Bioactive lipids as effectors and indicators of the deleterious effects of environmental exposure on chronic diseases
生物活性脂质作为环境暴露对慢性疾病有害影响的效应物和指标
基本信息
- 批准号:10400036
- 负责人:
- 金额:$ 75.68万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-06-15 至 2027-04-30
- 项目状态:未结题
- 来源:
- 关键词:AcidsAntibodiesBiochemicalBiological AssayBiological MarkersCellsCentral Nervous System DiseasesChemicalsChemotherapy-Oncologic ProcedureChronicChronic DiseaseCollaborationsCommunitiesCoupledDiabetes MellitusDietDietary InterventionDisciplineDiseaseDisease modelEducation and OutreachEnvironmentEnvironmental ExposureEnzymesEpoxide hydrolaseEpoxy CompoundsExcisionFatty AcidsFibrosisHealthHeart failureHomeostasisKnowledgeLife StyleLipidsMalignant NeoplasmsMediator of activation proteinMental DepressionMitochondriaMonitorNeoplasm MetastasisNon-Steroidal Anti-Inflammatory AgentsNutritionalOmega-3 Fatty AcidsOmega-6 Fatty AcidsOrganOutcomePainParkinson DiseasePathologicPathway interactionsPharmaceutical PreparationsPharmacologyProteinsReagentReportingResearchServicesSystemTestingToxic effectToxinTriclosanWorkanalytical methodanalytical toolbasebiochemical toolsdepressive symptomsendoplasmic reticulum stressenvironmental chemicalflexibilityinflammatory paininhibitormannanobodiesnovelnutritionpainful neuropathypreventprogramsresponsetooltumor
项目摘要
Man’s total environment including diet, lifestyle and environmental chemicals has a major impact on health. The
effects of environmental chemicals are most dramatic when they alter a regulatory system that amplifies the
toxicity. We will examine effects of toxins and disease on lipid chemical mediators or oxylipins. Deleterious effects
also are more global when the environmental chemicals alter a system fundamental to many cells and organs.
Thus, we will investigate how environmental chemicals increase endoplasmic reticulum stress resulting in
negative and often chronic outcomes in multiple organs. Natural epoxyfatty acids (EpFA) are a component of a
regulatory system that maintains homeostasis. We are using inhibitors of the soluble epoxide hydrolase (sEHI)
to stabilize these beneficial EpFA. A variety of environmental chemicals such as triclosan and nonsteroidal anti-
inflammatory drugs damage these pathways enhancing disease states. sEHI restore the homeostatic systems
leading to improvement in many disease models including for diabetes, heart failure, neuropathic and
inflammatory pain, fibrosis and toxicities. Recently, we reported sEHI beneficial for treating cancer as well as
Parkinson’s and depression. With the flexibility offered by the RIVER program, we will evaluate the relationships
among these disease states, determine biochemical mechanisms, and monitor the levels of EpFA and other
chemical mediators. Based on this knowledge we will develop cellular and biochemical biomarkers of health and
disease particularly for diseases related to endoplasmic reticulum stress. We will continue providing the
biochemical and analytical tools developed for this work for the broad scientific community. These tools include
clones and proteins of the sEH enzyme, sEH inhibitors as probes and drugs, novel bioassays, antibodies and
nanobodies, synthetic standards of regulatory lipids, and of course analytical methods. We will expand our
testing of the hypothesis that toxicity and disease can be altered by pharmacological and nutritional intervention
both in house and with collaborators. In particular, we will expand our recent studies that by stabilizing natural
omega 6 and omega 3 fatty acid epoxides, sEHI can prevent and reverse symptoms of depression, Parkinson’s
disease and other CNS disorders and block tumor resurgence and metastasis caused by cell debris from cancer
chemotherapy and resection. Thus, we will test the hypothesis that the mitochondrial–ROS–ER stress axis is a
common mechanism in the onset of many toxicities and pathological outcomes and that these effects can be
prevented or reversed by increasing epoxyfatty acids. While carrying out the above research we continue and
expand our work to reduce barriers to entering the oxylipin research field by providing service and reagents. Our
research will be coupled with a training and outreach component to encourage collaboration and free information
exchange in the oxylipin discipline. The work is transformative in emphasizing chronic rather than short-term
toxicities, illustrating a new mechanism of toxicity in ER stress, and in exploring approaches to prevent the
toxicities by manipulating endogenous chemical mediators.
人类的整体环境,包括饮食、生活方式和环境化学物质对健康有重大影响。的
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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BRUCE D HAMMOCK其他文献
BRUCE D HAMMOCK的其他文献
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{{ truncateString('BRUCE D HAMMOCK', 18)}}的其他基金
Soluble epoxide hydrolase and epoxide fatty acid involvement in corneal injury after ammonia exposure: Mechanisms of injury and potential therapeutics using sEH inhibitors and biostable EpFA mimics.
可溶性环氧化物水解酶和环氧化物脂肪酸参与氨暴露后角膜损伤:损伤机制和使用 sEH 抑制剂和生物稳定 EpFA 模拟物的潜在治疗方法。
- 批准号:
10708436 - 财政年份:2023
- 资助金额:
$ 75.68万 - 项目类别:
Bioactive lipids as effectors and indicators of the deleterious effects of environmental exposure on chronic diseases
生物活性脂质作为环境暴露对慢性疾病有害影响的效应物和指标
- 批准号:
10615675 - 财政年份:2019
- 资助金额:
$ 75.68万 - 项目类别:
Bioactive lipids as effectors and indicators of the deleterious effects of environmental exposure on chronic diseases
生物活性脂质作为环境暴露对慢性疾病有害影响的效应物和指标
- 批准号:
10153794 - 财政年份:2019
- 资助金额:
$ 75.68万 - 项目类别:
Clinical Paths for Soluble Epoxide Hydrolase Inhibitors at Experimental Biology 2018
2018 年实验生物学中可溶性环氧化物水解酶抑制剂的临床路径
- 批准号:
9544621 - 财政年份:2018
- 资助金额:
$ 75.68万 - 项目类别:
Role of Epoxygenated Fatty Acids in Modulating Pain
环氧化脂肪酸在调节疼痛中的作用
- 批准号:
8446055 - 财政年份:2013
- 资助金额:
$ 75.68万 - 项目类别:
Role of Epoxygenated Fatty Acids in Modulating Pain
环氧化脂肪酸在调节疼痛中的作用
- 批准号:
8619587 - 财政年份:2013
- 资助金额:
$ 75.68万 - 项目类别:
METHODS MONITOR TOXIC SUBSTAN AND/OR INDICATORS OF PRESENCE IN HUMANS&OTHER SPE
监测人类体内有毒物质和/或存在指标的方法
- 批准号:
8362756 - 财政年份:2011
- 资助金额:
$ 75.68万 - 项目类别:
ID AND DEV OF BIOLOGICAL MARKERS OF HUMAN EXPOSURE TO THE INSECTICIDE PERMETHRI
人类接触杀虫剂氯菊酯的生物标志物的识别和开发
- 批准号:
8362754 - 财政年份:2011
- 资助金额:
$ 75.68万 - 项目类别:
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