Literature DB >> 23223497

Alteration of the expression of pesticide-metabolizing enzymes in pregnant mice: potential role in the increased vulnerability of the developing brain.

Marie C Fortin1, Lauren M Aleksunes, Jason R Richardson.   

Abstract

Studies on therapeutic drug disposition in humans have shown significant alterations as the result of pregnancy. However, it is not known whether pesticide metabolic capacity changes throughout pregnancy, which could affect exposure of the developing brain. We sought to determine the effect of pregnancy on the expression of hepatic enzymes involved in the metabolism of pesticides. Livers were collected from virgin and pregnant C57BL/6 mice at gestational days (GD)7, GD11, GD14, GD17, and postpartum days (PD)1, PD15, and PD30. Relative mRNA expression of several enzymes involved in the metabolism of pesticides, including hepatic cytochromes (Cyp) P450s, carboxylesterases (Ces), and paraoxonase 1 (Pon1), were assessed in mice during gestation and the postpartum period. Compared with virgin mice, alterations in the expression occurred at multiple time points, with the largest changes observed on GD14. At this time point, the expression of most of the Cyps involved in pesticide metabolism in the liver (Cyp1a2, Cyp2d22, Cyp2c37, Cyp2c50, Cyp2c54, and Cyp3a11) were downregulated by 30% or more. Expression of various Ces isoforms and Pon1 were also decreased along with Pon1 activity. These data demonstrate significant alterations in the expression of key enzymes that detoxify pesticides during pregnancy, which could alter exposure of developing animals to these chemicals.

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Year:  2012        PMID: 23223497      PMCID: PMC3558862          DOI: 10.1124/dmd.112.049395

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  42 in total

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2.  Developmental exposure to the pesticide dieldrin alters the dopamine system and increases neurotoxicity in an animal model of Parkinson's disease.

Authors:  Jason R Richardson; W Michael Caudle; Minzheng Wang; E Danielle Dean; Kurt D Pennell; Gary W Miller
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3.  Changes in maternal liver Cyp2c and Cyp2d expression and activity during rat pregnancy.

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4.  Identification of rat and human cytochrome p450 isoforms and a rat serum esterase that metabolize the pyrethroid insecticides deltamethrin and esfenvalerate.

Authors:  Stephen J Godin; J Allen Crow; Edward J Scollon; Michael F Hughes; Michael J DeVito; Matthew K Ross
Journal:  Drug Metab Dispos       Date:  2007-06-18       Impact factor: 3.922

Review 5.  Prenatal and childhood exposure to pesticides and neurobehavioral development: review of epidemiological studies.

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6.  In vitro metabolism of pyrethroid pesticides by rat and human hepatic microsomes and cytochrome p450 isoforms.

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Journal:  Expert Opin Drug Metab Toxicol       Date:  2007-08       Impact factor: 4.481

8.  Synergism of glucocorticoid hormone with growth hormone for female-specific mouse Cyp3a44 gene expression.

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10.  Organophosphate pesticide exposure and neurodevelopment in young Mexican-American children.

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1.  Isoform-Specific Regulation of Mouse Carboxylesterase Expression and Activity by Prototypical Transcriptional Activators.

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2.  Nerve Growth Factor Protects Against Pyrethroid-Induced Endoplasmic Reticulum (ER) Stress in Primary Hippocampal Neurons.

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3.  Alternative microglial activation is associated with cessation of progressive dopamine neuron loss in mice systemically administered lipopolysaccharide.

Authors:  Eric E Beier; Matthew Neal; Gelerah Alam; Melissa Edler; Long-Jun Wu; Jason R Richardson
Journal:  Neurobiol Dis       Date:  2017-08-18       Impact factor: 5.996

Review 4.  Neurotoxicity of pesticides.

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6.  Drug metabolism and transport during pregnancy: how does drug disposition change during pregnancy and what are the mechanisms that cause such changes?

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7.  Pyrethroid Insecticides Directly Activate Microglia Through Interaction With Voltage-Gated Sodium Channels.

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Review 8.  Pathophysiological implications of neurovascular P450 in brain disorders.

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9.  Developmental pyrethroid exposure causes long-term decreases of neuronal sodium channel expression.

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