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Biomedical subjects

I T Diamond

Publications and source records attributed to I T Diamond.

At least 37 records · Page 2Linked to original sources
PubMed1980

Cortical connections of the pulvinar nucleus in Galago.

In the first series of experiments, small amounts of HRP were injected into areas 17, 18, and 19 and each of the cytoarchitectonic areas of the temporal lobe. The resulting distributions of labeled cells fell into a number of distinctive classes. For example, after injecting the temporal anterior area (Ta), the labeled cells occupied a band on the ventral border of the inferior division of the pulvinar complex; after injecting the temporal ventral area (Tv), the labeled cells were concentrated in the medial extremity of the superior division. In spite of the distinctiveness of these different distributions, there was evidence that in areas that we know to contain a representation of the visual field, the injection of the same part of the field led to labeled cells in the same part of the pulvinar nucleus. Thus, when the representation of the center of the field was injected in areas 17 or 18 or Tm (the temporal middle area), labeled cells were found in the dorsal part of the rostral half of the inferior division. The distinctiveness of the different distributions did not obscure certain features common to all experiments: labeled cells were always found in both subdivisions of the pulvinar complex, and there was always continuity between the population of labeled cells in the inferior division and the population of cells in the superior division. Wherever the site of the injection in the extrastriate region, some labeled cells were found in the causal half of the inferior division. Since the caudal half of the inferior division corresponds approximately to the tecto-recipient zone as defined earlier, the entire temporal lobe, except for the auditory areas, is visual cortex. Evidence was also found for an overlap in the striate cortex between the projections of the lateral geniculate body and the pulvinar nucleus. In conclusion, the pulvinar complex projects to a vast area of cortex, including all of the occipital lobe and most of the lateral surface of the temporal lobe. This entire region, which comprises a good part of the whole of the neocortex, can be regarded as visual cortex. A second series of experiments involved cortical injections of tritiated amino acids. The results showed that the projections from the thalamus to cortex were precisely reciprocated by descending projections from cortex to thalamus. The results also served as a way of confirming the results of the first set of experiments.

Animals↗
PubMed1979

Layer I of striate cortex of Tupaia glis and Galago senegalensis: projections from thalamus and claustrum revealed by retrograde transport of horseradish peroxidase.

We have examined the origin of the subcortical projections to the superficial layers of the striate cortex in Tupaia glis and Galago senegalensis by using the retrograde transport of HRP. Crystals of HRP were laid directly on the moist pial surface of the cortex which had been gently pricked with a small glass pipette. The diffusion of HRP was limited to layers I and II by restricting the length of time that the HRP was in contact with the surface. Following the application of HRP to the striate cortex, labeled cells were found in restricted regions of the lateral geniculate body of both species. Layers 4 and 5 of galago and layer 3 of tree shrew contained dense clusters of labeled cells. Labeled neurons were also found in the zones between the layers of the lateral geniculate body in both species and these cells were always in register with the labeled cells within the layers. In galago, curved columns of labeled cells were observed in the inferior and superior subdivisions of the pulvinar nucleus. These columns were arranged in the shape of two arcs, joined at the fiber bundle which separates the two subdivisions. The position of the bands in the pulvinar nucleus varied with the locus of the application in the striate cortex. While no labeled cells were seen in the body of the pulvinar nucleus of tree shrew, small labeled neurons were found in the external medullary lamina forming the capsule of the pulvinar nucleus. These cells were continuous with a larger population of labeled cells in the lateral intermediate nucleus. In both species, labeled cells were also found in the intralaminar nuclei (particularly the paracentral nucleus) and in the dorsal-caudal portion of the claustrum. In the claustrum, few unlabeled neurons were present within the zone containing labeled cells. In conclusion, layer I os striate cortex appears to be the site of convergence of several projection systems originating from principal and intralaminar thalamic nuclei as well as the claustrum. The significance of this overlap is discussed in terms of the total cortical extent of each system.

Animals↗
PubMed1979

Projections from cortex to tectum in the tree shrew, Tupaia glis.

Sensory neocortex of the tree shrew was divided into three main areas: the visual field, the auditory field, and the somatic field which includes motor cortex. Cortical cells which project to the tectum were identified by injecting HRP into superficial or deep layers of the superior colliculus and into various parts of the inferior colliculus. The main result is that these descending projections are well organized according to their origin in the three main sensory fields of the cortex. (1) Auditory field: labeled cells are found only in the core or auditory koniocortex, after injections of HRP in the pericentral area of the inferior colliculus; labeled cells are found in auditory belt areas after injections in posterior parts of the intermediate and deep layers of the superior colliculus, adjacent to the inferior colliculus. (2) Somatic field: labeled cells are also found in the somatic field after injections in the intermediate and deep layers of the superior colliculus, so that auditory and somatic fields probably overlap to some extent. The results do not exclude the possibility that somatic koniocortex has an exclusive target in the intermediate or deep layers of the superior colliculus. (3) Visual field: labeled cells are found only in the core or striate cortex after injections in the superficial layers of the superior colliculus. Labeled cells are found in the visual belt after injections in the rostral parts of the intermediate layers of the superior colliculus. When these results are related to ascending sensory pathways a picture emerges of a series of circuits or loops which interconnect parallel sensory pathways. These loops eventually reach the deep layers of the superior colliculus which of course have indirect access to motor neurons.

Animals↗
PubMed1979

Thalamic projections to layer I of striate cortex shown by retrograde transport of horseradish peroxidase.

The diffusion of horseradish peroxidase was restricted to layers I and II of the striate cortex in Tupaia glis and Galago senegalensis. In the lateral geniculate body of Tupaia labeled cells were found only in layer 3; some labeled cells were also found in the lateral nucleus. In Galago labeled cells were found only in layers 4 and 5 of the lateral geniculate body; a band of cells was also found in the pulvinar nucleus. These results support the distinction between two overlapping thalamic systems, a layer I and a layer IV system.

Animals↗
PubMed1978

Some further observations on the effects of unilateral cortical ablation on sound localization in the cat.

It has previously been shown that unilateral ablation of the whole auditory cortex in the cat disrupts the precedence effect, and also interferes with the ability of the normal animal to discriminate in the Y-maze between a single sound on one side and a double sound consisting of a signal on both left and right sides. The present work has confirmed these effects and has shown that both can be obtained with lesions confined to AI and AII. The "one-versus-two" deficit has invariably been seen in all the animals studied, but a proportion of animals do not show the precedence effect deficit. It has been confirmed that the apparent sucess of some animals can be due to the training effect of the one-versus-two paradigm, as was proposed in the earlier paper; however it has also been shown that this cannot be explanation in all cases. It has been demonstrated that cats are able to localize sound behind them with some success; turning around in the start box to reverse right and left space is therefore a possible strategy for overcoming a unilateral deficit. However, even with the head "fixed" in the forward-facing position, one animal was still able to run well above chance. The size of the lesion does not appear to be a correlate of the performance level.

Animals↗
PubMed1977

The visual cortex of the opossum: the retrograde transport of horseradish peroxidase to the lateral geniculate and lateral posterior nuclei.

The visual cortex of opossum was studied by injecting horseradish peroxidase into the cortex and identifying labeled neurons in the thalamus. The results show that the lateral geniculate nucleus projects to area 17 in a topographical manner: the rostral lateral geniculate is represented in caudal striate cortex, and the dorsal extremity of the lateral geniculate, which probably corresponds to the zero vertical meridian, is represented along the border of area 18. Small injections in area 17 produced restricted bands of labeled neurons across the medial-lateral extent of the lateral geniculate, suggesting a greater precision in the topography than previously shown by retrograde degeneration studies. Following injections into area 17, labeled cells were also found in the lateral posterior nucleus. Injections of peristriate cortex produced labeled cells in the lateral posterior nucleus, as well as the lateral intermediate, posterior and intralaminar nuclei. Since the lateral posterior nucleus receives visual projections from the superior colliculus, the results show two visual pathways: the geniculo-striate path projecting just to core area or area 17, and a more diffuse parallel path that projects to both the core and belt. Whether or not this overlap is characteristics of the mammalian prototype it seems to be present in widely separated species.

Animals↗
PubMed1977

Symmetrical lateralization of function in the auditory system of the cat: effects of unilateral ablation of cortex.

We have presented behavioral evidence suggesting that one function of auditory cortex is to attend to stimuli at the contralateral ear. Further, behavioral and anatomic evidence shows that the neural mechanisms for this function probably depend on a pathway that crosses at the level of the medulla, bypasses the superior olive, and ascends to the contralateral inferior colliculus. At higher centers there are several auditory pathways from thalamus to cortex, as well as descending pathways from cortex, and some of these pathways may play a role in selective listening with one ear.

Acoustic Stimulation↗
PubMed1976

Auditory pathways to the cortex in Tupaia glis.

The auditory system of the tree shrew, Tupaia glis, was investigated by identifying axonal degeneration after lesions of the lateral lemniscus, the inferior colliculus, the medial geniculate nucleus and the auditory cortex. The results show that the lateral lemniscus projects to the central nucleus of the inferior colliculus which in turn projects principally to the ventral division of the medial geniculate nucleus but to a lesser extent to the magnocellular division of the medial geniculate nucleus. The final step in the pathway to the cortex is achieved by a projection from the ventral division to the fourth layer of auditory koniocortex. There appear to be several auditory pathways parallel to this primary path. The lateral lemniscus projects to the dorsal division of the medial geniculate nucleus; the deeper layers of the superior colliculus project to the posterior nucleus; and both the dorsal division and the posterior nucleus project to the belt caudal to auditory koniocortex. The caudal division of the medial geniculate nucleus may constitute a relay in still another path from the pericentral division of the inferior colliculus. Finally, the magnocellular division also appears to be distinct insofar as its cortical projections are confined chiefly to the deeper layers. A comparison between the tree shrew and the cat reveals a similar organization in the two species. In the cat the starting point for understanding the organization of the several auditory pathways is the distinction between a core cortical zone which corresponds to konicortex and to AI and a peripheral belt. The core receives essential projections from the ventral division; the belt receives sustaining projections from the cell groups which surround the ventral division. It is reasonable to hypothesize that this difference between the core and the belt is characteristic of all mammals.

Animals↗