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Biomedical subjects

S O Ebbesson

Publications and source records attributed to S O Ebbesson.

At least 73 records · Page 4Linked to original sources
PubMed1980

The parcellation theory and its relation to interspecific variability in brain organization, evolutionary and ontogenetic development, and neuronal plasticity.

Recently discovered neocortical equivalents in anamniotes and certain patterns of interspecific variability in brain organization provide new insights into evolutionary and ontogenetic mechanisms of development. The new data suggest that nervous systems become more complex, not by one system invading another, but by a process of parcellation that involves the selective loss of connections of the newly formed daughter aggregates and subsystems. The parcellation process is reflected in the normal ontogenetic development of the CNS in a given species and can be manipulated, to a certain extent, by deprivation or surgically induced sprouting. The parcellation theory allows certain predictions about the range of variation of a given system at all levels of analysis including the cellular and aggregate levels. For example, the interspecific variability in organization of cortical columns, thalamic nuclei, cortical areas and tectal layers can be explained. The findings, summarized here, suggest that diffuse, undifferentiated systems existed in the beginning of vertebrate evolution and that during the evolution of complex behaviors, and analytical capacities related to these behaviors, a range of patterns of neural systems evolved that relate to these functions. One principle underlying the growth, differentiation and multiplication of neural systems appears to be the process of parcellation as defined by the theory.

Amphibians↗
PubMed1980

Bilateral retinal projections in the black piranha (Serrasalnus niger).

The retinal projections were studied in the black piranha (Serrasalmus niger) with degeneration and autoradiographic methods. The projections are bilateral to the hypothalamic optic nucleus, the dorsomedial optic nucleus, corpus geniculatum ipsum of Meader (1934) and the optic tectum. Unilateral, crossed projections were traced to the pretectal nucleus and the cortical nucleus. The visual system of the black piranha is exceptionally well developed but has retained many primitive features including the extensive bilateral projections.

Animals↗
PubMed1980

Retinal projections in the electric catfish (Malapterurus electricus).

The poorly developed visual system of the electric catfish was studied with silver-degeneration methods. Retinal projections were entirely contralateral to the hypothalamic optic nucleus, the lateral geniculate nucleus, the dorsomedial optic nucleus, the pretectal nuclei including the cortical nucleus, and the optic tectum. The small size and lack of differentiation of the visual system in the electric catfish suggest a relatively small role for this sensory system in this species.

Animals↗
PubMed1980

A visual thalamo-telencephalic pathway in a teleost fish (Holocentrus rufus).

Injections of large doses of horseradish peroxidase (HRP) into the telencephalon of the squirrel fish (Holocentrus rufus) revealed the first anatomical evidence for a visual thalamo-telencephalic projection in a teleost. The central optic nucleus of the thalamus appears to be the only visual thalamic nucleus projecting to the telencephalon in this species. Since the central optic nucleus has a large tectal input but not a direct one from the retina, it is suggested that a retino-geniculo-telencephalic pathway does not exist in this species.

Animals↗
PubMed1978

Visual discrimination following partial telencephalic ablations in nurse sharks (Ginglymostoma cirratum).

An instrumental conditioning task was used to examine the role of the nurse shark telencephalon in black-white (BW) and horizontal-vertical stripes (HV) discrimination performance. In the first experiment, subjects initially received either bilateral anterior telencephalic control lesions or bilateral posterior telencephalic lesions aimed at destroying the central telencephalic nuclei (CN), which are known to receive direct input from the thalamic visual area. Postoperatively, the sharks were trained first on BW and then on HV. Those with anterior lesions learned both tasks as rapidly as unoperated subjects. Those with posterior lesions exhibited visual discrimination deficits related to the amount of damage to the CN and its connecting pathways. Severe damage resulted in an inability to learn either task but caused no impairments in motivation or general learning ability. In the second experiment, the sharks were first trained on BW and HV and then operated. Suction ablations were used to remove various portions of the CN. Sharks with 10% or less damage to the CN retained the preoperatively acquired discriminations almost perfectly. Those with 11-50% damage had to be retrained on both tasks. Almost total removal of the CN produced behavioral indications of blindness along with an inability to perform above the chance level on BW despite excellent retention of both discriminations over a 28-day period before surgery. It appears, however, that such sharks can still detect light. These results implicate the central telencephalic nuclei in the control of visually guided behavior in sharks.

Animals↗
PubMed1976

Projections of the optic tectum in two teleost species.

The efferent pathways of the optic tectum have been investigated in the percomorph Eugerres and the berycomorph Holocentrus. A portion of the dorsal-dorsolateral region of the optic tectum was unilaterally resected by suction. The animals were perfused 6-30 days thereafter, and the brains were processed according to a modification (Method 7 in Ebbesson, '70) of the Fink-Heimer ('67) technique for the selective silver impregnation of degenerating axons and terminals. Three groups of fibers emerge from the lesioned region (a) a medial group, which runs towards the midline and terminates in the ipsilateral torus longitudinalis and the contralateral tectum; (b) an ascending group, which enters the dorsocaudal region of the diencephalon and terminates in pretectal cell groups, in the dorsomedial optic thalamic nucleus, and in the nucleus rotundus or prethalamicus; and (c) a descending group, which funnels down into the midbrain tegmentum. Here abundant terminals are given to dorsolateral cell groups and to the nucleus isthmi. A recurrent fascicle leaves the mainstream and ascends to terminate in scattered diencephalic cell groups, in the nucleus geniculatus posterior pars ventralis, and in the nucleus rotundus or prethalamicus. The bulk of descending fibers then forms an ipsilateral bundle, which gives terminals to the lateral reticular formation of mesencephalon and rhombencephalon, and a contralateral (i.e., the predorsal) bundle, which terminates in the medial reticular formation of mesencephalon and rhombencephalon.

Animals↗
PubMed1976

Telencephalic projections in two teleost species.

The efferent pathways of the telencephalon were investigated in the percomorph Eugerres and the berycomorph Holocentrus. One telencephalic hemisphere was resected by suction and the animals were perfused 7-35 days thereafter. The brains were processed according to a modification (Method 7 in Ebbesson, '70) of the Fink-Heimer ('67) technique for selective silver impregnation of degenerating axons and terminals. Some fibers emerging from the lesioned telencephalic hemisphere terminate upon the contralateral hemisphere. The large bulk of efferent fibers, however, descends into the ipsilateral diencephalon and gives off the so-called strio-tectal bundle (STB) as well as the medial forebrain bundle (MFB). The remaining contingent eventually splits into the so-called strio-lobar bundle (SLB) and the lateral forebrain (LFB), but, previous to splitting, it contributes most of the telencephalic projection to the optic tectum in Eugerres, and gives abundant terminals to the ipsilateral nucleus rotundus or prethalamicus in both Eugerres and Holocentrus. The STB conveys all telencephalo-tectal fibers in Holocentrus, and some of them in Eugerres. Telencephalic efferents teminate ipsilaterally in the middle level of the tectum's stratum griseum centrale; in Holocentrus there is also a small projection to the stratum opticum. The MFB terminates at the caudal hypothalamus and gives terminals all along its course. The LFB also gives terminals all along its course and terminates upon a nucleus located between the midline and the corpus glomerulosum. The SLB spreads out and terminates in the inferior lobe of the hypothalamus.

Animals↗
PubMed1975

The visual connections of the adult flatfish, Achirus lineatus.

Metamorphosis in the flatfish is characterized by the migration of one eye around the dorsal surface of the head to a position adjacent to the other eye on the new top side of the animal. The visual connections of the adult flatfish, Achirus lineatus, were examined. Either the migrating or non-migrating eye was removed and the animal allowed to survive for one to three weeks. Alternate sections of the brain were stained by a modification of the Fink-Heimer technique, or with cresyl violet. The diencephalic visual connections of the flatfish were similar to those of other teleosts with contralateral projections to the nuclei corticalis, dorsomedialis thalami, pretectalis, and the corpus geniculatum laterale. The distribution of the retinal efferents to the optic tectum is unique in the flatfish. In the medial one-third of the tectum, terminal degeneration was found in three bands in the stratum opticum (SO) and the stratum griseum et fibrosum superficiale (sgfs). In the middle part of the tectum, two bands of degeneration remained over the sgfs. The lateral part of the tectum has only a very small amount of degeneration distributed radomly in scattered clusters over the deep SO and superficial sgfs. The Nissl preparations also reflected the differences between the medial and lateral parts of the tectum. Distinct layer was lacking in the medial tectum with a conspicuously absent large cell layer in the stratum griseum centrale (sgc). In contrast, the lateral tectum had a typical tectal stratification. Most notable were the large neurons of the sgc.

Animals↗
PubMed1975

Cytoarchitecture of the optic tectum in the nurse shark.

The cytoarchitecture of the optic tectum of the nurse shark is described and related to the arrangements of afferents from retina, telencephalon and contralateral tectum. Its lamination is not pronounced when compared to tecta of most other non-mammalian species but more comparable to those of mammals. The absence of highly differentiated cells such as pyramidal and true horizontal cells is perhaps correlated with the poor differentiation in general, including the apparent partial overlap of inputs. Some neurons near the midline were found to possess dendrites extending into the contralateral tectum.

Animals↗
PubMed1973

Electrophysiological identification of a visual area in shark telencephalon.

Optic nerve stimulation in the shark evokes short-latency telencephalic field potentials localized to the ipsilateral, posterior central nucleus. Such a well-defined visual area in elasmobranch telencephalon further challenges classical formulations of forebrain evolution. Moreover, its ipsilateral representation confirms recent evidence for a crossed thalamotelencephalic visual projection.

Animals↗
PubMed1973

Visual discrimination in sharks without optic tectum.

After complete removal of the optic tectum, nurse sharks can learn to discriminate black versus white and horizontal versus vertical stripes. This finding is contrary to the traditional belief of exclusive tectal control over visuomotor behavior in lower vertebrates and suggests a role for the telencephalon in the vision of these primitive animals.

Animals↗