Neurotensin enhances glutamatergic EPSCs in VTA neurons by acting on different neurotensin receptors

被引:14
作者
Bose, Poulomee [1 ]
Rompre, Pierre-Paul [2 ]
Warren, Richard A. [1 ]
机构
[1] Univ Montreal, Dept Psychiat, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Dept Neurosci, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
Neurotensin; Ventral tegmental area; Glutamatergic EPSCs; SR142948A; SR48692; VENTRAL TEGMENTAL AREA; DOPAMINE NEURONS; BEHAVIORAL SENSITIZATION; ENDOGENOUS NEUROTENSIN; NUCLEUS-ACCUMBENS; RAT; BINDING; CONDUCTANCE; ACTIVATION; RELEASE;
D O I
10.1016/j.peptides.2015.08.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurotensin (NT) is an endogenous neuropeptide that modulates dopamine and glutamate neurotransmission in several limbic regions innervated by neurons located in the ventral tegmental area (VTA). While several studies showed that NT exerted a direct modulation on VTA dopamine neurons less is known about its role in the modulation of glutamatergic neurotransmission in this region. The present study was aimed at characterising the effects of NT on glutamate-mediated responses in different populations of VTA neurons. Using whole cell patch clamp recording technique in horizontal rat brain slices, we measured the amplitude of glutamatergic excitatory post-synaptic currents (EPSCs) evoked by electrical stimulation of VTA afferents before and after application of different concentrations of NT1-13 or its Cterminal fragment, NT8-13. Neurons were classified as either I-h(+) or I-h(-) based on the presence or absence of a hyperpolarisation activated cationic current (I-h). We found that NT1-13 and NT8-13 produced comparable concentration dependent increase in the amplitude of EPSCs in both Ih' and neurons. In I-h(+) neurons, the enhancement effect of NT8-13 was blocked by both antagonists, while in neurons it was blocked by the NTS1/NTS2 antagonist, SR142948A, but not the preferred NTS1 antagonist, SR48692. In as much as neurons are non-dopaminergic neurons and I-h(+) neurons represent both dopamine and nondopamine neurons, we can conclude that NT enhances glutamatergic mediated responses in dopamine, and in a subset of non-dopamine, neurons by acting respectively on NTS1 and an NT receptor other than NTS1. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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