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Diego Minciacchi

Publications and source records attributed to Diego Minciacchi.

4 recordsLinked to original sources

Spatial analysis reveals alterations of parvalbumin- and calbindin-positive local circuit neurons in the cerebral cortex of mutant mdx mice.

The aim of the present study was to investigate the spatial organization of selected populations of local circuit neurons in the cerebral cortex of the mutant mdx mouse, an acknowledged model of Duchenne Muscular Dystrophy. To this purpose, we quantified and compared the distribution of parvalbumin- and calbindin-positive neurons in the motor, somatosensory, visual, and anterior cingulate cortices of wild-type and mdx mice. The methodological approach was based on generation of two-dimensional Voronoi polygons from digital charts of the cell populations visualized immunohistochemically. Polygon areas were then analyzed and the derived coefficients of variation were statistically compared. Using this strategy, we were able to reveal, in mdx mice, changes involving both the above populations of interneurons. These changes were evident in the motor and anterior cingulate cortices but not in the somatosensory and visual cortices. In addition, the changes of coefficients of variation were area-specific in the cortex of mdx mice. The values increased in the motor cortex and decreased in the anterior cingulate cortex with respect to the corresponding values of wild-type animals. The present findings point out widespread alterations in the mdx cortex involving also areas not primarily related to sensorimotor integration. In addition, we demonstrate that cortical alterations of the local circuit machinery are characterized in mdx mice by individual regional differences.

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Cortical and brainstem neurons containing calcium-binding proteins in a murine model of Duchenne's muscular dystrophy: selective changes in the sensorimotor cortex.

In the muscular dystrophic (mdx) mouse, which is characterized by deficient dystrophin expression and provides a model of Duchenne's muscular dystrophy, we previously demonstrated marked central nervous system alterations and in particular a quantitative reduction of corticospinal and rubrospinal neurons and pathologic changes of these cells. Prompted by these findings and in view of the relations between calcium ions and dystrophin, we analyzed with immunohistochemistry the neurons containing the calcium-binding proteins parvalbumin, calbindin D28k, and calretinin in cortical areas and brainstem nuclei of mdx mice. In the sensorimotor cortex, parvalbumin-positive and calbindin-positive neurons, which represent a subset of cortical interneurons, were significantly more numerous in mdx mice than in wild-type ones. In addition, the laminar distribution of parvalbumin-positive neurons in the motor and somatosensory cortical areas of mdx mice was altered with respect to wild-type animals. No alterations in the number and distribution were found in the parvalbumin- or calbindin-expressing cell populations of the visual and anterior cingulate cortices of mdx mice. The pattern of calretinin immunoreactivity was normal in all investigated cortical areas. The cell populations containing either calcium-binding protein were similar in brainstem nuclei of mdx and wild-type mice. The present findings demonstrated selective changes of subsets of interneurons in the motor and somatosensory cortical areas of mdx mice. Therefore, the data showed that, in the cortices of these mutant animals, the previously demonstrated pathologic changes of corticospinal cell populations are accompanied by marked alterations in the local circuitry.

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Translation from neurobiological data to music parameters.

Composers have explored different ways to use biological information for the realization of music. Throughout the decades, biological findings have been repeatedly indicated as a source of inspiration or a reservoir of extramusical material for musical composition. More radical and fertile are attempts to produce music systematically using biological data in processes called data sonification or biofeedback techniques. Presented here is a novel strategy of translation where populations of neurobiological data are converted into relational structures from which sound objects are generated by flexible and homogeneous control of the sound parameters. All brain data originate from experiments performed with standard anatomical and physiological techniques, and results of studies based on these experimental materials have already been published. During the translation processes, the information for every sound parameter (such as pitch, duration, envelope, and dynamics) is never derived from fixed transcriptions of data properties. Rather, the space and/or the time interrelations of data populations are used to obtain indexes for sound construction. In this way, equivalent sets of information are exploited to model, or sculpt, the different parameters of sound objects. Three examples from the last decade's personal productions are given. The first refers to the microformal aspects of sound aggregation and is based on data from a microstimulation experiment in the motor cortex. The second describes the earliest translation process developed for live performance with conventional instruments and is based on experiments using a conventional tract tracing technique to compare selected spinal-projecting cell populations in two differently organized brains. The third outlines a recent music production for three pianos based on data from experiments using the multiple fluorescent tract-tracing technique to simultaneously label different populations of thalamocortical neurons. The approach here described can potentially contribute to a unitary view of the different sound parameters and of the micro- and macroformal aspects of the compositional process.

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