Transneuronal transport in the frog visual system

1976 ◽  
Vol 109 (3) ◽  
pp. 623-627 ◽  
Author(s):  
Gyula La´za´r
1977 ◽  
Vol 121 (2) ◽  
pp. 343-347 ◽  
Author(s):  
Jacques Repérant ◽  
Dom Miceli ◽  
Jean-Pierre Raffin

1997 ◽  
Vol 14 (2) ◽  
pp. 213-224 ◽  
Author(s):  
Dom Miceli ◽  
Jacques Repérant ◽  
Renuka Bavikati ◽  
Jean-Paul Rio ◽  
Michel Volle

AbstractBrain-stem afferents to the n. isthmo-opticus (NIO) and ectopic neurons (EN) of the centrifugal visual system (CVS) were determined in the pigeon using the retrograde transneuronal transport of the fluorescent dye Rhodamine β-isothiocyanate (RITC) after its intraocular injection. In other experiments, either RITC was injected into various periocular tissues (controls) or the retrograde tracer Fluoro-gold (FG) was injected stereotaxically in the NIO. Following intraocular injections, the RITC retrograde labeling of cell bodies was observed contralaterally in the NIO and EN and transneuronally in layers 9/10 of the optic tectum, area ventralis-Tsai, zona peri-NIII, mesencephalic and pontine reticular formation (PRF), n. linearis caudalis-raphe, and bilaterally within a region referred to as zona peri-n.NVI (Zp-n.NVI) immediately underlying the abducens nerve nucleus. None of the above structures were labeled after RITC periocular injections. The FG labeling revealed that the tectal efferent neurons were mainly medium-sized, multipolar cells whose dendrites extended superficially to retino-recipient tectal layers 6 and 5. Quantitative measurements of the distribution of layers 9/10 RITC-labeled neurons indicated the highest densities to be localized within the ventral tectum corresponding to the representation of the dorsal retina and inferior visual field. We suggest that visual and nonvisual brain-stem afferents upon NIO and EN may play a role in the proposed mechanism of the avian CVS in attention, ground-feeding behavior, and modulation of retinal sensitivity.


1977 ◽  
Vol 129 (2) ◽  
pp. 346-352 ◽  
Author(s):  
J.T. Weber ◽  
V.A. Casagrande ◽  
J.K. Harting

2020 ◽  
Author(s):  
Samson Chengetanai ◽  
Adhil Bhagwandin ◽  
Mads F. Bertelsen ◽  
Therese Hård ◽  
Patrick R. Hof ◽  
...  

Author(s):  
Klaus-Ruediger Peters

Differential hysteresis processing is a new image processing technology that provides a tool for the display of image data information at any level of differential contrast resolution. This includes the maximum contrast resolution of the acquisition system which may be 1,000-times higher than that of the visual system (16 bit versus 6 bit). All microscopes acquire high precision contrasts at a level of <0.01-25% of the acquisition range in 16-bit - 8-bit data, but these contrasts are mostly invisible or only partially visible even in conventionally enhanced images. The processing principle of the differential hysteresis tool is based on hysteresis properties of intensity variations within an image.Differential hysteresis image processing moves a cursor of selected intensity range (hysteresis range) along lines through the image data reading each successive pixel intensity. The midpoint of the cursor provides the output data. If the intensity value of the following pixel falls outside of the actual cursor endpoint values, then the cursor follows the data either with its top or with its bottom, but if the pixels' intensity value falls within the cursor range, then the cursor maintains its intensity value.


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