Tonic enhancement of endocannabinoid-mediated retrograde suppression of inhibition by cholinergic interneuron activity in the striatum

被引:107
作者
Narushima, Madoka
Uchigashima, Motokazu
Fukaya, Masahiro
Matsui, Minoru
Manabe, Toshiya
Hashimoto, Kouichi
Watanabe, Masahiko
Kano, Masanobu [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Cellular Neurosci, Suita, Osaka 5650871, Japan
[2] Kanazawa Univ, Grad Sch Med Sci, Dept Cellular Neurophysiol, Kanazawa, Ishikawa 9208640, Japan
[3] Japan Sci & Technol Agcy, Tokyo 1028666, Japan
[4] Hokkaido Univ, Sch Med, Dept Anat, Sapporo, Hokkaido 0608638, Japan
[5] Univ Tokyo, Inst Med Sci, Dept Basic Med Sci, Div Nueronal Network, Tokyo 1088639, Japan
关键词
CB1; receptor; acetylcholine; muscarinic receptor; DSI; medium spiny neuron; basal ganglia;
D O I
10.1523/JNEUROSCI.4644-06.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tonically active cholinergic interneurons in the striatum modulate activities of striatal outputs from medium spiny (MS) neurons and significantly influence overall functions of the basal ganglia. Cellular mechanisms of this modulation are not fully understood. Here we show that ambient acetylcholine (ACh) derived from tonically active cholinergic interneurons constitutively upregulates depolarizationinduced release of endocannabinoids from MS neurons. The released endocannabinoids cause transient suppression of inhibitory synaptic inputs to MS neurons through acting retrogradely onto presynaptic CB1 cannabinoid receptors. The effects were mediated by postsynaptic M-1 subtype of muscarinic ACh receptors, because the action of a muscarinic agonist to release endocannabinoids and the enhancement of depolarization-induced endocannabinoid release by ambient ACh were both deficient in M-1 knock-out mice and were blocked by postsynaptic infusion of guanosine-5'-O-(2-thiodiphosphate). Suppression of spontaneous firings of cholinergic interneurons by inhibiting I-h current reduced the depolarization-induced release of endocannabinoids. Conversely, elevation of ambient ACh concentration by inhibiting choline esterase significantly enhanced the endocannabinoid release. Paired recording from a cholinergic interneuron and an MS neuron revealed that the activity of single cholinergic neuron could influence endocannabinoid-mediated signaling in neighboring MS neurons. These results clearly indicate that striatal endocannabinoid-mediated modulation is under the control of cholinergic interneuron activity. By immunofluorescent and immunoelectron microscopic examinations, we demonstrated that M-1 receptor was densely distributed in perikarya and dendrites of dopamine D-1 or D-2 receptor-positive MS neurons. Thus, we have disclosed a novel mechanism by which the muscarinic system regulates striatal output and may contribute to motor control.
引用
收藏
页码:496 / 506
页数:11
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