Chemotherapy-Induced Peripheral Neuropathy: A Recent Update on Pathophysiology and Treatment

被引:4
|
作者
Mattar, Marina [1 ]
Umutoni, Florence [2 ]
Hassan, Marwa A. [1 ]
Wamburu, M. Wambui [3 ]
Turner, Reagan [4 ]
Patton, James S. [2 ]
Chen, Xin [5 ]
Lei, Wei [1 ,2 ]
机构
[1] Presbyterian Coll Sch Pharm, Dept Pharmaceut & Adm Sci, Clinton, SC 29325 USA
[2] Univ Manchester, Coll Hlth Sci Nursing & Pharm, Dept Pharmaceut & Grad Life Sci, Ft Wayne, IN 46845 USA
[3] Univ Manchester, Coll Hlth Sci Nursing & Pharm, Dept Pharm Practice, Ft Wayne, IN 46845 USA
[4] Presbyterian Coll, Dept Biol, Clinton, SC 29325 USA
[5] Campbell Univ, Coll Pharm & Hlth Sci, Dept Pharmaceut & Clin Sci, Buies Creek, NC 27506 USA
来源
LIFE-BASEL | 2024年 / 14卷 / 08期
关键词
chemotherapy-induced peripheral neuropathy; pathophysiology; duloxetine; cannabinoid; pain; OXALIPLATIN-INDUCED NEUROPATHY; PACLITAXEL-INDUCED NEUROPATHY; BREAST-CANCER PATIENTS; DORSAL-ROOT GANGLION; DOUBLE-BLIND; NICOTINAMIDE RIBOSIDE; INDUCED NEUROTOXICITY; SENSORY NEURONS; MURINE MODEL; PHASE-II;
D O I
10.3390/life14080991
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chemotherapy-induced peripheral neuropathy (CIPN) is a major long-lasting side effect of some chemotherapy drugs, which threatens cancer survival rate. CIPN mostly affects sensory neurons and occasionally motor neurons, causing numbness, tingling, discomfort, and burning pain in the upper and lower extremities. The pathophysiology of CIPN is not completely understood; however, it is believed that chemotherapies induce peripheral neuropathy via directly damaging mitochondria, impairing the function of ion channels, triggering immunological mechanisms, and disrupting microtubules. The treatment of CIPN is a medical challenge, and there are no approved pharmacological options. Currently, duloxetine and other antidepressants, antioxidant, anti-inflammatory, and ion-channel targeted therapies are commonly used in clinics to relieve the symptoms of CIPN. Several other types of drugs, such as cannabinoids, sigma-1 receptor antagonists, and nicotinamides ribose, are being evaluated in preclinical and clinical studies. This paper summarizes the information related to the physiology of CIPN and medicines that could be used for treating this condition.
引用
收藏
页数:25
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