N-type Calcium Channels in Nociceptive Neurons

伤害感受神经元中的 N 型钙通道

• 批准号: 7088279
• 负责人: Diane Lipscombe
• 金额: $ 23.34万
• 依托单位: BROWN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-08-02 至 2010-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7088279
• 关键词: G protein; calcium channel; dorsal horn; dorsal root; electrical potential; model; neurons; neurotransmitters; nociceptors; pain

DESCRIPTION (provided by applicant): In this proposal we study the physiological significance of cell-specific alternative splicing of the voltage-gated N-type calcium channel CaValpha1 subunit in nociceptive neurons of the dorsal root ganglia. N- type calcium channels regulate release of glutamate and substance P from primary sensory afferents in the superficial dorsal horn of the spinal cord. The N-type calcium channel is an important target in chronic pain therapy. Inhibition of presynaptic N-type calcium channels is also a therapeutically important site of action of opiates. We recently discovered a unique splice isoform of the N-type calcium channel CaV2.2 subunit, CaV2.2e[37a], that is expressed in many nociceptive neurons. Our recent data show that this unique CaV2.2 splice isoform has unique properties. In this proposal we have two main aims. The first is to understand the physiological significance of alternative splicing of CaV2.2 in regulating the activity of N-type channels in sensory neurons from normal animals. We aim to test the possibility that some of the unique electrical properties and pharmacology of nociceptive neurons originate from cell-specific alternative splicing of CaV2.2 (Aim 1). We will also investigate whether alternative splicing of CaV2.2 is modified following nerve injury using two neuropathic pain models (Aim 2). A change in the pattern of alternative splicing of the N-type channel could have profound effects on the efficacy of synaptic transmission and on the responsiveness of nociceptors to drugs that act by inhibiting the N-type channel. This proposal combines our extensive experience in molecular and electrophysiological studies of calcium channels with that of our collaborator Dr. Carl Saab who has expertise using models of neuropathic pain. We propose that alternative splicing optimizes the behavior and pharmacology of N-type channels in the pain pathway. A defect in alternative splicing following nerve injury could contribute to aberrant pain processing and the de-habilitating symptoms of neuropathic pain.

描述（由申请人提供）：在本提案中，我们研究了背根神经节伤害性神经元中电压门控 N 型钙通道 CaValpha1 亚基的细胞特异性选择性剪接的生理意义。 N 型钙通道调节脊髓浅表背角初级感觉传入神经中谷氨酸和 P 物质的释放。 N型钙通道是慢性疼痛治疗的重要靶点。突触前 N 型钙通道的抑制也是阿片类药物治疗上重要的作用位点。我们最近发现了 N 型钙通道 CaV2.2 亚基的独特剪接亚型 CaV2.2e[37a]，它在许多伤害性神经元中表达。我们最近的数据表明，这种独特的 CaV2.2 剪接亚型具有独特的特性。在这个提案中，我们有两个主要目标。首先是了解 CaV2.2 选择性剪接在调节正常动物感觉神经元 N 型通道活性中的生理意义。我们的目的是测试伤害性神经元的一些独特的电特性和药理学源自 CaV2.2 的细胞特异性选择性剪接的可能性（目标 1）。我们还将使用两种神经病理性疼痛模型研究神经损伤后 CaV2.2 的选择性剪接是否发生改变（目标 2）。 N型通道选择性剪接模式的改变可能对突触传递的功效以及伤害感受器对通过抑制N型通道起作用的药物的反应性产生深远的影响。该提案结合了我们在钙通道分子和电生理学研究方面的丰富经验以及我们的合作者 Carl Saab 博士的经验，后者拥有使用神经性疼痛模型的专业知识。我们提出选择性剪接优化了疼痛通路中 N 型通道的行为和药理学。神经损伤后选择性剪接的缺陷可能导致异常的疼痛处理和神经病理性疼痛的失能症状。