A Study on Neonatal Intake of Oleanolic Acid and Metformin in Rats (Rattus norvegicus) with Metabolic Dysfunction:

Mmahiine Molepo1, Ademola Ayeleso2, Trevor Nyakudya3

  • 1Department of Biochemistry, Faculty of Natural and Agricultural Science, North West University, Mafikeng Campus, Private Bag X2046, Mmabatho 2735, South Africa. chrissy.molepo@gmail.com.

Insights

Neonatal exposure to oleanolic acid and metformin may prevent metabolic dysfunction caused by high fructose diets. These treatments improved lipid profiles and gene expression related to metabolism in rats.

Area of Science:

  • Metabolic disorders and developmental origins of health and disease.
  • Pharmacology and toxicology of natural compounds and drugs.
  • Molecular biology and gene expression analysis.

Background:

  • Metabolic syndrome, encompassing diabetes, obesity, and cardiovascular diseases, is a growing global health crisis.
  • Early life developmental stages significantly influence the origins of metabolic diseases.
  • Neonatal interventions may offer a strategy to mitigate long-term metabolic health risks.

Purpose of the Study:

  • To investigate the effects of neonatal oral administration of oleanolic acid and metformin on lipid metabolism and glucose transport.
  • To assess both sub-acute and long-term impacts of these treatments in a rat model.
  • To determine the influence on free fatty acids (FFAs) and key genes involved in lipid and glucose regulation.

Main Methods:

  • Neonatal rat pups were administered distilled water, oleanolic acid (OA), metformin (MET), or high fructose (HF) diet from postnatal day 7.
  • Sub-acute study: termination on postnatal day 14; Long-term study: weaned to normal chow until adulthood (postnatal day 112).
  • Analyses included gas chromatography-mass spectrometry for FFAs and quantitative polymerase chain reaction (qPCR) for gene expression (glut-4, glut-5, fas, acc-1, nrf-1, cpt-1).

Main Results:

  • High fructose diet (HF) induced accumulation of saturated FFAs (stearic acid) in skeletal muscle, decreased glucose, suppressed key metabolic genes (glut-4, glut-5, nrf-1, cpt-1), and increased lipogenic genes (acc-1, fas).
  • Neonatal administration of OA + HF and MET + HF counteracted HF effects, increasing unsaturated FFAs (oleic, octadecadienoic acids).
  • These unsaturated FFAs correlated with upregulated glucose transporters (glut-4, glut-5) and metabolic regulators (nrf-1), and downregulated lipogenic genes (acc-1, fas).

Conclusions:

  • Neonatal oral administration of oleanolic acid and metformin demonstrates protective effects against fructose-induced metabolic dysfunction.
  • These benefits were observed in both short-term (sub-acute) and long-term (adult) outcomes in the rat model.
  • The findings suggest potential therapeutic strategies targeting early life to prevent metabolic syndrome development.

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