Modulation of MicroRNAs and Exosomal MicroRNAs after Dietary Interventions for Obesity and Insulin Resistance: A Narrative Review.
Karla G Hernández-GómezAzalia Avila-NavaLuis E González-SalazarLilia G NoriegaAurora Elizabeth Serralde-ZúñigaRocio Guizar-HerediaIsabel Medina-VeraAna Ligia Gutiérrez-SolisNimbe TorresArmando R TovarMartha Guevara-CruzPublished in: Metabolites (2023)
MicroRNAs (miRNAs) are small noncoding RNAs approximately 22 nucleotides in length. Their main function is to regulate gene expression at the posttranscriptional level by inhibiting the translation of messenger RNAs (mRNAs). miRNAs originate in the cell nucleus from specific genes, where they can perform their function. However, they can also be found in serum, plasma, or other body fluids travelling within vesicles called exosomes and/or bound to proteins or other particles such as lipoproteins. miRNAs can form complexes outside the cell where they are synthesized, mediating paracrine and endocrine communication between different tissues. In this way, they can modulate the gene expression and function of distal cells. It is known that the expression of miRNAs can be affected by multiple factors, such as the nutritional or pathological state of the individual, or even in conditions such as obesity, insulin resistance, or after any dietary intervention. In this review, we will analyse miRNAs whose expression and circulation are affected in conditions of obesity and insulin resistance, as well as the changes generated after a dietary intervention, with the purpose of identifying new possible biomarkers of early response to nutritional treatment in these conditions.
Keyphrases
- insulin resistance
- gene expression
- metabolic syndrome
- high fat diet induced
- adipose tissue
- high fat diet
- skeletal muscle
- type diabetes
- polycystic ovary syndrome
- poor prognosis
- randomized controlled trial
- dna methylation
- single cell
- cell therapy
- induced apoptosis
- mesenchymal stem cells
- glycemic control
- stem cells
- physical activity
- genome wide
- long non coding rna
- oxidative stress
- transcription factor
- cell death