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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.
Abstract:
Metabolic syndrome, a cluster of different disorders which include diabetes, obesity and cardiovascular diseases, is a global epidemic that is growing at an alarming rate. The origins of disease can be traced back to early developmental stages of life. This has increased mortalities and continues to reduce life expectancies of individuals across the globe. The aim of this study was to investigate the sub-acute and long term effects of neonatal oral administration of oleanolic acid and metformin on lipids (free fatty acids, FFAs) and genes associated with lipid metabolism and glucose transport using a neonatal rat experimental model. In the first study, seven days old pups were randomly grouped into control-distilled water (DW); oleanolic acid (60 mg/kg), metformin (500 mg/kg), high fructose diet (20% w/v, HF), oleanolic acid (OA) + high fructose diet (OA + HF), and Metformin + high fructose diet (MET + HF) groups. The pups were treated for 7 days, and then terminated on postnatal day (PD) 14. In the second study, rat pups were initially treated similarly to study 1 and weaned onto normal rat chow and plain drinking water on PD 21 till they reached adulthood (PD112). Tissue and blood samples were collected for further analyses. Measurement of the levels of free fatty acids (FFAs) was done using gas chromatography-mass spectrometry. Quantitative polymerase chain reaction (qPCR) was used to analyze the gene expression of glut-4, glut-5, fas, acc-1, nrf-1 and cpt-1 in the skeletal muscle. The results showed that HF accelerated accumulation of saturated FFAs within skeletal muscles. The HF fed neonatal rats had increased stearic acid, which was associated with decreased glucose, suppressed expression of glut-4, glut-5, nrf-1 and cpt-1 genes, and increased expression of acc-1 (p < 0.01) and fas. OA + HF and MET + HF treated groups had increased mono- and polyunsaturated FFAs; oleic, and octadecadienoic acids than the HF group. These unsaturated FFAs were associated with increased glut-4, glut-5 and nrf-1 (p < 0.01) and decreased acc-1 and fas (p < 0.05) in both OA + HF and MET + HF treated groups.
Conclusions:
The present study shows that neonatal oral administration of oleanolic acid and metformin potentially protects against the development of fructose-induced metabolic dysfunction in the rats in both short and long time periods.
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