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

被引:0
|
作者
Jarred Younger
Luke Parkitny
David McLain
机构
[1] Stanford University,Department of Anesthesia, Pain and Perioperative Medicine
[2] Stanford University,Department of Anesthesia, Pain and Perioperative Medicine
[3] McLain Medical Associates,undefined
[4] Stanford University,undefined
来源
Clinical Rheumatology | 2014年 / 33卷
关键词
Anti-inflammatory; Chronic pain; Fibromyalgia; Glial cell modulators; Low-dose naltrexone; Microglia;
D O I
暂无
中图分类号
学科分类号
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.
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页码:451 / 459
页数:8
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