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通过逆行神经元追踪和双标记免疫组织化学研究豚鼠肺和气管的感觉和交感神经支配。

The sensory and sympathetic innervation of guinea-pig lung and trachea as studied by retrograde neuronal tracing and double-labelling immunohistochemistry.

作者信息

Kummer W, Fischer A, Kurkowski R, Heym C

机构信息

Institute for Anatomy and Cell Biology, University of Heidelberg, F.R.G.

出版信息

Neuroscience. 1992 Aug;49(3):715-37. doi: 10.1016/0306-4522(92)90239-x.

DOI:10.1016/0306-4522(92)90239-x
PMID:1380140
Abstract

The sympathetic and sensory innervation of guinea-pig trachea and lung were studied by means of retrograde neuronal tracing using fluorescent dyes, and double-labelling immunofluorescence. Sympathetic neurons supplying the lung were located in stellate ganglia and in thoracic sympathetic chain ganglia T2-T4; those supplying the trachea resided in the superior cervical and stellate ganglia. Retrogradely labelled sympathetic neurons were usually immunoreactive to tyrosine hydroxylase; the majority also contained neuropeptide Y immunoreactivity. However, a small number were non-catecholaminergic (i.e. tyrosine hydroxylase negative), but neuropeptide Y immunoreactive. Within the airways, tyrosine hydroxylase/neuropeptide Y-immunoreactive axons were found in the smooth muscle layer, around blood vessels including the pulmonary artery and vein, and to a lesser extent in the lamina propria. Periarterial axons contained in addition dynorphin immunoreactivity. Sensory neurons supplying the lung were located in jugular and nodose vagal ganglia as well as in upper thoracic dorsal root ganglia; those supplying the trachea were most frequently found bilaterally in the nodose ganglia and less frequently in the jugular ganglia. A spinal origin of tracheal sensory fibres could not be consistently demonstrated. With regard to their immunoreactivity to peptides, three types of sensory neurons projecting to the airways could be distinguished: (i) substance P/dynorphin immunoreactive; (ii) substance P immunoreactive but dynorphin negative; and (iii) negative to all peptides tested. Substance P-immunoreactive neurons innervating the airways invariably contained immunoreactivity to neurokinin A and calcitonin gene-related peptide. Retrogradely labelled neurons located in the nodose ganglia belonged almost exclusively (greater than or equal to 99%) to the peptide-negative group, whereas the three neuron types each represented about one-third of retrogradely labelled neurons in jugular and dorsal root ganglia. Within the airways, axons immunoreactive to substance P/neurokinin A and substance P/calcitonin gene-related peptide were distributed within the respiratory epithelium of trachea and large bronchi, in the lamina propria and smooth muscle from the trachea down to the smallest bronchioli (highest density at the bronchial level), in the alveolar walls, around systemic and pulmonary blood vessels, and within airway ganglia. Those axons also containing dynorphin immunoreactivity were restricted to the lamina propria and smooth muscle. The origin of nerve fibres immunoreactive for vasoactive intestinal polypeptide, of which a part were also neuropeptide Y immunoreactive, could not be determined by retrograde tracing experiments. Vasoactive intestinal polypeptide-immunoreactive fibres terminating within airway ganglia may be of preganglionic parasympathetic origin, whereas others (e.g. those found in smooth muscle) may arise from intrinsic ganglia.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

采用荧光染料逆行神经元追踪法和双标免疫荧光法,对豚鼠气管和肺的交感神经与感觉神经支配进行了研究。支配肺的交感神经元位于星状神经节和胸交感链神经节T2 - T4;支配气管的交感神经元位于颈上神经节和星状神经节。逆行标记的交感神经元通常对酪氨酸羟化酶呈免疫反应;大多数还含有神经肽Y免疫反应性。然而,少数是非儿茶酚胺能的(即酪氨酸羟化酶阴性),但具有神经肽Y免疫反应性。在气道内,酪氨酸羟化酶/神经肽Y免疫反应性轴突见于平滑肌层、包括肺动脉和静脉在内的血管周围,在固有层中较少见。动脉周围的轴突还含有强啡肽免疫反应性。支配肺的感觉神经元位于颈静脉和结状迷走神经节以及上胸段背根神经节;支配气管的感觉神经元最常见于双侧的结状神经节,较少见于颈静脉神经节。未能始终如一地证实气管感觉纤维有脊髓起源。就其对肽的免疫反应性而言,可区分出投射到气道的三种感觉神经元类型:(i)P物质/强啡肽免疫反应性;(ii)P物质免疫反应性但强啡肽阴性;以及(iii)对所有测试肽均呈阴性。支配气道的P物质免疫反应性神经元始终含有对神经激肽A和降钙素基因相关肽的免疫反应性。位于结状神经节的逆行标记神经元几乎完全(≥99%)属于肽阴性组,而在颈静脉神经节和背根神经节中,这三种神经元类型各约占逆行标记神经元的三分之一。在气道内,对P物质/神经激肽A和P物质/降钙素基因相关肽呈免疫反应性的轴突分布于气管和大支气管呼吸上皮、从气管到最小细支气管的固有层和平滑肌(在支气管水平密度最高)、肺泡壁、全身和肺血管周围以及气道神经节内。那些也含有强啡肽免疫反应性的轴突局限于固有层和平滑肌。对血管活性肠肽呈免疫反应性的神经纤维起源(其中一部分也具有神经肽Y免疫反应性)无法通过逆行追踪实验确定。终止于气道神经节内的血管活性肠肽免疫反应性纤维可能起源于节前副交感神经,而其他纤维(如在平滑肌中发现的纤维)可能起源于内在神经节。(摘要截于400字)

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