Literature DB >> 21971745

Role of gap junctions in chronic pain.

Ann Wu1, Colin R Green, Ilva D Rupenthal, Gila Moalem-Taylor.   

Abstract

Gap junctions are specialized transmembrane channels that allow rapid electrical signalling and direct intercellular communication for maintenance and coordination of normal cellular activities and homeostasis. Although gap junction channels in the nervous system mediate intercellular coupling between glial cells and between neurons, they also contribute to the spread of secondary damage and inflammation under pathological conditions. There is now evidence of the involvement of gap junctions in chronic pain caused by nervous system damage or tissue inflammation. In this Mini-Review, we highlight recent studies demonstrating the dynamic plasticity of gap junctions in response to nervous system injury and the effects of gap junction blockade on neuronal survival and modulation of pain in animal models of neuropathic and inflammatory pain. The involvement of dorsal root ganglia and spinal cord gap junctions in mediating chronic pain and the potential for targeting connexins as a novel modality for the treatment of intractable pain syndromes arising from nervous system injury and disorders are discussed.
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21971745     DOI: 10.1002/jnr.22764

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  12 in total

1.  Reversal of TRESK Downregulation Alleviates Neuropathic Pain by Inhibiting Activation of Gliocytes in the Spinal Cord.

Authors:  Jun Zhou; Hongtao Chen; Chengxiang Yang; Jiying Zhong; Wanyou He; Qingming Xiong
Journal:  Neurochem Res       Date:  2017-02-03       Impact factor: 3.996

Review 2.  Gap junctions, pannexins and pain.

Authors:  David C Spray; Menachem Hanani
Journal:  Neurosci Lett       Date:  2017-06-22       Impact factor: 3.046

Review 3.  Revisiting APP secretases: an overview on the holistic effects of retinoic acid receptor stimulation in APP processing.

Authors:  José J M Vitória; Diogo Trigo; Odete A B da Cruz E Silva
Journal:  Cell Mol Life Sci       Date:  2022-01-28       Impact factor: 9.261

4.  Spinal astrocyte gap junctions contribute to oxaliplatin-induced mechanical hypersensitivity.

Authors:  Seo-Yeon Yoon; Caleb R Robinson; Haijun Zhang; Patrick M Dougherty
Journal:  J Pain       Date:  2013-02       Impact factor: 5.820

5.  CaMKII and CaV3.2 T-type calcium channel mediate Connexin-43-dependent inflammation by activating astrocytes in vincristine-induced neuropathic pain.

Authors:  Gui-Zhou Li; Ya-Hui Hu; Yi-Ni Lu; Qing-Yan Yang; Di Fu; Feng Chen; Yun-Man Li
Journal:  Cell Biol Toxicol       Date:  2021-07-20       Impact factor: 6.691

6.  Astrocytic CX43 hemichannels and gap junctions play a crucial role in development of chronic neuropathic pain following spinal cord injury.

Authors:  Michael J Chen; Benjamin Kress; Xiaoning Han; Katherine Moll; Weiguo Peng; Ru-Rong Ji; Maiken Nedergaard
Journal:  Glia       Date:  2012-08-01       Impact factor: 7.452

Review 7.  Gap junction proteins and their role in spinal cord injury.

Authors:  Ryan S Tonkin; Yilin Mao; Simon J O'Carroll; Louise F B Nicholson; Colin R Green; Catherine A Gorrie; Gila Moalem-Taylor
Journal:  Front Mol Neurosci       Date:  2015-01-06       Impact factor: 5.639

Review 8.  Applying the NIA Health Disparities Research Framework to Identify Needs and Opportunities in Chronic Musculoskeletal Pain Research.

Authors:  Monika Patel; Alisa J Johnson; Staja Q Booker; Emily J Bartley; Shreela Palit; Keesha Powell-Roach; Ellen L Terry; Dottington Fullwood; Lucas DeMonte; Angela M Mickle; Kimberly T Sibille
Journal:  J Pain       Date:  2021-07-17       Impact factor: 5.383

Review 9.  Intercellular communication and ion channels in neuropathic pain chronicization.

Authors:  Nunzio Vicario; Rita Turnaturi; Federica Maria Spitale; Filippo Torrisi; Agata Zappalà; Rosario Gulino; Lorella Pasquinucci; Santina Chiechio; Carmela Parenti; Rosalba Parenti
Journal:  Inflamm Res       Date:  2020-06-12       Impact factor: 6.986

10.  The role of Cx36 and Cx43 in 4-aminopyridine-induced rhythmic activity in the spinal nociceptive dorsal horn: an electrophysiological study in vitro.

Authors:  Christopher W P Kay; Daniel Ursu; Emanuele Sher; Anne E King
Journal:  Physiol Rep       Date:  2016-07
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