Revisiting dezocine for opioid use disorder: A narrative review of its potential abuse liability

IF 4.8 1区 医学 Q1 NEUROSCIENCES CNS Neuroscience & Therapeutics Pub Date : 2024-09-18 DOI:10.1111/cns.70034
Gordon A. Barr, Heath D. Schmidt, Ashish P. Thakrar, Henry R. Kranzler, Renyu Liu
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Abstract

Aims

Opioid use disorder (OUD) remains a serious public health problem. Opioid maintenance treatment is effective but under-utilized, hard to access under existing federal regulations, and, once patients achieve OUD stability, challenging to discontinue. Fewer than 2% of persons with OUD stop using opioids completely. There have been calls from public advocacy groups, governmental agencies, and public health officials for new treatments for OUD. Dezocine, a non-scheduled opioid previously used in the United States and currently widely prescribed in China for pain management, could be a candidate for a novel OUD treatment medication in the U.S. Nonetheless, to date, there have been no reviews of the clinical and preclinical literature detailing dezocine's abuse potential, a key consideration in assessing its clinical utility.

Discussion

There are no English language reports of human abuse, dependence, or overdose of dezocine, despite years of extensive clinical use. There are a few case reports of dezocine abuse in the Chinese literature, but there are no reports of overdose deaths. Dezocine is perceived as an opioid and is “liked” by opioid-experienced human and non-human primates, properties that are not dose-dependent and are mitigated by ceiling effects—higher doses do not result in more “liking.” There is little withdrawal, spontaneous or precipitated, in humans, monkeys, rats, or mice treated chronically with dezocine alone. However, at some doses, dezocine can precipitate withdrawal in humans and monkeys dependent on other opioids. In rodents, dezocine reduces the severity of morphine withdrawal and the rewarding properties of other opioids.

Conclusions

Although dezocine is reinforcing in humans and monkeys with prior or concurrent opioid use within a restricted dose range, there are only a few anecdotal reports of dezocine abuse despite of the long history of use in humans. Given the evidence of dezocine's limited abuse potential, it could be useful both as a treatment for OUD. However, in-depth studies would be required for dezocine to be re-considered for clinical use.

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重新审视治疗阿片类药物使用障碍的地佐辛:对其潜在滥用责任的叙述性回顾。
AIMSO 类阿片使用障碍(OUD)仍然是一个严重的公共卫生问题。阿片类药物维持治疗很有效,但利用率低,根据现行联邦法规很难获得治疗,而且一旦患者的阿片类药物使用达到稳定,中断治疗也很困难。只有不到 2% 的 OUD 患者完全停止使用阿片类药物。公众权益团体、政府机构和公共卫生官员一直呼吁为 OUD 提供新的治疗方法。尽管如此,迄今为止,还没有任何临床和临床前文献对地佐辛的滥用可能性进行详细评述,而滥用可能性是评估其临床效用的一个关键因素。中文文献中有几例滥用地佐辛的报道,但没有过量致死的报道。有阿片类经验的人类和非人灵长类动物认为地佐辛是一种阿片类药物,并 "喜欢 "这种药物。人类、猴子、大鼠或小鼠在长期单独使用地佐辛的情况下,几乎不会出现自发或诱发的戒断症状。不过,在某些剂量下,地佐辛会使依赖其他阿片类药物的人类和猴子出现戒断症状。在啮齿类动物中,地佐辛可减轻吗啡戒断的严重程度,并降低其他阿片类药物的奖赏特性。结论尽管地佐辛在限制剂量范围内对人类和曾使用或同时使用阿片类药物的猴子具有强化作用,但尽管地佐辛在人类中的使用历史悠久,但关于地佐辛滥用的传闻却寥寥无几。鉴于有证据表明地佐辛的滥用可能性有限,它既可以作为治疗 OUD 的药物,也可以作为治疗 OUD 的药物。不过,要重新考虑将地佐辛用于临床,还需要进行深入研究。
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来源期刊
CNS Neuroscience & Therapeutics
CNS Neuroscience & Therapeutics 医学-神经科学
CiteScore
7.30
自引率
12.70%
发文量
240
审稿时长
2 months
期刊介绍: CNS Neuroscience & Therapeutics provides a medium for rapid publication of original clinical, experimental, and translational research papers, timely reviews and reports of novel findings of therapeutic relevance to the central nervous system, as well as papers related to clinical pharmacology, drug development and novel methodologies for drug evaluation. The journal focuses on neurological and psychiatric diseases such as stroke, Parkinson’s disease, Alzheimer’s disease, depression, schizophrenia, epilepsy, and drug abuse.
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