Excitatory and inhibitory frequency response areas of 130 neurons of the central nucleus of the mouse inferior colliculus (ICC) were mapped by extracellular single-unit recordings and quantitatively evaluated with regard to thresholds, steepness of slopes of excitatory tuning, characteristic frequencies of excitation (CF(E)), inhibition (CFI), and bandwidths of response areas (sharpness of tuning). Two-tone stimuli were used to determine the shapes of inhibitory response areas. Class I neurons (n=54) had asymmetrical (with regard to the CF(E)) excitatory and inhibitory response areas, with inhibition above CF(E) having lower thresholds and covering larger areas than inhibition below CF(E). Quantitative relationships between CF(E) and CF(I) thresholds, and sharpness of tuning showed that the receptive fields of about two-thirds of these neurons had properties similar to auditory nerve fibers. Class II neurons (n=36) had small symmetrical or tilted excitatory areas of rather constant bandwidths and broad inhibitory areas reaching far into and often through the excitatory area, leading to closed excitatory areas in ten neurons. Class III neurons (n=32) had higher excitatory thresholds and the highest proportions of unilateral inhibitory areas compared with neurons of the other classes. Their excitatory area often widened symmetrically with increasing sound level. Their inhibitory areas did not overlap with the excitatory area. Class IV neurons (n=8) had two branches of excitatory areas (two-CFs(E)) and six of the neurons had a central inhibitory area in addition to the low- and high-frequency inhibitory areas. In most neurons, the shapes of excitatory response areas predicted the shapes of inhibitory areas. Altogether, 15 neurons from all 4 classes had areas of facilitation in addition to inhibitory areas. Facilitation in six class IV neurons occurred between the two branches of the excitatory area. All 130 neurons had large inhibitory areas, 106 of them on both sides of the excitatory area. That is, sound processing in the ICC shows strong inhibitory components. The close relationships between excitatory and inhibitory CFs found here indicate that inhibitory projections to and interactions within the ICC are tonotopically organized comparable to the excitatory ones.

Selectivity for processing of species-specific vocalizations and communication sounds has often been associated with the auditory cortex. The midbrain inferior colliculus, however, is the first center in the auditory pathways of mammals integrating acoustic information processed in separate nuclei and channels in the brainstem and, therefore, could significantly contribute to enhance the perception of species' communication sounds. Here, we used natural wriggling calls of mouse pups, which communicate need for maternal care to adult females, and further 15 synthesized sounds to test the hypothesis that neurons in the central nucleus of the inferior colliculus of adult females optimize their response rates for reproduction of the three main harmonics (formants) of wriggling calls. The results confirmed the hypothesis showing that average response rates, as recorded extracellularly from single units, were highest and spectral facilitation most effective for both onset and offset responses to the call and call models with three resolved frequencies according to critical bands in perception. In addition, the general on- and/or off-response enhancement in almost half the investigated 122 neurons favors not only perception of single calls but also of vocalization rhythm. In summary, our study provides strong evidence that critical-band resolved frequency components within a communication sound increase the probability of its perception by boosting the signal-to-noise ratio of neural response rates within the inferior colliculus for at least 20% (our criterion for facilitation). These mechanisms, including enhancement of rhythm coding, are generally favorable to processing of other animal and human vocalizations, including formants of speech sounds.

Neurons in the central nucleus of the auditory midbrain inferior colliculus divide into four classes according to the shapes of their receptive fields. Neurons of two of these classes - sharply tuned, inhibition-dominated neurons of class II, and broadly tuned neurons of class III - show systematic gradients in their abundance on isofrequency contours. Sharp tuning is most prevalent in the center, broad tuning in the periphery of the ICC. This new map of tuning-curve shape adds to the six previously described maps of neural response properties on isofrequency contours of the ICC and stresses the fact that very different sensitivities and selectivities to sound properties are combined in local clusters of collicular neurons.

Critical bands are perceptual filters that detect and separate spectral peaks in complex sounds. Here, we show that the main properties of psychophysically defined critical bands, as measured in narrow-band noise masking tests (species-specific frequency dependence and intensity independence of the bandwidths), are present in single neurons of the mouse's central nucleus of the inferior colliculus. Bandwidths of critical bands amount to, on average, 3/8-1/3 octave related to the neurons' characteristic frequencies. They are not determined by the shapes of the neurons' excitatory receptive fields. The results support the view that frequency resolution in the auditory system is shaped to its perceptual level in the main nucleus of the auditory midbrain.

Frequency resolution and spectral integration in acoustic perception is investigated psychacoustically by measuring critical bands (CBs) or equivalent quantities. In general, CB bandwidths increase with increasing sound frequency but remain constant over a large range of sound pressure levels (SPL; intensity independence). These CB properties have previously been found, on average, in responses of midbrain inferior colliculus neurons. Here, we use single-neuron recordings from the central nucleus of mouse inferior colliculus (ICC) to study neurons' excitatory and inhibitory frequency receptive fields together with neural critical bands (NCBs) measured in a narrowband noise-masking paradigm at SPLs up to 85 dB. We aim to clarify whether and how neurons with very different shapes of excitatory and inhibitory receptive fields express CB properties, whether and how inhibition contributes to set boundaries of NCBs, and where these boundaries are located in the excitatory-inhibitory receptive fields. The main results are: the above-mentioned general CB properties exist in neurons independent of the shapes of their receptive fields, that is, frequency filtering related to single tones (tuning curves) and frequency resolution related to complex sounds (NCBs) are different neuronal properties; NCB boundaries match the boundaries of an area devoid of inhibition around the characteristic frequencies in 67% of the neurons, that is, the inhibitory influence is adjusted to frequency resolution in part of the neurons; filter bandwidths of NCBs are, relative to their centre frequencies, about on average 1/3 octave wide, equaling the average frequency distance between frequency-band laminae as found in the cat ICC.