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      Morphological evidence for a neurotensinergic periaqueductal gray-rostral ventromedial medulla-spinal dorsal horn descending pathway in rat

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          Abstract

          Neurotensin (NT) is an endogenous neuropeptide that exerts potent opioid-independent analgesic effects, most likely via the type 2 NT receptor (NTR2). Previous morphological and electrophysiological studies suggested that the NT-NTR2 system is primarily localized in structures that constitute the descending pain control pathway, such as the periaqueductal gray (PAG), the rostral ventromedial medulla (RVM), and the spinal dorsal horn (SDH). However, relevant morphological evidence for this neurotensinergic (NTergic) circuit is lacking. Thus, the aim of the present study was to morphologically elucidate the potential sites and connections in the NT-NTR2 system that are involved in the descending pain control pathway. Based on light and electron microscopy combined with anterograde and retrograde tracing, we found evidence that NTR2-immunoreactive (IR) neurons in the RVM receive NT-IR projections originating from the PAG; express NT, serotonin (5-HT), or both; and send projections that terminate in laminae I and II of the SDH. These results suggest that NTR2 may contribute to pain control by binding to NT in the PAG-RVM-SDH pathway. In conclusion, our data provide morphological evidence for an NTergic PAG-RVM-SDH pathway, implicating novel mechanisms of NT-induced analgesia.

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          Most cited references36

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          The isolation of a new hypotensive peptide, neurotensin, from bovine hypothalami.

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            Neurotensin and neurotensin receptors.

            Neurotensin is a brain and gastrointestinal peptide that fulfils many central and peripheral functions through its interaction with specific receptors. Three subtypes of neurotensin receptors have been cloned. Two of them belong to the family of G protein-coupled receptors, whereas the third one is an entirely new type of neuropeptide receptor and is identical to gp95/sortilin, a 100 kDa-protein with a single transmembrane domain. In this review, the present knowledge regarding the molecular and pharmacological properties of the three cloned neurotensin receptors is summarized and the relationship between these receptors and the known pharmacological effects of neurotensin is discussed.
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              Pain genetics: past, present and future.

              Chronic pain is a classic example of gene × environment interaction: inflammatory and/or nerve injuries are known or suspected to be the etiology of most chronic pain syndromes, but only a small minority of those subjected to such injuries actually develop chronic pain. Once chronic pain has developed, pain severity and analgesic response are also highly variable among individuals. Although animal genetics studies have been ongoing for over two decades, only recently have comprehensive human twin studies and large-scale association studies been performed. Here, I review recent and accelerating progress in, and continuing challenges to, the identification of genes contributing to such variability. Success in this endeavor will hopefully lead to both better management of pain using currently available therapies and the development and/or prioritizing of new ones. Copyright © 2012 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Front Neuroanat
                Front Neuroanat
                Front. Neuroanat.
                Frontiers in Neuroanatomy
                Frontiers Media S.A.
                1662-5129
                09 October 2014
                2014
                : 8
                : 112
                Affiliations
                [1] 1Department of Anatomy, Histology and Embryology & K.K. Leung Brain Research Centre, Preclinical School of Medicine, The Fourth Military Medical University Xi’an, China
                [2] 2Department of Geriatrics, Xijing Hospital, The Fourth Military Medical University Xi’an, China
                Author notes

                Edited by: Javier DeFelipe, Cajal Institute, Spain

                Reviewed by: Alino Martinez-Marcos, Universidad de Castilla, Spain; Amber Virya King Buhler, Pacific University, USA

                *Correspondence: Jin-Shan Zhang and Yun-Qing Li, Department of Anatomy, Histology and Embryology & K.K. Leung Brain Research Centre, Preclinical School of Medicine, The Fourth Military Medical University, No.169, West Changle Road, Xi’an 710032, China e-mail: jszhang@ 123456fmmu.edu.cn ; deptanat@ 123456fmmu.edu.cn

                These authors have contributed equally to this work.

                This article was submitted to the journal Frontiers in Neuroanatomy.

                Article
                10.3389/fnana.2014.00112
                4191475
                25346662
                28678c43-116e-4be1-98a5-6f59b871f374
                Copyright © 2014 Wang, Zhang, Feng, Meng, Wu, Wang, Li, Zhang, Zhang and Li.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 02 July 2014
                : 22 September 2014
                Page count
                Figures: 6, Tables: 2, Equations: 0, References: 38, Pages: 11, Words: 7218
                Categories
                Neuroscience
                Original Research Article

                Neurosciences
                neurotensin,ntr2,periaqueductal gray matter,rostral ventromedial medulla (rvm),nociception,analgesia

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