Prolonged Cannabidiol Treatment Effects on Hippocampal Subfield Volumes in Current Cannabis Users

被引:55
作者
Beale, Camilla [1 ]
Broyd, Samantha J. [1 ]
Chye, Yann [2 ]
Suo, Chao [2 ]
Schira, Mark [1 ]
Galettis, Peter [3 ,4 ]
Martin, Jennifer H. [3 ,4 ]
Yuecel, Murat [2 ]
Solowij, Nadia [1 ,4 ]
机构
[1] Univ Wollongong, Illawarra Hlth & Med Res Inst, Sch Psychol, Wollongong, NSW, Australia
[2] Monash Univ, Monash Inst Cognit & Clin Neurosci, Sch Psychol Sci, Brain & Mental Hlth Lab, Clayton, Vic, Australia
[3] Univ Newcastle, Sch Med & Publ Hlth, Discipline Clin Pharmacol, Callaghan, NSW, Australia
[4] Australian Ctr Cannabinoid Clin & Res Excellence, New Lambton Hts, Australia
基金
澳大利亚研究理事会;
关键词
CA1; cannabidiol; cannabis; hippocampal subfields; hippocampus; subiculum; BRAIN; SYMPTOMS; DELTA-9-TETRAHYDROCANNABINOL; PSYCHOSIS; MEMORY; INDIVIDUALS; SUBICULUM; COGNITION; SHAPE; RISK;
D O I
10.1089/can.2017.0047
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Chronic cannabis use is associated with neuroanatomical alterations in the hippocampus. While adverse impacts of cannabis use are generally attributed to Delta (9)-tetrahydrocannabinol, emerging naturalistic evidence suggests cannabidiol (CBD) is neuroprotective and may ameliorate brain harms associated with cannabis use, including protection from hippocampal volume loss. This study examined whether prolonged administration of CBD to regular cannabis users within the community could reverse or reduce the characteristic hippocampal harms associated with chronic cannabis use. Materials and Methods: Eighteen regular cannabis users participated in an similar to 10-week open-label pragmatic trial involving daily oral administration of 200mg CBD, with no change to their ongoing cannabis use requested. Participants were assessed at baseline and post-CBD treatment using structural magnetic resonance imaging. Automated longitudinal hippocampal segmentation was performed to assess volumetric change over the whole hippocampus and within 12 subfields. Results: No change was observed in left or right hippocampus as a whole. However, left subicular complex (parasubiculum, presubiculum, and subiculum) volume significantly increased from baseline to post-treatment (p=0.017 uncorrected) by 1.58% (Cohen's d=0.63; 2.83% in parasubiculum). Heavy cannabis users demonstrated marked growth in the left subicular complex, predominantly within the presubiculum, and right cornu ammonis (CA)1 compared to lighter users. Associations between greater right subicular complex and total hippocampal volume and higher plasma CBD concentration were evident, particularly in heavy users. Conclusions: Our findings suggest a restorative effect of CBD on the subicular and CA1 subfields in current cannabis users, especially those with greater lifetime exposure to cannabis. While replication is required in a larger, placebo-controlled trial, these findings support a protective role of CBD against brain structural harms conferred by chronic cannabis use. Furthermore, these outcomes suggest that CBD may be a useful adjunct in treatments for cannabis dependence and may be therapeutic for a range of clinical disorders characterized by hippocampal pathology (e.g., schizophrenia, Alzheimer's disease, and major depressive disorder).
引用
收藏
页码:94 / 107
页数:14
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