Properties of the masticatory muscle piimary afferents from the trigeminal ganglion in the rats

大鼠三叉神经节咀嚼肌初级传入神经的特性

• 批准号: 14571731
• 负责人: MORITANI Masayuki
• 金额: $ 1.86万
• 依托单位: OSAKA UNIVERSITY
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for Scientific Research (C)
• 财政年份: 2002
• 资助国家: 日本
• 起止时间: 2002 至 2003
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/en/grant/KAKENHI-PROJECT-14571731/
• 关键词: trigeminal nerve; masticatory muscle; sensory; primary afferent nueron; trigeminal ganglion; pain; neuron tracer; neuro-transmitter

The main findings of this research project are as follows:(1) Rerogradely labeled muscle afferent neurons were significantly lager and fewer than retrogradely labeled cutaneous afferent neurons. (2) α-D-galactose specific lectin IB4 binding was found in 6% of muscle and 44% of cutaneous afferents indicating a target specific difference. (3) The experiments inducing muscle inflammation by injecting complete Freund's adjuvant (CFA) to masseter muscle indicate that the percentage of trigeminal ganglion muscle afferent neurons immunoreactive for CGRP or SP does not change significantly four days after inflammation. (4) Muscle inflammation resulted in increased number of CGRP and substance P positive trigeminal ganglion muscle afferent neurons 12 days after CFA injection. It is suggested that the increased number of peptidergic neurons following muscle inflammation is recruited equally from trigeminal group III and IV muscle afferents. (5) It is indicated that in trigeminal ganglia, P2X3 receptor is not exclusively expressed in IB4 neurons but includes larger neurons. Target specific differences exist in P2X3 and IB4 expression. Furthermore, it is suggested that deep tissue inflammation can modulate the number of neurons expressing the P2X3 receptor.

该研究项目的主要发现如下：（1）逆行标记的肌肉传入神经元明显大于逆行标记的皮肤传入神经元，（2）在6％的肌肉中发现α-D-半乳糖特异性凝集素IB4结合。 44％的皮肤传入表明存在目标特异性差异（3）通过向咬肌注射完全弗氏佐剂（CFA）诱导肌肉炎症的实验表明。炎症后四天，三叉神经节肌肉传入神经元对 CGRP 或 SP 产生免疫反应的百分比没有显着变化。 (4)注射 CFA 后 12 天，肌肉炎症导致 CGRP 和 P 物质阳性的三叉神经节肌肉传入神经元数量增加。 (5) 表明在三叉神经在神经节中，P2X3 受体不仅在 IB4 神经元中表达，还包括较大的神经元，P2X3 和 IB4 表达存在靶标特异性差异。此外，表明深层组织炎症可以调节表达 P2X3 受体的神经元数量。

项目成果

Bae YC.et al.: "Synaptic organization of tooth pulp afferent terminals in the rat trigeminal sensory nuclei."J Comp Neurol.. 463(1). 13-24 (2003)

Bae YC.等人：“大鼠三叉神经感觉核中牙髓传入末梢的突触组织。”J Comp Neurol.. 463(1)。

Moritani, M., et al.: "Quantitative analysis of the dendritic architectures of single jaw-closing and jaw-opening motoneurons in cats."Experimental Brain Research. 150(3). 265-275 (2003)

Moritani, M. 等人：“猫的单个下颌闭合和张开运动神经元的树突结构的定量分析。”实验性大脑研究。

Moritani, M., et al.: "Quantitative analysis of the dendritic architectures of single jaw-closing and jaw-opening motoneurons in cats"Experimental Brain Research. 150(3). 265-275 (2003)

Moritani, M. 等人：“猫单个下颌闭合和张开运动神经元的树突结构的定量分析”实验脑研究。

Moritani, M.: "Quantitative analysis of the dendritic architectures of single jaw-closing and jaw-opening motoneurons in cats"Experimental Brain Research. (In press). (2003)

Moritani, M.：“猫单个下颌闭合和张开运动神经元的树突结构的定量分析”实验脑研究。

Bae YC.et al.: "Quantitative ultrastructural analysis of glycine-and gamma-aminobutyric acid-immunoreactive terminals on trigeminal alpha-and gamma-motoneuron somata in the rat."J Comp Neurol. 442(2). 308-319 (2002)

Bae YC.等人：“大鼠三叉神经α-和γ-运动神经元胞体上甘氨酸和γ-氨基丁酸免疫反应末端的定量超微结构分析。”J Comp Neurol。