Literature DB >> 3998815

Stimulation of denervated rat soleus muscle with fast and slow activity patterns induces different expression of acetylcholinesterase molecular forms.

T Lømo, J Massoulié, M Vigny.   

Abstract

The relative amount and distribution of acetylcholinesterase (AChE) molecular forms were studied in slow soleus and (less extensively) in fast extensor digitorum longus (EDL) muscles of the rat before and after denervation and direct stimulation. Normal EDL muscles showed higher total and specific AChE activity than normal soleus muscles and contained essentially three different molecular AChE forms (G1, G4, and A12) as opposed to six forms (G1, G2, G4, A4, A8, and A12) in the soleus. Denervation reduced AChE activity in both muscles. In the soleus direct stimulation starting 2 to 3 weeks after denervation increased the specific AChE activity markedly. The increase started 12 to 24 hr after the onset of stimulation, reached 3 to 5 times normal values after 2 to 7 days, and then declined gradually toward normal values over the next 2 weeks. Furthermore, the effect on the different molecular forms depended strongly on the stimulus pattern. Thus, intermittent 100 Hz stimulation (fast pattern) induced essentially the three forms typical of the normal EDL, whereas continuous 10 Hz stimulation induced the six forms characteristic of normal soleus muscles but with some differences in their relative proportions. In the EDL, 2 days of continuous 10 Hz stimulation (the only duration and pattern examined) failed to induce a similar increase in AChE activity.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3998815      PMCID: PMC6565058     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  24 in total

1.  Golgi complex, endoplasmic reticulum exit sites, and microtubules in skeletal muscle fibers are organized by patterned activity.

Authors:  E Ralston; T Ploug; J Kalhovde; T Lomo
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

2.  Postnatal development of rat motor nerve terminals.

Authors:  O Waerhaug
Journal:  Anat Embryol (Berl)       Date:  1992

3.  Differences in expression of acetylcholinesterase and collagen Q control the distribution and oligomerization of the collagen-tailed forms in fast and slow muscles.

Authors:  E Krejci; C Legay; S Thomine; J Sketelj; J Massoulié
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

4.  Control of end-plate channel properties by neurotrophic effects and by muscle activity in rat.

Authors:  H R Brenner; T Lømo; R Williamson
Journal:  J Physiol       Date:  1987-07       Impact factor: 5.182

Review 5.  Acetylcholinesterase mRNA level and synaptic activity in rat muscles depend on nerve-induced pattern of muscle activation.

Authors:  J Sketelj; N Crne-Finderle; B Strukelj; J V Trontelj; D Pette
Journal:  J Neurosci       Date:  1998-03-15       Impact factor: 6.167

6.  Molecular forms and localization of acetylcholinesterase and nonspecific cholinesterase in regenerating skeletal muscles.

Authors:  J Sketelj; N Crne; M Brzin
Journal:  Neurochem Res       Date:  1987-02       Impact factor: 3.996

7.  Skeletal muscle IP3R1 receptors amplify physiological and pathological synaptic calcium signals.

Authors:  Haipeng Zhu; Bula J Bhattacharyya; Hong Lin; Christopher M Gomez
Journal:  J Neurosci       Date:  2011-10-26       Impact factor: 6.167

Review 8.  Mechanical regulation of musculoskeletal system development.

Authors:  Neta Felsenthal; Elazar Zelzer
Journal:  Development       Date:  2017-12-01       Impact factor: 6.868

Review 9.  The neuromuscular junction. Muscle fibre type differences, plasticity and adaptability to increased and decreased activity.

Authors:  M R Deschenes; J Covault; W J Kraemer; C M Maresh
Journal:  Sports Med       Date:  1994-06       Impact factor: 11.136

10.  Interactions between intrinsic regulation and neural modulation of acetylcholinesterase in fast and slow skeletal muscles.

Authors:  J Sketelj; N Crne-Finderle; S Ribaric; M Brzin
Journal:  Cell Mol Neurobiol       Date:  1991-02       Impact factor: 5.046

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.