Rytel L, Palus K, Całka J
Division of Clinical Physiology, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland.
Anat Histol Embryol. 2015 Apr;44(2):86-91. doi: 10.1111/ahe.12111. Epub 2014 Apr 9.
Our previous study revealed the expression of substance P (SP) and calcitonin gene-related peptide (CGRP) in sensory distal ganglion of the vagus (nodose ganglion) neurons in the pig. As these neuropeptides may be involved in nociception, the goal of these investigations was to determine possible expression of vasoactive intestinal polypeptide (VIP), SP and CGRP in the pituitary adenylate cyclase-activating polypeptide-immunoreactive (PACAP-IR) porcine nodose perikarya. Co-expression of these substances was examined using a double-labelling immunofluorescence technique. To reveal the ganglionic cell bodies, the pan-neuronal marker protein gene product 9.5 (PGP 9.5) was used. Quantitative analysis of the neurons revealed that 67.25% of the PGP 9.5+ somata in the right-side ganglion and 66.5% in the left side, respectively, co-expressed PACAP-IR. Moreover, 60.6% of the PACAP-IR cells in the right-side ganglion and 62.1% in the left, respectively, co-expressed VIP. SP-IR was observed in 52.2 and 39.9% of the right and left ganglia, respectively. CGRP was found in 27.7 and 34.1% of the right and left distal ganglion of the vagus, respectively. High level of co-expression of PACAP with VIP, SP and CGRP in the distal ganglia of the vagus sensory perikarya directly implicates studied peptides in their functional interaction during nociceptive vagal transduction.
我们之前的研究揭示了猪迷走神经(结状神经节)感觉远端神经节中P物质(SP)和降钙素基因相关肽(CGRP)的表达。由于这些神经肽可能参与伤害感受,这些研究的目的是确定血管活性肠肽(VIP)、SP和CGRP在垂体腺苷酸环化酶激活多肽免疫反应性(PACAP-IR)猪结状神经节周核中的可能表达。使用双标记免疫荧光技术检查这些物质的共表达情况。为了揭示神经节细胞体,使用了泛神经元标记蛋白基因产物9.5(PGP 9.5)。对神经元的定量分析显示,右侧神经节中67.25%的PGP 9.5+胞体和左侧66.5%的PGP 9.5+胞体共表达PACAP-IR。此外,右侧神经节中60.6%的PACAP-IR细胞和左侧62.1%的PACAP-IR细胞分别共表达VIP。在右侧和左侧神经节中,分别有52.2%和39.9%的细胞观察到SP-IR。在右侧和左侧迷走神经远端神经节中,分别有27.7%和34.1%的细胞发现有CGRP。迷走神经感觉周核远端神经节中PACAP与VIP、SP和CGRP的高水平共表达直接表明所研究的肽在伤害性迷走神经转导过程中的功能相互作用。