Pregled bibliografske jedinice broj: 1279176
Trial of a Novel Oral Cannabinoid Formulation in Patients with Hypertension: A Double-Blind, Placebo-Controlled Pharmacogenetic Study
Trial of a Novel Oral Cannabinoid Formulation in Patients with Hypertension: A Double-Blind, Placebo-Controlled Pharmacogenetic Study // MDPI Pharmaceuticals, 16 (2023), 5; 645-663 doi:10.3390/ph16050645 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1279176 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Trial of a Novel Oral Cannabinoid Formulation in
Patients with Hypertension: A Double-Blind,
Placebo-Controlled Pharmacogenetic Study
Autori
Batinić, Ana ; Sutlović, Davorka ; Kuret, Sendi ; Matana, Antonela ; Kumrić, Marko ; Božić, Joško ; Dujić, Željko
Izvornik
MDPI Pharmaceuticals (1424-8247) 16
(2023), 5;
645-663
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
cannabidiol ; blood pressure ; CYP P450 genes ; GC-MS analysis ; SNP genotyping
Sažetak
Cannabidiol (CBD) is a non-psychoactive cannabinoid, and available evidence suggests potential efficacy in the treatment of many disorders. DehydraTECHTM2.0 CBD is a patented capsule formulation that improves the bioabsorption of CBD. We sought to compare the effects of CBD and DehydraTECHTM2.0 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 emales and 12 males with reported hypertension were given either placebo capsules or DehydraTECHTM2.0 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 DehydraT- ECHTM2.0 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.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti, Farmacija
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Split,
Sveučilište u Splitu Sveučilišni odjel zdravstvenih studija
Profili:
Željko Dujić (autor)
Marko Kumrić (autor)
Joško Božić (autor)
Antonela Matana (autor)
Sendi Kuret (autor)
Davorka Sutlović (autor)