Suppr超能文献

向腹内侧前额叶皮质注射大麻二酚的抗抑郁样作用——5-HT1A和CB1受体的可能参与

Antidepressant-like effect of cannabidiol injection into the ventral medial prefrontal cortex-Possible involvement of 5-HT1A and CB1 receptors.

作者信息

Sartim A G, Guimarães F S, Joca S R L

机构信息

Department of Physical and Chemical, School of Pharmaceutical Science of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.

Department of Pharmacology, School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil; Center for Interdisciplinary Research on Applied Neurosciences (NAPNA), University of São Paulo, Brazil.

出版信息

Behav Brain Res. 2016 Apr 15;303:218-27. doi: 10.1016/j.bbr.2016.01.033. Epub 2016 Jan 20.

Abstract

RATIONALE

Systemic administration of cannabidiol (CBD), the main non-psychotomimetic constituent of Cannabis sativa, induces antidepressant-like effects. The mechanism of action of CBD is thought to involve the activation of 5-HT1A receptors and the modulation of endocannabinoid levels with subsequent CB1 activation. The brain regions involved in CBD-induced antidepressant-like effects remain unknown. The ventral medial prefrontal cortex (vmPFC), which includes the infralimbic (IL) and prelimbic (PL) subregions, receives dense serotonergic innervation and plays a significant role in stress responses.

OBJECTIVE

To test the hypothesis that the administration of CBD into the IL or PL would induce an antidepressant-like effect through 5-HT1A and CB1 activation.

METHODS

Rats received intra-IL or -PL microinjections of CBD (10-60 nmol/side), 8-OH-DPAT (5-HT1A agonist, 5-10 nmol/side), anandamide (AEA, 0.5 pmol/side) or vehicle (0.2 μl/side) and were submitted to the forced swimming (FST) or to the open field (OFT) tests. Independent CBD-treated groups were pre-treated with WAY100635 (10, 30 nmol/side, 5-HT1A antagonist) or AM251 (10 pmol/side, CB1 antagonist) and submitted to the same tests. An additional group was treated with WAY100635 followed by anandamide.

RESULTS

CBD (PL: 10-60 nmol; IL:45-60 nmol) and 8-OH-DPAT (10 nmol) administration significantly reduced the immobility time in the FST, without changing locomotor activity in the OFT. WAY100635 (30 nmol) did not induce effect per se but blocked CBD, 8-OH-DPAT and AEA effects. Additionally, AM251 blocked CBD-effects.

CONCLUSION

administration of CBD into the vmPFC induces antidepressant-like effects possibly through indirect activation of CB1 and 5-HT1A receptors.

摘要

理论依据

大麻二酚(CBD)是大麻的主要非致幻成分,全身给药可诱导出抗抑郁样效应。CBD的作用机制被认为涉及5-HT1A受体的激活以及内源性大麻素水平的调节,随后激活CB1。参与CBD诱导抗抑郁样效应的脑区尚不清楚。腹内侧前额叶皮层(vmPFC)包括下边缘区(IL)和前边缘区(PL),接受密集的5-羟色胺能神经支配,并在应激反应中起重要作用。

目的

验证向IL或PL注射CBD可通过激活5-HT1A和CB1诱导抗抑郁样效应这一假设。

方法

给大鼠在IL或PL内微量注射CBD(10 - 60 nmol/侧)、8-OH-DPAT(5-HT1A激动剂,5 - 10 nmol/侧)、花生四烯乙醇胺(AEA,0.5 pmol/侧)或溶剂(0.2 μl/侧),然后进行强迫游泳(FST)或旷场试验(OFT)。独立的CBD处理组预先用WAY100635(10、30 nmol/侧,5-HT1A拮抗剂)或AM251(10 pmol/侧,CB1拮抗剂)处理,然后进行相同试验。另一组先用WAY100635处理,随后用花生四烯乙醇胺处理。

结果

注射CBD(PL:10 - 60 nmol;IL:45 - 60 nmol)和8-OH-DPAT(10 nmol)可显著减少FST中的不动时间,而不改变OFT中的运动活性。WAY100635(30 nmol)本身无效应,但可阻断CBD、8-OH-DPAT和AEA的效应。此外,AM251可阻断CBD的效应。

结论

向vmPFC注射CBD可能通过间接激活CB1和5-HT1A受体诱导抗抑郁样效应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验