Literature DB >> 17698514

Quantitative comparisons of the acute neurotoxicity of toluene in rats and humans.

Vernon A Benignus1, William K Boyes, Elaina M Kenyon, Philip J Bushnell.   

Abstract

The behavioral and neurophysiological effects of acute exposure to toluene are the most thoroughly explored of all the hydrocarbon solvents. Behavioral effects have been experimentally studied in humans and other species, for example, rats. The existence of both rat and human dosimetric data offers the opportunity to quantitatively compare the relative sensitivity to acute toluene exposure. The purpose of this study was to fit dose-effect curves to existing data and to estimate the dose-equivalence equation (DEE) between rats and humans. The DEE gives the doses that produce the same magnitude of effect in the two species. Doses were brain concentrations of toluene estimated from physiologically based pharmacokinetic models. Human experiments measuring toluene effects on choice reaction time (CRT) were meta-analyzed. Rat studies employed various dependent variables: amplitude of visual-evoked potentials (VEPs), signal detection (SIGDET) accuracy (ACCU) and reaction time (RT), and escape-avoidance (ES-AV) behaviors. Comparison of dose-effect functions showed that human and rat sensitivity was practically the same for those two task regimens that exerted the least control over the behaviors being measured (VEP in rats and CRT in humans) and the sensitivity was progressively lower for SIGDET RT, SIGDET ACCU, and ES-AV behaviors in rats. These results suggested that the sensitivity to impairment by toluene depends on the strength of control over the measured behavior rather than on the species being tested. This interpretation suggests that (1) sensitivity to toluene would be equivalent in humans and rats if both species performed behaviors that were controlled to the same extent, (2) the most sensitive tests of neurobehavioral effects would be those in which least control is exerted on the behavior being measured, and (3) effects of toluene in humans may be estimated using the DEEs from rat studies despite differences in the amount of control exerted by the experimental regimen or differences in the behaviors under investigation.

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Year:  2007        PMID: 17698514     DOI: 10.1093/toxsci/kfm203

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  4 in total

1.  Specific impairments in instrumental learning following chronic intermittent toluene inhalation in adolescent rats.

Authors:  Alec L W Dick; Martin Axelsson; Andrew J Lawrence; Jhodie R Duncan
Journal:  Psychopharmacology (Berl)       Date:  2013-12-10       Impact factor: 4.530

2.  Chronic intermittent toluene inhalation in adolescent rats results in metabolic dysfunction with altered glucose homeostasis.

Authors:  A L W Dick; A Simpson; A Qama; Z Andrews; A J Lawrence; J R Duncan
Journal:  Br J Pharmacol       Date:  2015-10-22       Impact factor: 8.739

3.  Estimation of Equipotent Doses for Anti-Inflammatory Effects of Prednisolone and AZD9567, an Oral Selective Nonsteroidal Glucocorticoid Receptor Modulator.

Authors:  Joachim Almquist; Muhammad Waqas Sadiq; Ulf G Eriksson; Tove Hegelund Myrbäck; Susanne Prothon; Jacob Leander
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2020-08

4.  Neurological symptoms associated with oil spill response exposures: Results from the Deepwater Horizon Oil Spill Coast Guard Cohort Study.

Authors:  Jayasree Krishnamurthy; Lawrence S Engel; Li Wang; Erica G Schwartz; Kate Christenbury; Benjamin Kondrup; John Barrett; Jennifer A Rusiecki
Journal:  Environ Int       Date:  2019-08-02       Impact factor: 9.621

  4 in total

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