Microarray profiling of gene expression patterns in glomerular cells of astaxanthin-treated diabetic mice: A nutrigenomic approach
We have demonstrated that astaxanthin reduces glomerular oxidative stress as well as inhibits the increase in urinary albumin in diabetic db/db mice. The aim of the present study was to determine the gene expression patterns in the glomerular cells of the diabetic mouse kidney, and to investigate th...
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Veröffentlicht in: | International journal of molecular medicine 2006-10, Vol.18 (4), p.685-695 |
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Zusammenfassung: | We have demonstrated that astaxanthin reduces glomerular oxidative stress
as well as inhibits the increase in urinary albumin in diabetic db/db mice. The
aim of the present study was to determine the gene expression patterns in the
glomerular cells of the diabetic mouse kidney, and to investigate the effects
of astaxanthin on the expression of these genes using a high-density DNA microarray.
The diet administered to the astaxanthin-supplementation group was prepared by
mixing a control powder with astaxanthin at a concentration of 0.02%. Glomerular
cells were obtained from the kidneys of mice by laser capture microdissection.
Preparation of cRNA and target hybridization were performed according to the Affymetrix
GeneChip eukaryotic small sample target labeling assay protocol. The gene expression
profile was evaluated by the mouse expression set 430A GeneChip. Array data analysis
was carried out using Affymetrix GeneChip operating and Ingenuity Pathway analysis
software. Comparison between diabetic db/db and non-diabetic db/m mice revealed
that 779 probes (3.1%) were significantly affected, i.e. 550 probes were up-regulated,
and 229 probes were down-regulated, both at levels of ≥1.5-fold in the diabetic
mice. Ingenuity signal analysis of 550 up-regulated probes revealed the mitochondrial
oxidative phosphorylation pathway as the most significantly affected caronical
pathway. The affected genes were associated with complexes I, III, and IV located
on the mitochondrial inner membrane, and the expression levels of these genes
were decreased in mice treated with astaxanthin as compared to the levels in the
control mice. In addition, the expression of many genes associated with oxidative
stress, collagen synthesis, and transforming growth factor-β signaling was enhanced
in the diabetic mice, and this enhancement was slightly inhibited in the astaxanthin-treated
mice. In conclusion, this genome-wide nutrigenomics approach provided insight
into genes and putative genetic pathways that are thought to be affected by stimulation
by high-glucose concentrations. In addition, the present approach may help us
gain a better understanding of the genes and pathways involved in the anti-diabetic
mechanism of astaxanthin. |
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ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.18.4.685 |