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鞘氨醇-1-磷酸(S1P)受体调节剂在多发性硬化症治疗中的滥用和依赖潜力:文献和公共数据回顾。

Abuse and dependence potential of sphingosine-1-phosphate (S1P) receptor modulators used in the treatment of multiple sclerosis: a review of literature and public data.

机构信息

Altreos Research Partners, Inc, Toronto, Canada.

Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.

出版信息

Psychopharmacology (Berl). 2022 Jan;239(1):1-13. doi: 10.1007/s00213-021-06011-6. Epub 2021 Nov 13.

DOI:10.1007/s00213-021-06011-6
PMID:34773483
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8770388/
Abstract

Abuse and misuse of prescription drugs remains an ongoing concern in the USA and worldwide; thus, all centrally active new drugs must be assessed for abuse and dependence potential. Sphingosine-1-phosphate (S1P) receptor modulators are used primarily in the treatment of multiple sclerosis. Among the new S1P receptor modulators, siponimod, ozanimod, and ponesimod have recently been approved in the USA, European Union (EU), and other countries. This review of literature and other public data has been undertaken to assess the potential for abuse of S1P receptor modulators, including ozanimod, siponimod, ponesimod, and fingolimod, as well as several similar compounds in development. The S1P receptor modulators have not shown chemical or pharmacological similarity to known drugs of abuse; have not shown abuse or dependence potential in animal models for subjective effects, reinforcement, or physical dependence; and do not have adverse event profiles demonstrating effects of interest to individuals who abuse drugs (such as sedative, stimulant, mood-elevating, or hallucinogenic effects). In addition, no reports of actual abuse, misuse, or dependence were identified in the scientific literature for fingolimod, which has been on the market since 2010 (USA) and 2011 (EU). Overall, the data suggest that S1P receptor modulators are not associated with significant potential for abuse or dependence, consistent with their unscheduled status in the USA and internationally.

摘要

滥用和误用处方药物仍然是美国和全球持续关注的问题;因此,所有中枢活性新药都必须评估其滥用和依赖潜力。鞘氨醇-1-磷酸(S1P)受体调节剂主要用于治疗多发性硬化症。在新型 S1P 受体调节剂中,西尼莫德、奥扎尼莫德和培尼莫德最近已在美国、欧盟(EU)和其他国家获得批准。对文献和其他公开数据的审查旨在评估 S1P 受体调节剂(包括奥扎尼莫德、西尼莫德、培尼莫德和芬戈莫德)以及几种正在开发的类似化合物的滥用潜力。S1P 受体调节剂与已知的滥用药物在化学或药理学上没有相似性;在评估主观效应、强化或身体依赖的动物模型中没有显示出滥用或依赖潜力;并且没有不良事件谱表明药物滥用者(如镇静、兴奋剂、情绪提升或致幻作用)感兴趣的效果。此外,在科学文献中也没有发现芬戈莫德的实际滥用、误用或依赖报告,自 2010 年(美国)和 2011 年(欧盟)上市以来,芬戈莫德一直在市场上销售。总体而言,数据表明 S1P 受体调节剂与显著的滥用或依赖潜力无关,这与其在美国和国际上的非附表地位一致。

相似文献

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Abuse and dependence potential of sphingosine-1-phosphate (S1P) receptor modulators used in the treatment of multiple sclerosis: a review of literature and public data.鞘氨醇-1-磷酸(S1P)受体调节剂在多发性硬化症治疗中的滥用和依赖潜力:文献和公共数据回顾。
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本文引用的文献

1
Single-Dose Pharmacokinetics of Ozanimod and its Major Active Metabolites Alone and in Combination with Gemfibrozil, Itraconazole, or Rifampin in Healthy Subjects: A Randomized, Parallel-Group, Open-Label Study.在健康受试者中单剂量奥扎莫德及其主要活性代谢物单独及与吉非贝齐、伊曲康唑或利福平联合用药的药代动力学:一项随机、平行分组、开放标签研究。
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Siponimod: First Global Approval.西尼莫德:全球首次获批。
Drugs. 2019 Jun;79(9):1009-1015. doi: 10.1007/s40265-019-01140-x.
6
Different MRI patterns in MS worsening after stopping fingolimod.多发性硬化症停药后恶化的不同 MRI 模式。
Neurol Neuroimmunol Neuroinflamm. 2019 Apr 16;6(4):e566. doi: 10.1212/NXI.0000000000000566. eCollection 2019 Jul.
7
Ozanimod for the treatment of relapsing remitting multiple sclerosis.奥扎莫德治疗复发缓解型多发性硬化。
Expert Opin Pharmacother. 2018 Dec;19(18):2073-2086. doi: 10.1080/14656566.2018.1540592. Epub 2018 Nov 8.
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Adverse psychiatric effects of disease-modifying therapies in multiple Sclerosis: A systematic review.多发性硬化症中疾病修正疗法的不良精神影响:一项系统综述。
Mult Scler Relat Disord. 2018 Nov;26:124-156. doi: 10.1016/j.msard.2018.09.008. Epub 2018 Sep 12.
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Siponimod pharmacokinetics, safety, and tolerability in combination with rifampin, a CYP2C9/3A4 inducer, in healthy subjects.西尼莫德在健康受试者中与细胞色素P450 2C9/3A4诱导剂利福平联合使用时的药代动力学、安全性及耐受性
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Tumefactive multiple sclerosis lesions associated with fingolimod treatment: Report of 5 cases.与芬戈莫德治疗相关的肿块样多发性硬化病变:5 例报告。
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