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A preliminary study on DRGs and spinal cord of a galanin receptor 2-EGFP transgenic mouse

文献类型： 外文期刊

作者： Lyu, Chuang 1 ; Xia, Sheng 2 ; Lyu, Gong-Wei 3 ; Dun, Xin-Peng 2 ; Zheng, Kang 2 ; Su, Jie 4 ; Barde, Swapnali 2 ; Xu, Zh 1 ;

作者机构： 1.Chinese Acad Agr Sci, Harbin Vet Res Inst, State Key Lab Vet Biotechnol, Harbin 150069, Peoples R China

2.Karolinska Inst, Dept Neurosci, SE-17177 Stockholm, Sweden

3.Harbin Med Univ, Hosp 1, Dept Neurol, Harbin 150001, Peoples R China

4.Karolinska Inst, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden

5.Capital Med Univ, Dept Neurobiol, Beijing 100069, Peoples R China

6.Univ Bergen, Dept Biomed, N-5009 Bergen, Norway

关键词： Autoreceptor; Coexistence; G protein-coupled receptor; Nerve injury; Neuropeptides; Pain

期刊名称：NEUROPEPTIDES （ 影响因子：3.286； 五年影响因子：3.129 ）

ISSN： 0143-4179

年卷期： 2020 年 79 卷

页码：

收录情况： SCI

摘要： The neuropeptide galanin functions via three G-protein coupled receptors, Gal(1-3)-R. Both Gal(1)-R and (2)-R are involved in pain signaling at the spinal level. Here a Gal(2)-R-EGFP transgenic (TG) mouse was generated and studied in pain tests and by characterizing Gal(2)-R expression in both sensory ganglia and spinal cord. After peripheral spared nerve injury, mechanical allodynia developed and was ipsilaterally similar between wild type (WT) and TG mice. A Gal(2)-R-EGFP-positive signal was primarily observed in small and medium-sized dorsal root ganglion (DRG) neurons and in spinal interneurons and processes. No significant difference in size distribution of DRG neuronal profiles was found between TG and WT mice. Both percentage and fluorescence intensity of Gal(2)-R-EGFP-positive neuronal profiles were overall significantly upregulated in ipsilateral DRGs as compared to contralateral DRGs. There was an ipsilateral reduction in substance P-positive and calcitonin gene-related peptide (CGRP)-positive neuronal profiles, and this reduction was more pronounced in TG as compared to WT mice. Moreover, Gal(2)-R-EGFP partly co-localized with three pain-related neuropeptides, CGRP, neuropeptide Y and galanin, both in intact and injured DRGs, and with galanin also in local neurons in the superficial dorsal horn. Taken together, the present results provide novel information on the localization and phenotype of DRG and spinal neurons expressing the second galanin receptor, Gal(2)-R, and on phenotypic changes following peripheral nerve injury. Gal(2)-R may also be involved in autoreceptor signaling.

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