Neurodevelopmental Apoptosis

神经发育细胞凋亡

• 批准号: 7406603
• 负责人: NURI B FARBER
• 金额: $ 33.77万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-09-06 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7406603
• 关键词: Adolescence; Adult; Adverse effects; Affect; Age; Apoptosis; Apoptotic; Barbiturates; Benzodiazepines; Birth; Brain; Brain Mass; Brain region; Cerebral cortex; Cholinergic Agents; Class; Complex; Data; Development; Dimethyl Sulfoxide; Disinhibition; Dose; Drug Receptors; Drug usage; Drug vehicle; Emulsifying Agents; Encephalopathies; Ethanol; Fetal Alcohol Syndrome; Glutamate Receptor; Glutamates; Growth; Human; In Vitro; Injectable; Injury; Marketing; Medical; Medicine; Mus; N-Methyl-D-Aspartate Receptors; N-Methylaspartate; Nature; Nerve Degeneration; Neurons; Numbers; Pathway interactions; Pattern; Pediatric Neurology; Pharmaceutical Preparations; Phenobarbital; Phenytoin; Polyethylene Glycols; Population; Preclinical Drug Evaluation; Process; Property; Propylene Glycols; Propylene glycol; Rattus; Reaction; Research; Risk; Rodent; Solvents; Syndrome; Third Pregnancy Trimester; Toxic effect; Week; accomplished suicide; barbituric acid salt; biological research; cholinergic; gamma-Aminobutyric Acid; in vivo; inhibitory neuron; killings; manufacturing process; neonate; neurobehavioral; neurotoxic; neurotoxicity; neurotransmission; receptor; response; synaptogenesis

DESCRIPTION (provided by applicant): This is a second revision of a previously submitted application (R01-ES012443-01). It has recently been shown that apoptotic neurodegeneration can be triggered in the in vivo developing rodent CNS by any of several classes of drugs that have in common the property of abnormally suppressing neuronal activity. The period of vulnerability coincides with synaptogenesis, also known as the brain growth spurt period, which occurs postnatally in rodents (first 2 weeks after birth) and both prenatally and postnatally in humans (third trimester and several years after birth). Included among the offending agents are drugs that block NMDA glutamate receptors, drug that hyperactivate GABAA receptors and ethanol, which has both NMDA antagonist and GABAmimetic properties. The apoptogenic action of ethanol is a promising candidate to explain the reduced brain mass and neurobehavioral disturbances associated with the human Fetal Alcohol Syndrome. While interference with NMDA and GABAA neurotransmission during synaptogenesis is putatively responsible for much of ethanol's neurotoxic action, other mechanisms may also be operative in that ethanol kills some populations of neurons that are not affected by NMDA antagonist or GABAmimetic drugs. The applicants have recently discovered that an ethanol-like neurodegenerative syndrome can be induced in the developing rodent brain by certain solvents that are widely used in the industrial world to facilitate the manufacturing process or to dissolve and/or add functionality to marketed products, including injectable drugs used in human medicine. For example, we have found that dimethyl sulfoxide (DMSO) and propylene glycol, which are widely used throughout the world and are generally considered having a very low toxicity potential, trigger a robust neurodegenerative reaction in the developing rodent brain. This is not a property of all solvents in that polyethylene glycol, a very widely used solvent, does not display such activity. The Aims of the proposed research are to more fully characterize the neurodegenerative reactions induced by DMSO and propylene glycol, to screen other solvents for their ability to mimic this type of neurodegenerative phenomenon, to evaluate the degree of risk associated with using these agents as solvent vehicles for drugs administered intravenously to human neonates and, by a combined in vivo/in vitro approach, attempt to elucidate mechanisms underlying these newly discovered neurotoxic phenomena.

描述（由申请人提供）：这是先前提交的申请（R 01-ES 012443 -01）的第二次修订。最近已经表明，凋亡性神经变性可以在体内发育的啮齿动物CNS中由几类药物中的任何一类触发，所述药物具有异常抑制神经元活性的共同性质。脆弱期与突触发生相一致，也称为大脑生长突增期，其发生在啮齿动物的出生后（出生后的前2周）以及人类的出生前和出生后（妊娠晚期和出生后几年）。其中包括阻断NMDA谷氨酸受体的药物，超活化GABAA受体的药物和乙醇，乙醇具有NMDA拮抗剂和GABA模拟物的特性。乙醇的致脑损害作用是解释与人类胎儿酒精综合征相关的脑质量减少和神经行为障碍的一个有希望的候选者。虽然在突触发生过程中干扰NMDA和GABAA神经传递是乙醇神经毒性作用的主要原因，但其他机制也可能起作用，因为乙醇杀死了一些不受NMDA拮抗剂或GABA模拟药物影响的神经元群体。申请人最近发现，乙醇样神经变性综合征可以通过某些溶剂在发育中的啮齿动物脑中诱导，所述溶剂在工业世界中广泛使用以促进制造过程或溶解和/或向市售产品（包括用于人类医学的可注射药物）添加功能性。例如，我们已经发现，在世界各地广泛使用并且通常被认为具有非常低的毒性潜力的二甲基亚砜（DMSO）和丙二醇在发育中的啮齿动物大脑中引发强烈的神经退行性反应。这不是所有溶剂的性质，因为聚乙二醇（一种非常广泛使用的溶剂）不显示这种活性。拟议研究的目的是更全面地表征DMSO和丙二醇诱导的神经退行性反应，筛选其他溶剂模拟此类神经退行性现象的能力，评价使用这些试剂作为新生儿静脉给药药物的溶剂载体相关的风险程度，并通过体内/体外联合方法，试图阐明这些新发现的神经毒性现象的机制。

项目成果

Glucocorticoid receptor stimulation and the regulation of neonatal cerebellar neural progenitor cell apoptosis.

• DOI: 10.1016/j.nbd.2011.04.004
• 发表时间: 2011-08
• 期刊: NEUROBIOLOGY OF DISEASE
• 影响因子: 6.1
• 作者: Noguchi, Kevin K.;Lau, Karen;Smith, Derek J.;Swiney, Brant S.;Farber, Nuri B.
• 通讯作者: Farber, Nuri B.