1990
DOI: 10.1007/bf00228890
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Processing of amplitude modulated sounds in the medial geniculate body of squirrel monkeys

Abstract: The responses of single and multi units in the medial geniculate body of the squirrel monkey (Saimiri sciureus) to modulation frequency, modulation depth and changes in absolute intensity of sinusoidally amplitude modulated (AM) sounds were studied. Both spike-frequency and spike rate modulation were used as a measure for neuronal response. Spike rate modulation was derived from FFT (Fast-Fourier-Transformation) analysis of the PSTHs. In all cases (N = 133) spike rate modulation was shown to be dependent on th… Show more

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Cited by 60 publications
(39 citation statements)
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“…It is also important to consider the modulation frequencies that did not generate the expected suppression produced when S1 and S2 carrier frequencies matched. In some cases, the suppression probably mirrored the modulation frequency tuning of inputs that have already been formed at subcortical levels (Creutzfeldt et al 1980;Langner and Schreiner 1988;Preuss and Muller-Preuss 1990). However, many S1 stimuli drove the neuron and still did not produce suppression, supporting the assertion that suppression differed from spiking habituation.…”
Section: Sensitivity To S1 Modulation Frequencymentioning
confidence: 69%
“…It is also important to consider the modulation frequencies that did not generate the expected suppression produced when S1 and S2 carrier frequencies matched. In some cases, the suppression probably mirrored the modulation frequency tuning of inputs that have already been formed at subcortical levels (Creutzfeldt et al 1980;Langner and Schreiner 1988;Preuss and Muller-Preuss 1990). However, many S1 stimuli drove the neuron and still did not produce suppression, supporting the assertion that suppression differed from spiking habituation.…”
Section: Sensitivity To S1 Modulation Frequencymentioning
confidence: 69%
“…Another simplification we employed was to implement thalamic activity in response to AM stimuli as a smooth, rectified sinusoid that mirrored the stimulus (Eq. 4); thalamic activity in vivo shows more complex temporal profiles as well as diverse response tuning (Bartlett and Wang 2007;Creutzfeldt et al 1980;Miller et al 2002;Preuss and Muller-Preuss 1990). Nonetheless, the model provides insight into the qualitative effects that the modeled synaptic and intrinsic properties may have on cortical responses.…”
Section: Discussionmentioning
confidence: 95%
“…The synchronization of responses to SAM stimuli in the IC, the SPON's main projection target, is limited to MRs of ~ 200 Hz in all mammalian species tested, including rats (Rees and Moller, 1987), guinea pigs (Rees and Palmer, 1989), gerbils (Krishna and Semple, 2000), squirrel monkeys (MullerPreuss et al, 1994), and mice , and is similarly limited in the medial geniculate body (Creutzfeldt et al, 1980;Preuss and Muller-Preuss, 1990), another recently identified projection target of the SPON (Jin and Berrebi, 2006). Therefore, by providing a highly synchronized inhibitory input, the SPON may serve to shape responses in its target nuclei by segmenting their ongoing responses.…”
Section: Functional Implicationsmentioning
confidence: 99%