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      Structural and functional properties of spinal dorsal horn neurons after peripheral nerve injury change overtime via astrocyte activation

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          Summary

          Chronic pain remains challenging to treat, despite numerous reports of its pathogenesis, including neuronal plasticity in the spinal dorsal horn (SDH). We hypothesized that understanding plasticity only at a specific time point after peripheral nerve injury (PNI) is insufficient to solve chronic pain. Here, we analyzed the temporal changes in synaptic transmission and astrocyte-neuron interactions in SDH after PNI. We found that synaptic transmission in the SDH after PNI changed in a time-dependent manner, which was accompanied by astrocyte proliferation and loss of inhibitory and excitatory neurons. Furthermore, neuronal loss was accompanied by necroptosis. Short-term inhibition of astrocytes after PNI suppressed these physiological and morphological changes and long-term pain-related behaviors. These results are the first to demonstrate that the inhibition of astrocyte proliferation after PNI contributes to the long-term regulation of plasticity and of necroptosis development in the SDH.

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          Highlights

          • Synaptic transmission in SDH after PNI is altered over time

          • Astrocyte proliferation induces neuronal loss with necroptosis in the SDH

          • Astrocyte regulation prevents transition to chronic pain

          Abstract

          Molecular biology; Neuroscience; Cell biology

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          Most cited references48

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          Neurotoxic reactive astrocytes are induced by activated microglia

          A reactive astrocyte subtype termed A1 is induced after injury or disease of the central nervous system and subsequently promotes the death of neurons and oligodendrocytes.
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            Cellular and molecular mechanisms of pain.

            The nervous system detects and interprets a wide range of thermal and mechanical stimuli, as well as environmental and endogenous chemical irritants. When intense, these stimuli generate acute pain, and in the setting of persistent injury, both peripheral and central nervous system components of the pain transmission pathway exhibit tremendous plasticity, enhancing pain signals and producing hypersensitivity. When plasticity facilitates protective reflexes, it can be beneficial, but when the changes persist, a chronic pain condition may result. Genetic, electrophysiological, and pharmacological studies are elucidating the molecular mechanisms that underlie detection, coding, and modulation of noxious stimuli that generate pain.
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              A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man

              A peripheral mononeuropathy was produced in adult rats by placing loosely constrictive ligatures around the common sciatic nerve. The postoperative behavior of these rats indicated that hyperalgesia, allodynia and, possibly, spontaneous pain (or dysesthesia) were produced. Hyperalgesic responses to noxious radiant heat were evident on the second postoperative day and lasted for over 2 months. Hyperalgesic responses to chemogenic pain were also present. The presence of allodynia was inferred from the nocifensive responses evoked by standing on an innocuous, chilled metal floor or by innocuous mechanical stimulation, and by the rats' persistence in holding the hind paw in a guarded position. The presence of spontaneous pain was suggested by a suppression of appetite and by the frequent occurrence of apparently spontaneous nocifensive responses. The affected hind paw was abnormally warm or cool in about one-third of the rats. About one-half of the rats developed grossly overgrown claws on the affected side. Experiments with this animal model may advance our understanding of the neural mechanisms of neuropathic pain disorders in humans.
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                Author and article information

                Contributors
                Journal
                iScience
                iScience
                iScience
                Elsevier
                2589-0042
                11 November 2022
                22 December 2022
                11 November 2022
                : 25
                : 12
                : 105555
                Affiliations
                [1 ]Division of Anesthesiology, Niigata University Graduate School of Medical and Dental Sciences, Chuo-Ku, Niigata City 951-8510, Japan
                [2 ]Department of Neurophysiology, Hyogo College of Medicine, Nishinomiya 663-8501, Japan
                Author notes
                []Corresponding author miyuki915@ 123456med.niigata-u.ac.jp
                [3]

                Lead contact

                Article
                S2589-0042(22)01827-2 105555
                10.1016/j.isci.2022.105555
                9700017
                36444301
                1afd6dc7-e01e-4a18-8565-809ee2417a80
                © 2022 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 6 December 2021
                : 21 September 2022
                : 8 November 2022
                Categories
                Article

                molecular biology,neuroscience,cell biology
                molecular biology, neuroscience, cell biology

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