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Can Endocannabinoids Explain CBD-Mediated Reduction in Blood Pressure? Insights from a Randomized,
Marko Kumric1,2, Goran Dujic3, Josip Vrdoljak1,2
1Department of Pathophysiology, University of Split School of Medicine, Split, Croatia.
Insights
Cannabidiol (CBD) supplementation increased anandamide (AEA) levels in patients with hypertension. However, these changes in AEA did not explain the blood pressure-lowering effects of CBD.
Area of Science:
- Cardiovascular Pharmacology
- Endocannabinoid System Research
- Hypertension Therapeutics
Background:
- The HYPER-H21-4 trial demonstrated that chronic cannabidiol (CBD) reduces blood pressure (BP) in hypertensive patients.
- The endocannabinoid (EC) system is implicated in hypertension, prompting investigation into its role in CBD's cardiovascular effects.
Purpose of the Study:
- To investigate if changes in circulating endocannabinoids (ECs) mediate the blood pressure-lowering effects of CBD.
- To determine the impact of chronic CBD administration on plasma levels of anandamide (AEA) and 2-arachidonoylglycerol (2-AG).
Main Methods:
- A randomized, placebo-controlled, crossover trial involving 66 patients with primary hypertension.
- Patients received either CBD (225-450 mg/day) or placebo for 5 weeks, followed by a crossover period.
- Plasma AEA and 2-AG levels were measured throughout the study, alongside BP monitoring.
Main Results:
- Chronic CBD administration significantly increased plasma AEA levels compared to placebo.
- No significant association was found between changes in AEA levels and changes in systolic blood pressure.
- Chronic CBD administration did not significantly alter plasma 2-AG concentrations.
Conclusions:
- CBD supplementation increases circulating AEA levels in hypertensive patients.
- The observed increase in AEA levels does not conclusively explain the blood pressure-reducing effects of CBD.
- Further research is needed to elucidate the precise mechanisms underlying CBD's antihypertensive actions.
Abstract:
Background: HYPER-H21-4 trial, a randomized, placebo-controlled, crossover trial, showed that chronic cannabidiol (CBD) supplementation reduces blood pressure (BP) in patients with primary hypertension. Given the association between the endocannabinoid (EC) system and hypertension, we aimed to determine whether changes in circulating ECs, signaling molecules of the EC system, could explain CBD-mediated cardiovascular effects. Methods: For this purpose, anandamide (AEA) and 2-arachidonoylglycerol (2-AG) were measured in 66 patients with hypertension. Patients were assigned to receive CBD for 5 weeks (225-300 mg/day for the first 2.5 weeks, increasing to 375-450 mg/day for the subsequent 2.5 weeks), followed by 5 weeks of placebo, or 5 weeks of placebo followed by 5 weeks of CBD. Results: Administration of the CBD formulation for 5 weeks resulted in a significant increase in plasma AEA levels, whereas no such increase was observed during the placebo period (Placebo: 37.0 ± 18.0 ng/mL vs. 38.9 ± 20.8 ng/mL, CBD: 36.7 ± 18.0 ng/mL vs. 47.9 ± 24.6 ng/mL, F = 3.592, p = 0.042; ΔCBDAEA 11.1 ± 3.7 ng/mL, p = 0.025). Change in AEA levels following CBD administration (ΔCBDAEA) did not correlate with change in systolic BP following CBD administration (ΔCBDSBP) (r = -0.106, p = 0.428). Multivariate analysis showed that body mass index, current antihypertensive treatment, and fasting plasma glucose at baseline emerged as significant predictors of AEA increase, while BP reduction did not demonstrate a significant association. No significant association was found between chronic CBD administration and 2-AG plasma concentrations (placebo: 28.8 ± 4.3 ng/mL vs. 38.9 ± 20.8 ng/mL; CBD: 36.7 ± 18.0 ng/mL vs. 47.9 ± 24.6 ng/mL; F = 0.513, p = 0.478). Conclusions: Collectively, these findings suggest that although chronic CBD administration appears to increase AEA, but not 2-AG plasma levels, this study provides no conclusive evidence that such alterations explain CBD-mediated BP reduction.
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