Literature DB >> 8549464

The concern for developmental neurotoxicology: is it justified and what is being done about it?

H A Tilson1.   

Abstract

In general, it is believed that the possibility of an adverse developmental outcome following conception is relatively high. In most cases, the cause of the defect is not clear, although exposure to chemical agents at a critical period during development has been proposed to play a significant role. Consequently, regulatory agencies such as the U.S. Environmental Protection Agency (U.S. EPA) have promulgated testing guidelines for assessing developmental neurotoxicity of chemicals in animal testing protocols. Concerns have been expressed about the use of behavioral tests to evaluate chemicals for developmental neurotoxicity, since some investigators believe that they lack predictive validity for human developmental neurotoxicity. Other investigators have indicated that results from such studies are difficult to interpret because of a lack of standardization and sensitivity of the tests. Furthermore, it has been argued that the developing organism is not especially sensitive to chemicals or, if effects are observed, the developing organism is capable of compensating for the deficit. Recent research, however, has adequately demonstrated that developing organisms are especially vulnerable to chemical agents if the exposure occurs at a critical period during development, while other studies have supported the assumption that functional or behavioral effects observed in animal models can be extrapolated to humans. These findings support the routine assessment of chemicals for developmental neurotoxicity using functional end points and suggest that currently available methods could be used to determine more precisely the mechanism of chemical-induced developmental defects.

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Year:  1995        PMID: 8549464      PMCID: PMC1518918          DOI: 10.1289/ehp.95103s6147

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  16 in total

1.  The insensitivity of the developing rat foetus to the toxic effects of acrylamide.

Authors:  P M Ewards
Journal:  Chem Biol Interact       Date:  1976-01       Impact factor: 5.192

Review 2.  A review of acrylamide neurotoxicity. Part I. Properties, uses and human exposure.

Authors:  P S Spencer; H H Schaumburg
Journal:  Can J Neurol Sci       Date:  1974-05       Impact factor: 2.104

Review 3.  Human teratogenicity.

Authors:  T H Shepard
Journal:  Adv Pediatr       Date:  1986

4.  Behavioral consequences of interference with CNS development in the early fetal period.

Authors:  P M Rodier; S S Reynolds; W N Roberts
Journal:  Teratology       Date:  1979-06

5.  The effects of postpartum exposure to triethyl tin on the neurobehavioral functioning of rats.

Authors:  G J Harry; H A Tilson
Journal:  Neurotoxicology       Date:  1981-10       Impact factor: 4.294

6.  Treatment with methylazoxymethanol at different gestational days: two-way shuttle box avoidance and residential maze activity in rat offspring.

Authors:  W Balduini; J Elsner; G Lombardelli; G Peruzzi; F Cattabeni
Journal:  Neurotoxicology       Date:  1991       Impact factor: 4.294

7.  Measuring early pregnancy loss: laboratory and field methods.

Authors:  A J Wilcox; C R Weinberg; R E Wehmann; E G Armstrong; R E Canfield; B C Nisula
Journal:  Fertil Steril       Date:  1985-09       Impact factor: 7.329

8.  Effects of acrylamide given during gestation on dopamine receptor binding in rat pups.

Authors:  A K Agrawal; R E Squibb
Journal:  Toxicol Lett       Date:  1981-01       Impact factor: 4.372

9.  Postpartum exposure to triethyl tin produces long-term alterations in responsiveness to apomorphine.

Authors:  G J Harry; H A Tilson
Journal:  Neurotoxicology       Date:  1982-07       Impact factor: 4.294

10.  Critical periods for behavioral anomalies in mice.

Authors:  P M Rodier
Journal:  Environ Health Perspect       Date:  1976-12       Impact factor: 9.031

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  6 in total

1.  Maternal use of drugs and preeclampsia.

Authors:  Heidi Sahlman; Marjaana Koponen; Hani El-Nezami; Kirsi Vähäkangas; Leea Keski-Nisula
Journal:  Br J Clin Pharmacol       Date:  2019-12-15       Impact factor: 4.335

2.  The sea urchin embryo, an invertebrate model for mammalian developmental neurotoxicity, reveals multiple neurotransmitter mechanisms for effects of chlorpyrifos: therapeutic interventions and a comparison with the monoamine depleter, reserpine.

Authors:  Gennady A Buznikov; Lyudmila A Nikitina; Ljubisa M Rakić; Ivan Milosević; Vladimir V Bezuglov; Jean M Lauder; Theodore A Slotkin
Journal:  Brain Res Bull       Date:  2007-07-06       Impact factor: 4.077

Review 3.  Pesticides and inner-city children: exposures, risks, and prevention.

Authors:  P J Landrigan; L Claudio; S B Markowitz; G S Berkowitz; B L Brenner; H Romero; J G Wetmur; T D Matte; A C Gore; J H Godbold; M S Wolff
Journal:  Environ Health Perspect       Date:  1999-06       Impact factor: 9.031

4.  Screening for developmental neurotoxicity using PC12 cells: comparisons of organophosphates with a carbamate, an organochlorine, and divalent nickel.

Authors:  Theodore A Slotkin; Emiko A MacKillop; Ian T Ryde; Charlotte A Tate; Frederic J Seidler
Journal:  Environ Health Perspect       Date:  2007-01       Impact factor: 9.031

Review 5.  Potential developmental neurotoxicity of pesticides used in Europe.

Authors:  Marina Bjørling-Poulsen; Helle Raun Andersen; Philippe Grandjean
Journal:  Environ Health       Date:  2008-10-22       Impact factor: 5.984

6.  The MATEX cohort - a Finnish population register birth cohort to study health effects of prenatal exposures.

Authors:  Isabell K Rumrich; Kirsi Vähäkangas; Matti Viluksela; Mika Gissler; Heljä-Marja Surcel; Hanna de Ruyter; Jukka Jokinen; Otto Hänninen
Journal:  BMC Public Health       Date:  2017-11-07       Impact factor: 3.295

  6 in total

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