SWALLOWING--BUCCOPHARYNGEAL/ESOPHAGEAL COORDINATION

吞咽——颊咽/食管协调

• 批准号: 6176143
• 负责人: STEVEN M ALTSCHULER
• 金额: $ 22.42万
• 依托单位: CHILDREN'S HOSP OF PHILADELPHIA
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-04-01 至 2003-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6176143
• 关键词: Animalia; GABA receptor; NMDA receptors; attenuated microorganism; central neural pathway /tract; complementary RNA; esophagus; fluorescent dye /probe; glutamate receptor; immunocytochemistry; in situ hybridization; motor neurons; mouth; neuroanatomy; neuronal transport; nucleic acid probes; oligonucleotides; pharynxs; protein localization; receptor expression; suid alphaherpesvirus 1; swallowing

Swallowing, one of the more complex motor behaviors is programmed centrally by a medullary central pattern generator located in and around the nucleus of the solitary tract. The generation and modulation of neuronal patterned motor activity by the central pattern generator is dependent upon endogenous excitatory and inhibitory mechanisms and requisite central and peripheral afferent contacts. A significant imbalance in the relative contribution of excitation via NMDA and inhibition via GABA receptors may form the basis of dysfunctional swallowing present in neurological disease. Utilizing the rat as animal model, the anatomic basis of the excitatory and inhibitory processes critical to the coordination of the buccupharyngeal and esophageal phases of swallowing will be studied. Transsynaptic tracing with Pseudorabies Virus in conjunction with: (1) Fluorescent retrograde tracing will be utilized to study the anatomical connections between the buccopharyngeal and esophageal central pattern generator networks at the premotor neuron level; (2) In situ hybridization with oligonucleotide probes for the different N-Methyl-D-aspartate (NMDA) receptor subunits (R1, R2A- D) and GABAA receptor subunits (alpha1-6, beta1-3, gamma1-3, delta) will be utilized to determine the NMDA and GABAA receptor subunits expressed by our premotor neurons; (4) Immunocytochemistry for glutamate and GABA will be utilized to determined location and organization of glutaminergic and GABAergic neurons constituting and projecting to the central pattern generator; (5) Immunocytochemistry for NMDAR1 and GABAA alpha1 receptor subunit proteins will be utilized to investigate colocalization of the receptors on buccopharyngeal and esophageal premotor neurons (triple labeling method). Since alterations in excitatory and inhibitory synaptic function could contribute to the pathogenesis of swallowing disorders, these studies may have a direct bearing on the future clinical management of patients with dysphagia.

吞咽是一种较为复杂的运动行为，由位于孤束核内和周围的延髓中央模式发生器进行中枢编程。 中枢模式发生器对神经元模式运动活动的产生和调节依赖于内源性兴奋和抑制机制以及必要的中枢和外周传入接触。 通过NMDA的兴奋和通过GABA受体的抑制的相对贡献的显著不平衡可能形成神经系统疾病中存在的功能障碍性吞咽的基础。 利用大鼠作为动物模型，兴奋和抑制过程的解剖学基础，关键的协调口咽和食管阶段的吞咽将进行研究。 伪狂犬病病毒跨突触追踪结合：（1）荧光逆行追踪将用于研究前运动神经元水平上颊咽和食管中枢模式发生器网络之间的解剖学联系;（2）不同N-甲基-D-天冬氨酸（NMDA）受体亚单位的寡核苷酸探针原位杂交（R1，R2 A-D）和GABAA受体亚单位（α 1 -6，β 1 -3，γ 1 -3，δ）将用于确定由我们的前运动神经元表达的NMDA和GABAA受体亚单位;（四）将利用谷氨酸和GABA的免疫细胞化学来确定构成神经元的多巴胺能和GABA能神经元的位置和组织。（5）应用NMDAR 1和GABAA α 1受体亚单位蛋白的免疫细胞化学方法研究受体在颊咽和食管前运动神经元上的共定位（三重标记法）。 由于兴奋性和抑制性突触功能的改变可能有助于吞咽障碍的发病机制，这些研究可能对吞咽困难患者未来的临床管理有直接影响。