Table 2.
Reference | Subjects | Dosing THC/CBD | Results | Comments |
---|---|---|---|---|
Karniol et al. (64) | Healthy volunteers (n = 40) | 30 mg THC (oral); 15, 30 of 60 mg CBD (oral) or in combination with 30 mg THC (both oral) | Antagonizing (part of) the THC-induced effects | CBD decreased the anxiety component of THC effects; no effect of CBD alone |
Hollister and Gillespie (65) | Healthy volunteers (n = 30) | 20 mg THC + 40 mg CBD (both oral) | CBD delays onset of the effect of THC and prolongs the effects of THC | |
Dalton et al. (66) | Healthy volunteers (n = 15) | 25 μg/kg BW THC and 150 μg/kg BW CBD via smoking a joint | CBD reduces euphoric effect of THC | Only effective when CBD and THC are administered simultaneously |
Hollister (67) | Healthy volunteers (n = ?) | CBD 5–30 mg i.v. | No effects | |
Carlini and Cunha (68) | Healthy volunteers | Acute 600 mg CBD; 10 mg/kg/BW CBD 20 days | CBD does not have psychological or physical effects | Light drowsiness after CBD administration |
Zuardi et al. (42) | Healthy volunteers (n = 8) | 0.5 mg/kg BW THC + 1 mg/kg BW CBD (both oral) | CBD antagonizes psychological effects of THC (anxiety) | CBD itself has no effect and does not antagonize the physical effects of THC (HR, BP) |
Zuardi et al. (69) | Treatment resistant schizophrenic patients (n = 3) | CBD during 29 days upwards from 40 to 1280 mg/day (oral) | CBD does not antagonize symptoms | No side effects of CBD reported |
Crippa et al. (70) | Healthy volunteers (n = 10) | CBD 400 mg oral | Anxiolytic effects; light mental sedation | SPECT results: effects in left amygdala-hippocampus complex radiating to hypothalamus |
Leweke et al. (71) | Psychiatric patients (n = 43) | CBD oral 800 mg/day; during 4 weeks | CBD more effective as antipychotic than amsulpride | Less side effects of CBD than with amsulpride |
Zuardi et al. (72) | PD patients with psychoses | CBD 150 mg/day; during 4 weeks | CBD possibly effective for treatment of PD patients suffering from psychoses | No significant side effects of CBD reported |
Borgwardt et al. (73), Fusar-Poli et al. (74), Fusar-Poli et al. (75), Bhattacharyya et al. (76)a | Healthy volunteers (n = 15) | CBD oral 600 mg; 10 mg THC (not simultaneously); in comparison with placebo | No effect in contrast with THC; CBD activates other brain areas than THC no effects of CBD in verbal learning task and no induction of psychotic symptoms | No sedation and no inhibition of locomotion by CBD; THC induces psychotic symptoms, anxiety, and sedation |
Zuardi et al. (77) | Patients with bipolar disorder (n = 2) | CBD oral 600 – 1200 mg/day during 25 days | CBD has no effect on symptoms | No side effects of CBD reported |
Bhattacharyya et al. (43) | Healthy volunteers (n = 6) | CBD 5 mg i.v. immediately followed by 1.25 mg THC i.v. | CBD antagonizes THC-induced psychotic symptoms | CBD and THC have opposite effects on regional brain function |
Bergamaschi et al. (78) | Healthy controls (n = 12) and patients with social phobia (n = 24) | CBD oral 600 mg | Reduction of anxiety scores in patients, no effect in controls | No physical effects or side effects of CBD reported |
Crippa et al. (79) | Patients with social phobia (n = 10) | CBD oral 400 mg | No effect on psychological scores | No physical effects; SPECT: CBD exerts its effects via limbic and paralimbic areas |
Nicholson et al. (80) | Healthy volunteers (n = 8) | CBD 5 mg + THC 5 mg; CBD 15 mg + THC 15 mg, via mouth spray | THC (15 mg) increases drowsiness, antagonized by CBD (15 mg) | |
Hallak et al. (81) | Schizophrenic patients (n = 28) | CBD oral 300 and 600 mg acute | No positive effects in Stroop Color Word Test | No significant side effects of CBD reported |
Hallak et al. (82) | Healthy volunteers (n = 10) | CBD oral 600 mg and ketamine i.v. | CBD increases activating effects of ketamine (BPRS); reduction of ketamine-induced depersonalization (CADSS) | No effect of CBD on HR and BP |
a This concerns experiments with one group of 15 subjects from which the results have been spread over four different publications; BP, blood pressure; BW, body weight; CADSS, Clinician Administered Dissociative States Scale; HR, heart rate; i.v., intravenously; PD, Parkinson disease.