Literature DB >> 6747890

Turnover of acetylcholinesterase in innervated and denervated rat diaphragm.

J R Newman, J B Virgin, L H Younkin, S G Younkin.   

Abstract

The acetylcholinesterase (AChE) in rat diaphragms was labelled by intravenous injection of echothiophate in order to evaluate the turnover of AChE in innervated and denervated muscle in vivo. Echothiophate diethylphosphorylates AChE thereby inactivating it. Labelled (diethylphosphorylated) enzyme is rapidly and quantitatively reactivated with 1-methyl-2-hydroxyiminomethylpyridinium (2-PAM), so labelled (diethylphosphorylated) AChE was conveniently measured as 2-PAM-reactivatable AChE activity. In homogenates in vitro, label is lost spontaneously (diethylphosphorylated AChE spontaneously reactivates) with a half-time of 27 h. In innervated diaphragm, labelled non-end-plate AChE is lost with a half-time of 13 h. When correction is made for the spontaneous loss of label on the basis of in vitro measurements, this data indicates that non-end-plate AChE turns over with a half-time of about 26 h. In innervated diaphragm, labelled end-plate-specific AChE is lost more slowly than non-end-plate AChE and at a rate essentially identical to the rate of spontaneous loss of label in vitro. The rate of loss of labelled non-end-plate AChE is essentially identical in 18 h denervated and in paired innervated diaphragms. The rate of loss of labelled end-plate-specific AChE is significantly faster in 18 h denervated diaphragms than in paired innervated diaphragms. On the basis of these observations, hypotheses concerning the mechanisms of the denervation-induced decreases in non-end-plate and end-plate-specific AChE are formulated and discussed.

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Year:  1984        PMID: 6747890      PMCID: PMC1193212          DOI: 10.1113/jphysiol.1984.sp015292

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  33 in total

1.  Nerve stump length-dependent loss of acetycholinesterase activity in endplate regions of rat diaphragm.

Authors:  N A Ranish; W D Dettbarn; L Wecker
Journal:  Brain Res       Date:  1980-06-09       Impact factor: 3.252

2.  Partial purification and characterization of a nerve trophic factor regulating muscle acetylcholinesterase activity.

Authors:  T L Lentz; J S Addis; J Chester
Journal:  Exp Neurol       Date:  1981-08       Impact factor: 5.330

3.  Cellular localization of the molecular forms of acetylcholinesterase in rat diaphragm.

Authors:  S G Younkin; C Rosenstein; P L Collins; T L Rosenberry
Journal:  J Biol Chem       Date:  1982-11-25       Impact factor: 5.157

4.  Synthesis, transport and fate of acetylcholinesterase in cultured chick embryos muscle cells.

Authors:  R L Rotundo; D M Fambrough
Journal:  Cell       Date:  1980-11       Impact factor: 41.582

5.  Neurotrophic control of 16S acetylcholinesterase from mammalian skeletal muscle in organ culture.

Authors:  H L Fernandez; M R Patterson; M J Duell
Journal:  J Neurobiol       Date:  1980-11

6.  Secretion of acetylcholinesterase: relation to acetylcholine receptor metabolism.

Authors:  R L Rotundo; D M Fambrough
Journal:  Cell       Date:  1980-11       Impact factor: 41.582

7.  Control of junctional acetylcholinesterase by neural and muscular influences in the rat.

Authors:  T Lømo; C R Slater
Journal:  J Physiol       Date:  1980-06       Impact factor: 5.182

8.  16 S acetylcholinesterase in endplate-free regions of developing rat diaghragm.

Authors:  J Sketelj; M Brzin
Journal:  Neurochem Res       Date:  1980-06       Impact factor: 3.996

9.  Regulation of acetylcholinesterase appearance at neuromuscular junctions in vitro.

Authors:  L L Rubin; S M Schuetze; C L Weill; G D Fischbach
Journal:  Nature       Date:  1980-01-17       Impact factor: 49.962

10.  Effects of acute and chronic denervation on release of acetylcholinesterase and its molecular forms in rat diaphragms.

Authors:  J L Cater; S Brimijoin
Journal:  J Neurochem       Date:  1981-03       Impact factor: 5.372

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  2 in total

1.  Stabilization of collagen-tailed acetylcholinesterase in muscle cells through extracellular anchorage by transglutaminase-catalyzed cross-linking.

Authors:  D Hand; D Dias; L W Haynes
Journal:  Mol Cell Biochem       Date:  2000-01       Impact factor: 3.396

2.  Protection against the effects of anticholinesterases on the latencies of action potentials in mouse skeletal muscles.

Authors:  S S Kelly; C B Ferry; J P Bamforth; S K Das
Journal:  Br J Pharmacol       Date:  1992-11       Impact factor: 8.739

  2 in total

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