Chemotherapy-induced peripheral neuropathy: part 1-current state of knowledge and perspectives for pharmacotherapy

被引:93
作者
Salat, Kinga [1 ]
机构
[1] Jagiellonian Univ, Coll Med, Dept Pharmacodynam, Chair Pharmacodynam, 9 Medyczna St, PL-30688 Krakow, Poland
关键词
Chemotherapy-induced peripheral neuropathy; Neuronal hyperexcitability; Platinum derivatives; Paclitaxel; Vinca alkaloids; Bortezomib; DORSAL-ROOT GANGLION; INDUCED COLD ALLODYNIA; INDUCED MECHANICAL ALLODYNIA; RECEPTOR POTENTIAL CHANNELS; ANTINOCICEPTIVE ACTIVITY; INDUCED NEUROTOXICITY; CALCIUM-CHANNELS; UP-REGULATION; PHASE-II; PAIN;
D O I
10.1007/s43440-020-00109-y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Despite the increasing knowledge of the etiology of neuropathic pain, this type of chronic pain is resistant to available analgesics in approximately 50% of patients and therefore is continuously a subject of considerable interest for physiologists, neurologists, medicinal chemists, pharmacologists and others searching for more effective treatment options for this debilitating condition. Materials and methods The present review article is the first of the two articles focused on chemotherapy-induced peripheral neuropathy (CIPN). Results CIPN is regarded as one of the most common drug-induced neuropathies and is highly pharmacoresistant. The lack of efficacious pharmacological methods for treating CIPN and preventing its development makes CIPN-related neuropathic pain a serious therapeutic gap in current medicine and pharmacotherapy. In this paper, the most recent advances in the field of studies on CIPN caused by platinum compounds (namely oxaliplatin and cisplatin), taxanes, vinca alkaloids and bortezomib are summarized. Conclusions The prevalence of CIPN, potential causes, risk factors, symptoms and molecular mechanisms underlying this pharmacoresistant condition are discussed.
引用
收藏
页码:486 / 507
页数:22
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