Evidence map›Paper›PMID 38805554›Full record

ArticlePLoS computational biology2024

Dorsal and median raphe neuronal firing dynamics characterized by nonlinear measures.

Claudia Pascovich, Diego Serantes, Alejo Rodriguez, Diego Mateos, Joaquín González, Diego Gallo, Mayda Rivas, Andrea Devera, Patricia Lagos, Nicolás Rubido and 1 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Claudia PascovichLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.ORCID 0000-0003-2899-306X
Diego SerantesLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Alejo RodriguezLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Diego MateosAchucarro Basque Center for Neuroscience, Leioa (Bizkaia), Spain.
Joaquín GonzálezLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.ORCID 0000-0002-8721-4292
Diego GalloLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Mayda RivasLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Andrea DeveraLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Patricia LagosLaboratory of Neuropeptide Transmission, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Nicolás RubidoInstitute for Complex Systems and Mathematical Biology, King's College, University of Aberdeen, Aberdeen, United Kingdom.ORCID 0000-0002-0616-2479
Pablo TorteroloLaboratory of Sleep Neurobiology, Department of Physiology, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.

Funding

“Comisión Sectorial de Investigación Científica” (CSIC) I + D grupos 2022-22620220100148
6 · The paper itself

Abstract

The dorsal (DRN) and median (MRN) raphe are important nuclei involved in similar functions, including mood and sleep, but playing distinct roles. These nuclei have a different composition of neuronal types and set of neuronal connections, which among other factors, determine their neuronal dynamics. Most works characterize the neuronal dynamics using classic measures, such as using the average spiking frequency (FR), the coefficient of variation (CV), and action potential duration (APD). In the current study, to refine the characterization of neuronal firing profiles, we examined the neurons within the raphe nuclei. Through the utilization of nonlinear measures, our objective was to discern the redundancy and complementarity of these measures, particularly in comparison with classic methods. To do this, we analyzed the neuronal basal firing profile in both nuclei of urethane-anesthetized rats using the Shannon entropy (Bins Entropy) of the inter-spike intervals, permutation entropy of ordinal patterns (OP Entropy), and Permutation Lempel-Ziv Complexity (PLZC). Firstly, we found that classic (i.e., FR, CV, and APD) and nonlinear measures fail to distinguish between the dynamics of DRN and MRN neurons, except for the OP Entropy. We also found strong relationships between measures, including the CV with FR, CV with Bins entropy, and FR with PLZC, which imply redundant information. However, APD and OP Entropy have either a weak or no relationship with the rest of the measures tested, suggesting that they provide complementary information to the characterization of the neuronal firing profiles. Secondly, we studied how these measures are affected by the oscillatory properties of the firing patterns, including rhythmicity, bursting patterns, and clock-like behavior. We found that all measures are sensitive to rhythmicity, except for the OP Entropy. Overall, our work highlights OP Entropy as a powerful and useful quantity for the characterization of neuronal discharge patterns.

Indexed as

Action PotentialsModels, NeurologicalNeuronsNonlinear DynamicsAnimalsComputational BiologyMaleRaphe NucleiRatsRats, Sprague-Dawley

Identifiers

PMID38805554
PMCPMC11161118

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.