The role of stimulus complexity, spectral overlap, and pitch for gap-detection thresholds in young and old listeners.

Thresholds for detecting a gap between two complex tones were determined for young listeners with normal hearing and old listeners with mild age-related hearing loss. The leading tonal marker was always a 20-ms, 250-Hz complex tone with energy at 250, 500, 750, and 1000 Hz. The lagging marker, also tonal, could differ from the leading marker with respect to fundamental frequency (f0), the presence versus absence of energy at f0, and the degree to which it overlapped spectrally with the leading marker. All stimuli were presented with steeper (1 ms) and less steep (4 ms) envelope rise and fall times. F0 differences, decreases in the degree of spectral overlap between the markers, and shallower envelope shape all contributed to increases in gap-detection thresholds. Age differences for gap detection of complex sounds were generally small and constant when gap-detection thresholds were measured on a log scale. When comparing the results for complex sounds to thresholds obtained for pure-tones in a previous study by Heinrich and Schneider [(2006). J. Acoust. Soc. Am. 119, 2316-2326], thresholds increased in an orderly fashion from markers with identical (within-channel) pure tones to different (between-channel) pure tones to complex sounds. This pattern of results was true for listeners of both ages although younger listeners had smaller thresholds overall.

Masking-level differences in older adults: the effect of the level of the masking noise.

In Experiment 1, masking-level differences (MLDs) for a 500-Hz tone at five masker levels were obtained from younger and older adults. For both age groups, there were no reliable increases in MLD once the spectrum level of the masker exceeded 27 dB SPL. MLDs were larger for younger than for older adults over the range of masker levels tested. In Experiment 2, the levels of both the signal and the masker in one ear were attenuated by either 15 or 30 dB relative to their level in the other ear, which was fixed at a spectrum level of 47 dB SPL. MLDs for both age groups declined with increasing IAA and age-related differences were observed in all conditions. The findings of these experiments indicate that (1) age-related differences in MLDs exist even when the level of the masker is sufficiently high that older adults achieve their plateau performance, and (2) older listeners are not disadvantaged more than younger listeners by interaural differences in the level of the input.

Gap detection and the precedence effect in young and old adults.

Thresholds for detecting a gap between two Gaussian-enveloped (standard deviation = 0.5 ms), 2-kHz tones were determined in young and old listeners. The gap-detection thresholds of old adults were more variable and about twice as large as those obtained from young adults. Moreover, gap-detection thresholds were not correlated with audiometric thresholds in either group. Estimates of the width of the temporal window of young subjects, based on the detection of a gap between two tone pips, were smaller than those typically obtained when a relatively long duration pure tone is interrupted [Moore et al., J. Acoust. Soc. Am. 85, 1266-1275 (1989)]. Because the amount of time it takes to recover from an adapting stimulus is likely to affect gap detection thresholds [Glasberg et al., J. Acoust. Soc. Am. 81, 1546-1556 (1987)], smaller estimates of temporal window size would be expected in this paradigm if the amount of adaptation produced by the first tone pip was negligible. The larger gap-detection thresholds of old subjects indicate that they may have larger temporal windows than young subjects. The lack of correlation between audiometric and gap-detection thresholds indicates that this loss of temporal acuity is not related to the degree of sensorineural hearing loss. In a second experiment on the precedence effect using the same subjects, a Gaussian-enveloped tone was presented over earphones to the left ear followed by the same tone pip presented to the right ear. To more realistically approximate a sound field situation, the tone pip presented to each ear was followed 0.6 ms later by an attenuated version presented to the contralateral ear. The delay between the left- and right-ear tone-pips was varied and the transition point between hearing a single tone on the left, and hearing two such sounds in close succession (one coming from the left and the other from the right) was determined. The transition point in this experiment did not differ between young and old subjects nor were these transition points correlated with gap-detection thresholds. These results indicate that monaural temporal acuity and binaural echo suppression may be based on different processes.

Inhibition of the effects of 12-O-tetradecanoylphorbol-13-acetate on mouse epidermal glutathione peroxidase and ornithine decarboxylase activities by glutathione level-raising agents and selenium-containing compounds.

The present study was undertaken to determine the effect of 12-O-tetradecanoylphorbol-13-acetate (TPA), a potent tumor promoter known to inhibit superoxide dismutase (SOD) (superoxide: superoxide oxidoreductase, EC 1.15.1.1) and catalase (CAT) (H2O2: H2O2 oxidoreductase, EC 1.11.1.6) activities, on mouse epidermal glutathione (GSH) peroxidase (glutathione: H2O2 oxidoreductase, EC 1.11.1.9) activity in vivo and in vitro. TPA led to a rapid and transient increase in GSH peroxidase specific activity within 30 min followed by a decrease from 1 to 12 h. Incubation of isolated epidermal cells with GSH level-raising agents and/or selenium-containing compounds increased remarkably basal GSH peroxidase activity, and thus, abolished totally the prolonged inhibitory effects of TPA on this enzyme. The inhibitory effects of 0.2 mM cysteine (Cys) or 0.5 mM GSH and 2.5 microM Na2 SeO3 or 50 microM selenocystamine on TPA-decreased GSH peroxidase activity were additive, in relation with their additive inhibitory effects on TPA-induced ornithine decarboxylase (ODC) (L-ornithine carboxylase, EC 4.1.1.17) activity. These data support the hypothesis that the stimulators of the GSH-dependent antioxidant protective system of the epidermal cells may inhibit the oxidative challenge linked to skin tumor promotion by TPA.