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Procyanidins modulate microRNA expression in pancreatic islets
Anna Castell-Auví1, Lídia Cedó, Jamileh Movassat
1Nutrigenomics Research Group, Departament de Bioquímica i Biotecnologia, Universitat Rovira i Virgili, Marcel·lí Domingo s/n, 43007 Tarragona, Spain.
Abstract:
Procyanidins modulate glucose metabolism, partly due to its effects on pancreas. Given the role of microRNAs (miRNAs) in the regulation of diabetes and the fact that flavonoids modulate miRNAs in other tissues, we hypothesized that procyanidins might target miRNAs in the pancreas. We investigated the miRNA expression profile in pancreatic islets isolated from rats treated with a daily dose of grape seed procyanidin extract (GSPE) (25 mg/kg of body weight) for 45 days. The miRWalk database identified putative target genes of these miRNAs. We found that GSPE altered significantly the expression of miR-1249, miR-483, miR-30c-1*, and miR-3544. In silico prediction studies suggested that ion transport and response to glucose are among the regulated pathways. As a conclusion, this is the first study showing that procyanidins can also exert their bioactivity on pancreatic islets by modifying the miRNA expression pattern.
Insights
Grape seed procyanidins impact pancreatic islets by altering microRNA (miRNA) expression. This study reveals procyanidins
Area of Science:
- Endocrinology
- Molecular Biology
- Nutritional Science
Background:
- Procyanidins are known to influence glucose metabolism, with effects on the pancreas.
- MicroRNAs (miRNAs) play a crucial role in diabetes regulation.
- Flavonoids, including procyanidins, have been shown to modulate miRNA expression in various tissues.
Purpose of the Study:
- To investigate the hypothesis that procyanidins target pancreatic miRNAs.
- To examine the effect of grape seed procyanidin extract (GSPE) on miRNA expression in pancreatic islets.
Main Methods:
- Rats were treated daily with GSPE (25 mg/kg) for 45 days.
- Pancreatic islets were isolated for miRNA expression profiling.
- The miRWalk database was used to identify putative target genes of differentially expressed miRNAs.
Main Results:
- GSPE significantly altered the expression of specific miRNAs: miR-1249, miR-483, miR-30c-1*, and miR-3544.
- In silico analysis predicted that regulated pathways include ion transport and response to glucose.
- This is the first study to demonstrate procyanidin-induced changes in miRNA expression within pancreatic islets.
Conclusions:
- Procyanidins exert bioactivity on pancreatic islets by modulating miRNA expression patterns.
- This mechanism contributes to the known effects of procyanidins on glucose metabolism.
- The findings open new avenues for understanding the therapeutic potential of procyanidins in metabolic diseases.
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