Trial of a Novel Oral Cannabinoid Formulation in Patients with Hypertension: A Double-Blind, Placebo-Controlled Pharmacogenetic Study

被引:7
作者
Batinic, Ana [1 ]
Sutlovic, Davorka [2 ,3 ]
Kuret, Sendi [2 ]
Matana, Antonela [2 ]
Kumric, Marko [4 ]
Bozic, Josko [4 ]
Dujic, Zeljko [5 ]
机构
[1] Pharm Split Dalmatia Cty, Split 21000, Croatia
[2] Univ Split, Univ Dept Hlth Studies, Split 21000, Croatia
[3] Univ Split, Sch Med, Dept Toxicol & Pharmacogenet, Split 21000, Croatia
[4] Univ Split, Sch Med, Dept Pathophysiol, Split 21000, Croatia
[5] Univ Split, Sch Med, Dept Integrat Physiol, Split 21000, Croatia
关键词
cannabidiol; blood pressure; CYP P450 genes; GC-MS analysis; SNP genotyping; CANNABIDIOL; EPILEPSY;
D O I
10.3390/ph16050645
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cannabidiol (CBD) is a non-psychoactive cannabinoid, and available evidence suggests potential efficacy in the treatment of many disorders. DehydraTECH (TM) 2.0 CBD is a patented capsule formulation that improves the bioabsorption of CBD. We sought to compare the effects of CBD and DehydraTECH (TM) 2.0 CBD based on polymorphisms in CYP P450 genes and investigate the effects of a single CBD dose on blood pressure. In a randomized and double-blinded order, 12 females and 12 males with reported hypertension were given either placebo capsules or DehydraTECH (TM) 2.0 CBD (300 mg of CBD, each). Blood pressure and heart rate were measured during 3 h, and blood and urine samples were collected. In the first 20 min following the dose, there was a greater reduction in diastolic blood pressure (p = 0.025) and mean arterial pressure MAP (p = 0.056) with DehydraTECH (TM) 2.0 CBD, which was probably due to its greater CBD bioavailability. In the CYP2C9*2*3 enzyme, subjects with the poor metabolizer (PM) phenotype had higher plasma CBD concentrations. Both CYP2C19*2 (p = 0.037) and CYP2C19*17 (p = 0.022) were negatively associated with urinary CBD levels (beta = -0.489 for CYP2C19*2 and beta = -0.494 for CYP2C19*17). Further research is required to establish the impact of CYP P450 enzymes and the identification of metabolizer phenotype for the optimization of CBD formulations.
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页数:18
相关论文
共 41 条
  • [1] Cannabidiol and Cannabidiol Metabolites: Pharmacokinetics, Interaction with Food, and Influence on Liver Function
    Abbotts, Kieran Shay Struebin
    Ewell, Taylor Russell
    Butterklee, Hannah Michelle
    Bomar, Matthew Charles
    Akagi, Natalie
    Dooley, Gregory P.
    Bell, Christopher
    [J]. NUTRIENTS, 2022, 14 (10)
  • [2] [Anonymous], HARD WEINB EQ
  • [3] [Anonymous], ON WAY AN CALC
  • [4] [Anonymous], ?About us"
  • [5] Bachtiar M, 2013, Curr. Genet. Med. Rep, V1, P162, DOI DOI 10.1007/S40142-013-0017-3
  • [6] Cytochrome P450-Catalyzed Metabolism of Cannabidiol to the Active Metabolite 7-Hydroxy-Cannabidiol
    Beers, Jessica L.
    Fu, Dong
    Jackson, Klarissa D.
    [J]. DRUG METABOLISM AND DISPOSITION, 2021, 49 (10) : 882 - 891
  • [7] Bioscience L., DEHYDRATECH
  • [8] Pharmacokinetics, Safety, and Tolerability of a Medicinal Cannabis Formulation in Patients with Chronic Non-cancer Pain on Long-Term High Dose Opioid Analgesia: A Pilot Study
    Bonomo, Yvonne
    Norman, Amanda
    Collins, Lisa
    O'Neill, Helen
    Galettis, Peter
    Trinca, Jane
    Strauss, Nigel
    Martin, Jennifer
    Castle, David
    [J]. PAIN AND THERAPY, 2022, 11 (01) : 171 - 189
  • [9] Bozina N, 2003, CROAT MED J, V44, P425
  • [10] Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome
    Devinsky, Orrin
    Cross, J. Helen
    Laux, Linda
    Marsh, Eric
    Miller, Ian
    Nabbout, Rima
    Scheffer, Ingrid E.
    Thiele, Elizabeth A.
    Wright, Stephen
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (21) : 2011 - 2020