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Renaud, L.

Publications and source records attributed to Renaud, L..

5 recordsLinked to original sources

Chamber Implant for Chronic Optical Recordings from the Cerebral Cortex of Marmosets

We describe a novel imaging chamber for chronic optical recordings from the marmoset cerebral cortex, together with the surgery needed for its implantation and that of an associated headpost. MRI data allow optimizing positioning on the skull. The chamber is implanted into a precisely matched craniotomy, improving mechanical stability. For maximal biocompatibility, chamber and headpost are made out of titanium. It consists of an outer cylinder into which screws adjustably an inner one, called "well", with a glass window on its bottom. This allows easy opening and closing whenever access to the cortex is needed, while preserving a sterile seal when closed. Moreover, simply rotating the well allows fine adjustment of the windows distance with respect to the underlying cortex. Together with using a curved - rather than flat - glass window, this allows achieving gentle but continuous contact with the underlying cortex, which helps to delay tissue regrowth, notably of a neomembrane that must otherwise be surgically removed. The chambers sealing system combines a silicone elastomer and O-ring, minimizing infection risk and CSF leakage. Data from longitudinal two-photon imaging using genetically encoded fluorescent calcium sensors reveal high optical quality over months, with excellent resolution of neurons and their activity. We also demonstrate the feasibility of two-photon imaging of genetically encoded voltage sensors in the marmoset cortex in-vivo. Finally, although the chamber provides a durable, adaptable solution for long-term imaging studies in marmosets already in its current version, we discuss a few straightforward modifications that could likely improve its performance even further.

neuroscience↗

Dynamic Norm-Based Coding of Vocal Identity in the Primate Auditory Cortex

Recognition of vocal identity is essential for primate social behavior, yet the neural mechanisms supporting this ability remain poorly understood. Cognitive models suggest that the brain may represent identity based on an average voice prototype. Here, we tested this hypothesis by recording spiking activity from single neurons in an fMRI-localized voice-selective region of the anterior temporal lobe in two rhesus macaques. Using synthetic "coo" calls systematically morphed along identity trajectories from "anti-voices" to caricatures, we found that early neuronal responses ([~]100 ms post-stimulus) exhibited robust V-shaped tuning to distance from the average voice. This pattern reflects an energy-efficient representational strategy in which neural activity increases with identity distinctiveness, also applied to face stimuli. Unexpectedly, a distinct subpopulation of neurons showed a delayed ([~]200 ms) rebound response selectively enhanced for the average voice. These findings reveal two temporally dissociable mechanisms for vocal identity encoding in primate auditory cortex, suggesting that the brain emphasizes both distinctiveness and prototypicality to support efficient and flexible voice recognition. Significance statementRecognizing who is speaking is fundamental to primate social life, yet how the brain encodes vocal identity remains poorly understood. Cognitive theories suggest that the brain may represent identity relative to an internal "average" voice, but direct neural evidence has been lacking. Here, we recorded single-neuron activity in a voice-selective brain region of rhesus macaques and found two distinct coding strategies: one that increases neural activity with identity distinctiveness, and another that selectively enhances the average voice itself. These results reveal dual mechanisms for vocal identity encoding in the primate brain, highlighting how the brain balances flexibility and efficiency in social communication.

neuroscience↗

Voice identity invariance by anterior temporal lobe neurons

The ability to recognize speakers by their voice despite acoustical variation plays a significant role in primate social interactions. While neurons in the macaque anterior temporal lobe (ATL) show invariance to face viewpoint, whether they also encode abstract representations of caller identity is not known. Here we show that neurons in the voice-selective ATL of two macaques show invariance to voice identity via dynamic representations that minimize within-caller neuronal distances while maintaining distinct neural trajectories for different individuals. A small proportion of highly identity-selective neurons plays a central role although less selective neurons are also informative. Our findings provide a neural basis for voice identity recognition in primates and highlight the ATL as a key hub for integrating perceptual voice features into higher-level identity representations.

neuroscience↗

Argon neuroprotection in a non-human primate model of transient endovascular ischemic stroke.

BackgroundPrevious studies have demonstrated the efficacy of argon neuroprotection in rodent models of cerebral ischemia. The objective of the present study was to confirm a potential neuroprotective effect of argon in a non-human primate model of endovascular ischemic stroke as an essential step before considering the use of argon as a neuroprotective agent in humans. MethodsThirteen adult monkeys (Macaca mulatta) were allocated to two groups: a control group (n=8) without neuroprotection and an argon group (n=5) in which argon inhalation (90 min) was initiated 30 minutes after onset of ischemia. Animals in both groups underwent brain MRI (pre-ischemic) at least 7 days before the intervention. The monkeys were subjected to focal cerebral ischemia induced by a transient (90 min) middle cerebral artery occlusion (tMCAO). After tMCAO, MRI was performed 1 hour after cerebral reperfusion. The ischemic core volume was defined by the apparent diffusion coefficient (aDC) and edema in fluid attenuated inversion recovery (FLAIR) acquisitions. MRI masks were applied to distinguish between cortical and subcortical abnormalities. In addition, a modified version of the Rankin scale was used to neurologically assess post-tMCAO. ResultsDespite variability in the ischemic core and edema volumes in the control group, argon significantly reduced ischemic core volume after ischemia compared to the control group (1.1{+/-}1.6 cm3 vs. 8.5{+/-}8.1 cm3; p=0.03). This effect was limited to cortical structures (0.6{+/-}1.1 cm3 vs. 7.4{+/-}7.2 cm3; p=0.03). No significant differences were observed in the edema volumes. Measures of neurological clinical outcome suggested a better prognosis in argon-treated animals. ConclusionsIn the tMCAO macaque model, argon induced effective neuroprotective effects, leading to a reduced ischemic core in cortical areas. These results support the potential use of this therapeutic approach for future clinical studies in stroke patients.

neuroscience↗

Planum Temporale grey matter volume asymmetries in new-born monkeys (Papio anubis)

The Planum Temporale (PT) is one of the key hubs of the language network in the human brain. The gross asymmetry of this perisylvian region toward the left brain was considered as the most emblematic marker of hemispheric specialization of language processes in the brain. Interestingly, this neuroanatomical signature was documented also in newborn infants and preterms, suggesting the early brains readiness for language acquisition. Nevertheless, this latter interpretation was questioned by a recent report in nonhuman primates of a potential similar signature in newborn baboons Papio anubis based on PT surface measures. Whether this "tip of the iceberg" PT asymmetry is actually reflecting asymmetry of its underlying grey matter volume remain unclear but critical to investigate potential continuities of cortical specialization with human infants. Here we report a population-level leftward asymmetry of the Planum Temporale grey matter volume in in vivo 34 newborn baboons Papio anubis, which showed intra-individual positive correlation with PT surfaces asymmetry measures but also a more pronounced degree of leftward asymmetry at the population-level. This finding demonstrates that PT leftward structural asymmetry in this Old World monkey species is a robust phenomenon in early primate development, which clearly speaks for a continuity with early human brain specialization. Results also strengthen the hypothesis that early PT asymmetry might be not a human-specific marker for the pre-wired language-ready brain in infants.

neuroscience↗