Endocannabinoid receptors contribute significantly to multiple forms of long-term depression in the rat dentate gyrus

被引:8
|
作者
Fontaine, Christine J. [1 ]
Grafe, Erin L. [1 ]
Pinar, Cristina [1 ]
Bonilla-Del Rio, Itziar [2 ,3 ]
Grandes, Pedro [1 ,2 ,3 ]
Christie, Brian R. [1 ,4 ,5 ]
机构
[1] Univ Victoria, Div Med Sci, Victoria, BC V8W 2Y2, Canada
[2] Univ Basque Country UPV EHU, Fac Med & Nursing, Dept Neurosci, E-48940 Leioa, Spain
[3] Univ Basque Country UPV EHU, Achucarro Basque Ctr Neurosci, Sci Pk, E-48940 Leioa, Spain
[4] Univ British Columbia, Isl Med Program, Victoria, BC, Canada
[5] Univ British Columbia, Dept Cellular & Physiol Sci, Victoria, BC, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
OCULAR DOMINANCE COLUMNS; PATH-GRANULE CELL; SYNAPTIC PLASTICITY; AMPA RECEPTORS; CA2+ CHANNELS; FLIP SIDE; AREA CA1; HIPPOCAMPUS; INDUCTION; LTD;
D O I
10.1101/lm.050666.119
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cannabinoid receptors are widely expressed throughout the hippocampal formation, but are particularly dense in the dentate gyrus (DG) subregion. We, and others, have shown in mice that cannabinoid type 1 receptors (CB1Rs) are involved in a long-term depression (LTD) that can be induced by prolonged 10 Hz stimulation of the medial perforant path (MPP)-granule cell synaptic input to the DG. Here, we extend this work to examine the involvement of CB1Rs in other common forms of LTD in the hippocampus of juvenile male and female Sprague-Dawley rats (Rattus norvegicus). We found, as in mice, that prolonged 10 Hz stimulation (6000 pulses) could reliably induce a form of LTD that was dependent upon CB1R activation. In addition, we also discovered a role for both CB1R and mGluR proteins in LTD induced with 1 Hz low-frequency stimulation (1 Hz-LTD; 900 pulses) and in LTD induced by bath application of the group I mGluR agonist (RS)-3,5-Dihydroxyphenylglycine (DHPG; DHPG-LTD). This study elucidates an essential role for endocannabinoid receptors in a number of forms of LTD in the rat DG, and identifies a novel role for CB1Rs as potential therapeutic targets for conditions that involve impaired LTD in the DG.
引用
收藏
页码:380 / 389
页数:10
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