Singh Uday, Kumar Santosh, Shelkar Gajanan P, Yadav Manoj, Kokare Dadasaheb M, Goswami Chandan, Lechan Ronald M, Singru Praful S
School of Biological Sciences, National Institute of Science Education and Research (NISER)-Bhubaneswar, 752050, Odisha, India.
Department of Pharmaceutical Sciences, R.T.M. Nagpur University, Nagpur, 440033, Maharashtra, India.
Neuropharmacology. 2016 Nov;110(Pt A):198-210. doi: 10.1016/j.neuropharm.2016.04.012. Epub 2016 Apr 12.
While dopamine (DA) neurons in the ventral tegmental area (VTA) drive the mesolimbic-reward pathway, confluent lines of evidence underscore the importance of transient receptor potential vanilloid (TRPV) channels as novel regulators of these neurons. Among the TRPV-subfamily, TRPV3 is of particular interest in reward, since active ingredients of flavour-enhancing spices in food serve as TRPV3 agonists and modulate DAergic neurotransmission. The nature of TRPV3 elements in the VTA and their role in driving the mesolimbic-DA-reward pathway has however, remained unexplored. We observed TRPV3 mRNA as well as TRPV3-immunoreactive neurons in the VTA of Wistar rats. We therefore explored whether these ion channels participate in modulating mesolimbic-DA reward pathway. In the posterior VTA (pVTA), 82 ± 2.6% of the TRPV3 neurons co-express tyrosine hydroxylase and 68 ± 5.5% of these neurons project to the nucleus accumbens shell (Acb shell). While ex vivo treatment of midbrain slices with TRPV3-agonist, thymol increased [Ca(2+)]i-activity in pVTA neurons, intra-pVTA injections of thymol in freely-moving, satiated rats enhanced positive reinforcement for active lever pressings in an operant chamber to self-administer sweet pellets. This behavior was attenuated by prior treatment with intra-Acb shell DA D1- and D2-like receptor antagonists. These results demonstrate a role for TRPV3 in driving mesolimbic-DA food-reward pathway, and underscores the importance of these channels in the VTA as key components processing reward.
虽然腹侧被盖区(VTA)中的多巴胺(DA)神经元驱动中脑边缘奖赏通路,但一系列证据强调了瞬时受体电位香草酸(TRPV)通道作为这些神经元新型调节因子的重要性。在TRPV亚家族中,TRPV3在奖赏方面特别受关注,因为食物中增强风味香料的活性成分可作为TRPV3激动剂并调节多巴胺能神经传递。然而,VTA中TRPV3元件的性质及其在驱动中脑边缘多巴胺奖赏通路中的作用仍未得到探索。我们在Wistar大鼠的VTA中观察到了TRPV3 mRNA以及TRPV3免疫反应性神经元。因此,我们探究了这些离子通道是否参与调节中脑边缘多巴胺奖赏通路。在VTA后部(pVTA),82±2.6%的TRPV3神经元共表达酪氨酸羟化酶,其中68±5.5%的神经元投射到伏隔核壳(Acb壳)。虽然用TRPV3激动剂百里酚对中脑切片进行离体处理可增加pVTA神经元中的[Ca(2+)]i活性,但在自由活动、已饱食的大鼠中向pVTA内注射百里酚可增强其在操作性条件反射箱中主动按压杠杆以自我给药甜味颗粒的正强化作用。这种行为可被预先用Acb壳内多巴胺D1和D2样受体拮抗剂处理所减弱。这些结果证明了TRPV3在驱动中脑边缘多巴胺食物奖赏通路中的作用,并强调了VTA中这些通道作为处理奖赏的关键成分的重要性。