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
[21]   Neuropathic pain [J].
Colloca, Luana ;
Ludman, Taylor ;
Bouhassira, Didier ;
Baron, Ralf ;
Dickenson, AnthonyH. ;
Yarnitsky, David ;
Freeman, Roy ;
Truini, Andrea ;
Attal, Nadine ;
Finnerup, Nanna B. ;
Eccleston, Christopher ;
Kalso, Eija ;
Bennett, David L. ;
Dworkin, RobertH. ;
Raja, Srinivasa N. .
NATURE REVIEWS DISEASE PRIMERS, 2017, 3
[22]   Role of connexin-based gap junction channels and hemichannels in ischemia-induced cell death in nervous tissue [J].
Contreras, JE ;
Sánchez, HA ;
Véliz, LP ;
Bukauskas, FF ;
Bennett, MVL ;
Sáez, JC .
BRAIN RESEARCH REVIEWS, 2004, 47 (1-3) :290-303
[23]   Neuropathic Pain: A Maladaptive Response of the Nervous System to Damage [J].
Costigan, Michael ;
Scholz, Joachim ;
Woolf, Clifford J. .
ANNUAL REVIEW OF NEUROSCIENCE, 2009, 32 :1-32
[24]   Physiological and pathological functions of P2X7 receptor in the spinal cord [J].
Cotrina, Maria Luisa ;
Nedergaard, Maiken .
PURINERGIC SIGNALLING, 2009, 5 (02) :223-232
[25]   Expression and function of astrocytic gap junctions in aging [J].
Cotrina, ML ;
Gao, Q ;
Lin, JHC ;
Nedergaard, M .
BRAIN RESEARCH, 2001, 901 (1-2) :55-61
[26]   Blocking connexin43 expression reduces inflammation and improves functional recovery after spinal cord injury [J].
Cronin, Michael ;
Anderson, Patrick N. ;
Cook, Jererny E. ;
Green, Colin R. ;
Becker, David L. .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2008, 39 (02) :152-160
[27]   Glutamate uptake [J].
Danbolt, NC .
PROGRESS IN NEUROBIOLOGY, 2001, 65 (01) :1-105
[28]   Battle of the hemichannels - Connexins and Pannexins in ischemic brain injury [J].
Davidson, J. O. ;
Green, C. R. ;
Bennet, L. ;
Gunn, A. J. .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2015, 45 :66-74
[29]   Chronic Neuropathic Pain in SCI: Evaluation and Treatment [J].
Felix, Elizabeth Roy .
PHYSICAL MEDICINE AND REHABILITATION CLINICS OF NORTH AMERICA, 2014, 25 (03) :545-+
[30]   Sodium channel alpha-subunit mRNAs I, II, III, NaG, Na6 and hNE (PN1): Different expression patterns in developing rat nervous system [J].
Felts, PA ;
Yokoyama, S ;
DibHajj, S ;
Black, JA ;
Waxman, SG .
MOLECULAR BRAIN RESEARCH, 1997, 45 (01) :71-82