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Can marijuana compounds show more than diabetes drugs? Early discovery shows potential, but more research is needed

Cannabinoids such as THC, CBD and CBN may help regulate blood sugar levels, possibly exceeding some existing diabetes medications, a new study suggests. However, it should be noted that since this study was not peer-reviewed and was purely theoretical, any potential application remains speculative at this stage. This study requires further validation before any clinical application is considered.

Research highlights the multi-target potential of cannabinoids

From University of Liberty State and Yaoundé University 1 A silicon molecule docking study was conducted to evaluate the interaction between six cannabinoids and four key enzymes involved in glucose metabolism: dipeptidyl peptidase-4 (DPP-4), alpha-glucosidase, alpha – Amylase and convertase. These enzymes play an important role in breaking down carbohydrates and regulating postprandial glucose peaks, making them the main targets for type 2 diabetes treatment.

According to the study, cannabinoids show stronger binding affinity for these enzymes compared to certain standard diabetes drugs, except for DPP-4 inhibitors. THC and CBN exhibit particularly strong interactions, suggesting that they may regulate multiple metabolic pathways simultaneously.

The study shows that cannabinoids have a multi-target binding to key type 2 diabetes drug targets, indicating their potential as further research on antidiabetic drugs.

Why this matters

With 537 million people suffering from diabetes worldwide, the demand for effective and safer treatment options continues to grow. Although traditional diabetes medications focus on a single pathway, cannabinoids may provide a multi-target approach that may improve glucose control while reducing side effects.

Previous studies have suggested the metabolic effects of cannabis compounds, and studies have shown that CBD may reduce insulin resistance and inflammation, while THCV has been associated with appetite suppression and improved metabolic function. However, the exact mechanism is not yet clear.

Warning: This study has not proven

Despite the encouraging results, this study is still theoretical. It relies solely on computer simulations, which means no clinical trials or real-life tests were conducted to confirm the effect of cannabinoids on blood sugar regulation.

Furthermore, although studies have shown that cannabinoids bind well to key enzymes, binding affinity alone does not guarantee therapeutic efficacy. Before any conclusions are drawn, factors such as bioavailability, metabolism and dosage need to be studied in laboratory and human trials.

It is also important to note that this study has not been peer-reviewed, meaning it has not undergone rigorous scientific review. Cannabinoids should not be considered a reliable treatment for diabetes until further studies validate these findings. Although these findings are interesting, they do not constitute medical evidence. Without clinical validation, the effects of cannabinoids on organisms cannot be determined as seen in computer models.

What’s next?

In order for cannabinoids to be carefully considered in diabetes management, animal and human trials must confirm their efficacy and safety. Future studies should also explore how different cannabinoids interact and if non-psychoactive compounds such as CBG and THCV can provide metabolic benefits without being associated with THC.

Although cannabis-based drugs have been explored in diseases such as epilepsy and chronic pain, their potential in diabetes remains largely untapped. If future research supports these findings, we may see the development of novel cannabinoid-based therapies for blood sugar control.

For now, this study is a stepping stone, not a breakthrough, and it is a signal that further investigation is necessary rather than a replacement for existing treatments.

Leadership Images by shutterstock

The content was partially produced with the help of AI tools and was reviewed and published by Benzinga editors.

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