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Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation
Spinal cord plays a central role in the development and progression of pathogenesis of obstinate pruritus. In the current study, four groups of adult male C57Bl/6 mice were investigated; one group treated with saline, while the other groups intradermally injected with compound 48/80, histamine, α-Me...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650352/ https://www.ncbi.nlm.nih.gov/pubmed/29088797 http://dx.doi.org/10.18632/oncotarget.20148 |
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author | Liu, Bao-Wen Li, Zhi-Xiao He, Zhi-Gang Liu, Cheng Xiong, Jun Xiang, Hong-Bing |
author_facet | Liu, Bao-Wen Li, Zhi-Xiao He, Zhi-Gang Liu, Cheng Xiong, Jun Xiang, Hong-Bing |
author_sort | Liu, Bao-Wen |
collection | PubMed |
description | Spinal cord plays a central role in the development and progression of pathogenesis of obstinate pruritus. In the current study, four groups of adult male C57Bl/6 mice were investigated; one group treated with saline, while the other groups intradermally injected with compound 48/80, histamine, α-Me-5-HT and capsaicin (algogenic substance), respectively. The intradermal microinjection of pruritic and algogenic compound resulted in a dramatic increase in the itch/algogenic behavior. Analysis of the microarray data showed that 15 genes in spinal cord (C5-C8) were differentially expressed between control group and 48/80 group, in which 9 genes were up-regulated and 6 genes were down-regulated. Furthermore, the results of RT-qPCR validation studies in C5-C8 spinal cord revealed that the 9 mRNA (Sgk1, Bag4, Fos, Ehd2, Edn3, Wdfy, Corin, 4921511E18Rik and 4930423020Rik) showed very different patterns for these different drugs, especially when comparing α-Me-5-HT and capsaicin. In three itch models, Fos and Ehd2 were up-regulated whereas Corin, 4921511E18Rik and 4930423020Rik were down-regulated. Furthermore, Corin and 4930423020Rik were down-regulated in itch model group compared to capsaicin group. Thus the application of microarray technique, coupled with RT-qPCR validation, further explain the mechanism behind itching evoked by pruritic compounds. It can contribute to our understanding of pharmacological methods for prevention or treatment of obstinate pruritus. |
format | Online Article Text |
id | pubmed-5650352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56503522017-10-30 Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation Liu, Bao-Wen Li, Zhi-Xiao He, Zhi-Gang Liu, Cheng Xiong, Jun Xiang, Hong-Bing Oncotarget Research Paper Spinal cord plays a central role in the development and progression of pathogenesis of obstinate pruritus. In the current study, four groups of adult male C57Bl/6 mice were investigated; one group treated with saline, while the other groups intradermally injected with compound 48/80, histamine, α-Me-5-HT and capsaicin (algogenic substance), respectively. The intradermal microinjection of pruritic and algogenic compound resulted in a dramatic increase in the itch/algogenic behavior. Analysis of the microarray data showed that 15 genes in spinal cord (C5-C8) were differentially expressed between control group and 48/80 group, in which 9 genes were up-regulated and 6 genes were down-regulated. Furthermore, the results of RT-qPCR validation studies in C5-C8 spinal cord revealed that the 9 mRNA (Sgk1, Bag4, Fos, Ehd2, Edn3, Wdfy, Corin, 4921511E18Rik and 4930423020Rik) showed very different patterns for these different drugs, especially when comparing α-Me-5-HT and capsaicin. In three itch models, Fos and Ehd2 were up-regulated whereas Corin, 4921511E18Rik and 4930423020Rik were down-regulated. Furthermore, Corin and 4930423020Rik were down-regulated in itch model group compared to capsaicin group. Thus the application of microarray technique, coupled with RT-qPCR validation, further explain the mechanism behind itching evoked by pruritic compounds. It can contribute to our understanding of pharmacological methods for prevention or treatment of obstinate pruritus. Impact Journals LLC 2017-08-10 /pmc/articles/PMC5650352/ /pubmed/29088797 http://dx.doi.org/10.18632/oncotarget.20148 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liu, Bao-Wen Li, Zhi-Xiao He, Zhi-Gang Liu, Cheng Xiong, Jun Xiang, Hong-Bing Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation |
title | Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation |
title_full | Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation |
title_fullStr | Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation |
title_full_unstemmed | Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation |
title_short | Altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by RT-qPCR validation |
title_sort | altered expression of target genes of spinal cord in different itch models compared with capsaicin assessed by rt-qpcr validation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650352/ https://www.ncbi.nlm.nih.gov/pubmed/29088797 http://dx.doi.org/10.18632/oncotarget.20148 |
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