Sodium withdrawal contractures in developing and regenerating rat extensor digitorum longus muscles.

Abstract:

:During postnatal development of extensor digitorum longus (EDL) muscle, sodium withdrawal contractures were observed during the first 6 days after birth, and not after this time. In regenerating EDL muscles, zero-Na contractures were demonstrated: (1) 7 days after bupivacaine injection, but not 14 or 90 days after this injection; (2) 7, 14, and 90 days after autotransplantation; and (3) 7, 14, and 90 days after the intervention in sliced muscles. The present findings emphasize the role of the denervation in the development of zero-Na contractures in the regenerating muscles and suggest that a calcium-sodium exchange across the sarcolemma may appear in these muscles.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Louboutin JP,Noireaud J

doi

10.1002/(sici)1097-4598(199811)21:11<1530::aid-mus

subject

Has Abstract

pub_date

1998-11-01 00:00:00

pages

1530-2

issue

11

eissn

0148-639X

issn

1097-4598

pii

10.1002/(SICI)1097-4598(199811)21:11<1530::AID-MUS

journal_volume

21

pub_type

杂志文章
  • Danon disease due to a novel splice mutation in the LAMP2 gene.

    abstract::Danon disease is a rare X-linked dominant disorder caused by lysosomal-associated membrane protein 2 (LAMP2) deficiency and is characterized by hypertrophic cardiomyopathy, cardiac conduction abnormalities, skeletal vacuolar myopathy, variable degree of mental retardation, and peripheral pigmentary retinopathy. We des...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20930

    authors: Nadeau A,Therrien C,Karpati G,Sinnreich M

    更新日期:2008-03-01 00:00:00

  • Peripheral nerve atrophy together with higher cerebrospinal fluid progranulin indicate axonal damage in amyotrophic lateral sclerosis.

    abstract:INTRODUCTION:We aimed to investigate whether sonographic peripheral cross-sectional nerve area (CSA) and progranulin (PGRN), a neuritic growth factor, are related to each other and whether they interact to predict clinical and paraclinical measures in amyotrophic lateral sclerosis (ALS). METHODS:We included 55 ALS pat...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25682

    authors: Schreiber S,Debska-Vielhaber G,Abdulla S,Machts J,Schreiber F,Kropf S,KÖrtvelyessy P,KÖrner S,Kollewe K,Petri S,Dengler R,Kunz WS,Nestor PJ,Vielhaber S

    更新日期:2018-02-01 00:00:00

  • Interaction of monoclonal antibodies to Torpedo acetylcholine receptor with the receptor of skeletal muscle.

    abstract::Several monoclonal antibodies (mcAbs) elicited against the nicotinic acetylcholine receptor (AChR) from Torpedo react also with skeletal muscle AChR. Such mcAbs were used to define antigenic determinants on muscle AChR and to elucidate their effect on muscle AChR functions. Primary chick muscle cultures were used as a...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880060410

    authors: Souroujon MC,Mochly-Rosen D,Gordon AS,Fuchs S

    更新日期:1983-05-01 00:00:00

  • Botulinum toxin improves sialorrhea and quality of living in bulbar amyotrophic lateral sclerosis.

    abstract::Sialorrhea is frequently a socially disabling symptom in patients with bulbar amyotrophic lateral sclerosis (ALS). In this open-label prospective study, we report the effect of botulinum toxin A (Botox) injection into the parotid glands in 10 patients with bulbar ALS and socially disabling sialorrhea. We applied three...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/mus.20545

    authors: Verma A,Steele J

    更新日期:2006-08-01 00:00:00

  • The electrodiagnostic findings in polyneuropathies associated with IgM monoclonal gammopathies.

    abstract::Electrodiagnostic studies were analyzed in patients with neuropathy associated with IgM monoclonal proteins, 7 with anti-myelin associated glycoprotein reactivity (MAG) and 7 nonreactive to MAG. The findings were distinctly different in the two groups. The electrodiagnostic studies of all the MAG-reactive patients had...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880131205

    authors: Kelly JJ Jr

    更新日期:1990-12-01 00:00:00

  • Neural hyperexcitability in hyperkalemic periodic paralysis.

    abstract::An electrophysiologic study of peripheral nerve excitability was performed in patients with hyperkalemic periodic paralysis (HPP) and in normal controls. It was found that a marked degree of neural hyperexcitability existed in all patients with HPP who showed cold sensitivity. The results suggest involvement of the ne...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880020402

    authors: Segura RP,Petajan JH

    更新日期:1979-07-01 00:00:00

  • Addressing heterogeneity in amyotrophic lateral sclerosis CLINICAL TRIALS.

    abstract::Amyotrophic lateral sclerosis (ALS) is a debilitating neurodegenerative disorder with complex biology and significant clinical heterogeneity. Many preclinical and early phase ALS clinical trials have yielded promising results that could not be replicated in larger phase 3 confirmatory trials. One reason for the lack o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.26801

    authors: Goyal NA,Berry JD,Windebank A,Staff NP,Maragakis NJ,van den Berg LH,Genge A,Miller R,Baloh RH,Kern R,Gothelf Y,Lebovits C,Cudkowicz M

    更新日期:2020-08-01 00:00:00

  • Immunohistochemical characterization of human masseter muscle spindles.

    abstract::An enzyme- and immunohistochemical study has been performed on human masseter muscle spindles. Antibodies selective for different myosin heavy chain (MHC) isoforms and M-band proteins (M-protein, myomesin, and MM-CK) were used. The expression of these proteins was determined in the different intrafusal fiber types. Nu...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880170105

    authors: Eriksson PO,Butler-Browne GS,Thornell LE

    更新日期:1994-01-01 00:00:00

  • The dropped head syndrome with chronic inflammatory demyelinating polyneuropathy.

    abstract::The dropped head syndrome occurs in a variety of neuromuscular disorders. We present a woman with chronic inflammatory demyelinating polyneuropathy who developed this syndrome, likely reflecting severe demyelination of nerves to cervical paraspinal muscles. ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880170717

    authors: Hoffman D,Gutmann L

    更新日期:1994-07-01 00:00:00

  • Plasticity of dynamic muscle performance with strength training in elderly humans.

    abstract::Data are scarce relating to the plasticity with strength training of dynamic muscle performance in older humans. Hence, we investigated alterations in the torque-velocity relation with strength training in old age, and their origin. Knee extension and leg-press exercises were performed three times per week for 14 week...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20275

    authors: Reeves ND,Maganaris CN,Narici MV

    更新日期:2005-03-01 00:00:00

  • A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenita.

    abstract::At least 50 disease-causing mutations in the skeletal muscle voltage-gated chloride channel gene (CLCN1), almost all of which originate from Caucasian families, have been identified. We investigated a Japanese family with Thomsen's myotonia congenita that included 16 affected individuals (8 men and 8 women) through fi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/1097-4598(200103)24:3<357::aid-mus1006>3.0

    authors: Sasaki R,Ito N,Shimamura M,Murakami T,Kuzuhara S,Uchino M,Uyama E

    更新日期:2001-03-01 00:00:00

  • GNE myopathy in the bedouin population of Kuwait: Genetics, prevalence, and clinical description.

    abstract:INTRODUCTION:GNE myopathy is a rare recessive myopathy caused by mutations in the GNE gene. It is mainly a distal myopathy with relative sparing of the quadriceps muscle. METHODS:Patients with distal myopathies from Kuwait were examined and tested for the Middle Eastern GNE gene founder mutation, p.M743T. Patients wer...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26337

    authors: Alrohaif H,Pogoryelova O,Al-Ajmi A,Aljeryan LA,Alrashidi NH,Alefasi SA,Urtizberea A,Lochmüller H,Bastaki L

    更新日期:2018-11-01 00:00:00

  • Ultrasound appears to be a reliable technique for the diagnosis of piriformis syndrome.

    abstract:INTRODUCTION:Piriformis muscle syndrome (PS) is a disorder encompassing a constellation of symptoms, including buttock and hip pain. In this study we aimed to assess the value of ultrasound (US) in the diagnosis of PS. METHODS:Thirty-three clinically diagnosed PS patients and 26 healthy volunteers underwent a clinical...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26418

    authors: Zhang W,Luo F,Sun H,Ding H

    更新日期:2019-04-01 00:00:00

  • Organization of the motor-unit pool for different directions of isometric contraction of the first dorsal interosseous muscle.

    abstract:INTRODUCTION:Muscle force generation involves recruitment and firing rate modulation of motor units (MUs). The control of MUs in producing multidirectional forces remains unclear. METHODS:We studied MU recruitment and firing properties, recorded from the first dorsal interosseous muscle, for 3 different directions of ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25963

    authors: Lei Y,Suresh NL,Rymer WZ,Hu X

    更新日期:2018-01-01 00:00:00

  • Epidemiology of cauda equina and conus medullaris lesions.

    abstract::The epidemiology of cauda equina and conus medullaris lesions is not well known, and this study aimed to provide further information on this topic. In the period 1996-2004, patients fulfilling the clinical, electrodiagnostic, and radiological criteria for such lesions were identified. For cauda equina/conus medullaris...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20696

    authors: Podnar S

    更新日期:2007-04-01 00:00:00

  • Differences between young and older women in maximal force, force fluctuations, and surface EMG during isometric knee extension and elbow flexion.

    abstract::The loss of muscle strength with aging appears to be greater in the lower than upper limbs, but strength and its neural control have never been compared in the same population of individuals in both upper and lower limbs. The aim of this study was to investigate differences between eight young (20-31 years) and eight ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20151

    authors: Bazzucchi I,Felici F,Macaluso A,De Vito G

    更新日期:2004-11-01 00:00:00

  • Potential implications of a ciliary neurotrophic factor gene mutation in a German population of patients with motor neuron disease.

    abstract::The frequency of a recently described point mutation of the ciliary neurotrophic factor (CNTF) gene was investigated in a population of 154 German patients with motor neuron disease (MND). Twenty-two percent of the patients were heterozygous, 2% homozygous for the CNTF mutation. Since the gene defect is per se not lin...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199802)21:2<236::aid-mus12

    authors: Giess R,Goetz R,Schrank B,Ochs G,Sendtner M,Toyka K

    更新日期:1998-02-01 00:00:00

  • I-Z-I complexes in congenital myopathy.

    abstract::A 3-month-old boy with hypotonia at birth succumbed to a congenital myopathy. The major finding in his muscle biopsy corresponded to I-Z-I complexes described previously in embryonic skeletal muscle. A few previous myopathy cases have described findings suggestive of I-Z-I-like complexes. A mutation affecting mononucl...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21575

    authors: Rhodes RH,Sharer LR

    更新日期:2010-05-01 00:00:00

  • Near-infrared spectroscopy during exercise and recovery in children with juvenile dermatomyositis.

    abstract:INTRODUCTION:We hypothesized that microvascular disturbances in muscle tissue play a role in the reduced exercise capacity in juvenile dermatomyositis (JDM). METHODS:Children with JDM, children with juvenile idiopathic arthritis (clinical controls), and healthy children performed a maximal incremental cycloergometric ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23484

    authors: Habers GE,De Knikker R,Van Brussel M,Hulzebos E,Stegeman DF,Van Royen A,Takken T

    更新日期:2013-01-01 00:00:00

  • The thoracic outlet syndromes.

    abstract::The term thoracic outlet syndrome (TOS) refers to a heterogeneous group of disorders, all of which have in common compression of one or more neurovascular elements at some point within the thoracic outlet. Of the five disorders comprising this group, four have all of the features expected of a syndrome-a recognized co...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.23235

    authors: Ferrante MA

    更新日期:2012-06-01 00:00:00

  • Evidence for new isoform of fast myosin heavy chain in rat skeletal muscle.

    abstract::The purpose of this study was to investigate whether the previously demonstrated heterogeneity of myosin heavy chain (MHC) in type 2B fibers of the superficial portion of the lateral gastrocnemius (SLG) muscle of the rat may be due to presence of type 2D/X fibers. Immunohistochemical identification of MHC heterogeneit...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880151210

    authors: Sawchak JA,Leung B,Shafiq SA

    更新日期:1992-12-01 00:00:00

  • Proteasome inhibitors for malignancy-related Lambert-Eaton myasthenic syndrome.

    abstract::Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disorder characterized by autoantibodies against presynaptic voltage-gated calcium channels that impair neuromuscular transmission. Malignancies, especially small cell lung cancer (SCLC), have been associated with LEMS and account for approximately 60% of cases...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24122

    authors: Wang C,Chen S,Feng B,Guan Y

    更新日期:2014-03-01 00:00:00

  • Calmodulin levels in developing muscle tissues and primary cultures of normal and dystrophic (UM-X7.1) hamsters.

    abstract::Calmodulin levels have been assessed in whole muscle and primary culture extracts in order to examine the relationship between calmodulin and the accumulation of calcium in dystrophic hamster muscle tissues. Significant decreases in both normal and dystrophic skeletal muscle, tongue, and heart calmodulin levels were o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880100113

    authors: Klamut HJ,Kotarba JA,Strickland KP

    更新日期:1987-01-01 00:00:00

  • Diagnostic utility of somatosensory evoked potentials in chronic polyradiculopathy without electrodiagnostic signs of peripheral demyelination.

    abstract:INTRODUCTION:Diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP) remains uncertain when nerve conduction studies (NCS) fail to show demyelination. METHODS:We conducted a retrospective study of patients who presented with clinical criteria of CIDP in whom electrodiagnostic (EDx) criteria of definite o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24693

    authors: Devic P,Petiot P,Mauguiere F

    更新日期:2016-01-01 00:00:00

  • Modification of the peripheral nerve disturbance in ciguatera poisoning in rats with lidocaine.

    abstract::Electrophysiological studies were performed on the ventral tail nerve of adult rats following intraperitoneal injection of a crude extract of ciguatoxin from known toxic fish flesh. Ciguatoxin induced significant slowing of both mixed and motor nerve conduction velocities and also significant reductions in both motor ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880160714

    authors: Cameron J,Flowers AE,Capra MF

    更新日期:1993-07-01 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

  • Basic polyaminoacids and protamine stimulate enzyme release from frog muscles.

    abstract::Polylysines, polyornithine, and protamine increased the release of creatine kinase (CK) and lactate dehydrogenase (LDH) from frog muscles. With 5 micrograms/ml (50 nM) of a polylysine of molecular weight 100,000, enzyme release reached peak values (ten-fold above control) within 30 minutes; subsequent removal of the p...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880080212

    authors: Suarez-Kurtz G

    更新日期:1985-02-01 00:00:00

  • Failure to detect HTLV-I by in situ hybridization in the biopsied muscles of viral carriers with polymyositis.

    abstract::Direct infection of muscle fibers by human T-lymphotropic virus type I (HTLV-I) has recently been reported in a patient with polymyositis infected with both HTLV-I and human immunodeficiency virus (HIV). Coinfections of these viruses are frequently found in the United States. In Kagoshima, Japan, patients with polymyo...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150108

    authors: Higuchi I,Nerenberg M,Yoshimine K,Yoshida M,Fukunaga H,Tajima K,Osame M

    更新日期:1992-01-01 00:00:00

  • Statistical motor unit number estimation: reproducibility and sources of error in patients with amyotrophic lateral sclerosis.

    abstract::The reliability of motor unit number estimation (MUNE) for assessment of the long-term course of ALS is dependent on the reproducibility of the technique. We report our results with the statistical method of MUNE on the ulnar nerve/hypothenar muscle in 16 ALS patients who were studied on 52 occasions. On each occasion...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/(sici)1097-4598(200002)23:2<193::aid-mus8>

    authors: Olney RK,Yuen EC,Engstrom JW

    更新日期:2000-02-01 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