Dorsal hippocampus cannabinoid type 1 receptors modulate the expression of contextual fear conditioning in rats: Involvement of local glutamatergic/nitrergic and GABAergic neurotransmissions

被引:18
|
作者
Spiacci, Gabriela B. L. [1 ]
Antero, Leandro S. [1 ]
Reis, Daniel G. [1 ]
Lisboa, Sabrina F. [1 ]
Resstel, Leonardo B. [1 ]
机构
[1] Univ Sao Paulo, Med Sch Ribeirao Preto, Dept Pharmacol, Av Bandeirantes 3900, BR-14049900 Ribeirao Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Endocannabinoid system; CB1; receptors; NMDA receptors; Nitric oxide; Freezing behavior; Autonomic responses; ELEVATED PLUS-MAZE; DORSOLATERAL PERIAQUEDUCTAL GRAY; PREFRONTAL CORTEX MODULATE; ANXIETY-LIKE BEHAVIOR; OXIDE-CGMP PATHWAY; NITRIC-OXIDE; RESTRAINT STRESS; REVERSIBLE INACTIVATION; ENDOCANNABINOID SYSTEM; VENTRAL HIPPOCAMPUS;
D O I
10.1016/j.euroneuro.2016.08.010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The cannabinoid receptor type 1 (CB1) is highly expressed in the dorsal portion of hippocampus - a brain region that has been involved in the control of conditioned emotional response (CER) in the contextual fear conditioning (CFC) model. These responses are characterized by increased freezing behavior and autonomic parameters. Moreover, CB1 receptors activation negatively modulate the release of several neurotransmitters, including glutamate and GABA, which also have been related to modulation of CER. Therefore, our aim was to investigate the involvement of CB1 receptors in the dorsal hippocampus on CER expression. Independent groups of male Wistar rats submitted to the contextual fear conditioning received bilateral intrahippocampal injections (500 nL/side) of the following drugs or vehicle before re-exposure to the aversive context: AM251 (CB1 antagonist; 0.1, 0.3 and 1 nmol); AP7 (NMDA antagonist; 1nmol)+AM251 (0.3 nmol); NPLA (0.01 nmol; nNOS inhibitor)+AM251 (0.3 nmol); Bicuculline (1.3 pmol; GABA(A) antagonist)+AM251 (0.1 and 1 nmol). In the present paper, AM251 (0.3 nmol) increased CER, while this response was prevented by both AP7 and NPLA pretreatment. After pretreatment with Bicuculline, the lower and higher ineffective doses of AM251 were able to increase the CER, supporting the balance between GABAergic and glutamatergic mechanisms controlling this response. Our results suggest that increased CER evoked by CB1 blockade in the dorsal hippocampus depends on NMDA receptor activation and NO formation. Moreover, a fine-tune control promoted by GABAergic and glutamatergic mechanisms in this brain area modulate the CER after CBI blockade. (C) 2016 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:1579 / 1589
页数:11
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