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Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney
BACKGROUND: A number of dysregulated miRNAs have been identified and are proposed to have significant roles in the pathogenesis of type 2 diabetes mellitus or renal pathology. Alpinia oxyphylla has shown significant anti-inflammatory properties and play an anti-diabetes role. The objective of this s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331689/ https://www.ncbi.nlm.nih.gov/pubmed/28249617 http://dx.doi.org/10.1186/s40659-017-0111-1 |
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author | Du, Guankui Xiao, Man Zhang, Xuezi Wen, Maoyu Pang, Chi Jiang, Shangfei Sang, Shenggang Xie, Yiqiang |
author_facet | Du, Guankui Xiao, Man Zhang, Xuezi Wen, Maoyu Pang, Chi Jiang, Shangfei Sang, Shenggang Xie, Yiqiang |
author_sort | Du, Guankui |
collection | PubMed |
description | BACKGROUND: A number of dysregulated miRNAs have been identified and are proposed to have significant roles in the pathogenesis of type 2 diabetes mellitus or renal pathology. Alpinia oxyphylla has shown significant anti-inflammatory properties and play an anti-diabetes role. The objective of this study was to detect the alteration of miRNAs underlying the anti-diabetes effects of A. oxyphylla extract (AOE) in a type II diabetic animal model (C57BIKsj db-/db-). RESULTS: Treatment with AOE for 8 weeks led to lower concentrations of blood glucose, urine albumin, and urine creatinine. 17 and 13 miRNAs were statistically identified as differentially regulated in the DB/DB and db-/db- AOE mice, respectively, compared to the untreated db-/db- mice. Of these, 7 miRNAs were identified in both comparison groups, and these 7 miRNAs were verified by quantitative real-time PCR. Functional bioinformatics showed that the putative target genes of 7 miRNAs were associated with several diabetes effects and signaling pathways. CONCLUSIONS: These founding suggest that the potential of AOE as a medicinal anti-diabetes treatment through changes in the expressions of specific miRNAs. The results provide a useful resource for future investigation of the role of AOE-regulated miRNAs in diabetes mellitus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40659-017-0111-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5331689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53316892017-03-06 Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney Du, Guankui Xiao, Man Zhang, Xuezi Wen, Maoyu Pang, Chi Jiang, Shangfei Sang, Shenggang Xie, Yiqiang Biol Res Research Article BACKGROUND: A number of dysregulated miRNAs have been identified and are proposed to have significant roles in the pathogenesis of type 2 diabetes mellitus or renal pathology. Alpinia oxyphylla has shown significant anti-inflammatory properties and play an anti-diabetes role. The objective of this study was to detect the alteration of miRNAs underlying the anti-diabetes effects of A. oxyphylla extract (AOE) in a type II diabetic animal model (C57BIKsj db-/db-). RESULTS: Treatment with AOE for 8 weeks led to lower concentrations of blood glucose, urine albumin, and urine creatinine. 17 and 13 miRNAs were statistically identified as differentially regulated in the DB/DB and db-/db- AOE mice, respectively, compared to the untreated db-/db- mice. Of these, 7 miRNAs were identified in both comparison groups, and these 7 miRNAs were verified by quantitative real-time PCR. Functional bioinformatics showed that the putative target genes of 7 miRNAs were associated with several diabetes effects and signaling pathways. CONCLUSIONS: These founding suggest that the potential of AOE as a medicinal anti-diabetes treatment through changes in the expressions of specific miRNAs. The results provide a useful resource for future investigation of the role of AOE-regulated miRNAs in diabetes mellitus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40659-017-0111-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-01 /pmc/articles/PMC5331689/ /pubmed/28249617 http://dx.doi.org/10.1186/s40659-017-0111-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Du, Guankui Xiao, Man Zhang, Xuezi Wen, Maoyu Pang, Chi Jiang, Shangfei Sang, Shenggang Xie, Yiqiang Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney |
title | Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney |
title_full | Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney |
title_fullStr | Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney |
title_full_unstemmed | Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney |
title_short | Alpinia oxyphylla Miq. extract changes miRNA expression profiles in db-/db- mouse kidney |
title_sort | alpinia oxyphylla miq. extract changes mirna expression profiles in db-/db- mouse kidney |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331689/ https://www.ncbi.nlm.nih.gov/pubmed/28249617 http://dx.doi.org/10.1186/s40659-017-0111-1 |
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