Literature DB >> 465887

Relationship between inhibition of acetylcholinesterase and response of the rat phrenic nerve-diaphragm preparation to indirect stimulation at higher frequencies.

P F Heffron, F Hobbiger.   

Abstract

1 Rat isolated diaphragm preparations were stimulated indirectly either intermittently at 20, 50 or 100 Hz or continuously at 0.2 Hz.2 Addition of 1.8 muM paraoxon (which inhibits acetylcholinesterase by forming a phosphorylated enzyme which undergoes slow spontaneous reactivation) for 5 min to the organ bath produced a failure of the muscle to maintain tetanic tension (tetanic fade, Wedensky inhibition) and potentiated the neuromuscular blocking activity of exogenous acetylcholine. The rates of recovery from both these effects were recorded.3 In a series of experiments with dyflos (which inhibits acetylcholinesterase by forming a phosphorylated enzyme which does not undergo spontaneous reactivation) the relationship between functional acetylcholinesterase activity and neuromuscular blocking activity of exogenous acetylcholine was also determined.4 From the data obtained, the relationship between functional acetylcholinesterase activity and tetanic fade was calculated. These calculations show that (i) a considerable reduction in functional acetylcholinesterase activity is required before the diaphragm loses its ability to respond with a sustained tetanus to indirect stimulation at higher frequencies, (ii) the minimum (critical) level of functional acetylcholinesterase activity required for a normal tetanic response is directly related to the frequency of stimulation and (iii) once functional acetylcholinesterase activity has been reduced to the critical level, a very small further reduction leads to a complete tetanic fade.5 The meaning of functional acetylcholinesterase assays and of conclusions which can be drawn from them, is discussed.

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Year:  1979        PMID: 465887      PMCID: PMC2043639          DOI: 10.1111/j.1476-5381.1979.tb13683.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  16 in total

1.  Comparison of the effects of inhibition of external, internal and total acetylcholinesterase upon ganglionic transmission.

Authors:  R J McISAAC; G B KOELLE
Journal:  J Pharmacol Exp Ther       Date:  1959-05       Impact factor: 4.030

2.  The mechanism of action of anti-cholinesterases. III. The action of anti-cholinesterases on the phrenic nerve-diaphragm preparation of the rat.

Authors:  J A COHEN; C H POSTHUMUS
Journal:  Acta Physiol Pharmacol Neerl       Date:  1957-10

3.  The cerebral distributions of a tertiary and a quaternary anticholinesterase agent following intravenous and intraventricular injection.

Authors:  G B KOELLE; E C STEINER
Journal:  J Pharmacol Exp Ther       Date:  1956-12       Impact factor: 4.030

4.  The role of cholinesterase at the myoneural junction.

Authors:  J M BARNES; J I DUFF
Journal:  Br J Pharmacol Chemother       Date:  1953-09

5.  Distribution of acetylcholine receptors at frog neuromuscular junctions with a discussion of some physiological implications.

Authors:  J Matthews-Bellinger; M M Salpeter
Journal:  J Physiol       Date:  1978-06       Impact factor: 5.182

6.  The inhibition of cholinesterases by alkyl-phosphates and alkylphenolphosphates.

Authors:  A S V BURGEN; F HOBBIGER
Journal:  Br J Pharmacol Chemother       Date:  1951-12

7.  Effects of 1,1'-trimethylene bis(4-formylpyridinium bromide) dioxime (TMB-4) on cholinesterase activity and neuromuscular block following poisoning with sarin and DEP.

Authors:  J H FLEISHER; J HANSA; P J KILLOS; C S HARRISON
Journal:  J Pharmacol Exp Ther       Date:  1960-12       Impact factor: 4.030

8.  The generation of nerve and muscle repetivie activity in the rat phrenic nerve-diaphragm preparation following inhibition of cholinesterase by ecothiopate.

Authors:  J D Morrison
Journal:  Br J Pharmacol       Date:  1977-05       Impact factor: 8.739

9.  Synthesis, storage and release of [14C]acetylcholine in isolated rat diaphragm muscles.

Authors:  L T Potter
Journal:  J Physiol       Date:  1970-01       Impact factor: 5.182

10.  The binding of acetylcholine to receptors and its removal from the synaptic cleft.

Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

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  8 in total

1.  In vitro oxime-induced reactivation of various molecular forms of soman-inhibited acetylcholinesterase in striated muscle from rat, monkey and human.

Authors:  J G Clement; N Erhardt
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

2.  Survivors of soman poisoning: recovery of the soman LD50 to control value in the presence of extensive acetylcholinesterase inhibition.

Authors:  J G Clement
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

3.  Role of acetylcholinesterase on the structure and function of cholinergic synapses: insights gained from studies on knockout mice.

Authors:  Michael Adler; Richard E Sweeney; Tracey A Hamilton; Oksana Lockridge; Ellen G Duysen; Angela L Purcell; Sharad S Deshpande
Journal:  Cell Mol Neurobiol       Date:  2011-05-03       Impact factor: 5.046

4.  Inactivation of end-plate acetylcholinesterase during the course of organophosphate intoxications.

Authors:  R Besser; L Gutman; L S Weilemann
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

5.  Effects of nicotine receptor agonists on acetylcholine release from the isolated motor nerve, small intestine and trachea of rats and guinea-pigs.

Authors:  I Wessler; C Apel; M Garmsen; A Klein
Journal:  Clin Investig       Date:  1992 Mar-Apr

6.  Twitch potentiation by organophosphate anticholinesterases in rat phrenic nerve diaphragm preparations.

Authors:  A L Clark; F Hobbiger
Journal:  Br J Pharmacol       Date:  1983-01       Impact factor: 8.739

7.  Mechanisms of the inhibition by neostigmine of tetanic contraction in the mouse diaphragm.

Authors:  C C Chang; S J Hong; J L Ko
Journal:  Br J Pharmacol       Date:  1986-04       Impact factor: 8.739

8.  Structural analysis of human glycoprotein butyrylcholinesterase using atomistic molecular dynamics: The importance of glycosylation site ASN241.

Authors:  Austen Bernardi; Karl N Kirschner; Roland Faller
Journal:  PLoS One       Date:  2017-11-30       Impact factor: 3.240

  8 in total

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