Understanding Complex Toxicological Mechanisms of Glyphosate and Mechanism-Sharing Environmental Chemical Mixtures
Understanding Complex Toxicological Mechanisms of Glyphosate and Mechanism-Sharing Environmental Chemical Mixtures
批准号:
9326789
负责人:
Breanna Ford
金额:
$3.84万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-05-01 至 2020-04-30
关键词:
AcetatesAgricultureAmino AcidsAnalytical ChemistryCarcinogensChemical ExposureChemicalsComplexCysteineDataDegradation PathwayDyslipidemiasEnvironmental Risk FactorEnzymesExposure toFatty AcidsFatty LiverFatty acid glycerol estersFunctional disorderHealthHerbicidesHome environmentHumanHypertrophyIcebergIndividualIndustrializationInternational Agency for Research on CancerLinkLipidsLiverMammalsMapsMetabolicMetabolismMethodsMusNutritionalObesityOxidesPathway interactionsPesticidesProteinsProteomeRoundupSerumTechnologyTestingTissuesToxic effectToxicologybasebiological systemschemoproteomicscomplex biological systemsenvironmental chemicalfatty acid oxidationglyoxylateglyphosatein vivoinnovationlipid metabolismnovelprotein profiling
中文摘要
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英文摘要
Glyphosate, the active ingredient in RoundUp produced by Monsanto, is the most commonly used
pesticides in the US across agricultural, industrial, and home settings with 180-185 million pounds used in the
US in 2007. \ While glyphosate exposure has been linked to adverse health effects, there is a surprising lack of
mechanistic information concerning the full scope of long-term health effects and potential toxicities associated
with glyphosate exposure. Understanding how glyphosate interacts with biological systems in vivo in mammals
is absolutely necessary to assess the prolonged effects and mechanism of toxicity of glyphosate on human
health. This project will apply innovative chemical technologies to map the direct proteome-wide
targets of glyphosate and its potentially reactive metabolites in vivo, as well as investigate the effects
co-exposures to glyphosate and chemical mixtures that act through overlapping mechanisms. Here, we
will use an innovative chemoproteomic strategy termed reactivity-based protein profiling (RBPP), which
uses reactivity-based chemical probes to identify hyper-reactive protein hotspots in complex proteomes, to
map direct proteome-wide targets of glyphosate. Using the RBPP platform, we have found that glyphosate
as well as several high usage environmental chemicals of concern commonly inhibit several metabolic
enzymes involved in fatty acid degradation and metabolism. We hypothesize that cumulative exposure to
glyphosate and other environmental chemicals that commonly inhibit fatty acid degradation enzymes will
directly cause additive or synergistic lipid dysregulation, tissue adiposity, and serum dyslipidemia in vivo in
mice. We propose to apply innovative chemoproteomic platforms to map proteome-wide targets of
glyphosate to reveal novel toxicological mechanisms of this widely used and controversial herbicide,
with a particular focus on understanding how exposure to glyphosate and other chemical and
nutritional exposures may synergize to impact fat metabolism.
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