Abstract
The most important psychoactive constituent of Cannabis sativa L. is Δ9-tetrahydrocannabinol (THC). Cannabidiol (CBD), another important constituent, is
able to modulate the distinct unwanted psychotropic effect of THC. In natural plant
extracts of C. sativa, large amounts of THC and CBD appear in the form of THCA-A (THC-acid-A) and CBDA
(cannabidiolic acid), which can be transformed to THC and CBD by heating. Previous
reports of medicinal use of cannabis or cannabis preparations with higher CBD/THC
ratios and use in its natural, unheated form have demonstrated that pharmacological
effects were often accompanied with a lower rate of adverse effects. Therefore, in
the present study, the pharmacokinetics and metabolic profiles of two different C. sativa extracts (heated and unheated) with a CBD/THC ratio > 1 were compared to synthetic
THC (dronabinol) in a double-blind, randomized, single center, three-period cross-over
study involving 9 healthy male volunteers. The pharmacokinetics of the cannabinoids
was highly variable. The metabolic pattern was significantly different after administration
of the different forms: the heated extract showed a lower median THC plasma AUC24 h than the unheated extract of 2.84 vs. 6.59 pmol h/mL, respectively. The later was
slightly higher than that of dronabinol (4.58 pmol h/mL). On the other hand, the median
sum of the metabolites (THC, 11-OH-THC, THC-COOH, CBN) plasma AUC24 h was higher for the heated than for the unheated extract. The median CBD plasma AUC24 h was almost 2-fold higher for the unheated than for the heated extract. These results
indicate that use of unheated extracts may lead to a beneficial change in metabolic
pattern and possibly better tolerability.
Key words
Cannabis sativa L. - Cannabaceae - tetrahydrocannabinol - THC - THC metabolites - CBD - pharmacokinetics
References
- 1
Clark A J, Ware M A, Yazer E, Murray T J, Lynch M E.
Patterns of cannabis use among patients with multiple sclerosis.
Neurology.
2004;
62
2098-2100
- 2
Furler M D, Einarson T R, Millson M, Walmsley S, Bendayan R.
Medicinal and recreational marijuana use by patients infected with HIV.
AIDS Patient Care STDS.
2004;
18
215-228
- 3
Gorter R W, Butorac M, Cobian E P.
Cutaneous resorption of lead after external use of lead-containing ointments in volunteers
with healthy skin.
Am J Ther.
2005;
12
17-21
- 4
Tramer M R, Carroll D, Campbell F A, Reynolds D J, Moore R A, McQuay H J.
Cannabinoids for control of chemotherapy induced nausea and vomiting: quantitative
systematic review.
Br Med J.
2001;
323
16-21
- 5
Ware M A, Adams H, Guy G W.
The medicinal use of cannabis in the UK: results of a nationwide survey.
Int J Clin Pract.
2005;
59
291-295
- 6
Wood S.
Evidence for using cannabis and cannabinoids to manage pain.
Nurs Times.
2004;
100
38-40
- 7
Hollister L E, Gillespie H K, Ohlsson A, Lindgren J E, Wahlen A, Agurell S.
Do plasma concentrations of delta 9-tetrahydrocannabinol reflect the degree of intoxication?.
J Clin Pharmacol.
1981;
21
171S-177S
- 8
Lemberger L, Weiss J L, Watanabe A M, Galanter I M, Wyatt R J, Cardon P V.
Delta-9-tetrahydrocannabinol. Temporal correlation of the psychologic effects and
blood levels after various routes of administration.
N Engl J Med.
1972;
286
685-688
- 9
Ohlsson A, Lindgren J E, Wahlen A, Agurell S, Hollister L E, Gillespie H K.
Plasma delta-9 tetrahydrocannabinol concentrations and clinical effects after oral
and intravenous administration and smoking.
Clin Pharmacol Ther.
1980;
28
409-416
- 10
Garrett E R, Hunt C A.
Pharmacokinetics of delta9-tetrahydrocannabinol in dogs.
J Pharm Sci.
1977;
66
395-407
- 11
Ashton C H.
Pharmacology and effects of cannabis: a brief review.
Br J Psychiatry.
2001;
178
101-106
- 12
Williams C M, Kirkham T C.
Observational analysis of feeding induced by Delta9-THC and anandamide.
Physiol Behav.
2002;
76
241-250
- 13
Ameri A.
The effects of cannabinoids on the brain.
Prog Neurobiol.
1999;
58
315-348
- 14
Nahas G, Leger C, Tocque B, Hoellinger H.
The kinetics of cannabinoid distribution and storage with special reference to the
brain and testis.
J Clin Pharmacol.
1981;
21
208S-214S
- 15
Rawitch A B, Rohrer R, Vardaris R M.
Delta-9-Tetrahydrocannabinol uptake by adipose tissue: preferential accumulation in
gonadal fat organs.
Gen Pharmacol.
1979;
10
525-529
- 16
Maykut M O.
Health consequences of acute and chronic marihuana use.
Prog Neuropsychopharmacol Biol Psychiatry.
1985;
9
209-238
- 17
Anderson P O, McGuire G G.
Delta-9-tetrahydrocannabinol as an antiemetic.
Am J Hosp Pharm.
1981;
38
639-646
- 18
Huestis M A, Cone E J.
Urinary excretion half-life of 11-nor-9-carboxy-delta9-tetrahydrocannabinol in humans.
Ther Drug Monit.
1998;
20
570-576
- 19
Wall M E, Sadler B M, Brine D, Taylor H, Perez-Reyes M.
Metabolism, disposition, and kinetics of delta-9-tetrahydrocannabinol in men and women.
Clin Pharmacol Ther.
1983;
34
352-363
- 20
Burstein S H.
The cannabinoid acids: nonpsychoactive derivatives with therapeutic potential.
Pharmacol Ther.
1999;
82
87-96
- 21
Brenneisen R.
Psychotropic drugs. II. Determination of cannabinoids in Cannabis sativa L. and in cannabis products with high pressure liquid chromatography (HPLC).
Pharm Acta Helv.
1984;
59
247-259
- 22
Grotenhermen F.
Pharmacokinetics and pharmacodynamics of cannabinoids.
Clin Pharmacokinet.
2003;
42
327-360
- 23
Verhoeckx K C, Korthout H A, van Meeteren-Kreikamp A P, Ehlert K A, Wang M, van der
Greef J, Rodenburg R J, Witkamp R F.
Unheated Cannabis sativa extracts and its major compound THC-acid have potential immuno-modulating properties
not mediated by CB1 and CB2 receptor coupled pathways.
Int Immunopharmacol.
2006;
6
656-665
- 24
El-Remessy A B, Al-Shabrawey M, Khalifa Y, Tsai N T, Caldwell R B, Liou G I.
Neuroprotective and blood-retinal barrier-preserving effects of cannabidiol in experimental
diabetes.
Am J Pathol.
2006;
168
235-244
- 25
Hampson A J, Grimaldi M, Axelrod J, Wink D.
Cannabidiol and (−)Delta9-tetrahydrocannabinol are neuroprotective antioxidants.
Proc Natl Acad Sci USA.
1998;
95
8268-8273
- 26
Iuvone T, Esposito G, Esposito R, Santamaria R, Di Rosa M, Izzo A A.
Neuroprotective effect of cannabidiol, a non-psychoactive component from Cannabis sativa, on beta-amyloid-induced toxicity in PC12 cells.
J Neurochem.
2004;
89
134-141
- 27
Mechoulam R, Hanus L.
Cannabidiol: an overview of some chemical and pharmacological aspects. Part I: chemical
aspects.
Chem Phys Lipids.
2002;
121
35-43
- 28
Teare L, Zajicek J.
The use of cannabinoids in multiple sclerosis.
Expert Opin Investig Drugs.
2005;
14
859-869
- 29
Grauwiler S B, Scholer A, Drewe J.
Development of a LC/MS/MS method for the analysis of cannabinoids in human EDTA-plasma
and urine after small doses of Cannabis sativa extracts.
J Chromatogr B Analyt Technol Biomed Life Sci.
2007;
850
515-522
1 These authors contributed equally to the work.
Prof. Juergen Drewe, MD, MSc
Department of Gastroenterology & Hepatology
University Hospital Basel
Petersgraben 4
4031 Basel
Switzerland
Phone: +41 7 89 23 27 44
Fax: +41 61 2 65 85 81
Email: juergen.drewe@unibas.ch