TOXICITY OF CATECHOL THIOETHER ADDUCTS
TOXICITY OF CATECHOL THIOETHER ADDUCTS
批准号:
2521659
负责人:
MATTHEW J PICKLO
金额:
$3.02万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
未结题
起止时间:
1998-08-01 至
中文摘要
特发性帕金森病(PD)是一种使人衰弱的、进行性的、
神经退行性疾病 流行病学研究表明,
以及暴露于金属和其他有毒物质作为PD的危险因素。
氧化应激和线粒体功能障碍被假设为
帕金森病神经元死亡的基本原因。 本研究的目的
建议是确定儿茶酚加合的作用,
警局邻苯二酚可以经历过渡金属催化的自氧化,
醌,然后在称为
氧化还原循环 儿茶酚到醌的氧化还原循环导致了
细胞毒性活性氧物质的产生和
邻苯二酚硫醚加合物通过将硫醇加成到醌上。
儿茶酚硫醚加合物具有较低的氧化电位,
氧化还原循环的速率比母体儿茶酚快。 前两
这项研究的具体目的是测试儿茶酚是否
硫醚加合物可以产生更多的活性氧物种和加合物
比天然儿茶酚更高的速率。 这将是
通过测量邻苯二酚硫醚的氧化电位来完成
加合物,由这些加合物产生的活性氧物质,以及
这些加合物的蛋白质加合速率。 最后一个具体目标
这项建议是为了测试邻苯二酚加合对
线粒体功能 这将通过研究
儿茶酚加合物对线粒体呼吸的影响,特异性
呼吸复合体和线粒体电子载体。
英文摘要
Idiopathic Parkinson's disease (PD) is a debilitating, progressive,
neurodegenerative disease. Epidemiological studies have identified age
and exposure to metals and other toxicants as risk factors for PD.
Oxidative stress and mitochondrial dysfunction are hypothesized to be
the basic causes of neuron death in PD. The objective of this research
proposal is to define the role of catechol adduction in the genesis of
PD. Catechols can undergo transition metal-catalyzed autoxidation to
quinones and then be reduced to catechols again in a process termed
redox cycling. The redox cycling of catechols to quinones leads to the
generation of cytotoxic reactive oxygen species and to the formation of
catechol thioether adducts via the addition of a thiol to the quinone.
A catechol thioether adduct has a lower oxidation potential and may
redox cycle at a faster rate than the parent catechol. The first two
specific aims of this research are designed to test whether catechol
thioether adducts can generate more reactive oxygen species and adduct
proteins at a greater rate than native catechols. This will be
accomplished by measuring the oxidation potentials of catechol thioether
adducts, the reactive oxygen species generated by these adducts, and the
rate of protein adduction by these adducts. The last specific aim of
this proposal is to test the effects of catechol adduction upon
mitochondrial function. This will be accomplished by studying the
effects of catechol adducts upon mitochondrial respiration, specific
respiratory complexes, and mitochondrial electron carriers.
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会议论文
OXIDATIVE DAMAGE, DNA, AND ETHANOL WITHDRAWAL
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批准号:7720891
-
项目类别:
-
资助金额:$5.28万
-
财政年份:2008
-
负责人:MATTHEW J PICKLO
-
依托单位:
COBRE: UND: CARBONYL DETOXIFICATION IN CNS
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批准号:7610477
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项目类别:
-
资助金额:$18.95万
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财政年份:2007
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负责人:MATTHEW J PICKLO
-
依托单位:
COBRE: UND: CARBONYL DETOXIFICATION IN CNS
-
批准号:7381901
-
项目类别:
-
资助金额:$18.36万
-
财政年份:2006
-
负责人:MATTHEW J PICKLO
-
依托单位:
COBRE: UND: CARBONYL DETOXIFICATION IN CNS
-
批准号:7171126
-
项目类别:
-
资助金额:$18.82万
-
财政年份:2005
-
负责人:MATTHEW J PICKLO
-
依托单位:
COBRE: UND: CARBONYL DETOXIFICATION IN CNS
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批准号:6981803
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项目类别:
-
资助金额:$18.81万
-
财政年份:2004
-
负责人:MATTHEW J PICKLO
-
依托单位:
Ethanol, 4-hydroxy-2-nonenal and the Central Nervous Sys
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批准号:6814462
-
项目类别:
-
资助金额:$20.15万
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财政年份:2004
-
负责人:MATTHEW J PICKLO
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依托单位:
Ethanol, HNE, and the CNS
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批准号:6932048
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项目类别:
-
资助金额:$16.65万
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财政年份:2004
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负责人:MATTHEW J PICKLO
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依托单位:
LIPID PEROXIDATION, TOXICANTS, AND MITOCHONDRIA
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批准号:6652467
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项目类别:
-
资助金额:$10.8万
-
财政年份:2001
-
负责人:MATTHEW J PICKLO
-
依托单位:
LIPID PEROXIDATION, TOXICANTS, AND MITOCHONDRIA
-
批准号:6524701
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项目类别:
-
资助金额:$10.8万
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财政年份:2001
-
负责人:MATTHEW J PICKLO
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依托单位:
LIPID PEROXIDATION, TOXICANTS, AND MITOCHONDRIA
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批准号:6133026
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项目类别:
-
资助金额:$10.3万
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财政年份:2001
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负责人:MATTHEW J PICKLO
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依托单位:
TOXICITY OF CATECHOL THIOETHER ADDUCTS
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批准号:6164604
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项目类别:
-
资助金额:$4.09万
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财政年份:2000
-
负责人:MATTHEW J PICKLO
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依托单位:
TOXICITY OF CATECHOL THIOETHER ADDUCTS
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批准号:2882826
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项目类别:
-
资助金额:$3.84万
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财政年份:1999
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负责人:MATTHEW J PICKLO
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依托单位:
海外基金