Literature DB >> 7246542

Cholinesterase Newfoundland: a new succinylcholine-sensitive variant of cholinesterase at locus 1.

N E Simpson, C R Elliott.   

Abstract

A family from Newfoundland was found to have a new rare variant for plasma cholinesterase (E.C.3.1.1.8) recognized by a high-percentage inhibition by dibucaine (DN), particularly when succinyldithiocholine was used as substrate (DNSDTC) but also somewhat high when benzoylcholine was substrate (DNBZCH). The family data demonstrated that the variant is determined by an allele of the usual and atypical alleles at locus 1, and the new allele is designated CHE1*NFLD. The proband who was heterozygous for the Newfoundland and atypical alleles had shown sensitivity to succinylcholine. It is postulated that cholinesterase Newfoundland (NFLD) has a reduced affinity for succinylcholine. Samples selected for high DNs with a benzoylcholine from 200 Canadian Caucasians and 70 Newfoundlanders did not have the variant, and, therefore, it is assumed that the remainder of the samples did not have the variant.

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Year:  1981        PMID: 7246542      PMCID: PMC1685028     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  25 in total

1.  Human serum cholinesterase, a tetramer.

Authors:  E M Scott; R F Powers
Journal:  Nat New Biol       Date:  1972-03-22

2.  Kinetics of succinyldithiocholine hydrolysis by serum cholinesterase: comparison to dibucaine and succinylcholine numbers.

Authors:  L B Hersh; P P Raj; D Ohlweiler
Journal:  J Pharmacol Exp Ther       Date:  1974-05       Impact factor: 4.030

3.  Polyacrylamide electrophoresis used for the detection of C5+ cholinesterase in Canadian caucasians, Indians, and Eskimos.

Authors:  N E Simpson
Journal:  Am J Hum Genet       Date:  1972-05       Impact factor: 11.025

4.  Evidence for different "silent genes" in the human serum pseudocholinesterase polymorphism.

Authors:  H W Goedde; K Altland
Journal:  Ann N Y Acad Sci       Date:  1968-06-14       Impact factor: 5.691

5.  Discrimination of phenotypes in human serum cholinesterase deficiency.

Authors:  E M Scott; D D Weaver; R C Wright
Journal:  Am J Hum Genet       Date:  1970-07       Impact factor: 11.025

6.  A pseudocholinesterase variant (E Cynthiana) associated with elevated plasma enzyme activity.

Authors:  A Yoshida; A G Motulsky
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

7.  The pseudocholinesterase variants. Differentiation by means of sodium chloride.

Authors:  M Whittaker
Journal:  Acta Genet Stat Med       Date:  1968

8.  Silent cholinesterase gene: variations in the properties of serum enzyme in apparent homozygotes.

Authors:  H M Rubinstein; A A Dietz; L K Hodges; T Lubrano; V Czebotar
Journal:  J Clin Invest       Date:  1970-03       Impact factor: 14.808

9.  Increased plasma cholinesterase activity and succinylcholine resistance: a genetic variant.

Authors:  H W Neitlich
Journal:  J Clin Invest       Date:  1966-03       Impact factor: 14.808

10.  Sulphur and selenium compounds related to acetylcholine and choline. 8. Comparative studies of succinoylcholine, succinoylthiolcholine and succinoylselenolcholine.

Authors:  P Goodyer; H G Mautner
Journal:  Biochem Pharmacol       Date:  1967-10       Impact factor: 5.858

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  2 in total

1.  Immunological comparison of the usual and atypical human serum cholinesterase phenotypes.

Authors:  H W Eckerson; A Oseroff; O Lockridge; B N La Du
Journal:  Biochem Genet       Date:  1983-02       Impact factor: 1.890

2.  Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing.

Authors:  B N La Du; C F Bartels; C P Nogueira; M Arpagaus; O Lockridge
Journal:  Cell Mol Neurobiol       Date:  1991-02       Impact factor: 5.046

  2 in total

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