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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/6762


    Title: Dextromethorphan attenuated inflammation and combined opioid use in humans undergoing methadone maintenance treatment
    Authors: Chen, SL;Lee, SY;Tao, PL;Chang, YH;Chen, SH;Chu, CH;Chen, PS;Lee, IH;Yeh, TL;Yang, YK;Hong, JS;Lu, RB
    Contributors: Division of Mental Health and Addiction Medicine
    Abstract: Recent studies show that proinflammatory cytokines might be related to the development of opioid dependence (physiological, psychological, or both). In a double-blind, randomly stratified clinical trial investigating whether add-on dextromethorphan (60-120 mg/day) attenuated inflammation and the combined use of opioids in heroin-dependent patients undergoing methadone maintenance treatment, we evaluated whether inflammation is related to the progression of opioid dependence. All participants (107 heroin-dependent patients and 84 nondependent healthy controls) were recruited from National Cheng Kung University Hospital. Their plasma cytokine levels were measured to evaluate the effect of add-on dextromethorphan. Plasma TNF-α and IL-8 levels were significantly higher in long-term heroin-dependent patients than in healthy controls (p < 0.001). Chronic heroin-use-induced TNF-α and IL-8 levels were significantly (p < 0.05) attenuated in patients treated for 12 weeks with add-on dextromethorphan. Moreover, both tolerance to methadone and the combined use of opioids were significantly (p < 0.05) attenuated in patients taking dextromethorphan. We conclude that dextromethorphan might be a feasible adjuvant therapeutic for attenuating inflammation and inhibiting methadone tolerance and combined opioid use in heroin-dependent patients.
    Date: 2012-12
    Relation: Journal of Neuroimmune Pharmacology. 2012 Dec;7(4):1025-1033.
    Link to: http://dx.doi.org/10.1007/s11481-012-9400-1
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1557-1890&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000312363500030
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84875829064
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