Effect of maximal voluntary contraction on the amplitude of the compound muscle action potential: implications for the interpolated twitch technique.

Abstract:

:The compound muscle action potential (M(MAX)) during a maximal voluntary contraction (MVC) may be measured to determine if the motor nerve has been supramaximally stimulated during the interpolated twitch technique (ITT). Ten males performed isometric knee extension MVCs. M(MAX) for the vastus medialis was recorded during MVC and rest. To examine the effect of stimulating electrode movement, the M(MAX) of the thenar group and antidromic sensory nerve action potentials (SNAPs) to the third digit were recorded in a separate experiment. M(MAX) during MVC was reduced by 18% (P < 0.0001) and 43% (p < 0.0001) for the quadriceps and thenar group, respectively. The SNAP amplitude was not different between rest and MVC (P = 0.18). Reduction of M(MAX) during MVC suggests that some motor axons are refractory and unable to respond to a superimposed maximal stimulus. These results have implications for the sensitivity of the interpolated twitch technique.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Berger MJ,Watson BV,Doherty TJ

doi

10.1002/mus.21692

subject

Has Abstract

pub_date

2010-10-01 00:00:00

pages

498-503

issue

4

eissn

0148-639X

issn

1097-4598

journal_volume

42

pub_type

杂志文章
  • Subacute demyelinating polyradiculoneuropathy complicating Epstein-Barr virus infection in GATA2 haploinsufficiency.

    abstract:INTRODUCTION:Autosomal dominant haploinsufficiency of GATA2 causes monocytopenia and natural killer cell lymphopenia, resulting in predisposition to mycobacterial, fungal, and viral infections. METHODS:Herein we report on the clinical, serologic, electrophysiologic, and pathologic evaluations of a 29-year-old woman wi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25581

    authors: Kazamel M,Klein CJ,Benarroch EE,Patnaik MM,Tracy JA

    更新日期:2018-01-01 00:00:00

  • Passive transfer of seronegative myasthenia gravis to mice.

    abstract::Muscle weakness in myasthenia gravis is due to autoantibody-induced loss of functional acetylcholine receptors (AChR). About 15% of myasthenia gravis patients, however, do not have detectable anti-AChR antibodies. To investigate the effect of their plasma immunoglobulins on neuromuscular transmission, mice were inject...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880171208

    authors: Burges J,Vincent A,Molenaar PC,Newsom-Davis J,Peers C,Wray D

    更新日期:1994-12-01 00:00:00

  • Chronic idiopathic axonal polyneuropathy: Electrophysiological progression and human leukocyte antigen associations.

    abstract:BACKGROUND:We aimed to describe the electrophysiological progression rate of chronic idiopathic axonal polyneuropathy (CIAP) and look into the potential role of human leukocyte antigen (HLA) genetic susceptibility in its development. METHODS:We recruited 57 patients with CIAP (mean age at diagnosis 67, mean follow-up ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.27164

    authors: Zis P,Sarrigiannis PG,Artemiadis A,Skarlatou V,Hadjivassiliou M

    更新日期:2021-01-13 00:00:00

  • Clinical and prognostic features in unilateral femoral neuropathies.

    abstract::We have examined the clinical features of patients with femoral neuropathy and the factors that influence the prognosis. Of 80 consecutive patients referred for neurophysiological evaluations of proximal lower limb weakness, 32 fulfilled strict inclusion criteria and had adequate information, including estimates of ax...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199702)20:2<205::aid-mus11

    authors: Kuntzer T,van Melle G,Regli F

    更新日期:1997-02-01 00:00:00

  • Orofacial strength, dysarthria, and dysphagia in congenital myotonic dystrophy.

    abstract:INTRODUCTION:Herein we present an exploratory study of orofacial function in children with congenital myotonic dystrophy (CDM) vs. healthy controls. METHODS:We evaluated 41 children with CDM and 29 healthy controls for speech and swallow function and for lingual and labial strength. RESULTS:The Iowa Oral Performance ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26176

    authors: Berggren KN,Hung M,Dixon MM,Bounsanga J,Crockett B,Foye MD,Gu Y,Campbell C,Butterfield RJ,Johnson NE

    更新日期:2018-09-01 00:00:00

  • Comparing the function of the corticospinal system in different species: organizational differences for motor specialization?

    abstract::An appreciation of the comparative functions of the corticospinal tract is of direct relevance to the understanding of how results from animal models can advance knowledge of the human motor system and its disorders. Two critical functions of the corticospinal tract are discussed: first, the role of descending project...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20333

    authors: Lemon RN,Griffiths J

    更新日期:2005-09-01 00:00:00

  • Therapeutic trial of isaxonine in Duchenne muscular dystrophy.

    abstract::A randomized double-blind therapeutic trial of isaxonine was completed over a 2-year period for 20 ambulant boys with Duchenne muscular dystrophy aged 5 1/2-10 years. The effect of the drug was monitored by measurement of walking times over 28 and 150 ft, motor ability score, MRC score based on 32 muscle groups, and m...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/mus.880110807

    authors: Heckmatt JZ,Hyde SA,Gabain A,Dubowitz V

    更新日期:1988-08-01 00:00:00

  • Does impaired glucose metabolism cause polyneuropathy? Review of previous studies and design of a prospective controlled population-based study.

    abstract::In spite of extensive studies it is unclear whether impaired fasting glucose (IFG) or impaired glucose tolerance (IGT), i.e., impaired glucose metabolism (IGM), causes diabetic sensorimotor polyneuropathy (DSPN) or chronic idiopathic axonal polyneuropathy (CIAP); the results and conclusions vary considerably in differ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20846

    authors: Dyck PJ,Dyck PJ,Klein CJ,Weigand SD

    更新日期:2007-10-01 00:00:00

  • In vivo bioluminescent imaging of Schwann cells in a poly(DL-lactide-epsilon-caprolactone) nerve guide.

    abstract::Nerve guides seeded with Schwann cells (SCs) promote axonal regeneration in peripheral nerve lesions. We examined the applicability of bioluminescent imaging (BLI) for monitoring the fate of SCs in nerve guides after implantation. Rat SCs were transfected with the firefly luciferase (Fluc) gene and subsequently seeded...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21372

    authors: Ma MS,Van Dam G,Meek M,Boddeke E,Copray S

    更新日期:2009-11-01 00:00:00

  • Toxoplasmic myositis as a presenting manifestation of idiopathic CD4 lymphocytopenia.

    abstract::Toxoplasma gondii encysts in skeletal muscle. Although only rarely found at muscle biopsy, this parasite has previously been regarded as a possible cause of polymyositis. We report a case of biopsy-proven toxoplasmic myositis in a non-HIV-infected patient that led to recognition of idiopathic CD4 lymphocytopenia (ICL)...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10376

    authors: Plonquet A,Bassez G,Authier FJ,Dray JM,Farcet JP,Gherardi RK

    更新日期:2003-06-01 00:00:00

  • Effects of isaxonine on skeletal muscle reinnervation in the rat: an electrophysiologic evaluation.

    abstract::Electrophysiologic detection of the first signs of gastrocnemius muscle reinnervation shows that after a single localized freezing of the rat sciatic nerve, isaxonine does not significantly increase the rate of axonal regeneration. However, this drug does significantly enhance axonal sprouting, as it induces an increa...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880080205

    authors: Pecot-Dechavassine M,Mira JC

    更新日期:1985-02-01 00:00:00

  • Application of differentiated human tonsil-derived stem cells to trembler-J mice.

    abstract:INTRODUCTION:Mesenchymal stem cells (MSCs) can differentiate into various cell types. METHODS:In this study we investigated the potential of human tonsil-derived MSCs (T-MSCs) for neuromuscular regeneration in trembler-J (Tr-J) mice, a model for Charcot-Marie-Tooth disease type 1A (CMT1A). RESULTS:T-MSCs differentiat...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25763

    authors: Park S,Choi Y,Kwak G,Hong YB,Jung N,Kim J,Choi BO,Jung SC

    更新日期:2018-03-01 00:00:00

  • Mononeuropathy multiplex associated with acute hepatitis B infection.

    abstract::Immunologic syndromes are associated with hepatitis B viral (HBV) infection. However, mononeuropathy multiplex (MM), a syndrome in which immune factors may play a role, is rare in acute HBV infection. Few cases of MM associated with HBV infection have been reported. We report a case of acute HBV infection in which MM ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880130304

    authors: Cohen JA,Wilborn SL,Rector WG Jr,Golitz LE

    更新日期:1990-03-01 00:00:00

  • Peripheral neuropathy in glycogen storage disease type III: Fact or myth?

    abstract:INTRODUCTION:The aim of this study was to assess whether peripheral neuropathy is a feature of glycogen storage disease type IIIa (GSD IIIa) in adult patients. METHODS:Medical records of a cohort of adult GSD IIIa patients who underwent electromyography (EMG) and nerve conduction studies (NCS) were reviewed, and the r...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24977

    authors: Herlin B,Laforět P,Labrune P,Fournier E,Stojkovic T

    更新日期:2016-02-01 00:00:00

  • Muscle fiber size in healthy children and adults in relation to sex and fiber types.

    abstract:BACKGROUND:In adult males, cross-sectional area (CSA) for type II muscle fibers is generally larger than for type I fibers. In this cross-sectional study the aim was to compare sex-related CSAs of various muscle fiber types during childhood-to-adulthood transition. METHODS:Percutaneous biopsy samples were obtained fro...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.27151

    authors: Esbjörnsson ME,Dahlström MS,Gierup JW,Jansson EC

    更新日期:2020-12-21 00:00:00

  • Repetitive nerve stimulation of facial muscles in MuSK antibody-positive myasthenia gravis.

    abstract::To better define electrophysiological abnormalities in myasthenia gravis (MG) patients with muscle-specific tyrosine kinase (MuSK) antibodies (Ab), we compared electrophysiological features of 14 MuSK Ab-positive, 73 acetylcholine receptor antibody (AChR Ab)-positive, and 22 MuSK and AChR Ab-negative (seronegative) pa...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20498

    authors: Oh SJ,Hatanaka Y,Hemmi S,Young AM,Scheufele ML,Nations SP,Lu L,Claussen GC,Wolfe GI

    更新日期:2006-04-01 00:00:00

  • Cognitive impairment in neuromuscular disorders.

    abstract::Several studies have suggested the presence of central nervous system involvement manifesting as cognitive impairment in diseases traditionally confined to the peripheral nervous system. The aim of this review is to highlight the character of clinical, genetic, neurofunctional, cognitive, and psychiatric deficits in n...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20535

    authors: D'Angelo MG,Bresolin N

    更新日期:2006-07-01 00:00:00

  • SMA valiant trial: a prospective, double-blind, placebo-controlled trial of valproic acid in ambulatory adults with spinal muscular atrophy.

    abstract:INTRODUCTION:An open-label trial suggested that valproic acid (VPA) improved strength in adults with spinal muscular atrophy (SMA). We report a 12-month, double-blind, cross-over study of VPA in ambulatory SMA adults. METHODS:There were 33 subjects, aged 20–55 years, included in this investigation. After baseline asse...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/mus.23904

    authors: Kissel JT,Elsheikh B,King WM,Freimer M,Scott CB,Kolb SJ,Reyna SP,Crawford TO,Simard LR,Krosschell KJ,Acsadi G,Schroth MK,D'Anjou G,LaSalle B,Prior TW,Sorenson S,Maczulski JA,Swoboda KJ,Project Cure Spinal Muscular Atr

    更新日期:2014-02-01 00:00:00

  • Characterization of skeletal muscle effects associated with daptomycin in rats.

    abstract::Daptomycin is a lipopeptide antibiotic with strong bactericidal effects against Gram-positive bacteria and minor side effects on skeletal muscles. The type and magnitude of the early effect of daptomycin on skeletal muscles of rats was quantified by histopathology, examination of contractile properties, Evans Blue Dye...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21691

    authors: Kostrominova TY,Hassett CA,Rader EP,Davis C,Larkin LM,Coleman S,Oleson FB,Faulkner JA

    更新日期:2010-09-01 00:00:00

  • Diffuse large B-cell lymphoma presenting as piriformis syndrome.

    abstract::Piriformis syndrome (PS) is a rare condition characterized by pain and paresthesia of the buttock, often radiating to the posterior thigh. A patient with sciatica that was clinically suspicious for PS, underwent diagnostic work-up. A diagnosis of diffuse large B-cell lymphoma with neurolymphomatosis (NL) was made. To ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21538

    authors: Ye BS,Sunwoo IN,Suh BC,Park JP,Shim DS,Kim SM

    更新日期:2010-03-01 00:00:00

  • Two patients with GMPPB mutation: The overlapping phenotypes of limb-girdle myasthenic syndrome and limb-girdle muscular dystrophy dystroglycanopathy.

    abstract:INTRODUCTION:Mutations in the guanosine diphosphate-mannose pyrophosphorylase-B gene (GMPPB) have been identified in congenital muscular dystrophies, limb-girdle muscular dystrophy (LGMD2T), and congenital myasthenic syndromes (CMSs); overall, 41 patients have been described. METHODS:Two patients presented with a myas...

    journal_title:Muscle & nerve

    pub_type:

    doi:10.1002/mus.25485

    authors: Montagnese F,Klupp E,Karampinos DC,Biskup S,Gläser D,Kirschke JS,Schoser B

    更新日期:2017-08-01 00:00:00

  • Sensory physiology assessed by evoked potentials in survivors of poliomyelitis.

    abstract::Evidence suggests that sensory loss may occur in a proportion of patients affected by poliomyelitis. We hypothesize that sensory problems may be a lasting sequela in some polio survivors. Sensory pathways in polio survivors were evaluated clinically and electrophysiologically using sensory evoked potentials (SEPs). Pa...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21093

    authors: Prokhorenko OA,Vasconcelos OM,Lupu VD,Campbell WW,Jabbari B

    更新日期:2008-10-01 00:00:00

  • Electrical impedance myography discriminates congenital muscular dystrophy from controls.

    abstract:INTRODUCTION:Electrical impedance myography (EIM) is an emerging non-invasive, highly reproducible electrophysiological technique that objectively characterizes muscle structure and composition by measuring bioimpedance. We assessed the ability of EIM ability to discriminate 2 forms of congenital muscular dystrophy (CM...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24770

    authors: Schwartz DP,Dastgir J,Salman A,Lear B,Bönnemann CG,Lehky TJ

    更新日期:2016-03-01 00:00:00

  • Spontaneous electrical muscle fiber activity in polymyositis and dermatomyositis.

    abstract::Forty patients with polymyositis or dermatomyositis underwent detailed electromyographic evaluation. The paraspinal muscles of all patients were examined, as were several extremity muscles. The distribution of fibrillation potentials (FPs) in different muscles is discussed. FPs were most frequent in paraspinal muscles...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880020103

    authors: Streib EW,Wilbourn AJ,Mitsumoto H

    更新日期:1979-01-01 00:00:00

  • Macroglossia in advanced amyotrophic lateral sclerosis.

    abstract:INTRODUCTION:An enlarged tongue (macroglossia) has been reported in advanced-stage patients with amyotrophic lateral sclerosis (ALS). METHODS:In this study we examined the prevalence of macroglossia and analyzed clinical correlations in 65 ALS patients on tracheostomy-invasive ventilation (TIV). RESULTS:Macroglossia ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25058

    authors: Matsuda C,Shimizu T,Nakayama Y,Haraguchi M,Hakuta C,Itagaki Y,Ogura A,Murata K,Taira M,Numayama T,Kinoshita M

    更新日期:2016-09-01 00:00:00

  • Evoked potentials elicited by stimulation of the lateral and anterior femoral cutaneous nerves in meralgia paresthetica.

    abstract::Seventy-five consecutive patients with clinical symptoms and signs of meralgia paresthetica underwent bilateral somatosensory evoked potential (SEP) studies involving stimulation of skin areas innervated by the lateral and anterior femoral cutaneous nerves of the thighs. The most common abnormality was an absolute lat...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10515

    authors: Cordato DJ,Yiannikas C,Stroud J,Halpern JP,Schwartz RS,Akbunar M,Cook M

    更新日期:2004-01-01 00:00:00

  • Stretch-induced spinal accessory nerve palsy.

    abstract::Left spinal accessory nerve palsy occurred in a young man when he quickly turned his head to the right while his shoulders were pulled down by heavy hand-held objects. Electrophysiologic studies demonstrated partial axonotmesis of the spinal accessory nerve branches innervating the sternocleidomastoid and upper and mi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110210

    authors: Logigian EL,McInnes JM,Berger AR,Busis NA,Lehrich JR,Shahani BT

    更新日期:1988-02-01 00:00:00

  • Differential response of heat shock proteins to hindlimb unloading and reloading in the soleus.

    abstract::Hindlimb unloading (HU) results in oxidative stress, skeletal muscle atrophy, and increased damage upon reloading. Heat shock proteins (HSPs) protect against oxidative stress. However, it is unknown whether HSPs are depressed with long-term unloading (28 days) or reloading. We tested the hypotheses that long-term HU w...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20454

    authors: Lawler JM,Song W,Kwak HB

    更新日期:2006-02-01 00:00:00

  • Body weight-supported training in Becker and limb girdle 2I muscular dystrophy.

    abstract:INTRODUCTION:We studied the functional effects of combined strength and aerobic anti-gravity training in severely affected patients with Becker and Limb-Girdle muscular dystrophies. METHODS:Eight patients performed 10-week progressive combined strength (squats, calf raises, lunges) and aerobic (walk/run, jogging in pl...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25039

    authors: Jensen BR,Berthelsen MP,Husu E,Christensen SB,Prahm KP,Vissing J

    更新日期:2016-08-01 00:00:00

  • Comparison of interpolation and central activation ratios as measures of muscle inactivation.

    abstract::The objective of this study was to investigate different methods of estimating muscle inactivation, derived from single and multiple voluntary contractions. Ten subjects performed maximal and submaximal leg extensor contractions to determine an interpolation (IT) or central activation ratio (CAR). A superimposed evoke...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.1090

    authors: Behm D,Power K,Drinkwater E

    更新日期:2001-07-01 00:00:00