Literature DB >> 30943091

A supervised machine learning approach to characterize spinal network function.

A N Dalrymple1, S A Sharples2,3, N Osachoff4, A P Lognon2,3, P J Whelan2,4.   

Abstract

Spontaneous activity is a common feature of immature neuronal networks throughout the central nervous system and plays an important role in network development and consolidation. In postnatal rodents, spontaneous activity in the spinal cord exhibits complex, stochastic patterns that have historically proven challenging to characterize. We developed a software tool for quickly and automatically characterizing and classifying episodes of spontaneous activity generated from developing spinal networks. We recorded spontaneous activity from in vitro lumbar ventral roots of 16 neonatal [postnatal day (P)0-P3] mice. Recordings were DC coupled and detrended, and episodes were separated for analysis. Amplitude-, duration-, and frequency-related features were extracted from each episode and organized into five classes. Paired classes and features were used to train and test supervised machine learning algorithms. Multilayer perceptrons were used to classify episodes as rhythmic or multiburst. We increased network excitability with potassium chloride and tested the utility of the tool to detect changes in features and episode class. We also demonstrate usability by having a novel experimenter use the program to classify episodes collected at a later time point (P5). Supervised machine learning-based classification of episodes accounted for changes that traditional approaches cannot detect. Our tool, named SpontaneousClassification, advances the detail in which we can study not only developing spinal networks, but also spontaneous networks in other areas of the nervous system. NEW & NOTEWORTHY Spontaneous activity is important for nervous system network development and consolidation. Our software uses machine learning to automatically and quickly characterize and classify episodes of spontaneous activity in the spinal cord of newborn mice. It detected changes in network activity following KCl-enhanced excitation. Using our software to classify spontaneous activity throughout development, in pathological models, or with neuromodulation, may offer insight into the development and organization of spinal circuits.

Entities:  

Keywords:  machine learning; neural recording; spinal cord; spontaneous activity

Year:  2019        PMID: 30943091      PMCID: PMC6620704          DOI: 10.1152/jn.00763.2018

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  45 in total

1.  Changes in correlation between spontaneous activity of dorsal horn neurones lead to differential recruitment of inhibitory pathways in the cat spinal cord.

Authors:  D Chávez; E Rodríguez; I Jiménez; P Rudomin
Journal:  J Physiol       Date:  2012-01-23       Impact factor: 5.182

Review 2.  Spontaneous patterned retinal activity and the refinement of retinal projections.

Authors:  Christine L Torborg; Marla B Feller
Journal:  Prog Neurobiol       Date:  2005-11-08       Impact factor: 11.685

3.  Development of precise maps in visual cortex requires patterned spontaneous activity in the retina.

Authors:  Jianhua Cang; René C Rentería; Megumi Kaneko; Xiaorong Liu; David R Copenhagen; Michael P Stryker
Journal:  Neuron       Date:  2005-12-08       Impact factor: 17.173

4.  Analytical characterization of spontaneous activity evolution during hippocampal development in the rabbit.

Authors:  L Menendez de la Prida; S Bolea; J V Sanchez-Andres
Journal:  Neurosci Lett       Date:  1996-11-08       Impact factor: 3.046

5.  Conversion of the modulatory actions of dopamine on spinal reflexes from depression to facilitation in D3 receptor knock-out mice.

Authors:  Stefan Clemens; Shawn Hochman
Journal:  J Neurosci       Date:  2004-12-15       Impact factor: 6.167

6.  Regional distribution of the locomotor pattern-generating network in the neonatal rat spinal cord.

Authors:  K C Cowley; B J Schmidt
Journal:  J Neurophysiol       Date:  1997-01       Impact factor: 2.714

7.  Early olfactory-induced rhythmic limb activity in the newborn rat.

Authors:  J C Fady; M Jamon; F Clarac
Journal:  Brain Res Dev Brain Res       Date:  1998-06-15

8.  Ventricular fibrillation and tachycardia classification using a machine learning approach.

Authors:  Qiao Li; Cadathur Rajagopalan; Gari D Clifford
Journal:  IEEE Trans Biomed Eng       Date:  2013-07-26       Impact factor: 4.538

9.  Early postnatal switch in GABAA receptor α-subunits in the reticular thalamic nucleus.

Authors:  Susanne Pangratz-Fuehrer; Werner Sieghart; Uwe Rudolph; Isabel Parada; John R Huguenard
Journal:  J Neurophysiol       Date:  2015-12-02       Impact factor: 2.714

10.  Multimodal and Multiscale Deep Neural Networks for the Early Diagnosis of Alzheimer's Disease using structural MR and FDG-PET images.

Authors:  Donghuan Lu; Karteek Popuri; Gavin Weiguang Ding; Rakesh Balachandar; Mirza Faisal Beg
Journal:  Sci Rep       Date:  2018-04-09       Impact factor: 4.379

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  3 in total

1.  A supervised machine learning approach to characterize spinal network function.

Authors:  A N Dalrymple; S A Sharples; N Osachoff; A P Lognon; P J Whelan
Journal:  J Neurophysiol       Date:  2019-04-03       Impact factor: 2.714

2.  Contributions of h- and Na+/K+ Pump Currents to the Generation of Episodic and Continuous Rhythmic Activities.

Authors:  Simon A Sharples; Jessica Parker; Alex Vargas; Jonathan J Milla-Cruz; Adam P Lognon; Ning Cheng; Leanne Young; Anchita Shonak; Gennady S Cymbalyuk; Patrick J Whelan
Journal:  Front Cell Neurosci       Date:  2022-02-04       Impact factor: 5.505

3.  A dynamic role for dopamine receptors in the control of mammalian spinal networks.

Authors:  Simon A Sharples; Nicole E Burma; Joanna Borowska-Fielding; Charlie H T Kwok; Shane E A Eaton; Glen B Baker; Celine Jean-Xavier; Ying Zhang; Tuan Trang; Patrick J Whelan
Journal:  Sci Rep       Date:  2020-10-02       Impact factor: 4.379

  3 in total

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