BDNF-Endocannabinoid Interactions in the Cerebral Cortex

大脑皮层中的 BDNF-内源性大麻素相互作用

• 批准号: 8660336
• 负责人: Eric S Levine
• 金额: $ 38.29万
• 依托单位: UNIVERSITY OF CONNECTICUT SCH OF MED/DNT
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-08-01 至 2017-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8660336
• 关键词: 1,2-diacylglycerol; 2-arachidonylglycerol; Antidepressive Agents; Anxiety; Biological; Brain-Derived Neurotrophic Factor; CNR1 gene; Cannabinoids; Cerebral cortex; Cognitive; Coupled; Development; Diglycerides; Disease; Electrophysiology (science); Employee Strikes; Endocannabinoids; Enzymes; Epilepsy; Excitatory Synapse; Functional disorder; Glutamates; Goals; Inhibitory Synapse; Knowledge; Link; Mediating; Memory; Mental Depression; Mental disorders; Molecular; Monitor; Mood Disorders; Motor; Motor Cortex; Multiple Sclerosis; Mus; N-Methyl-D-Aspartate Receptors; Nerve Growth Factor Receptors; Neurologic; Neuromodulator; Neurotrophic Tyrosine Kinase Receptor Type 2; Perception; Phospholipase C; Play; Process; Production; Pyramidal Cells; RNA Interference; Receptor Activation; Regulation; Role; Schizophrenia; Sensory; Signal Pathway; Signal Transduction; Signaling Molecule; Somatosensory Cortex; Synapses; Synaptic Potentials; Synaptic plasticity; System; Work; association cortex; base; immunocytochemistry; insight; interest; lipoprotein lipase; neocortical; nervous system disorder; neurotrophic factor; novel; novel therapeutic intervention; novel therapeutics; painful neuropathy; patch clamp; postsynaptic; presynaptic; receptor; research study; response; sensory cortex

DESCRIPTION (provided by applicant): The goal of this project is to explore previously-unknown interactions between brain-derived neurotrophic factor (BDNF) and the endocannabinoid system in the cerebral cortex. Both BDNF and endocannabinoids are highly expressed throughout the sensory, motor, and association cortices, and there is a striking overlap of expression of trkB neurotrophin receptors and type 1 cannabinoid (CB1) receptors across cortical layers, with highest levels of expression in cortical layers 2/3 and 5. Disruption f either of these neuromodulatory systems has been implicated in several neurologic and psychiatric diseases, including anxiety, depression, schizophrenia, and seizure disorders, and both systems are currently major targets for the development of novel therapeutics. We found that the effects of BDNF at inhibitory cortical synapses are mediated by the BDNF-induced mobilization of endocannabinoids acting at presynaptic CB1 receptors. The proposed studies will explore the signaling mechanisms underlying BDNF-evoked synthesis and release of endocannabinoids at inhibitory synapses using electrophysiological, molecular biological, and pharmacological approaches. The proposed studies will also extend these findings to examine BDNF-cannabinoid interactions at excitatory synapses, and explore the functional relevance of these interactions in regulating activity-dependent synaptic plasticity. Knowledge gained from these studies will provide insights into the regulation and interdependence of BDNF and endocannabinoid signaling. New mechanistic insights regarding the interaction between these neuromodulators could provide the basis for novel therapeutic approaches to neurologic and psychiatric disease.

描述（由申请人提供）：本项目的目标是探索脑源性神经营养因子（BDNF）与大脑皮层内源性大麻素系统之间先前未知的相互作用。BDNF和内源性大麻素在感觉皮质、运动皮质和关联皮质中都有高表达，trkB神经营养因子受体和1型大麻素（CB1）受体在皮质层中的表达明显重叠，在皮质层2/3和5中表达水平最高。这两种神经调节系统中的任何一种的破坏都与几种神经和精神疾病有关，包括焦虑、抑郁、精神分裂症和癫痫性疾病，这两种系统目前都是开发新疗法的主要目标。我们发现BDNF对抑制性皮质突触的作用是通过BDNF诱导的内源性大麻素的动员作用于突触前CB1受体介导的。拟开展的研究将利用电生理学、分子生物学和药理学方法探讨bdnf诱发的抑制性突触内源性大麻素合成和释放的信号机制。这些研究还将扩展这些发现，以检查bdnf -大麻素在兴奋性突触中的相互作用，并探索这些相互作用在调节活动依赖性突触可塑性中的功能相关性。从这些研究中获得的知识将为BDNF和内源性大麻素信号的调节和相互依赖提供见解。关于这些神经调节剂之间相互作用的新的机制见解可以为神经和精神疾病的新治疗方法提供基础。