Literature DB >> 15845326

Inhibition of gap junction currents by the abused solvent toluene.

Angelo M Del Re1, John J Woodward.   

Abstract

Abused inhalants are a large class of compounds that are inhaled for their intoxicating and mood altering effects. They include chemicals with known therapeutic uses such as anesthetic gases as well as volatile organic solvents like toluene that are found in paint thinners and adhesives. Because of their widespread commercial use and availability, inhalants are often among the first drugs that children encounter and use of these compounds is often associated with adverse acute and long-term consequences. The cellular and molecular sites of action for abused inhalants is not well known although recent studies report that toluene and other organic solvents alter the activity of specific ligand- and voltage-gated ion channels that regulate cellular excitability. As part of an ongoing effort to define molecular sites of action for abused inhalants, this study examined the effect of toluene on the function of gap junction proteins endogenously expressed in human embryonic kidney (HEK 293) cells. Gap junctions allow cell-to-cell electrical communication as well as passage of small molecular weight substances and are critical for synchronizing cellular activity in certain tissues. Gap junction currents in HEK 293 cells were measured during brief voltage steps using patch-clamp electrophysiology and were blocked by known gap junction blockers confirming expression of connexin proteins in these cells. Toluene dose-dependently inhibited these conductances with threshold effects appearing at approximately 0.4 mM and near complete inhibition occurring at concentrations of 1 mM and higher. The estimated EC50 value for toluene inhibition of gap junction currents in HEK 293 cells was 0.57 mM. The results of these studies suggest that volatile solvents including toluene may produce some of their effects by disrupting inter-cellular communication mediated by gap junction proteins.

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Year:  2004        PMID: 15845326     DOI: 10.1016/j.drugalcdep.2004.10.005

Source DB:  PubMed          Journal:  Drug Alcohol Depend        ISSN: 0376-8716            Impact factor:   4.492


  6 in total

1.  Review of toluene action: clinical evidence, animal studies and molecular targets.

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Journal:  J Drug Alcohol Res       Date:  2014

Review 2.  Volatile solvents as drugs of abuse: focus on the cortico-mesolimbic circuitry.

Authors:  Jacob T Beckley; John J Woodward
Journal:  Neuropsychopharmacology       Date:  2013-08-19       Impact factor: 7.853

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Authors:  Eliseo A Eugenin; Silvana Valdebenito; Anna Maria Gorska; Agustin D Martínez; Marcela Bitran; Juan C Sáez
Journal:  J Neurochem       Date:  2019-10-20       Impact factor: 5.372

4.  Screening fluorescent voltage indicators with spontaneously spiking HEK cells.

Authors:  Jeehae Park; Christopher A Werley; Veena Venkatachalam; Joel M Kralj; Sulayman D Dib-Hajj; Stephen G Waxman; Adam E Cohen
Journal:  PLoS One       Date:  2013-12-31       Impact factor: 3.240

5.  Human concentrative nucleoside transporter 3 transfection with ultrasound and microbubbles in nucleoside transport deficient HEK293 cells greatly increases gemcitabine uptake.

Authors:  Robert J Paproski; Sylvia Y M Yao; Nicole Favis; David Evans; James D Young; Carol E Cass; Roger J Zemp
Journal:  PLoS One       Date:  2013-02-18       Impact factor: 3.240

6.  A robotic multidimensional directed evolution approach applied to fluorescent voltage reporters.

Authors:  Kiryl D Piatkevich; Erica E Jung; Christoph Straub; Changyang Linghu; Demian Park; Ho-Jun Suk; Daniel R Hochbaum; Daniel Goodwin; Eftychios Pnevmatikakis; Nikita Pak; Takashi Kawashima; Chao-Tsung Yang; Jeffrey L Rhoades; Or Shemesh; Shoh Asano; Young-Gyu Yoon; Limor Freifeld; Jessica L Saulnier; Clemens Riegler; Florian Engert; Thom Hughes; Mikhail Drobizhev; Balint Szabo; Misha B Ahrens; Steven W Flavell; Bernardo L Sabatini; Edward S Boyden
Journal:  Nat Chem Biol       Date:  2018-02-26       Impact factor: 15.040

  6 in total

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