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Unlocking the Antidiabetic Potential of CBD: In Vivo Preclinical Studies
Elena Rafailovska1, Elona Xhemaili2, Zorica Naumovska3
1Institute of Biology, Faculty of Natural Sciences and Mathematics, Ss. Cyril and Methodius University in Skopje, Arhimedova 3, 1000 Skopje, North Macedonia.
Abstract:
Background/Objectives: Diabetes mellitus is a growing global health concern, driving the exploration of new therapies like cannabidiol (CBD), which shows potential in improving insulin sensitivity and glycemic control, though its effects on glucose metabolism remain unclear. This study evaluates CBD's dose-dependent effects on glycemia, insulin, and hepatic carbohydrate metabolism in diabetic rats. Methods: The Oral Glucose Tolerance Test (OGTT) was performed in healthy rats to compare intragastric vs. intraperitoneal CBD (0.5, 5, 50 mg/kg). Diabetic rats were treated with intragastric CBD (25, 50, 100 mg/kg) or metformin (70 mg/kg) for 8 days. Blood glucose, insulin, lipid profiles, and key carbohydrate-metabolizing enzymes were analyzed. Results: In the OGTT, intragastric CBD reduced glycemic AUC, with 50 mg/kg showing the strongest effect, while intraperitoneal CBD had no impact. In diabetic rats, metformin and 25 mg/kg CBD lowered blood glucose, but only CBD increased insulin. The 50 mg/kg dose caused the greatest glucose reduction and moderate insulin rise, while 100 mg/kg had no effect. At 25 mg/kg, CBD inhibited glucose-6-phosphatase and increased glucose-6-phosphate. The 50 mg/kg dose further suppressed gluconeogenic enzymes, reduced glycogen phosphorylase and liver glucose, and enhanced glucose-6-phosphate, showing the strongest metabolic effects. The 100 mg/kg dose increased hexokinase but had weaker metabolic effects. Metformin improved glucose utilization and glycogen storage. CBD at 25 and 50 mg/kg reduced triacylglycerols and increased HDL, while 100 mg/kg had no effect. Conclusions: This study provides strong evidence of CBD's antidiabetic potential, especially at 50 mg/kg, particularly through its modulation of glucose metabolism and tendency to regulate insulin levels.
Insights
Cannabidiol (CBD) shows promise in managing diabetes by improving glucose metabolism and insulin levels in diabetic rats. The 50 mg/kg dose demonstrated the most significant antidiabetic effects, highlighting CBD
Area of Science:
- Endocrinology
- Metabolic Disorders
- Pharmacology
Background:
- Diabetes mellitus presents a significant global health challenge.
- Cannabidiol (CBD) is being investigated for its potential antidiabetic properties, including improving insulin sensitivity.
- The precise impact of CBD on glucose metabolism requires further elucidation.
Purpose of the Study:
- To investigate the dose-dependent effects of cannabidiol (CBD) on glycemia, insulin levels, and hepatic carbohydrate metabolism in a rat model of diabetes.
- To compare the efficacy of intragastric versus intraperitoneal administration of CBD.
Main Methods:
- Oral Glucose Tolerance Tests (OGTT) were conducted in healthy rats to assess CBD administration routes.
- Diabetic rats received intragastric CBD (25, 50, 100 mg/kg) or metformin (70 mg/kg) for eight days.
- Analysis included blood glucose, insulin, lipid profiles, and key carbohydrate-metabolizing enzymes.
Main Results:
- Intragastric CBD, particularly at 50 mg/kg, reduced glycemic area under the curve (AUC) in OGTT, while intraperitoneal administration was ineffective.
- In diabetic rats, CBD (25 and 50 mg/kg) lowered blood glucose and increased insulin levels, with the 50 mg/kg dose showing the most pronounced effects.
- CBD modulated hepatic enzymes involved in glucose metabolism, including inhibition of glucose-6-phosphatase and gluconeogenic enzymes, and altered glucose-6-phosphate and hexokinase activity.
Conclusions:
- Cannabidiol exhibits significant antidiabetic potential, particularly at a 50 mg/kg dose, in a rat model.
- CBD's therapeutic effects are linked to its ability to modulate glucose metabolism and influence insulin regulation.
- CBD also demonstrated positive effects on lipid profiles, reducing triacylglycerols and increasing HDL cholesterol.
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