Department of Psychology, Utah State University, Logan, UT, USA.
Department of Biology, Utah State University, Logan, UT, USA.
Transl Psychiatry. 2022 May 31;12(1):217. doi: 10.1038/s41398-022-01967-1.
Neuroscience research presents contradictory evidence in support of both the protective and destructive effects of cannabinoids in depression. Therefore, this systematic review and meta-analysis summarizes the existing preclinical literature on the effects of cannabinoid administration in the chronic unpredictable stress model of depression in order to evaluate the effects of cannabinoids and identify gaps in the literature. After protocol registration (PROSPERO #CRD42020219986), we systematically searched Scopus, Embase, Psychology & Behavioral Sciences Collection, APA PsychINFO, PubMed, CINAHL Complete, and ProQuest Dissertations & Theses Global from the earliest record of the databases, February 1964, to November 2020 for articles that met inclusion criteria (e.g., rodent subjects and administration of a cannabinoid. A total of 26 articles were included representing a sample size estimate of 1132 rodents with the majority of articles administering daily intraperitoneal injections during chronic unpredictable stress. These articles were evaluated using a modified SYRCLE's risk-of-bias tool. For each continuous behavioral measure, the standardized mean difference was calculated between cannabinoid and vehicle groups in rodents subjected to chronic unpredictable stress. The effects of cannabinoids on depressive-like behavior was evaluated using a multilevel mixed-effects model with effect size weights nested within control groups. Cannabinoid administration moderately improved the pooled negative effects of chronic unpredictable stress on anhedonia, learned helplessness, novelty suppressed feeding, time in the anxiogenic context, and entries into the anxiogenic context. Although the interpretations are limited, these findings suggest that with further investigation, cannabinoids may be a viable long-term treatment for stress-related psychopathologies such as depression.
神经科学研究提供了相互矛盾的证据,支持大麻素在抑郁症中有保护和破坏作用。因此,本系统评价和荟萃分析总结了现有的关于大麻素给药在慢性不可预测应激抑郁模型中的作用的临床前文献,以评估大麻素的作用并确定文献中的空白。在方案注册(PROSPERO #CRD42020219986)后,我们系统地检索了 Scopus、Embase、心理学与行为科学收藏、APA PsychINFO、PubMed、CINAHL Complete 和 ProQuest Dissertations & Theses Global,从数据库最早的记录(1964 年 2 月)到 2020 年 11 月,以查找符合纳入标准的文章(例如,啮齿动物受试者和大麻素给药。共有 26 篇文章符合纳入标准,代表了 1132 只啮齿动物的样本量估计,其中大多数文章在慢性不可预测应激期间每天进行腹膜内注射。使用改良的 SYRCLE 偏倚风险工具对这些文章进行了评估。对于每个连续的行为测量,在经历慢性不可预测应激的啮齿动物中,计算大麻素和载体组之间的标准化均数差值。使用多层混合效应模型,根据对照组嵌套的效应大小权重,评估大麻素对抑郁样行为的影响。大麻素给药适度改善了慢性不可预测应激对快感缺失、习得性无助、新奇抑制性摄食、焦虑环境中的时间和进入焦虑环境的负面综合影响。尽管解释有限,但这些发现表明,随着进一步研究,大麻素可能是一种可行的治疗与压力相关的精神病理疾病(如抑郁症)的长期治疗方法。