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Title:
The intrauterine metabolic environment modulates the gene expression pattern in fetal rat islets: prevention by maternal taurine supplementation | Diabetologia
Description:
Aims/hypothesis Events during fetal life may in critical time windows programme tissue development leading to organ dysfunction with potentially harmful consequences in adulthood such as diabetes. In rats, the beta cell mass of progeny from dams fed with a low-protein (LP) diet during gestation is decreased at birth and metabolic perturbation lasts through adulthood even though a normal diet is given after birth or after weaning. Maternal and fetal plasma taurine levels are suboptimal. Maternal taurine supplementation prevents these induced abnormalities. In this study, we aimed to reveal changes in gene expression in fetal islets affected by the LP diet and how taurine may prevent these changes. Methods Pregnant Wistar rats were fed an LP diet (8% [wt/wt] protein) supplemented or not with taurine in the drinking water or a control diet (20% [wt/wt] protein). At 21.5 days of gestation, fetal pancreases were removed, digested and cultured for 7 days. Neoformed islets were collected and transcriptome analysis was performed. Results Maternal LP diet significantly changed the expression of more than 10% of the genes. Tricarboxylic acid cycle and ATP production were highly targeted, but so too were cell proliferation and defence. Maternal taurine supplementation normalised the expression of all altered genes. Conclusions/interpretation Development of the beta cells and particularly their respiration is modulated by the intrauterine environment, which may epigenetically modify expression of the genome and programme the beta cell towards a pre-diabetic phenotype. This mis-programming by maternal LP diet was prevented by early taurine intervention.
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Keywords {🔍}
diet, islets, taurine, maternal, expression, fetal, genes, cell, google, scholar, pubmed, article, cas, gene, beta, protein, diabetes, control, glucose, mitochondrial, reusens, significantly, involved, analysis, development, table, rat, supplementation, rats, atp, increased, lpt, low, remacle, changed, insulin, cycle, islet, igf, identified, fig, content, diabetologia, rna, data, fed, gestation, proliferation, altered, cells,
Topics {✒️}
uk/srsbin/cgi-bin/wgetz background-corrected probe values long-term consequences b60–b69 el-khattabi hot-start dna polymerase cmd=search&db=pubmed ucp2-overexpressing b-cells confocal laser-scanning microscope /cgi-bin/source/sourcesearch igf gene/protein family gov/projects/genome/genemap99/ low-protein diet supplemented fetal insulin-secreting cell inadequate maternal nutrition impaired glucose homeostasis beta cell mass beta-cell mass maternal low-protein related subjects high-fat diet early postnatal malnutrition low protein diet quantitative rt-pcr privacy choices/manage cookies transcriptome analysis fetal beta cell maternal protein restriction early taurine intervention remove probe sets gestational protein restriction low lactate dehydrogenase maternal lp diet pre-diabetic phenotype low-energy diet gestational diabetes leads glyceraldehyde-3-phosphate dehydrogenase beta cell maturation maternal lp targeted il-1beta sensitivity electronic supplementary material maternal diet manipulation fetal wistar rats beta cell development fat-rich diet protein restricted diet thrifty phenotype hypothesis peripheral insulin signalling superscript ii system raw image files rt-pcr analyses
Questions {❓}
- One question that remains is: is the altered phenotype that we observed the consequence of few modifications of gene expression leading to many beta cell secondary effects, or does it result from induction of a wide network of relatively minor imbalances?
- Uk/srsbin/cgi-bin/wgetz?
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mainEntity:
headline:The intrauterine metabolic environment modulates the gene expression pattern in fetal rat islets: prevention by maternal taurine supplementation
description:Events during fetal life may in critical time windows programme tissue development leading to organ dysfunction with potentially harmful consequences in adulthood such as diabetes. In rats, the beta cell mass of progeny from dams fed with a low-protein (LP) diet during gestation is decreased at birth and metabolic perturbation lasts through adulthood even though a normal diet is given after birth or after weaning. Maternal and fetal plasma taurine levels are suboptimal. Maternal taurine supplementation prevents these induced abnormalities. In this study, we aimed to reveal changes in gene expression in fetal islets affected by the LP diet and how taurine may prevent these changes. Pregnant Wistar rats were fed an LP diet (8% [wt/wt] protein) supplemented or not with taurine in the drinking water or a control diet (20% [wt/wt] protein). At 21.5 days of gestation, fetal pancreases were removed, digested and cultured for 7 days. Neoformed islets were collected and transcriptome analysis was performed. Maternal LP diet significantly changed the expression of more than 10% of the genes. Tricarboxylic acid cycle and ATP production were highly targeted, but so too were cell proliferation and defence. Maternal taurine supplementation normalised the expression of all altered genes. Development of the beta cells and particularly their respiration is modulated by the intrauterine environment, which may epigenetically modify expression of the genome and programme the beta cell towards a pre-diabetic phenotype. This mis-programming by maternal LP diet was prevented by early taurine intervention.
datePublished:2008-03-03T00:00:00Z
dateModified:2008-03-03T00:00:00Z
pageStart:836
pageEnd:845
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keywords:
Diabetes
Early programming
Fetal islets
Maternal low-protein diet
Rats
Taurine
Transcriptome
Internal Medicine
Metabolic Diseases
Human Physiology
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ScholarlyArticle:
headline:The intrauterine metabolic environment modulates the gene expression pattern in fetal rat islets: prevention by maternal taurine supplementation
description:Events during fetal life may in critical time windows programme tissue development leading to organ dysfunction with potentially harmful consequences in adulthood such as diabetes. In rats, the beta cell mass of progeny from dams fed with a low-protein (LP) diet during gestation is decreased at birth and metabolic perturbation lasts through adulthood even though a normal diet is given after birth or after weaning. Maternal and fetal plasma taurine levels are suboptimal. Maternal taurine supplementation prevents these induced abnormalities. In this study, we aimed to reveal changes in gene expression in fetal islets affected by the LP diet and how taurine may prevent these changes. Pregnant Wistar rats were fed an LP diet (8% [wt/wt] protein) supplemented or not with taurine in the drinking water or a control diet (20% [wt/wt] protein). At 21.5 days of gestation, fetal pancreases were removed, digested and cultured for 7 days. Neoformed islets were collected and transcriptome analysis was performed. Maternal LP diet significantly changed the expression of more than 10% of the genes. Tricarboxylic acid cycle and ATP production were highly targeted, but so too were cell proliferation and defence. Maternal taurine supplementation normalised the expression of all altered genes. Development of the beta cells and particularly their respiration is modulated by the intrauterine environment, which may epigenetically modify expression of the genome and programme the beta cell towards a pre-diabetic phenotype. This mis-programming by maternal LP diet was prevented by early taurine intervention.
datePublished:2008-03-03T00:00:00Z
dateModified:2008-03-03T00:00:00Z
pageStart:836
pageEnd:845
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Diabetes
Early programming
Fetal islets
Maternal low-protein diet
Rats
Taurine
Transcriptome
Internal Medicine
Metabolic Diseases
Human Physiology
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Analytics and Tracking {📊}
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