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Parigi, A.

Publications and source records attributed to Parigi, A..

3 recordsLinked to original sources

Novel cerebello-amygdala connections provide missing link between cerebellum and limbic system

The cerebellum is emerging as a powerful regulator of cognitive and affective processing and memory in both humans and animals and has been implicated in affective disorders. How the cerebellum supports affective function remains poorly understood. The short-latency (just a few ms) functional connections that were identified between the cerebellum and amygdala -a structure crucial for the processing of emotion and valence-more than 4 decades ago raise the exciting, yet untested, possibility that a cerebellum-amygdala pathway communicates information important for emotion. The major hurdle in rigorously testing this possibility is the lack of knowledge about the anatomy and functional connectivity of this pathway. Our initial anatomical tracing studies in mice excluded the existence of a direct monosynaptic pathway between cerebellum and amygdala. Using transneuronal tracing techniques, we have identified a novel disynaptic pathway that connects the cerebellar output nuclei to the basolateral amygdala. This pathway recruits the understudied intralaminar thalamus as a node. Using ex vivo optophysiology and super-resolution microscopy, we provide the first evidence for the functionality of the pathway, thus offering a missing mechanistic link between the cerebellum and amygdala. This discovery provides a connectivity blueprint between the cerebellum and a key structure of the limbic system. As such, it is the requisite first step toward obtaining new knowledge about cerebellar function in emotion, thus fundamentally advancing understanding of the neurobiology of emotion, which is perturbed in mental and autism spectrum disorders.

neuroscience↗

High-frequency stimulation of ventral CA1 neurons reduces amygdala activity and inhibits fear

The hippocampus can be divided into distinct segments that make unique contributions to learning and memory. The dorsal hippocampus supports cognitive processes like spatial learning and navigation while the ventral hippocampus regulates emotional behaviors related to fear, anxiety and reward. In the current study, we determined how pyramidal cells in ventral CA1 respond to spatial cues and aversive stimulation during a context fear conditioning task. We also examined the effects of high and low frequency stimulation of these neurons on defensive behaviors. Similar to previous work in the dorsal hippocampus, we found that cells in ventral CA1 expressed high-levels of c-Fos in response to a novel spatial environment. Surprisingly, however, the number of activated neurons did not increase when the environment was subsequently paired with footshock. This was true even in the subpopulation of ventral CA1 pyramidal cells that send direct projections to the amygdala. When these cells were stimulated at high-frequencies (20-Hz), we observed feedforward inhibition of basal amygdala neurons and impaired expression of context fear. In contrast, low-frequency stimulation (4-Hz) did not inhibit principal cells in the amygdala and produced a slight increase in fear generalization. Similar results have been reported in dorsal CA1. Therefore, despite the clear differences between the dorsal and ventral hippocampus, CA1 neurons in each segment appear to make similar contributions to context fear conditioning.

neuroscience↗

Hybridisation or Incomplete Lineage Sorting: The convoluted story about the origin of the capped-golden langur lineage (Cercopithecidae: Colobinae)

Hybridisation and incomplete lineage sorting (ILS) are two of the many naturally occurring evolutionary processes that contribute to variability in individual gene histories. However, distinguishing between hybridisation and ILS is challenging and these processes can lead to serious difficulties in inferring phylogenies. These processes have been invoked as a possible explanation for the evolution of the endangered golden langur and its sister species, the capped langur. Previous molecular studies have retrieved conflicting phylogenies, with mitochondrial tree grouping capped and golden langur (CG) lineage with a largely Indian genus Semnopithecus while nuclear markers supporting their affiliation with a Southeast Asian genus, Trachypithecus. However, as pointed by others, the use of nuclear copies of mitochondrial DNA in the above studies might have generated the discordance. Because of this discordance, the phylogenetic position of CG lineage has been much debated in recent times. In this study, we have used nine nuclear and eight mitochondrial markers in conjunction with coalescent based species tree approach to better understand the evolutionary origin of CG lineage. Concatenated nuclear as well as the mitochondrial dataset recovered congruent relationships where CG lineage was sister to Trachypithecus. However nuclear species tree estimated using different multispecies coalescent methods were incongruent with the above result, suggesting presence of ILS/hybridisation. Furthermore, CG lineage is morphologically intermediate between Semnopithecus and Trachypithecus with respect to skull and body measurements. Based on these evidences, we argue that CG lineage evolved through hybridisation between Semnopithecus and Trachypithecus. Taxonomic and conservation implications of these results are also discussed.

evolutionary biology↗