非肽能初级传入纤维在大鼠脊髓中神经激肽-1 受体免疫反应性Ⅰ层投射神经元的突触前。

Non-peptidergic primary afferents are presynaptic to neurokinin-1 receptor immunoreactive lamina I projection neurons in rat spinal cord.

机构信息

Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec H3G 1Y6, Canada.

出版信息

Mol Pain. 2012 Sep 10;8:64. doi: 10.1186/1744-8069-8-64.

Abstract

BACKGROUND

Pain-related (nociceptive) information is carried from the periphery to the dorsal horn of the spinal cord mostly by two populations of small diameter primary afferents, the peptidergic and the non-peptidergic. The peptidergic population expresses neuropeptides, such as substance P and calcitonin gene-related peptide, while the non-peptidergic fibers are devoid of neuropeptides, express the purinergic receptor P2X3, and bind the isolectin B4 (IB4). Although it has been known for some time that in rat the peptidergic afferents terminate mostly in lamina I and outer lamina II and non-peptidergic afferents in inner lamina II, the extent of the termination of the latter population in lamina I was never investigated as it was considered as very minor. Because our preliminary evidence suggested otherwise, we decided to re-examine the termination of non-peptidergic afferents in lamina I, in particular with regards to their innervation of projection neurons expressing substance P receptors (NK-1r). We used retrograde labeling of neurons from the parabrachial nucleus combined with lectin IB4 binding and immunocytochemistry. Samples were examined by confocal and electron microscopy.

RESULTS

By confocal microscopy, we studied the termination of non-peptidergic afferents in lamina I using IB4 binding and P2X3 immunoreactivity as markers, in relation to CGRP immunoreactivy, a marker of peptidergic afferents. The number of IB4 or P2X3-labeled fibers in lamina I was higher than previously thought, although they were less abundant than CGRP-labeled afferents. There were very few fibers double-labeled for CGRP and either P2X3 or IB4. We found a considerable number of IB4-positive fiber varicosities in close apposition to NK-1r-positive lamina I projection neurons, which were distinct from peptidergic varicosities. Furthermore, we confirmed at the ultrastructural level that there were bona fide synapses between P2X3-immunoreactive non-peptidergic boutons and neurokinin-1 receptor-positive lamina I dendrites.

CONCLUSIONS

These results indicate the presence of direct innervation by non-peptidergic nociceptive afferents of lamina I projection neurons expressing NK-1r. Further investigations are needed to better understand the role of these connections in physiological conditions and chronic pain states.

摘要

背景

疼痛相关(伤害性)信息主要由两种小直径初级传入纤维传递到脊髓背角,即肽能和非肽能纤维。肽能纤维表达神经肽,如 P 物质和降钙素基因相关肽,而无神经肽的非肽能纤维表达嘌呤能受体 P2X3,并结合同工凝集素 B4(IB4)。尽管已经有一段时间人们知道在大鼠中,肽能传入纤维主要终止于 I 层和外 II 层,而非肽能传入纤维终止于内 II 层,但从未研究过后者在 I 层的终止程度,因为它被认为是非常次要的。因为我们的初步证据表明并非如此,所以我们决定重新检查非肽能传入纤维在 I 层的终止情况,特别是关于它们对表达 P 物质受体(NK-1r)的投射神经元的支配。我们使用臂旁核神经元的逆行标记与凝集素 IB4 结合和免疫细胞化学结合。通过共聚焦和电子显微镜检查样本。

结果

通过共聚焦显微镜,我们使用 IB4 结合和 P2X3 免疫反应性作为标记物,研究了非肽能传入纤维在 I 层中的终止情况,与 CGRP 免疫反应性(肽能传入纤维的标记物)有关。IB4 或 P2X3 标记纤维的数量高于先前的想法,尽管它们比 CGRP 标记的传入纤维少。很少有纤维同时标记 CGRP 和 P2X3 或 IB4。我们发现相当数量的 IB4 阳性纤维末梢与 NK-1r 阳性 I 层投射神经元紧密接近,这些末梢与肽能末梢不同。此外,我们在超微结构水平上证实了 P2X3 免疫反应性非肽能末梢与神经激肽-1 受体阳性 I 层树突之间存在真正的突触。

结论

这些结果表明,表达 NK-1r 的 I 层投射神经元存在非肽能伤害性传入纤维的直接支配。需要进一步的研究来更好地理解这些连接在生理条件和慢性疼痛状态下的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e7e/3495683/2f8e7c832b8e/1744-8069-8-64-1.jpg

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