Contribution of human melanopsin retinal ganglion cells to steady-state pupil responses.

The recent discovery of melanopsin-containing retinal ganglion cells (mRGCs) has led to a fundamental reassessment of non-image forming processing, such as circadian photoentrainment and the pupillary light reflex. In the conventional view of retinal physiology, rods and cones were assumed to be the only photoreceptors in the eye and were, therefore, considered responsible for non-image processing. However, signals from mRGCs contribute to this non-image forming processing along with cone-mediated luminance signals; although both signals contribute, it is unclear how these signals are summed. We designed and built a novel multi-primary stimulation system to stimulate mRGCs independently of other photoreceptors using a silent-substitution technique within a bright steady background. The system allows direct measurements of pupillary functions for mRGCs and cones. We observed a significant change in steady-state pupil diameter when we varied the excitation of mRGC alone, with no change in luminance and colour. Furthermore, the change in pupil diameter induced by mRGCs was larger than that induced by a variation in luminance alone: that is, for a bright steady background, the mRGC signals contribute to the pupillary pathway by a factor of three times more than the L- and M-cone signals.

Representation of cardinal contour overlaps less with representation of nearby angles in cat visual cortex.

Extensive attempts have been made to explain the neurobiological basis of the greater sensitivity of the visual system to vertically or horizontally oriented information than to information presented at oblique angles. However, investigators have largely ignored the overlap of the representation of a given angle with the representation of nearby angles. Recordings based on intrinsic optical signals were obtained in area 17 from 12 adult cats during the presentation of contours in various orientations. A method investigating both amplitude and statistical significance of changes was proposed to evaluate the orientation tuning properties for cell populations in the central area retinotopically corresponding to 0-15 degrees of visual field. Cardinal orientations were found to activate significantly greater areas in the exposed cortical area than the areas activated by oblique orientations. Areas activated by cardinal or oblique contours and those separated from them by 10 degrees were compared. A significantly lower degree of overlap was seen between areas activated by presentation of cardinal contours and areas activated by neighboring orientations compared with those for oblique orientations which overlapped more extensively with neighboring orientations. In addition, areas activated only by cardinal contours were significantly larger than areas activated only by oblique contours. These results demonstrated in cell population level that more cells prefer horizontal or vertical orientations, and these cells are tuned more sharply than oblique selective cells.

Difference in the representation of cardinal and oblique contours in cat visual cortex.

Optical imaging based on intrinsic signals was used to analyze the structure of orientation column in area 18 of cat visual cortex. Recordings were obtained in 12 adult cats during presentation of contours in various orientations. In order to quantitatively evaluate the size of the response area, a method combining both information on the amplitude of the changes and the statistical significance of the changes was proposed. The results showed that the proportion of the cortical area activated reached a peak during the presentation of horizontal or vertical contours, whereas the areas activated by oblique contours were relatively smaller. Cardinal contours (0 degrees and 90 degrees ) activated 50.63 +/- 1.88% (mean +/- SE) of the cortical area in the recording site, whereas oblique contours (45 degrees and 135 degrees ) activated only 45.25 +/- 2.02% of the area. This difference in area was statistically significant (t = 2.38, d.f. = 11, and P < 0.05). The results demonstrated a difference in the representations of the cardinal and oblique contours in area 18 of the cat visual cortex.

Glutamate-induced increases in intracellular Ca2+ in cultured rat neocortical neurons.

In neurons, changes in intracellular Ca2+ concentration ([Ca2+]i) trigger neurotransmitter release, regulate membrane excitability, affect gene expression, and govern short- and long-term forms of synaptic plasticity. Rises in cytoplasmic Ca2+ are thought to underlie the various effects of glutamatergic neurotransmitters within the central nervous system. In the present study, we applied a calcium imaging technique using a confocal laser scanning microscope to investigate the effects of excitatory amino acids on glutamate induced calcium influx in primary cultured neocortical neurons. Glutamate (5 microM) induced increases in [Ca2+]i in both the soma and dendritic processes of the cells. The increase was partially blocked by 10 microM DL-2-amino-5-phosphovaleric acid (APV), a NMDA antagonist. The reduction was higher in the dendritic process than in the cell body: the reduction was 58% in the cell body and 67% in the dendritic processes. In contrast, 5 microM 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), a non-NMDA antagonist, had less effect on the response. We observed an 11% reduction in the dendritic processes, but no change in the cell bodies. The results demonstrated the heterogeneous distribution of APV- and CNQX-sensitive channels in primary cultured neocortical neurons. In both the cell body and dendritic processes, [Ca2+]i increase induced by low concentrations of glutamate was mainly due to the activation of NMDA receptors.