Excitatory orexinergic innervation of rat nucleus incertus - Implications for ascending arousal, motivation and feeding control

被引:30
作者
Blasiak, Anna [1 ]
Siwiec, Marcin [1 ]
Grabowiecka, Agnieszka [1 ]
Blasiak, Tomasz [1 ]
Czerw, Anna [1 ]
Blasiak, Ewa [2 ]
Kania, Alan [1 ]
Rajfur, Zenon [3 ]
Lewandowski, Marian H. [1 ]
Gundlach, Andrew L. [4 ,5 ,6 ]
机构
[1] Jagiellonian Univ, Dept Neurophysiol & Chronobiol, Inst Zool, PL-30387 Krakow, Poland
[2] Jagiellonian Univ, Dept Phys Biochem, Fac Biochem Biophys & Biotechnol, PL-30387 Krakow, Poland
[3] Jagiellonian Univ, Inst Phys, Fac Phys Astron & Appl Comp Sci, PL-30348 Krakow, Poland
[4] Florey Inst Neurosci & Mental Hlth, Parkville, Vic 3052, Australia
[5] Univ Melbourne, Florey Dept Neurosci & Mental Hlth, Melbourne, Vic 3010, Australia
[6] Univ Melbourne, Dept Anat & Neurosci, Melbourne, Vic 3010, Australia
关键词
Arousal; In vitro electrophysiology; Motivated behaviours; Neural tract-tracing; Orexin/OX1/2; Relaxin-3/RXFP3; VENTRAL TEGMENTAL AREA; REGULATES ALCOHOL-SEEKING; RECEPTOR MESSENGER-RNA; ANXIETY-LIKE BEHAVIOR; CALCIUM-CHANNELS; DORSAL RAPHE; LATERODORSAL TEGMENTUM; LOCUS-COERULEUS; KNOCKOUT MICE; WEIGHT-GAIN;
D O I
10.1016/j.neuropharm.2015.08.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Orexin/hypocretin peptides play a central role in the integrated control of feeding/reward and behavioural activation, principally via interactions with other neural systems. A brainstem area involved in behavioural activation is the nucleus incertus (NI), located in the posterior ventromedial central grey. Several studies have implicated NI in control of arousal/stress and reward/feeding responses. Orexin receptor mRNA expression identifies NI as a putative target of orexin modulation. Therefore, in this study we performed neural tract-tracing and immunofluorescence staining to characterise the orexinergic innervation of NI. Our results indicate a convergent innervation of the NI area by different orexin neuron populations, with an abundance of orexin-A-containing axons making putative synaptic contacts with relaxin-3-positive NI neurons. The influence of orexin-A on NI neuron activity was investigated using patch-clamp recordings. Orexin-A depolarised the majority (64%) of recorded neurons and this effect was maintained in the presence of tetrodotoxin and glutamate and GABA receptor antagonists, indicating a likely postsynaptic action. Voltage-clamp experiments revealed that in 'type I' NI neurons comprising relaxin-3-positive cells, orexin-A acted via L-type calcium channels, whereas in 'type II' relaxin-3-negative neurons, activation of a sodium/calcium exchanger was involved. A majority of the orexin-A sensitive neurons tested for the presence of orexin receptor mRNA, were OX2 mRNA-positive. Immunohistochemical staining for putative orexin receptors on NI neurons, confirmed stronger expression of OX2 than OX1 receptors. Our data demonstrate a strong influence of orexin-A on NI neurons, consistent with an important role for this hypothalamic/tegmental circuit in the regulation of arousal/vigilance and motivated behaviours. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:432 / 447
页数:16
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