Developmental neurotoxicity of pyrethroid insecticides: Critical review and future research needs

被引:384
作者
Shafer, TJ
Meyer, DA
Crofton, KM
机构
[1] US EPA, Div Neurotoxicol, Natl Hlth & Environm Effects Res Lab, Off Res & Dev, Res Triangle Pk, NC 27711 USA
[2] Univ N Carolina, Curriculum Toxicol, Chapel Hill, NC USA
关键词
age-dependent toxicity; biologically based dose-response model; developmental neurotoxicity; mode of action; physiologically based pharmacokinetic model; pyrethroid; risk assessment; voltage-sensitive sodium channel;
D O I
10.1289/ehp.7254
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Pyrethroid insecticides have been used for more than 40 years and account for 25% of the worldwide insecticide market. Although their acute neurotoxicity to adults has been well characterized, information regarding the potential developmental neurotoxicity of this class of compounds is limited. There is a large age dependence to the acute toxicity of pyrethroids in which neonatal rats are at least an order of magnitude more sensitive than adults to two pyrethroids. There is no information on age-dependent toxicity for most pyrethroids. In the present review we examine the scientific data related to potential for age-dependent and developmental neurotoxicity of pyrethroids. As a basis for understanding this neurotoxicity, we discuss the heterogeneity and ontogeny of voltage-sensitive sodium channels, a primary neuronal target of pyrethroids. We also summarize 22 studies of the developmental neurotoxicity of pyrethroids and review the strengths and limitations of these studies. These studies examined numerous end points, with changes in motor activity and muscarinic acetylcholine receptor density the most common. Many of the developmental neurotoxicity studies suffer from inadequate study design, problematic statistical analyses, use of formulated products, and/or inadequate controls. These factors confound interpretation of results. To better understand the potential for developmental exposure to pyrethroids to cause neurotoxicity, additional, well-designed and well-executed developmental neurotoxicity studies are needed. These studies should employ state-of-the-science methods to promote a greater understanding of the mode of action of pyrethroids in the developing nervous system.
引用
收藏
页码:123 / 136
页数:14
相关论文
共 117 条
  • [31] A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus -: and prevalence of variants in patients with epilepsy
    Escayg, A
    Heils, A
    MacDonald, BT
    Haug, K
    Sander, T
    Meisler, MH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (04) : 866 - 873
  • [32] Sodium channel alpha-subunit mRNAs I, II, III, NaG, Na6 and hNE (PN1): Different expression patterns in developing rat nervous system
    Felts, PA
    Yokoyama, S
    DibHajj, S
    Black, JA
    Waxman, SG
    [J]. MOLECULAR BRAIN RESEARCH, 1997, 45 (01): : 71 - 82
  • [33] 2 CLASSES OF PYRETHROID ACTION IN THE COCKROACH
    GAMMON, DW
    BROWN, MA
    CASIDA, JE
    [J]. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 1981, 15 (02) : 181 - 191
  • [34] Nomenclature of voltage-gated sodium channels
    Goldin, AL
    Barchi, RL
    Caldwell, JH
    Hofmann, F
    Howe, JR
    Hunter, JC
    Kallen, RG
    Mandel, G
    Meisler, MH
    Netter, YB
    Noda, M
    Tamkun, MM
    Waxman, SG
    Wood, JN
    Catterall, WA
    [J]. NEURON, 2000, 28 (02) : 365 - 368
  • [35] GOMES MD, 1991, VET HUM TOXICOL, V33, P427
  • [36] GOMES MD, 1991, VET HUM TOXICOL, V33, P315
  • [37] GRAY AJ, 1985, INSECTICIDES, P193
  • [38] Gupta A, 1999, J APPL TOXICOL, V19, P67, DOI 10.1002/(SICI)1099-1263(199901/02)19:1&lt
  • [39] 67::AID-JAT540&gt
  • [40] 3.0.CO