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Verdier, D.

Publications and source records attributed to Verdier, D..

2 recordsLinked to original sources

Integration of sensory and cortical information in the brainstem during mastication in mice

Mastication is a vital function that relies on precise synchronization among multiple brainstem regions, known as being part of a central pattern generator (CPG). Movements can be triggered either by stimulating a sensory-motor region called the cortical masticatory area (CMA), well-documented in various species but not yet formally identified in mice, or by stimulating the oro-facial sensory primary afferents which fibers form the trigeminal tract (Vtr). However, its unclear whether these different inputs activate distinct components of the CPG or converge on the same. This study aims at mapping brainstem areas activated by cortical and sensory inputs using immunohistochemistry against the cellular activity marker, c-Fos and Ca2+-imaging, respectively. Optogenetic stimulation of the cortical masticatory area (CMA) in awake, head-fixed mice reliably induced rhythmic jaw movements (RJMs) and increased c-Fos expression in multiple brainstem regions, with strongest activation in the peritrigeminal area (PeriV) and parvocellular reticular formation (PCRt) ventral to the trigeminal motor nucleus (NVmt). In contrast, in vitro electrical stimulation of trigeminal sensory afferents (Vtr) predominantly activated neurons and astrocytes in the main sensory nucleus (NVsnpr), the dorsal area of PeriV, adjacent to it, and PCRt. The areas containing the highest numbers of activated cells differed clearly according to the type of inputs and overlapped only in the PCRt, ventral and slightly medial to the trigeminal motor nucleus and the most dorso-medial part of PeriV. These findings demonstrate that cortical and sensory inputs take part in distinct components of the brainstem masticatory circuitry, with PCRt emerging as a point of convergence and provide new insights into the components of the CPG of mastication.

neuroscience↗

Astrocyte-induced firing in primary afferent axons

The mesencephalic trigeminal nucleus is unique in that it contains the cell bodies of large-caliber primary afferents that are usually located in the periphery in the dorsal root ganglia or trigeminal ganglia. The activity of these afferents is typically associated with proprioception of the jaw-closing muscles or mechanoreception on the teeth and periodontal ligament. However, like other large-caliber afferents from the body which display ectopic firing in neuropathic pain models, these afferents exhibit increased excitability and ectopic discharges even in a relatively mild muscle pain model. These discharges normally emerge from subthreshold membrane oscillations (SMOs) supported by a persistent sodium current (INaP) which is exquisitely sensitive to extracellular Ca2+-decreases. We have shown in the trigeminal main sensory nucleus that the release of a Ca2+-binding astrocytic protein, S100{beta}, is sufficient to modulate this sodium current. Here, we explore if this astrocyte-dependent mechanism contributes to emergence of this hyperexcitability and aim to localize the cellular site where ectopic discharge may arise using whole-cell patch-clamp recordings, confocal imaging, and immunohistochemistry methods on mice brain slices. We found that astrocytes, by lowering [Ca2+]e at focal points along the axons of NVmes neurons through S100{beta}, enhance the amplitude of the NaV1.6-dependent SMOs leading to ectopic firing. These findings suggest a crucial role for astrocytes in excitability regulation and raise questions about this neuron-astrocyte interaction as a key contributor to hyperexcitability in several pathologies.

neuroscience↗