Electrophysiological-histological studies on some functional properties of visual cells and second order neurons of an insect retina

1973 ◽  
Vol 136 (2) ◽  
pp. 291-306 ◽  
Author(s):  
M. J�rvilehto ◽  
F. Zettler

The optic nerve fibres project on to the optic lobe in a regular manner, being precisely re-assorted after passing through a chiasma. In the outer plexiform zone the optic nerve fibres end in contact with the dendrites of second-order visual cells. These presumably serve to classify the visual input and four types can be recognized anatomically: (1) The smallest have minute circular dendritic fields, in contact with one or few optic nerve fibres. (2) There are also larger circular fields. (3) Many cells have very elongated narrow dendritic fields each running straight in one direction and thus perhaps sensitive to edges. (4) The largest second-order visual cells have enormous oval dendritic fields, several millimetres long, orientated in the long axis of the lobe. Each type of field occupies a different level, producing the characteristic layering of the outer plexiform zone. Numerous amacrine cell processes end in the outer plexiform layer, some are very small with restricted branches, others have wide trees with fibres passing first inwards then outwards several times. There are thus possibilities of establishing uniform conditions of excitation or inhibition over small or large areas of the visual field. The dendrites of the centrifugal cells with axons passing to the retina spread in the various layers of the plexiform zone. They could serve to project information of the areas excited, or inhibited, out to the retina. The axons of the second-order visual cells form radial columns in the outer part of the medulla of the optic lobe. Those with the smaller dendritic fields end more superficially, the largest ones about half-way through the lobe. Each column contains fibres and neuropil at its centre, surrounded by multipolar and bipolar amacrine cells, whose branches enter the neuropil among the endings of the second-order visual cells. Horizontal multipolar cells of various sizes link the columns. Third-order visual cells send dendrites into these columns and axons deeper into the lobe, some directly to the optic tract. The giant cells of the magnocellular lobe can thus be activated by a visual pathway involving only two previous synapses (as well as by a direct static pathway involving none). Central to the zone of radial columns is a zone where many of the connexions are tangential. There is an increasing number of large cells passing centrally, many being presumably fourth-order visual neurons. They send axons either elsewhere within the lobe or to the optic tract. Fibres reaching the lobe from the central brain or opposite lobe are distributed in this region and also reach out into the radial columns. In many of the tracts leaving the optic lobes for other centres the fibres maintain precise topographical relations, as also do those of the optic commissure. This regularity is especially clear in the bundles that pass to the motor centres (peduncle lobes and anterior basal lobes) but may be present in others. There is thus a regular mapping of the visual field throughout much of the system. Other pathways show complex interweaving, for instance those for colour control, where the response pattern is not topographically related to the visual input.


1973 ◽  
Vol 61 (4) ◽  
pp. 444-461 ◽  
Author(s):  
Daniel L. Alkon

Intracellular recording was used to study the response to light of second order visual cells within the optic ganglion of Hermissenda crassicornis. Simultaneous recordings revealed that type B but not type A photoreceptors inhibit the second order cells. Additional details of the neural organization of the visual system were obtained. Possible functional implications of this neural organization are discussed.


Author(s):  
T. Wichertjes ◽  
E.J. Kwak ◽  
E.F.J. Van Bruggen

Hemocyanin of the horseshoe crab (Limulus polyphemus) has been studied in nany ways. Recently the structure, dissociation and reassembly was studied using electron microscopy of negatively stained specimens as the method of investigation. Crystallization of the protein proved to be possible and X-ray crystallographic analysis was started. Also fluorescence properties of the hemocyanin after dialysis against Tris-glycine buffer + 0.01 M EDTA pH 8.9 (so called “stripped” hemocyanin) and its fractions II and V were studied, as well as functional properties of the fractions by NMR. Finally the temperature-jump method was used for assaying the oxygen binding of the dissociating molecule and of preparations of isolated subunits. Nevertheless very little is known about the structure of the intact molecule. Schutter et al. suggested that the molecule possibly consists of two halves, combined in a staggered way, the halves themselves consisting of four subunits arranged in a square.


Author(s):  
W. L. Bell

Disappearance voltages for second order reflections can be determined experimentally in a variety of ways. The more subjective methods, such as Kikuchi line disappearance and bend contour imaging, involve comparing a series of diffraction patterns or micrographs taken at intervals throughout the disappearance range and selecting that voltage which gives the strongest disappearance effect. The estimated accuracies of these methods are both to within 10 kV, or about 2-4%, of the true disappearance voltage, which is quite sufficient for using these voltages in further calculations. However, it is the necessity of determining this information by comparisons of exposed plates rather than while operating the microscope that detracts from the immediate usefulness of these methods if there is reason to perform experiments at an unknown disappearance voltage.The convergent beam technique for determining the disappearance voltage has been found to be a highly objective method when it is applicable, i.e. when reasonable crystal perfection exists and an area of uniform thickness can be found. The criterion for determining this voltage is that the central maximum disappear from the rocking curve for the second order spot.


Author(s):  
Kazushige Hirosawa ◽  
Eichi Yamada

The pigment epithelium is located between the choriocapillary and the visual cells. The pigment epithelial cell is characterized by a large amount of the smooth endoplasmic reticulum (SER) in its cytoplasm. In addition, the pigment epithelial cell of some lower vertebrate has myeloid body as a specialized form of the SER. Generally, SER is supposed to work in the lipid metabolism. However, the functions of abundant SER and myeloid body in the pigment epithelial cell are still in question. This paper reports an attempt, to depict the functions of these organelles in the frog retina by administering one of phospholipid precursors.


2001 ◽  
Vol 268 (6) ◽  
pp. 1739-1748
Author(s):  
Aitor Hierro ◽  
Jesus M. Arizmendi ◽  
Javier De Las Rivas ◽  
M. Angeles Urbaneja ◽  
Adelina Prado ◽  
...  

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