Literature DB >> 36180709

Neurotransmission Recovery by Melatonin Measured by CMAP.

Samuele Negro1, Marco Stazi1, Michela Rigoni2,3, Aram Megighian4,5.   

Abstract

Compound muscle action potential (CMAP) recordings provide a sensitive electromyographic approach to measure nerve conduction and assess neuromuscular junction functionality in humans and rodents. In humans, it represents a diagnostic tool for neuromuscular disorders. In rodents, this approach is widely employed to dissect the molecular mechanisms driving peripheral nerve degeneration/regeneration, as well as to evaluate the effect of candidate pro-regenerative compounds. The method described here allows recording CMAP from the gastrocnemius muscle of mice after sciatic nerve stimulation. We report some representative traces of CMAP recorded from adult, healthy mice, after sciatic nerve compression and during neurotransmission recovery stimulated by melatonin administration.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Compound muscle action potential; Electromyography; Melatonin; Neurodegeneration; Neuromuscular disorders; Neuroregeneration; Sciatic nerve

Mesh:

Substances:

Year:  2022        PMID: 36180709     DOI: 10.1007/978-1-0716-2593-4_40

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  12 in total

1.  Prognostic value of decremental responses to repetitive nerve stimulation in ALS patients.

Authors:  F C Wang; V De Pasqua; P Gérard; P J Delwaide
Journal:  Neurology       Date:  2001-09-11       Impact factor: 9.910

2.  Significant CMAP decrement by repetitive nerve stimulation is more frequent in median than ulnar nerves of patients with amyotrophic lateral sclerosis.

Authors:  Satoshi Yamashita; Hideya Sakaguchi; Akira Mori; En Kimura; Yasushi Maeda; Teruyuki Hirano; Makoto Uchino
Journal:  Muscle Nerve       Date:  2012-03       Impact factor: 3.217

3.  CMAP decrement as a potential diagnostic marker for ALS.

Authors:  A Mori; S Yamashita; M Nakajima; H Hori; A Tawara; Y Matsuo; Y Misumi; Y Ando
Journal:  Acta Neurol Scand       Date:  2015-10-04       Impact factor: 3.209

4.  Macrophages Regulate Schwann Cell Maturation after Nerve Injury.

Authors:  Jo Anne Stratton; Alexandra Holmes; Nicole L Rosin; Sarthak Sinha; Mohit Vohra; Nicole E Burma; Tuan Trang; Rajiv Midha; Jeff Biernaskie
Journal:  Cell Rep       Date:  2018-09-04       Impact factor: 9.423

5.  Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

Authors:  K M Krajewski; R A Lewis; D R Fuerst; C Turansky; S R Hinderer; J Garbern; J Kamholz; M E Shy
Journal:  Brain       Date:  2000-07       Impact factor: 13.501

Review 6.  Electrodiagnostic criteria for diagnosis of ALS.

Authors:  Mamede de Carvalho; Reinhard Dengler; Andrew Eisen; John D England; Ryuji Kaji; Jun Kimura; Kerry Mills; Hiroshi Mitsumoto; Hiroyuki Nodera; Jeremy Shefner; Michael Swash
Journal:  Clin Neurophysiol       Date:  2007-12-27       Impact factor: 3.708

7.  Tubulation repair mitigates misdirection of regenerating motor axons across a sciatic nerve gap in rats.

Authors:  Dan Liu; Daguo Mi; Tuanjie Zhang; Yanping Zhang; Junying Yan; Yaxian Wang; Xuefeng Tan; Ying Yuan; Yumin Yang; Xiaosong Gu; Wen Hu
Journal:  Sci Rep       Date:  2018-02-21       Impact factor: 4.379

8.  A CXCR4 receptor agonist strongly stimulates axonal regeneration after damage.

Authors:  Giulia Zanetti; Samuele Negro; Aram Megighian; Andrea Mattarei; Florigio Lista; Silvia Fillo; Michela Rigoni; Marco Pirazzini; Cesare Montecucco
Journal:  Ann Clin Transl Neurol       Date:  2019-11-14       Impact factor: 4.511

9.  Melatonin promotes regeneration of injured motor axons via MT1 receptors.

Authors:  Marco Stazi; Samuele Negro; Aram Megighian; Giorgia D'Este; Michele Solimena; Ralf Jockers; Florigio Lista; Cesare Montecucco; Michela Rigoni
Journal:  J Pineal Res       Date:  2020-09-17       Impact factor: 13.007

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