Voltage-Gated Ion Channels in the PNS: Novel Therapies for Neuropathic Pain?

被引:96
作者
Tibbs, Gareth R. [1 ]
Posson, David J. [1 ]
Goldstein, Peter A. [1 ,2 ]
机构
[1] Weill Cornell Med Coll, Dept Anesthesiol, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Dept Med, New York, NY 10065 USA
关键词
T-TYPE CALCIUM; DORSAL-ROOT GANGLION; NA(V)1.8 SODIUM-CHANNEL; HYPERPOLARIZATION-ACTIVATED CURRENT; RAT SENSORY NEURONS; OF-FUNCTION MUTATION; OMEGA-CONOTOXIN GVIA; SPINAL NERVE INJURY; CURRENT I-H; N-TYPE;
D O I
10.1016/j.tips.2016.05.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neuropathic pain arises from injury to the nervous system. Conditions associated with neuropathic pain are diverse, and lesions and/or pathological changes in the central nervous system (CNS) or peripheral nervous system (PNS) can frequently, but not always, be identified. It is difficult to treat, with patients often on multiple, different classes of medications, all with appreciable adverse side effect profiles. Consequently, there is a pressing need for the development of new medications. The development of such therapeutics is predicated on a clear understanding of the relevant molecular and cellular processes that contribute to the development, and maintenance, of the neuropathic pain state. One proposed mechanism thought to contribute to the ontogeny of neuropathic pain is altered expression, trafficking, and functioning of ion channels expressed by primary sensory neurons. Here, we will focus on three voltage gated ion channel families, Ca-V, HCN, and Na-V, first reviewing the preclinical data and then the human data where it exists.
引用
收藏
页码:522 / 542
页数:21
相关论文
共 240 条
[1]   Heteromeric HCN1-HCN4 channels: a comparison with native pacemaker channels from the rabbit sinoatrial node [J].
Altomare, C ;
Terragni, B ;
Brioschi, C ;
Milanesi, R ;
Pagliuca, C ;
Viscomi, C ;
Moroni, A ;
Baruscotti, M ;
DiFrancesco, D .
JOURNAL OF PHYSIOLOGY-LONDON, 2003, 549 (02) :347-359
[2]  
An GH, 2015, AAPS J, V17, P481, DOI 10.1208/s12248-015-9725-9
[3]   MicroRNAs as modulators and biomarkers of inflammatory and neuropathic pain conditions [J].
Andersen, Hjalte H. ;
Duroux, Meg ;
Gazerani, Parisa .
NEUROBIOLOGY OF DISEASE, 2014, 71 :159-168
[4]   Novel, nonreflex tests detect analgesic action in rodents at clinically relevant concentrations [J].
Andrews, Nick ;
Harper, Sinead ;
Issop, Yasmin ;
Rice, Andrew S. C. .
ANIMAL MODELS: THEIR VALUE IN PREDICTING DRUG EFFICACY AND TOXICITY, 2011, 1245 :11-13
[5]  
[Anonymous], 1986, Pain Suppl, V3, pS1
[6]  
[Anonymous], BRAIN STRUCT FUNCT
[7]   Pain and the brain: Specificity and plasticity of the brain in clinical chronic pain [J].
Apkarian, A. Vania ;
Hashmi, Javeria A. ;
Baliki, Marwan N. .
PAIN, 2011, 152 (03) :S49-S64
[8]   Platinum-Induced Neurotoxicity and Preventive Strategies: Past, Present, and Future [J].
Avan, Abolfazl ;
Postma, Tjeerd J. ;
Ceresa, Cecilia ;
Avan, Amir ;
Cavaletti, Guido ;
Giovannetti, Elisa ;
Peters, Godefridus J. .
ONCOLOGIST, 2015, 20 (04) :411-432
[9]   Voltage gated sodium channels as drug discovery targets [J].
Bagal, Sharan K. ;
Marron, Brian E. ;
Owen, Robert M. ;
Storer, R. Ian ;
Swain, Nigel A. .
CHANNELS, 2015, 9 (06) :360-366
[10]   Discovery and Optimization of Selective Nav1.8 Modulator Series That Demonstrate Efficacy in Preclinical Models of Pain [J].
Bagal, Sharan K. ;
Bungay, Peter J. ;
Denton, Stephen M. ;
Gibson, Karl R. ;
Glossop, Melanie S. ;
Hay, Tanya L. ;
Kemp, Mark I. ;
Lane, Charlotte A. L. ;
Lewis, Mark L. ;
Maw, Graham N. ;
Million, William A. ;
Payne, C. Elizabeth ;
Poinsard, Cedric ;
Rawson, David J. ;
Stammen, Blanda L. ;
Stevens, Edward B. ;
Thompson, Lisa R. .
ACS MEDICINAL CHEMISTRY LETTERS, 2015, 6 (06) :650-654