Literature DB >> 3928894

Isomers of long-chain alkane derivatives and nervous impulse blockage.

J Requena, M E Velaz, J R Guerrero, J D Medina.   

Abstract

The potency to block nervous impulse of members of normal aliphatic homologous series of primary and secondary isomers of functional derivatives of alkanes was tested in bundles of a few axons from sciatic nerves of the toad Bufo marinus. For the primary substituted functional derivates of pentane, the relative potency series was I greater than H approximately equal to Br greater than Cl greater than COOCH3 greater than F greater than CH2OH greater than COCH3 greater than OH approximately equal to NH2 greater than COOH. For the homologous series of primary alkanols, and from saturated Ringer's solutions, the time required to reversibly reduce the amplitude of the action potential to one-half its initial value were determined. The cut-off effect was detected at the level of dodecan-1-ol, while for the primary bromoalkanes it was bromooctane. However, solutions of the secondary isomer of the inactive primary homologues, such as tridecan-5-ol and tridecan-7-ol or 2-bromononane, were able to block nervous impulse conduction reversibly. From the concentration required for an equipotent effect it was calculated that the standard free energy for adsorption of primary alkanols was -705 cal mol- CH2. Similarly, for primary bromoalkanes a value of -733 cal mol-1 CH2 was obtained. The concentration required for an equipotent effect for primary isomer (either of alkanols or bromoalkanes) is lower than those obtained for the secondary isomers. Therefore, the latter are less potent than the former. Among secondary isomers the potency decreases as the functional group is moved away from the terminal carbon. The differential effect of structural isomers of long-chain alkane derivates around the point of cut-off cannot be explained in terms of differences in chemical properties, concentration in aqueous and membrane phases, or mean molecular volume. It is concluded that a volume related to that of the hydrophobic region of the agent and not its mean molecular volume should be responsible for an expansion of the target region.

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Year:  1985        PMID: 3928894     DOI: 10.1007/bf01871386

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  19 in total

1.  Anaesthesia by the n-alkanes. A comparative study of nerve impulse blockage and the properties of black lipid bilayer membranes.

Authors:  D A Haydon; B M Hendry; S R Levinson; J Requena
Journal:  Biochim Biophys Acta       Date:  1977-10-03

2.  Structural isomers of tetradecenol discriminate between the lipid fluidity and phase transition theories of anesthesia.

Authors:  M J Pringle; K W Miller
Journal:  Biochem Biophys Res Commun       Date:  1978-12-14       Impact factor: 3.575

3.  The membrane concentrations of alcohol anesthetics.

Authors:  P Seeman; S Roth; H Schneider
Journal:  Biochim Biophys Acta       Date:  1971-02-02

4.  A dynamic X-ray diffraction study of anaesthesia action. Changes in myelin structure and electrical activity recorded simultaneously from frog sciatic nerves treated with n-alkanes.

Authors:  R Padrón; L Mateu; J Requena
Journal:  Biochim Biophys Acta       Date:  1980-11-04

5.  Where do general anaesthetics act?

Authors:  N P Franks; W R Lieb
Journal:  Nature       Date:  1978-07-27       Impact factor: 49.962

6.  Intrinsic perturbing ability of alkanols in lipid bilayers.

Authors:  M K Jain; J Gleeson; A Upreti; G C Upreti
Journal:  Biochim Biophys Acta       Date:  1978-05-04

7.  Degenerate perturbations of protein structure as the mechanism of anaesthetic action.

Authors:  C D Richards; K Martin; S Gregory; C A Keightley; T R Hesketh; G A Smith; G B Warren; J C Metcalfe
Journal:  Nature       Date:  1978 Dec 21-28       Impact factor: 49.962

8.  Can the lipid theories of anesthesia account for the cutoff in anesthetic potency in homologous series of alcohols?

Authors:  M J Pringle; K B Brown; K W Miller
Journal:  Mol Pharmacol       Date:  1981-01       Impact factor: 4.436

9.  The action of alcohols and other non-ionic surface active substances on the sodium current of the squid giant axon.

Authors:  D A Haydon; B W Urban
Journal:  J Physiol       Date:  1983-08       Impact factor: 5.182

10.  Fatty acid and alcohol partitioning with intestinal brush border and erythrocyte membranes.

Authors:  V L Sallee
Journal:  J Membr Biol       Date:  1978-10-19       Impact factor: 1.843

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  3 in total

1.  The mechanisms of sodium current inhibition by benzocaine in the squid giant axon.

Authors:  J R Elliott; D A Haydon; B M Hendry
Journal:  Pflugers Arch       Date:  1987-08       Impact factor: 3.657

2.  Nonanesthetic alcohols dissolve in synaptic membranes without perturbing their lipids.

Authors:  K W Miller; L L Firestone; J K Alifimoff; P Streicher
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

3.  The interaction of homologous series of alkanols with sodium channels in nerve membrane vesicles.

Authors:  N Rodríguez; R Villegas; J Requena
Journal:  J Membr Biol       Date:  1988-09       Impact factor: 1.843

  3 in total

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