Oscar Gerardo Silva-Gaona, J. M. Guzmán-Flores, M. Hernández-Ortiz, K. Vargas-Ortiz, J. Ramírez-Emiliano, S. Encarnación-Guevara, V. Pérez-Vázquez
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Three WT\nand three diabetic db/db mice received a standard diet (SD; WT and db/db groups, respectively); three WT and three\ndiabetic db/db mice received a SD supplemented with 0.75 % (w/w) curcumin (WT+C and db/db+C groups, respectively).\nLiver proteins were separated by 2D electrophoresis. Differential protein expression analysis was performed on\nImageMaster 2D Platinum software, and selected proteins were identified by MALDI-TOF-MS and subjected to enrichment\nanalysis using STRING and DAVID databases.\n\n\n\nThirty-six proteins with differential expression due to the diabetic background and curcumin treatment were found;\nthese proteins participate in the metabolism of amino acids, carbohydrates, and lipids. Interestingly, the altered expression of\nseven proteins was prevented in the liver of the diabetic mice that received curcumin.\n\n\n\nAmong all differentially expressed proteins, curcumin reverted the altered expression of seven proteins. Thus,\nalthough it was observed that curcumin did not affect the biochemical parameters, it does modify the expression of some\nliver proteins in diabetic mice.\n","PeriodicalId":50601,"journal":{"name":"Current Proteomics","volume":"40 1","pages":""},"PeriodicalIF":0.5000,"publicationDate":"2021-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Curcumin Reverts the Protein Differential Expression in the Liver of the Diabetic Obese db/db mice\",\"authors\":\"Oscar Gerardo Silva-Gaona, J. M. Guzmán-Flores, M. Hernández-Ortiz, K. Vargas-Ortiz, J. Ramírez-Emiliano, S. Encarnación-Guevara, V. Pérez-Vázquez\",\"doi\":\"10.2174/1570164618666210114112642\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\n In type 2 diabetic mouse liver, hyperglycemia, and insulin modify gene expression. Curcumin is a\\npowerful antioxidant and antidiabetic agent that regulates the gene expression of different signaling pathways through\\nvarious transcription factors. Therefore, we hypothesized that curcumin modifies the protein expression profile in the liver\\nof diabetic db/db mice.\\n\\n\\n\\nTo determine the effects of curcumin on the liver protein profile of diabetic db/db mice.\\n\\n\\n\\n\\ndb/db and wild type (WT) male mice were allocated in four groups, and they were fed for eight weeks. Three WT\\nand three diabetic db/db mice received a standard diet (SD; WT and db/db groups, respectively); three WT and three\\ndiabetic db/db mice received a SD supplemented with 0.75 % (w/w) curcumin (WT+C and db/db+C groups, respectively).\\nLiver proteins were separated by 2D electrophoresis. 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Curcumin Reverts the Protein Differential Expression in the Liver of the Diabetic Obese db/db mice
In type 2 diabetic mouse liver, hyperglycemia, and insulin modify gene expression. Curcumin is a
powerful antioxidant and antidiabetic agent that regulates the gene expression of different signaling pathways through
various transcription factors. Therefore, we hypothesized that curcumin modifies the protein expression profile in the liver
of diabetic db/db mice.
To determine the effects of curcumin on the liver protein profile of diabetic db/db mice.
db/db and wild type (WT) male mice were allocated in four groups, and they were fed for eight weeks. Three WT
and three diabetic db/db mice received a standard diet (SD; WT and db/db groups, respectively); three WT and three
diabetic db/db mice received a SD supplemented with 0.75 % (w/w) curcumin (WT+C and db/db+C groups, respectively).
Liver proteins were separated by 2D electrophoresis. Differential protein expression analysis was performed on
ImageMaster 2D Platinum software, and selected proteins were identified by MALDI-TOF-MS and subjected to enrichment
analysis using STRING and DAVID databases.
Thirty-six proteins with differential expression due to the diabetic background and curcumin treatment were found;
these proteins participate in the metabolism of amino acids, carbohydrates, and lipids. Interestingly, the altered expression of
seven proteins was prevented in the liver of the diabetic mice that received curcumin.
Among all differentially expressed proteins, curcumin reverted the altered expression of seven proteins. Thus,
although it was observed that curcumin did not affect the biochemical parameters, it does modify the expression of some
liver proteins in diabetic mice.
Current ProteomicsBIOCHEMICAL RESEARCH METHODS-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
1.60
自引率
0.00%
发文量
25
审稿时长
>0 weeks
期刊介绍:
Research in the emerging field of proteomics is growing at an extremely rapid rate. The principal aim of Current Proteomics is to publish well-timed in-depth/mini review articles in this fast-expanding area on topics relevant and significant to the development of proteomics. Current Proteomics is an essential journal for everyone involved in proteomics and related fields in both academia and industry.
Current Proteomics publishes in-depth/mini review articles in all aspects of the fast-expanding field of proteomics. All areas of proteomics are covered together with the methodology, software, databases, technological advances and applications of proteomics, including functional proteomics. Diverse technologies covered include but are not limited to:
Protein separation and characterization techniques
2-D gel electrophoresis and image analysis
Techniques for protein expression profiling including mass spectrometry-based methods and algorithms for correlative database searching
Determination of co-translational and post- translational modification of proteins
Protein/peptide microarrays
Biomolecular interaction analysis
Analysis of protein complexes
Yeast two-hybrid projects
Protein-protein interaction (protein interactome) pathways and cell signaling networks
Systems biology
Proteome informatics (bioinformatics)
Knowledge integration and management tools
High-throughput protein structural studies (using mass spectrometry, nuclear magnetic resonance and X-ray crystallography)
High-throughput computational methods for protein 3-D structure as well as function determination
Robotics, nanotechnology, and microfluidics.