Electroacupuncture Attenuates Hyperalgesia in Rats Withdrawn from Chronic Alcohol Drinking via Habenular Mu Opioid Receptors

被引:18
|
作者
Li, Jing [1 ]
Fu, Caihong [2 ]
Liu, Hongwei [2 ]
Fu, Rao [1 ]
Zuo, Wanhong [1 ]
Kang, Seungwoo [1 ]
Chen, Pei [2 ]
Gregor, Danielle [1 ]
Paulose, Rose [1 ]
Bekker, Alex [1 ]
Ye, Jiang-Hong [1 ]
机构
[1] Rutgers New Jersey Med Sch, Dept Anesthesiol, 185 South Orange Ave, Newark, NJ 07103 USA
[2] Beijing Univ Chinese Med, Dept Neurol, Dong Zhi Men Hosp, Key Lab Internal Chinese Med,Minist Educ, Beijing, Peoples R China
关键词
Electroacupuncture; Pain; Ethanol Withdrawal; Mu Opioid Receptor; Lateral Habenula; ETHANOL WITHDRAWAL; LATERAL HABENULA; PERIAQUEDUCTAL GRAY; NUCLEUS-ACCUMBENS; ANALGESIA; PAIN; BRAIN; CONSUMPTION; NOCICEPTION; ACUPUNCTURE;
D O I
10.1111/acer.13332
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Hyperalgesia or increased sensitivity to pain is often found in alcoholics during alcohol withdrawal and may contribute to relapse drinking. Alternative therapies such as acupuncture and electroacupuncture (EA), through mechanisms involving opioid receptors, may reduce pain and substance dependence and withdrawal syndromes. The lateral habenula (LHb), an epithalamic structure rich in mu opioid receptors (MORs), is a critical target for both drugs of abuse and pain. We previously observed hyperalgesia in rats withdrawn from chronic ethanol (EtOH) drinking and found that EA at the acupoint Zusanli (ST36) reduced EtOH intake. This raised question of whether EA can alleviate hyperalgesia during alcohol withdrawal and, if so, whether the mechanism involves MORs in the LHb. Methods: We trained male rats to drink EtOH using the intermittent access 20% EtOH 2-bottle free-choice drinking paradigm for 8weeks, after which the alcohol supply was discontinued. We measured pain sensitivity using radiant heat (a light beam directed at the hind paw of rats) and compared the paw withdrawal latencies (PWLs) with and without EA at ST36. Results: The PWLs were significantly shorter in rats at 24, 48, and 72hours and 7days after the discontinuation of EtOH when compared to EtOH-naive rats. After a single administration of 2-Hz EA for 20minutes at ST36, the PWLs at 24hours after the withdrawal of EtOH were significantly greater than those of the sham group (2-Hz EA at the tail). Furthermore, the effect of EA on PWLs was significantly attenuated by bilateral intrahabenula infusion of the MOR antagonist naltrexone. Conclusions: These results suggest that EA can alleviate hyperalgesia during EtOH withdrawal through a mechanism involving MORs in the habenula. Based on this, EA could be of potential value as a therapy for hyperalgesia in alcohol dependence.
引用
收藏
页码:637 / 643
页数:7
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