.de terminate in a distinctive pattern within precerebellar brainstem nuclei: densely throughout the middle third of nucleus reticularis tegmenti pontis; in a longitudinal zone of each of the three pontine gray subnuclei; in the principal and dorsal accessory nuclei of the inferior olive; and sparsely within nucleus reticularis paramedianus. Fibers in the B.C.de also terminate within the magnocellular nuclei of the reticular formation, principally the nuclei reticularis pontis oralis and caudalis.

Animals↗
PubMed1983

Cortical and thalamic afferent connections of the insular and adjacent cortex of the rat.

Thalamic and cortical afferents to the insular and perirhinal cortex of the rat were investigated. Unilateral injections of horseradish peroxidase (HRP) were made iontophoretically along the rhinal sulcus. HRP injections covered or invaded areas along the rhinal fissure from about the level of the middle cerebral artery to the posterior end of the fissure. The most anterior injection labeled a few cells in the mediodorsal nucleus. More posterior injections labeled neurons in the basal portion of the nucleus ventralis medialis, thus suggesting that this cortical region constitutes the rat's gustatory (insular) cortex. We consider the cortex situated posterior to the gustatory cortex in and above the rhinal sulcus as the core region of the rat's (associative) insular cortex, as this cortex receives afferents from the regions of and between the nuclei suprageniculatus and geniculatus medialis, pars magnocellularis. It includes parts of the cortex termed perirhinal in other studies. The cortex dorsal and posterior to the insular cortex we consider auditory cortex, as it receives afferents from the principal part of the medial geniculate nucleus, and the cortex ventral to the insular cortex (below the fundus of the rhinal sulcus) we consider to constitute the prepiriform cortex, which is athalamic. The posterior part of the perirhinal cortex (area 35) receives afferents from nonspecific thalamic nuclei (midline nuclei). Cortical afferents to the injection loci arise from a number of regions, above all from regions of the medial and sulcal prefrontal cortex. Those injections confined to the projection cortex of the suprageniculate-magnocellular medial geniculate nuclear complex also led to labeling in contralateral prefrontal regions, particularly in area 25 (infralimbic region). A comparison of our results with those on the insular cortex of cats and monkeys suggests that on the basis of thalamocortical connections, topographical relations, and involvements of neurons in information processing and overt behavior, the insular cortex has to be regarded as a heterogeneous region which may be separated into prefrontal insular, gustatory (somatosensory) insular, and associative insular portions.

Afferent Pathways↗
PubMed1983

Extrinsic and intrinsic fiber connections of the telencephalon in a teleost, Sebastiscus marmoratus.

Extrinsic and intrinsic fiber connections of the telencephalic subdivisions of Nieuwenhuys ('62) in a teleost, Sebastiscus marmoratus, were studied by means of horseradish peroxidase (HRP) and Fink-Heimer methods. The olfactory bulb projects bilaterally to area dorsalis pars posterior, area ventralis pars ventralis, pars lateralis, pars posterior, pars intermedia, and the nucleus posterior tuberis of Peter et al. ('75) and receives fibers from ipsilateral area dorsalis pars centralis, pars posterior, area ventralis pars dorsalis, and pars supracommissuralis. Area dorsalis pars posterior sends numerous fibers to the ipsilateral ventral region of area dorsalis pars medialis, from which fibers of the medial forebrain bundle arise and terminate in the inferior lobe and nucleus posterior tuberis. Area dorsalis pars lateralis, pars dorsalis, and the dorsal region of pars medialis are the main targets of extratelencephalic ascending afferents. Area dorsalis pars lateralis receives fibers from the ipsilateral nucleus prethalamicus of Meader ('34), where tectal projections terminate massively. Area dorsalis pars dorsalis and the dorsal region of pars medialis receive afferents from the ipsilateral nucleus preglomerulosus of Schnitzlein ('62), nucleus posterior tuberis, area preoptica pars medialis of Crosby and Showers ('69), and nucleus entopeduncularis of Sheldon ('12). Raphe nuclei and locus ceruleus project bilaterally to area dorsalis pars centralis, pars dorsalis, pars lateralis, and the dorsal region of pars medialis. Area dorsalis pars centralis, pars dorsalis, and the dorsal region of pars medialis are important sources of extratelencephalic efferents. These subdivisions give rise to the lateral forebrain bundle and project to the ipsilateral nucleus prethalamicus, nucleus preglomerulosus, inferior lobe, nucleus paracommissuralis of Ito et al. ('82), optic tectum, torus semicircularis, and the bilateral mesencephalic tegmentum. Within the telencephalon, most of the ventral subdivisions project to ipsilateral area dorsalis pars centralis, pars dorsalis, pars lateralis, and the dorsal region of pars medialis. Area dorsalis pars centralis has reciprocal connections with ipsilateral area dorsalis pars lateralis, pars dorsalis, pars posterior, and the dorsal region of pars medialis. A dorsal part of the anterior commissure is composed of axons of the ventral region of area dorsalis pars medialis destined to the contralateral ventral region of area dorsalis pars medialis. A ventral part of the anterior commissure contains axons of area dorsalis pars centralis destined to contralateral area dorsalis pars lateralis.

Animals↗
PubMed1989

Two distinct visual pathways through the superficial pretectum in a percomorph teleost.

The connections of the superficial pretectum and of nucleus isthmi were examined in a percomorph teleost, Lepomis cyanellus. Horseradish peroxidase was injected either with a pin into the parvicellular nucleus of the superficial pretectum or pressure injected into nucleus isthmi; the isthmal injections retrogradely labelled the neurons of the magnocellular nucleus of the superficial pretectum. Two main visual pathways can be recognized: The first projects from the retina to the parvicellular nucleus, and then to the intermediate nucleus of the superficial pretectum, the inferior raphe nucleus, and the trochlear nucleus. The second projects from the retina via the optic tectum to the magnocellular nucleus of the superficial pretectum, and from there to nucleus isthmi and the lateral thalamic nucleus; nucleus isthmi and the lateral thalamic nucleus project back to the optic tectum, and nucleus isthmi also projects back to the magnocellular nucleus. The two pathways are interconnected to some extent because both nucleus isthmi and the optic tectum project to the parvicellular nucleus; nevertheless, we suggest that they may be functionally and evolutionarily distinct. Compared to percomorphs, the first pathway appears reduced in cyprinid teleosts such as goldfish. Furthermore, the magnocellular nucleus of the second pathway is completely different in cyprinids, both in cellular architecture and in efferent connections. A phylogenetic analysis suggests that cyprinid ancestors went through a period of reduced vision and that the magnocellular nucleus of the superficial pretectum in modern cyprinids has been either extensively modified from the primitive condition or lost entirely and replaced by a superficially similar structure.

Animals↗
PubMed1993

Connections of somatosensory cortex in megachiropteran bats: the evolution of cortical fields in mammals.

The cortical connections of the primary somatosensory area (SI or 3b), a caudal somatosensory field (area 1/2), the second somatosensory area (SII), the parietal ventral area (PV), the ventral somatosensory area (VS), and the lateral parietal area (LP) were investigated in grey headed flying foxes by injecting anatomical tracers into electrophysiologically identified locations in these fields. The receptive fields for clusters of neurons were mapped with sufficient density for injection sites to be related to the boundaries of fields, and to representations of specific body parts within the fields. In all cases, cortex was flattened and sectioned parallel to the cortical surface. Sections were stained for myelin and architectonic features of cortex were related to physiological mapping and connection patterns. We found patterns of topographic and nontopographic connections between 3b and adjacent anterior parietal fields 3a and 1/2, and fields caudolateral to 3b (SII and PV). Area 1/2 had both topographic and nontopographic connections with 3b, PP, and SII. Connections of SII and PV with areas 3b, 3a, and 1/2 were roughly topographic, although there was clear evidence for nontopographic connections between these fields. SII was most densely connected with area 1/2, while PV was most densely connected with 3b. SII had additional connections with fields in lateral parietal cortex and with subdivisions of motor cortex. Other connections of PV were with subdivisions of motor cortex and pyriform cortex. Laminar differences in connection patterns of SII and PV with surrounding cortex were also observed. Injections in the ventral somatosensory area revealed connections with SII, PV, area 1/2, auditory cortex, entorhinal cortex, and pyriform cortex. Finally, the lateral parietal field had very dense connections with posterior parietal cortex, caudal temporal cortex, and with subdivisions of motor cortex. Our results indicate that the 3b region is not homogeneous, but is composed of myelin dense and light regions, associated with 3b proper and invaginations of area 1/2, respectively. Connections of myelin dense 3b were different from invaginating portions of myelin light area 1/2. Our findings that 3b is densely interconnected with PV and moderately to lightly interconnected with SII supports the notion that SII and PV have been confused across mammals and across studies. Our connectional evidence provides further support for our hypothesis that area 1/2 is partially incorporated in 3b and has led to theories of the evolution of cortical fields in mammals.

Animals↗
PubMed1988

Antisera probes to an atypical pseudocholinesterase from surgeonfish reveal immunochemical variability and tissue-specific molecular polymorphism.

Polyclonal antisera were raised in rabbits against the purified sialated, presumed-globular tetrameric pseudocholinesterase (pseudo-ChE) from surgeonfish (Leibel: Journal of Experimental Zoology 1988b) and against commercially obtained Electrophorus electroplax AChE. The resulting antisera probes were absolutely specific for their respective antigens and failed to titrate ChE activities heterologously. However, each antisera probe did crossreact with its other respective globular and asymmetric aggregational isozymes. The resultant specific probes were then used to examine interspecific evolutionary conservation of the two ChE activities and, in conjunction with velocity sedimentation analysis and differential paraoxon inhibition, the tissue distribution and molecular polymorphism of these same two enzyme systems in surgeonfish. These experiments suggest the tight evolutionary conservation of AChE in contrast to the apparent high variability of pseudo-ChE amongst the wide range of teleost fishes tested. The native atypical pseudo-ChE was shown to exist, like AChE, as a series of sialated and asialated globular and asymmetric aggregational isozymes whose relative distribution exhibits marked tissue specificity. The extremely high levels of pseudo-ChE characteristic of white skeletal (epaxial) muscle, in particular, was conspicuous, and its occurrence in the sarcolemma is discussed in the context of its possible function and in relation to the apparent lack of evolutionary conservation amongst marine teleosts.

Animals↗
PubMed2006

Genetic identification of AChE as a positive modulator of addiction to the psychostimulant D-amphetamine in zebrafish.

Addiction is a complex maladaptive behavior involving alterations in several neurotransmitter networks. In mammals, psychostimulants trigger elevated extracellular levels of dopamine, which can be modulated by central cholinergic transmission. Which elements of the cholinergic system might be targeted for drug addiction therapies remains unknown. The rewarding properties of drugs of abuse are central for the development of addictive behavior and are most commonly measured by means of the conditioned place preference (CPP) paradigm. We demonstrate here that adult zebrafish show robust CPP induced by the psychostimulant D-amphetamine. We further show that this behavior is dramatically reduced upon genetic impairment of acetylcholinesterase (AChE) function in ache/+ mutants, without involvement of concomitant defects in exploratory activity, learning, and visual performance. Our observations demonstrate that the cholinergic system modulates drug-induced reward in zebrafish, and identify genetically AChE as a promising target for systemic therapies against addiction to psychostimulants. More generally, they validate the zebrafish model to study the effect of developmental mutations on the molecular neurobiology of addiction in vertebrates.

Acetylcholine↗
PubMed1998

Lateralized agonistic responses and hindlimb use in toads.

The recent discovery of forepaw preferences (handedness) in toad species has provided some insight into the evolution of brain lateralization. We tested the prediction that, as in higher vertebrates, visual lateralization and other motor preferences (footedness) also exists in toad species. During feeding periods, South American cane toads, Bufo marinus, showed a population bias to strike with the tongue at other toads occupying their left visual field. This is the first demonstration of lateralized visual behaviour in an amphibian species. Tongue striking at an individual's eyes or head may sometimes delay its approach to prey already seen by the attacker, or may dislodge prey from its mouth. In addition, we report hindlimb preferences (footedness) for contact righting in three species of toad (B. marinus, the European green toad, B. viridis, and the European common toad, B. bufo). After being fully overturned on to their back on a horizontal surface, toads initiated and completed righting using the hindlimbs and with only perfunctory use of the forepaws. Together, the findings of visual lateralization and footedness demonstrate that in toads, as in higher vertebrates, behavioural lateralization is not restricted to handedness. The hypothesis that lateralized brain functions in birds and mammals might have arisen from a common lateralized ancestor is therefore supported. Copyright 1998 The Association for the Study of Animal Behaviour.

Journal Article↗
PubMed1993

A novel mouse gene highly conserved throughout evolution: regulation in adipocyte differentiation and in tumorigenic cell lines.

A cDNA clone referred to as 168 was previously isolated from mouse 1246 adipocytes by differential hybridization on the basis of its down regulation in adipocytes when compared to preadipocytes. 5' RACE was used to obtain a full length clone of 761 bp encoding for a highly basic 25 kD polypeptide that is extremely conserved in several diverse species of eukaryotes. There is a single amino acid substitution at position 202 compared to the human homolog, QM, a putative tumor suppressor. Clone 168 mRNA decreases 80% in rat primary culture of adipocytes compared to preadipocytes and does not decrease when differentiation is blocked by PGF2 alpha or EGF, indicating that the decrease is correlated with expression of the differentiation phenotype. Finally, two 1246 cell line variants that exhibit altered growth and increased tumorigenicity have a similar level of 168 mRNA when compared to the non tumorigenic adipogenic parent cell line.

Adipocytes↗
PubMed2000

Motor control by vision and the evolution of cerebral lateralization.

Chicks (4 or 5 days old), which are able to use either eye freely, use the right eye (RE) preferentially in approach to a food dish when a lid, which has to be removed, is visible during approach. They use the left eye (LE) instead when no manipulation is required, but the same dish is similarly visible. The RE is also used preferentially in selecting food grains scattered over the floor; RE use in these two contexts is thus associated with visual control which brings the bill in planned contact with a visible target rather than with approach to a site where it is anticipated that feeding will occur. Zebrafish also use the RE preferentially when preparing to bite a target; during purely visual examination of the same target, this preference disappears. This evidence is used together with evolutionary evidence to support a new hypothesis for the origin of cerebral lateralization: paired anterior eyes evolved in filter-feeding ancestors of the vertebrates as part of the acquisition of prey catching. A key use for early vision was to predict likely contact with prey so as to inhibit reflexes of rejection and avoidance normally elicitated by tactile input to the mouth and so to allow ingestion. Innervation of mouth structures by the left side of the CNS caused control of mouth reflexes to become predominantly a left CNS affair. As visual abilities developed this starting condition meant that control of manipulation (which is by the mouth for most vertebrates) remained predominantly with the left side of the CNS.

Animals↗