MicroRNA-mediated regulation of hepatic metabolism in pregnancy: current understanding and future perspectives

Jesus Monroy-Rodriguez1, Mónica Navarro-Meza2

  • 1División de Ciencias de la Salud. Departamento de Ciencias Básicas para la Salud, Centro Universitario del Sur, Universidad de Guadalajara, Ciudad Guzmán, Jalisco, 49000, Mexico.

PubMed

Pregnancy represents a unique physiological state that involves closely coordinated hormonal, immunological, and metabolic adaptations that ensure an optimal distribution of nutrients between the mother and the fetus. The maternal liver undergoes adaptive changes throughout the anabolic and catabolic phases of this reproductive process, where carbohydrate, lipid, and protein metabolism participate to sustain embryonic development, fetal growth, and maternal energy balance. This mini-review integrates recent in vitro, animal, and clinical evidence on the regulatory functions of microRNAs (miRNAs) small non-coding RNAs that fine-tune gene expression post-transcriptionally in maternal hepatic metabolism during pregnancy. Highlighted miRNAs include miR-29a, miR-351, miR-16-5p, miR-155-5p, miR-146b, and miR-1323, which collectively influence insulin signaling, gluconeogenesis, lipid mobilization, and inflammatory responses in hepatic tissue. Dysregulation of these miRNAs has been linked to metabolic disorders such as obesity, insulin resistance, and gestational diabetes mellitus (GDM). This review focuses on liver-specific expression patterns and pregnancy-associated miRNA pathways, underscoring their potential as early, non-invasive biomarkers as well as therapeutic targets. By deepening the understanding of epigenetic regulation in maternal-fetal metabolic adaptation, this review provides insights into molecular findings with clinical perspectives as key components of translational research.

Related Concept Videos

Regulation of Metabolism01:19

Regulation of Metabolism

Cellular needs and conditions vary from cell to cell and change within individual cells over time. For example, the required enzymes and energetic demands of stomach cells are different from those of fat storage cells, skin cells, blood cells, and nerve cells. Furthermore, a digestive cell works much harder to process and break down nutrients during the time that closely follows a meal compared with many hours after a meal. As these cellular demands and conditions vary, so do the amounts and...
11.3K
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.7K
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After...
23.8K
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion01:20

Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion

Drug metabolism, a critical process in the liver, involves two primary phases: Phase I reactions and Phase II conjugation. Obesity introduces significant alterations in this metabolic process, primarily due to fatty infiltration of the liver, leading to conditions such as nonalcoholic fatty liver disease (NAFLD). This condition can modify the activities of both Phase I and II enzymes, impacting how drugs are metabolized in obese patients.Phase I metabolism sees variable effects across...
153
Hepatic Drug Excretion: Influencing Factors01:16

Hepatic Drug Excretion: Influencing Factors

The biliary system of the liver, crucial for bile secretion and drug excretion, comprises intrahepatic bile ducts that merge to form the common hepatic duct. This duct, carrying hepatic bile, combines with the cystic duct, draining the gallbladder and forming the common bile duct, which empties into the duodenum. Bile, produced by hepatic cells lining the bile canaliculi, is composed primarily of water, bile salts, pigments, electrolytes, and lesser amounts of cholesterol and fatty acids. Bile...
502
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
171