Study: CBD Protects Insulin-Producing Cells in Obesity, Boosts Key Metabolic Pathway
- New research indicates that cannabidiol (CBD) may protect insulin-producing pancreatic beta-cells in obese rats, potentially addressing metabolic dysfunction caused by high-fat diets.
- In a study with obese rats, CBD alone or combined with aerobic exercise significantly improved beta-cell function, while exercise alone did not show significant benefits.
- All interventions increased pancreatic gene expression of PI3K, AKT, and PDX1, key elements in cell survival and insulin regulation, with the combined treatment showing the strongest effect.
- Researchers concluded that CBD activates the PI3K/AKT/PDX1 pathway, enhancing beta-cell function in obesity, suggesting a cannabinoid-based approach for protecting pancreatic health, pending further human studies.
New research published in Molecular Biology Reports finds that CBD may help protect insulin-producing pancreatic cells in the context of obesity, potentially pointing to a new avenue for addressing metabolic dysfunction linked to high-fat diets. The study was conducted by researchers from Islamic Azad University, who examined the effects of cannabidiol (CBD) and aerobic training, both individually and in combination, on beta-cell function in an animal model of diet-induced obesity. Beta-cells are responsible for producing insulin, and their dysfunction plays a central role in the development of type 2 diabetes.
To induce obesity, 32 male Wistar rats were fed a high-fat diet for eight weeks. The animals were then divided into four groups: sedentary obese rats, obese rats given CBD (10 mg/kg five times weekly), obese rats undergoing aerobic treadmill training (30 minutes at 50% to 80% maximal speed, five times weekly), and a group receiving both CBD and aerobic training. The interventions continued for another eight weeks.
Rats treated with CBD alone or in combination with exercise showed significant improvements in beta-cell function, measured using the HOMA-Beta index, compared to sedentary obese rats. The improvements were statistically significant, with p-values of 0.002 for CBD alone and 0.001 for the combined treatment. Aerobic training by itself did not significantly improve beta-cell function.
At the molecular level, all three intervention groups experienced significant increases in pancreatic gene expression of PI3K, AKT and PDX1, key components of a pathway involved in cell survival and insulin regulation. The combined CBD and exercise group demonstrated a synergistic effect, with greater gene expression increases than either treatment alone.
Researchers concluded that CBD activates the PI3K/AKT/PDX1 signaling pathway and improves functional beta-cell mass in obese rats. While aerobic training also stimulated this pathway, only CBD produced measurable improvements in beta-cell function. The findings highlight a potential mechanism through which cannabinoids may help protect pancreatic health in obesity, though further research in humans will be necessary.