Biomedical subjects

M J Pianta

Publications and source records attributed to M J Pianta.

4 recordsLinked to original sources

PubMed1998

Developing a clinical probability density function for automated perimetry.

BACKGROUND: Automated perimetry is associated with lengthy test times, but Baysean predictions can be applied to speed up testing. A critical component of such methods is the starting probability density function (PDF). METHODS/RESULTS: In the present study we show that a unimodal PDF, suggested n the literature as adequate for clinical data, fails to describe the thresholds of diseased eyes and we develop a bi-modal PDF representative of a clinical population. CONCLUSION: We suggest that the implementation of a bi-modal PDF will save test time and retain test accuracy.

Adult↗

PubMed1998

Characteristics of anisometropic suppression: simple reaction time measurements.

The characteristics of artificially induced anisometropic suppression were investigated in observers with normal and abnormal binocular vision (anisometropic amblyopia) by using a simple reaction time paradigm. Reaction time was measured as a function of stimulus intensity for various stimulus durations. For all conditions, the reaction time increased as stimulus intensity decreased toward threshold. We found that traditional techniques for modeling this trend were inadequate, so we developed a simple visuogram method for comparing these functions. Using this technique, reaction time versus intensity functions are shown to be shape-invariant for all conditions examined. This means that, although reaction times are longer during induced anisometropic suppression or in anisometropic amblyopia, they are the same if contrast is normalized to equate threshold. The shape-invariant nature of these functions is also consistent with the notion that a single mechanism mediates detection under these conditions. Temporal summation was investigated at both threshold (method of limits) and suprathreshold (criterion reaction time) levels. Again, because of shape invariance, the suprathreshold results mirror the threshold results. The critical duration (the duration at the intersection of the complete summation and zero summation regions) is not affected by any of the conditions. However, the critical intensity (the intensity for the zero summation region) is higher for the amblyopic eyes, as compared with the normal or nonamblyopic eyes. Induced anisometropic suppression always increases the critical intensity, with a smaller increase occurring for the amblyopic eyes. This suggests that amblyopic eyes do not have a need for strong suppression.

Anisometropia↗

PubMed1997

L and M cone input into spectral sensitivity functions: a reanalysis.

In order to better understand the nature of long-wavelength (L) and middle-wavelength (M) cone input into spectral sensitivity functions and determine the reliability with which it is possible to predict L:M cone inputs, we developed analytical methods to determine confidence intervals for L:M cone input for spectral sensitivity functions or data transformed to cone-contrast space. Spectral sensitivity functions measured by direct heterochromatic brightness matches are dominated by the L/M opponent channel over most of the spectral range. For detection of large/ long test stimuli, spectral sensitivity functions show a characteristic "notch" at the adapting wavelength, with the L/M opponent channel dominating most of the spectral range. Flicker increment threshold (FIT) spectral sensitivity functions display many of the characteristics of the luminance flicker mechanism described by Stromeyer et al. (1987). [Vision Research, 27, 1113-1137]. Previous modelling of FIT spectral sensitivity functions proposed a 2:1 L:M cone input for most of testing conditions. We show that FIT spectral sensitivity functions are dominated by L cones but show L cone suppression under bright red adapting fields. For the fitted spectral sensitivity functions or simulated data sets, we found small confidence intervals for L:M cone input into the L/M opponent channel and conclude that it is possible to reliably predict L:M cone input ratios. However, for similar data sets of additive spectral sensitivity functions, we found large confidence intervals for L:M cone input ratios and conclude that it is not possible reliably predict L:M cone input into the L/M non-opponent channel using available spectral sensitivity functions.

Adaptation, Ocular↗

PubMedDate not supplied

Reduced glutamate uptake by retinal glial cells under ischemic/hypoxic conditions.

The high-affinity uptake of glutamate by glial cells and neurons of the central nervous system, including the retina, serves to inactivate synaptically released glutamate and maintains glutamate at low concentrations in the extracellular space. This uptake prevents accumulation of glutamate extracellularly and thus minimizes the possibility of glutamate neurotoxicity secondary to ischemic insult. One mechanism whereby glutamate neurotoxicity may occur in ischemic/hypoxic insult is through increased extracellular K+ reversing the electrogenic glutamate uptake into retinal glial (Müller) cells. We investigated glial uptake of the amino acids glutamate, GABA, and D-aspartate in the intact isolated rat retina under high extracellular K+ conditions and under conditions simulating ischemia. Immunocytochemical findings showed that uptake of glutamate and GABA by MIller cells in the intact isolated rat retina continues under conditions simulating ischemia and high extracellular K+ conditions, and uptake of D-aspartate also continues under high K+ conditions. However, under high K+ conditions, the glutamate uptake system saturates at a lower concentration of exogenous glutamate than in the normal K+ condition. These findings provide evidence that disruption of glutamate uptake by Müller cells is likely to be a significant contributing factor to excess glutamate accumulation in the extracellular space which can lead to neurotoxicity.

Animals↗