The use of low-dose naltrexone (LDN) as a novel anti-inflammatory treatment for chronic pain

被引:182
作者
Younger, Jarred [1 ,2 ]
Parkitny, Luke [2 ]
McLain, David [3 ]
机构
[1] Stanford Univ, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Anesthesia Pain & Perioperat Med, Palo Alto, CA 94304 USA
[3] McLain Med Associates, Birmingham, AL USA
关键词
Anti-inflammatory; Chronic pain; Fibromyalgia; Glial cell modulators; Low-dose naltrexone; Microglia; QUALITY-OF-LIFE; OPIOID-RECEPTOR; CELL-PROLIFERATION; NEUROPATHIC PAIN; NALOXONE; ANTAGONIST; ACTIVATION; MORPHINE; THERAPY; INFLAMMATION;
D O I
10.1007/s10067-014-2517-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Low-dose naltrexone (LDN) has been demonstrated to reduce symptom severity in conditions such as fibromyalgia, Crohn's disease, multiple sclerosis, and complex regional pain syndrome. We review the evidence that LDN may operate as a novel anti-inflammatory agent in the central nervous system, via action on microglial cells. These effects may be unique to low dosages of naltrexone and appear to be entirely independent from naltrexone's better-known activity on opioid receptors. As a daily oral therapy, LDN is inexpensive and well-tolerated. Despite initial promise of efficacy, the use of LDN for chronic disorders is still highly experimental. Published trials have low sample sizes, and few replications have been performed. We cover the typical usage of LDN in clinical trials, caveats to using the medication, and recommendations for future research and clinical work. LDN may represent one of the first glial cell modulators to be used for the management of chronic pain disorders.
引用
收藏
页码:451 / 459
页数:9
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