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      Early Neonatal Pain—A Review of Clinical and Experimental Implications on Painful Conditions Later in Life

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          Abstract

          Modern health care has brought our society innumerable benefits but has also introduced the experience of pain very early in life. For example, it is now routine care for newborns to receive various injections or have blood drawn within 24 h of life. For infants who are sick or premature, the pain experiences inherent in the required medical care are frequent and often severe, with neonates requiring intensive care admission encountering approximately fourteen painful procedures daily in the hospital. Given that much of the world has seen a steady increase in preterm births for the last several decades, an ever-growing number of babies experience multiple painful events before even leaving the hospital. These noxious events occur during a critical period of neurodevelopment when the nervous system is very vulnerable due to immaturity and neuroplasticity. Here, we provide a narrative review of the literature pertaining to the idea that early life pain has significant long-term effects on neurosensory, cognition, behavior, pain processing, and health outcomes that persist into childhood and even adulthood. We refer to clinical and pre-clinical studies investigating how early life pain impacts acute pain later in life, focusing on animal model correlates that have been used to better understand this relationship. Current knowledge around the proposed underlying mechanisms responsible for the long-lasting consequences of neonatal pain, its neurobiological and behavioral effects, and its influence on later pain states are discussed. We conclude by highlighting that another important consequence of early life pain may be the impact it has on later chronic pain states—an area of research that has received little attention.

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          Most cited references200

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          Different immune cells mediate mechanical pain hypersensitivity in male and female mice.

          A large and rapidly increasing body of evidence indicates that microglia-to-neuron signaling is essential for chronic pain hypersensitivity. Using multiple approaches, we found that microglia are not required for mechanical pain hypersensitivity in female mice; female mice achieved similar levels of pain hypersensitivity using adaptive immune cells, likely T lymphocytes. This sexual dimorphism suggests that male mice cannot be used as proxies for females in pain research.
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            Pathological pain and the neuroimmune interface.

            Reciprocal signalling between immunocompetent cells in the central nervous system (CNS) has emerged as a key phenomenon underpinning pathological and chronic pain mechanisms. Neuronal excitability can be powerfully enhanced both by classical neurotransmitters derived from neurons, and by immune mediators released from CNS-resident microglia and astrocytes, and from infiltrating cells such as T cells. In this Review, we discuss the current understanding of the contribution of central immune mechanisms to pathological pain, and how the heterogeneous immune functions of different cells in the CNS could be harnessed to develop new therapeutics for pain control. Given the prevalence of chronic pain and the incomplete efficacy of current drugs--which focus on suppressing aberrant neuronal activity--new strategies to manipulate neuroimmune pain transmission hold considerable promise.
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              Role of the immune system in chronic pain.

              During the past two decades, an important focus of pain research has been the study of chronic pain mechanisms, particularly the processes that lead to the abnormal sensitivity - spontaneous pain and hyperalgesia - that is associated with these states. For some time it has been recognized that inflammatory mediators released from immune cells can contribute to these persistent pain states. However, it has only recently become clear that immune cell products might have a crucial role not just in inflammatory pain, but also in neuropathic pain caused by damage to peripheral nerves or to the CNS.
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                Author and article information

                Contributors
                Journal
                Front Pediatr
                Front Pediatr
                Front. Pediatr.
                Frontiers in Pediatrics
                Frontiers Media S.A.
                2296-2360
                07 February 2020
                2020
                : 8
                : 30
                Affiliations
                [1] 1Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University , Raleigh, NC, United States
                [2] 2Translational Research in Pain Program, North Carolina State University , Raleigh, NC, United States
                [3] 3Comparative Medicine Institute, North Carolina State University , Raleigh, NC, United States
                [4] 4Thurston Arthritis Research Center, University of North Carolina at Chapel Hill , Chapel Hill, NC, United States
                [5] 5Center for Translational Pain Medicine, Duke University , Durham, NC, United States
                Author notes

                Edited by: Udo Rolle, University Hospital Frankfurt, Germany

                Reviewed by: Burak Tander, Acibadem University, Turkey; Karel Allegaert, University Hospitals Leuven, Belgium

                *Correspondence: B. Duncan X. Lascelles dxlascel@ 123456ncsu.edu

                This article was submitted to Children and Health, a section of the journal Frontiers in Pediatrics

                Article
                10.3389/fped.2020.00030
                7020755
                32117835
                f39c50b7-1c7b-4f6d-8718-5a8bcd0d2fab
                Copyright © 2020 Williams and Lascelles.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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
                : 18 November 2019
                : 20 January 2020
                Page count
                Figures: 0, Tables: 7, Equations: 0, References: 236, Pages: 18, Words: 15818
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Categories
                Pediatrics
                Review

                neonatal pain,early life,consequences,neurobiology,mechanisms,animal models,chronic pain

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