Abused Inhalant Actions at GABA and Glutamate Synapses

GABA 和谷氨酸突触的滥用吸入行为

• 批准号: 7253420
• 负责人: M. Bruce MacIver
• 金额: $ 22.19万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-07-01 至 2009-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7253420
• 关键词: AMPA Receptors; Accounting; Acids; Address; Amino Acids; Amphetamines; Anesthesia procedures; Anesthetics; Animals; Aromatic Hydrocarbons; Behavioral; Brain; Brain Stem; Breathing; Buffers; Calcium; Calcium Channel; Cells; Chemicals; Chromosome Pairing; Class; Cocaine Abuse; Color; Conscious; Cytoplasmic Granules; Dantrolene; Dendrites; Depressed mood; Disinhibition; Disruption; Drug effect disorder; Educational process of instructing; Electrodes; Euphoria; Excitatory Amino Acid Antagonists; Excitatory Postsynaptic Potentials; Fiber; Frequencies; GABA Receptor; GTP-Binding Proteins; Glutamate Receptor; Glutamates; Goals; Halogenated Hydrocarbons; Halothane; Hippocampus (Brain); Inhalant dose form; Inhibitory Synapse; Interneurons; Intoxication; Ionophores; Isoflurane; Laboratories; Lead; Link; Literature; Measures; Mediating; Membrane; Mental Depression; Methods; Modification; Molecular; Motor; Mus; N-Methyl-D-Aspartate Receptors; N-Methylaspartate; Narcotics; Nerve; Neuraxis; Neurons; Neurotransmitters; Numbers; Outcome; Pathway interactions; Pattern; Perception; Perforant Pathway; Pharmaceutical Preparations; Physiologic pulse; Play; Population; Preparation; Prevention; Principal Investigator; Pulse taking; Pyramidal Cells; Rattus; Recording of previous events; Relative (related person); Research; Research Personnel; Role; Role playing therapy; Ryanodine; Sensory; Site; Slice; Solvents; Structure; Students; Study Section; Synapses; Synaptic Transmission; System; Teenagers; Testing; Thalamic structure; Thinking; Time; Toluene; Trichloroethanes; Trichloroethylene; Work; addiction; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; amino 3 hydroxy 5 methylisoxazole 4 propionate; channel blockers; clinically relevant; experience; extracellular; gamma-Aminobutyric Acid; hippocampal pyramidal neuron; in vivo; inhalation drug abuse; inhibitor/antagonist; mossy fiber; neuronal cell body; patch clamp; postsynaptic; presynaptic; programs; receptor; release of sequestered calcium ion into cytoplasm; research study; response; sevoflurane; synaptic function; synaptic inhibition; transmission process; uptake; voltage

DESCRIPTION (provided by applicant): Inhaled solvent abuse is a growing problem among U.S. teenagers and may lead to the abuse of other drugs. The long-term goal of our research is to gain a better understanding of the mechanisms of action of these drugs, in order to provide rational strategies for the treatment and prevention of inhaled solvent abuse. Evidence exists for inhaled solvent actions at central nervous system (CMS) synapses, but the importance of effects at glutamate and gamma-aminobutyric acid (GABA) synapses remains unknown. Some solvents (e.g. toluene) appear to enhance GABA-mediated inhibitory transmission while others appear to disrupt CMS function by altering glutamate-mediated excitation. Preliminary results from our laboratory indicate that toluene can act at both types of synapses and that combined effects disprupt the normal circuit function of neurons. The proposed research will use the well-characterized CA 1 neuron circuit in rat hippocampal brain slices. The CA 1 circuit uses GABA and glutamate for fast monosynaptic transmission and evoked responses can be completely blocked by a combination of GABA and glutamate receptor antagonists. The specific aims are as follows: 1) To determine whether inhaled solvents alter GABA-mediated transmission. 2) To determine whether solvents alter glutamate-mediated synaptic responses. 3) To investigate the cellular and molecular mechanisms of solvent effects at amino acid synapses. Electrophysiological recordings will be combined with selective NMDA and AMPA receptor antagonists to investigate solvent-induced effects on glutamate-mediated excitatory postsynaptic potentials. Parallel studies will determine the extent to which solvent-induced effects on CA 1 neuron discharge come about via effects on GABA receptor/CI- channels. Inhaled solvents will likely produce effects similar to inhalational anesthetics, which we have studied for over 15 years in our laboratory. Taken together, the results will allow a quantitative comparison of drug effects on glutamate and GABA-mediated transmission for commonly abused solvents including: toluene, 1,1,1-trichloroethane and trichloroethylene.

描述（由申请人提供）：吸入溶剂滥用是美国青少年中一个日益严重的问题，并可能导致其他药物的滥用。我们研究的长期目标是更好地了解这些药物的作用机制，为吸入性溶剂滥用的治疗和预防提供合理的策略。有证据表明吸入溶剂对中枢神经系统（CMS）突触有作用，但对谷氨酸和γ-氨基丁酸（GABA）突触影响的重要性仍不清楚。一些溶剂（例如甲苯）似乎可以增强 GABA 介导的抑制传递，而其他溶剂似乎可以通过改变谷氨酸介导的兴奋来破坏 CMS 功能。我们实验室的初步结果表明，甲苯可以作用于两种类型的突触，并且综合作用会破坏神经元的正常回路功能。拟议的研究将使用大鼠海马脑切片中已充分表征的 CA 1 神经元回路。 CA 1 回路使用 GABA 和谷氨酸进行快速单突触传递，并且 GABA 和谷氨酸受体拮抗剂的组合可以完全阻断诱发反应。具体目标如下： 1) 确定吸入溶剂是否会改变 GABA 介导的传播。 2) 确定溶剂是否改变谷氨酸介导的突触反应。 3）研究氨基酸突触溶剂效应的细胞和分子机制。电生理记录将与选择性 NMDA 和 AMPA 受体拮抗剂相结合，研究溶剂诱导的对谷氨酸介导的兴奋性突触后电位的影响。平行研究将确定溶剂对 CA 1 神经元放电的影响在多大程度上是通过对 GABA 受体/CI 通道的影响而产生的。吸入溶剂可能会产生类似于吸入麻醉剂的效果，我们在实验室对此进行了超过 15 年的研究。总而言之，这些结果将能够定量比较药物对谷氨酸盐和 GABA 介导的传输的影响，这些溶剂包括：甲苯、1,1,1-三氯乙烷和三氯乙烯。