Delta-9-tetrahydrocannabinol effects in schizophrenia: Implications for cognition, psychosis, and addiction

被引:429
作者
D'Souza, DC
Abi-Saab, WM
Madonick, S
Forselius-Bielen, K
Doersch, A
Braley, G
Gueorguieva, R
Cooper, TB
Krystal, JH
机构
[1] VA Connecticit Healthcare Syst, Schizophrenia Biol Res Ctr, West Haven, CT 06516 USA
[2] Connecticut Mental Hlth Ctr, Abraham Ribicoff Res Facil, New Haven, CT 06519 USA
[3] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[4] Inst Living, Hartford, CT USA
[5] Pfizer Global Res & Dev, Groton, CT USA
[6] Univ Connecticut, Div Biostat, Dept Epidemiol & Publ Hlth, Storrs, CT USA
[7] Columbia Univ, Coll Phys & Surg, Dept Psychiat, New York, NY USA
[8] Nathan S Kline Inst Psychiat Res, Orangeburg, NY USA
关键词
delta-9-tetrahydrocannabinol; cannabinoids; cannabis; self-medication; cognition; schizophrenia;
D O I
10.1016/j.biopsych.2004.12.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Recent advances in the neurobiology of cannabinoids have renewed interest in the association between cannabis and psychotic disorders. Methods: In a 3-day, double-blind, randomized, placebo-controlled study, the behavioral, cognitive, motor, and endocrine effects of 0 mg, 2.5 mg, and 5 mg intravenous Delta-9-tetrabydrocannabinol (Delta-9-7HC) were characterized in 13 stable, antipsycbotic-treated schizophrenia patients. These data were compared with effects in healthy subjects reported elsewhere. Results: Delta-9-tetrabydrocannabinol transiently increased 1) learning and recall deficits; 2) positive, negative, and general schizophrenia symptoms; 3) perceptual alterations; 4) akatbisia, rigidity, and dyskinesia; 5) deficits in vigilance; and 6) plasma prolactin and cortisol. Schizophrenia patients were more vulnerable to Delta-9-7HC effects on recall relative to control subjects. There were no serious short- or long-term adverse events associated with study participation. Conclusions: Delta-9-tetrabydrocannabinol is associated with transient exacerbation in core psychotic and cognitive deficits in schizophrenia. These data do not provide a reason to explain why schizophrenia patients use or misuse cannabis. Furthermore, Delta-9-7HC might differentially affect schizophrenia patients relative to control subjects. Finally, the enhanced sensitivity to the cognitive effects of Delta-9-THC warrants further study into whether brain cannabinoid receptor dysfunction contributes to the pathophysiology of the cognitive deficits associated with schizophrenia.
引用
收藏
页码:594 / 608
页数:15
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