Cholinergic and glutamatergic transmission at synapses between pedunculopotine tegmental nucleus axonal terminals and A7 catecholamine cell group noradrenergic neurons in the rat

被引:1
|
作者
Li, Meng-Jiyuan [1 ,2 ]
Chang, Tien-Wei [1 ,2 ]
Hung, Wei-Chen [1 ,2 ]
Wu, Chieh-Yi [1 ,2 ]
Luo, Yu-Cheng [1 ,2 ]
Chang, Ting-Hsuan [2 ]
Lin, Chingju [4 ]
Yang, Chi-Sheng [5 ]
Yang, Hsiu-Wen [6 ,7 ]
Min, Ming-Yuan [1 ,2 ,3 ]
机构
[1] Natl Taiwan Univ, Inst Zool, Taipei 107, Taiwan
[2] Natl Taiwan Univ, Dept Life Sci, 1 Roosevelt Rd,Sec 4, Taipei 107, Taiwan
[3] Natl Taiwan Univ, Ctr Neurobiol & Cognit Sci, Taipei 107, Taiwan
[4] China Med Univ, Sch Med, Dept Physiol, Taichung 402, Taiwan
[5] Hung Kuang Univ, Dept Nutr, Taichung, Taiwan
[6] Chung Shan Med Univ, Dept Biomed Sci, Taichung 401, Taiwan
[7] Chung Shan Med Univ, Dept Med Res, Taichung 401, Taiwan
关键词
Asynchronous release; Locus coeruleus; Muscarinic receptor; Pain; MEDIATED TONIC INHIBITION; LOCUS-CERULEUS ACTIVATION; ASYNCHRONOUS RELEASE; TRP CHANNELS; COERULEUS; ANTINOCICEPTION; PAIN; ACETYLCHOLINE; STIMULATION; MODULATION;
D O I
10.1016/j.neuropharm.2016.07.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We characterized transmission from the pedunculopotine tegmental nucleus (PPTg), which contains cholinergic and glutamatergic neurons, at synapses with noradrenergic (NAergic) A7 neurons. Injection of an anterograde neuronal tracer, biotinylated-dextran amine, into the PPTg resulted in labeling of axonal terminals making synaptic connection with NAergic A7 neurons. Consistent with this, extracellular stimulation using a train of 10 pulses at 100 Hz evoked both fast and slow excitatory synaptic currents (EPSCs) that were blocked, respectively, by DNQX, a non-N-methyl-D-aspartate receptor blocker, or atropine, a cholinergic muscarinic receptor (mAChR) blocker. Interestingly, many spontaneous-like, but stimulation-dependent, EPSCs, were seen for up to one second after the end of stimulation and were blocked by DNQX and decreased by EGTA-AM, a membrane permeable form of EGTA, showing they are glutamatergic EPSCs causing by asynchronous release of vesicular quanta. Moreover, application of atropine or carbachol, an mAChR agonist, caused, respectively, an increase in the number of asynchronous EPSCs or a decrease in the frequency of miniature EPSCs, showing that mAChRs mediated pre synaptic inhibition of glutamatergic transmission of the PPTg onto NAergic A7 neurons. In conclusion, our data show direct synaptic transmission of PPTg afferents onto pontine NAergic neurons that involves cooperation of cholinergic and glutamatergic transmission. This dual-transmitter transmission drives the firing rate of NAergic neurons, which may correlate with axonal and somaticidendritic release of NA. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:237 / 250
页数:14
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