Intercellular communication and ion channels in neuropathic pain chronicization

被引:35
作者
Vicario, Nunzio [1 ]
Turnaturi, Rita [2 ]
Spitale, Federica Maria [1 ]
Torrisi, Filippo [1 ]
Zappala, Agata [1 ]
Gulino, Rosario [1 ]
Pasquinucci, Lorella [2 ]
Chiechio, Santina [3 ,4 ]
Parenti, Carmela [3 ]
Parenti, Rosalba [1 ]
机构
[1] Univ Catania, Dept Biomed & Biotechnol Sci, Physiol Sect, Catania, Italy
[2] Univ Catania, Dept Drug Sci, Sect Med Chem, Catania, Italy
[3] Univ Catania, Dept Drug Sci, Sect Pharmacol, Catania, Italy
[4] Oasi Res Inst IRCCS, Troina, Italy
关键词
Connexin; Glia; Gap junction; Neuropathic pain; Neurodegeneration; DORSAL-ROOT GANGLION; GAP-JUNCTION CHANNELS; GATED POTASSIUM CHANNELS; SPINAL SENSORY NEURONS; SUBUNIT UP-REGULATION; SODIUM-CHANNEL; NERVE INJURY; CENTRAL SENSITIZATION; THERAPEUTIC TARGETS; EXPRESSION;
D O I
10.1007/s00011-020-01363-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background Neuropathic pain is caused by primary lesion or dysfunction of either peripheral or central nervous system. Due to its complex pathogenesis, often related to a number of comorbidities, such as cancer, neurodegenerative and neurovascular diseases, neuropathic pain still represents an unmet clinical need, lacking long-term effective treatment and complex case-by-case approach. Aim and methods We analyzed the recent literature on the role of selective voltage-sensitive sodium, calcium and potassium permeable channels and non-selective gap junctions (GJs) and hemichannels (HCs) in establishing and maintaining chronic neuropathic conditions. We finally focussed our review on the role of extracellular microenvironment modifications induced by resident glial cells and on the recent advances in cell-to-cell and cell-to-extracellular environment communication in chronic neuropathies. Conclusion In this review, we provide an update on the current knowledge of neuropathy chronicization processes with a focus on both neuronal and glial ion channels, as well as on channel-mediated intercellular communication.
引用
收藏
页码:841 / 850
页数:10
相关论文
共 105 条
[1]   Connexin 43 in Astrocytes Contributes to Motor Neuron Toxicity in Amyotrophic Lateral Sclerosis [J].
Almad, Akshata A. ;
Doreswamy, Arpitha ;
Gross, Sarah K. ;
Richard, Jean-Philippe ;
Huo, Yuqing ;
Haughey, Norman ;
Maragakis, Nicholas J. .
GLIA, 2016, 64 (07) :1154-1169
[2]   The voltage-gated sodium channel Nav1.9 is an effector of peripheral inflammatory pain hypersensitivity [J].
Amaya, Fumimasa ;
Wang, Haibin ;
Costigan, Michael ;
Allchorne, Andrew J. ;
Hatcher, Jon P. ;
Egerton, Julie ;
Stean, Tania ;
Morisset, Valerie ;
Grose, David ;
Gunthorpe, Martin J. ;
Chessell, Iain P. ;
Tate, Simon ;
Green, Paula J. ;
Woolf, Clifford J. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (50) :12852-12860
[3]   Ion channels and neuronal hyperexcitability in chemotherapy-induced peripheral neuropathy; cause and effect? [J].
Aromolaran, Kelly A. ;
Goldstein, Peter A. .
MOLECULAR PAIN, 2017, 13
[4]   Peripheral Input and Its Importance for Central Sensitization [J].
Baron, Ralf ;
Hans, Guy ;
Dickenson, Anthony H. .
ANNALS OF NEUROLOGY, 2013, 74 (05) :630-636
[5]   The Increased Trafficking of the Calcium Channel Subunit α2δ-1 to Presynaptic Terminals in Neuropathic Pain Is Inhibited by the α2δ Ligand Pregabalin [J].
Bauer, Claudia S. ;
Nieto-Rostro, Manuela ;
Rahman, Wahida ;
Tran-Van-Minh, Alexandra ;
Ferron, Laurent ;
Douglas, Leon ;
Kadurin, Ivan ;
Ranjan, Yorain Sri ;
Fernandez-Alacid, Laura ;
Millar, Neil S. ;
Dickenson, Anthony H. ;
Lujan, Rafael ;
Dolphin, Annette C. .
JOURNAL OF NEUROSCIENCE, 2009, 29 (13) :4076-4088
[6]   DIFFERENTIAL REGULATION OF 3 SODIUM-CHANNEL MESSENGER-RNAS IN THE RAT CENTRAL NERVOUS-SYSTEM DURING DEVELOPMENT [J].
BECKH, S ;
NODA, M ;
LUBBERT, H ;
NUMA, S .
EMBO JOURNAL, 1989, 8 (12) :3611-3616
[7]   Functional up-regulation of Nav1.8 sodium channel in Aβ afferent fibers subjected to chronic peripheral inflammation [J].
Belkouch, Mounir ;
Dansereau, Marc-Andre ;
Tetreault, Pascal ;
Biet, Michael ;
Beaudet, Nicolas ;
Dumaine, Robert ;
Chraibi, Ahmed ;
Melik-Parsadaniantz, Stephane ;
Sarret, Philippe .
JOURNAL OF NEUROINFLAMMATION, 2014, 11
[8]   Upregulation of a silent sodium channel after peripheral, but not central, nerve injury in DRG neurons [J].
Black, JA ;
Cummins, TR ;
Plumpton, C ;
Chen, YH ;
Hormuzdiar, W ;
Clare, JJ ;
Waxman, SG .
JOURNAL OF NEUROPHYSIOLOGY, 1999, 82 (05) :2776-2785
[9]   Expression of Nav1.7 in DRG neurons extends from peripheral terminals in the skin to central preterminal branches and terminals in the dorsal horn [J].
Black, Joel A. ;
Frezel, Noemie ;
Dib-Hajj, Sulayman D. ;
Waxman, Stephen G. .
MOLECULAR PAIN, 2012, 8
[10]   Basic Anatomy and Physiology of Pain Pathways [J].
Bourne, Sarah ;
Machado, Andre G. ;
Nagel, Sean J. .
NEUROSURGERY CLINICS OF NORTH AMERICA, 2014, 25 (04) :629-+