CB1 cannabinoid receptor-mediated anandamide signalling reduces the defensive behaviour evoked through GABAA receptor blockade in the dorsomedial division of the ventromedial hypothalamus

被引:35
作者
dos Anjos-Garcia, Tayllon [1 ]
Ullah, Farhad [1 ]
Falconi-Sobrinho, Luiz Luciano [1 ]
Coimbra, Norberto Cysne [1 ,2 ]
机构
[1] Univ Sao Paulo, Lab Neuroanat & Neuropsychobiol, Dept Pharmacol, Ribeirao Preto Med Sch, Av Bandeirantes 3900, BR-14049900 Ribeirao Preto, SP, Brazil
[2] FMRP USP, NAP Neurobiol Emot NuPNE, Res Ctr, Ribeirao Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Endocannabinoid neuromodulators; GABA(A) receptor; Ventromedial hypothalamus; Defensive behaviour; CB1 cannabinoid receptor; TRPV1; channel; FEAR-INDUCED ANTINOCICEPTION; DORSOLATERAL PERIAQUEDUCTAL GRAY; GLUTAMIC-ACID DECARBOXYLASE; MESENCEPHALIC CENTRAL GRAY; ANXIETY-LIKE BEHAVIOR; PANIC-LIKE RESPONSES; PREFRONTAL CORTEX; TRPV1; RECEPTORS; RAT-BRAIN; MODULATION;
D O I
10.1016/j.neuropharm.2016.04.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of cannabinoids in brain areas expressing cannabinoid receptors, such as hypothalamic nuclei, are not yet well known. Several studies have demonstrated the role of hypothalamic nuclei in the organisation of behavioural responses induced through innate fear and panic attacks. Panic-prone states are experimentally induced in laboratory animals through a reduction in the GABAergic activity. The aim of the present study was to examine panic-like elaborated defensive behaviour evoked by GABA(A) receptor blockade with bicuculline (BIC) in the dorsomedial division of the ventromedial hypothalamus (VMHdm). We also aimed to characterise the involvement of endocannabinoids and the CB1 cannabinoid receptor in the modulation of elaborated defence behavioural responses organised with the VMHdm. The guide-cannula was stereotaxicaly implanted in VMHdm and the animals were treated with anandamide (AEA) at different doses, and the effective dose was used after the pre-treatment with the CB1 receptor antagonist AM251, followed by GABA(A) receptor blockade in VMHdm. The results showed that the intra-hypothalamic administration of AEA at an intermediate dose (5 pmol) attenuated defence responses induced through the intra-VMHdm microinjection of bicuculline (40 ng). This effect, however, was inhibited when applied central microinjection of the CB1 receptor antagonist AM251 in the VMHdm. Moreover, AM251 potentiates de non-oriented escape induced by bicuculline, effect blocked by pretreatment with the TRPV1 channel antagonist 6-I-CPS. These results indicate that AEA modulates the pro-aversive effects of intra-VMHdm-bicuculline treatment, recruiting CB1 cannabinoid receptors and the TRPV1 channel is involved in the AM251-related potentiation of bicuculline effects on non-oriented escape behaviour. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:156 / 166
页数:11
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