Suppr超能文献

伊维菌素治疗酒精使用障碍的安全性和初始疗效的初步研究。

A Pilot Study of the Safety and Initial Efficacy of Ivermectin for the Treatment of Alcohol Use Disorder.

作者信息

Roche Daniel J O, Yardley Megan M, Lunny Katy F, Louie Stan G, Davies Daryl L, Miotto Karen, Ray Lara A

机构信息

Department of Psychology, University of California, Los Angeles, California.

Titus Family Department of Clinical Pharmacy, University of Southern California, Los Angeles, California.

出版信息

Alcohol Clin Exp Res. 2016 Jun;40(6):1312-20. doi: 10.1111/acer.13064. Epub 2016 Apr 18.

Abstract

BACKGROUND

Ivermectin (IVM) is an antiparasitic agent that has been shown to reduce alcohol intake in mice, suggesting IVM as a potential treatment for alcohol use disorder (AUD). However, the safety profile of IVM administered in combination with an intoxicating dose of alcohol has not been characterized in humans.

METHODS

This pilot project sought to provide the first clinical evidence that IVM could be repositioned as an AUD pharmacotherapy by examining (i) the safety of combining IVM (30 mg oral , once a day [QD]) with an intoxicating dose of intravenous alcohol (0.08 g/dl) and (ii) the effects of IVM on alcohol cue-induced craving and subjective response to alcohol. Eleven individuals with AUD participated in a randomized, placebo-controlled, crossover study in which they received the study medication, participated in a cue exposure paradigm followed by intravenous alcohol administration, and remained in an inpatient unit overnight for observation.

RESULTS

IVM treatment, versus placebo, did not increase the number or severity of adverse effects during alcohol administration or throughout the visit. However, IVM did not reduce cue-induced craving nor did it significantly affect subjective response to alcohol.

CONCLUSIONS

These results suggest that IVM (30 mg oral, QD) is safe in combination with an intoxicating dose of alcohol, but do not provide evidence that this dose of IVM is effective in reducing alcohol craving or its reinforcing effects. Given the preclinical data suggesting IVM is effective in reducing alcohol consumption in mice, additional studies testing larger samples and alternate dosing regimens are warranted to further characterize the potential efficacy of IVM as an AUD treatment.

摘要

背景

伊维菌素(IVM)是一种抗寄生虫药物,已被证明可减少小鼠的酒精摄入量,这表明IVM可能是治疗酒精使用障碍(AUD)的潜在药物。然而,IVM与中毒剂量酒精联合使用时的安全性在人类中尚未得到明确。

方法

本试点项目旨在通过研究(i)将IVM(口服30毫克,每日一次[QD])与中毒剂量的静脉酒精(0.08克/分升)联合使用的安全性,以及(ii)IVM对酒精线索诱导的渴望和对酒精的主观反应的影响,提供首个临床证据,证明IVM可重新定位为AUD的药物治疗方法。11名患有AUD的个体参与了一项随机、安慰剂对照、交叉研究,他们接受了研究药物,参与了线索暴露范式,随后进行静脉酒精给药,并在住院单元过夜观察。

结果

与安慰剂相比,IVM治疗在酒精给药期间或整个就诊过程中并未增加不良反应的数量或严重程度。然而,IVM并未减少线索诱导的渴望,也未显著影响对酒精的主观反应。

结论

这些结果表明,IVM(口服30毫克,QD)与中毒剂量酒精联合使用是安全的,但没有证据表明该剂量的IVM在减少酒精渴望或其强化作用方面有效。鉴于临床前数据表明IVM可有效减少小鼠的酒精摄入量,有必要进行更多研究,测试更大样本和不同给药方案,以进一步明确IVM作为AUD治疗方法的潜在疗效。

相似文献

1
A Pilot Study of the Safety and Initial Efficacy of Ivermectin for the Treatment of Alcohol Use Disorder.
Alcohol Clin Exp Res. 2016 Jun;40(6):1312-20. doi: 10.1111/acer.13064. Epub 2016 Apr 18.
5
Ivermectin reduces alcohol intake and preference in mice.
Neuropharmacology. 2012 Aug;63(2):190-201. doi: 10.1016/j.neuropharm.2012.03.014. Epub 2012 Mar 23.
6
Development of the Neuroimmune Modulator Ibudilast for the Treatment of Alcoholism: A Randomized, Placebo-Controlled, Human Laboratory Trial.
Neuropsychopharmacology. 2017 Aug;42(9):1776-1788. doi: 10.1038/npp.2017.10. Epub 2017 Jan 16.
7
Heartworm and Wolbachia: therapeutic implications.
Vet Parasitol. 2008 Dec 10;158(3):204-14. doi: 10.1016/j.vetpar.2008.09.008. Epub 2008 Sep 7.
8
Efficacy of ivermectin and oxfendazole against Taenia solium cysticercosis and other parasitoses in naturally infected pigs.
Acta Trop. 2013 Oct;128(1):48-53. doi: 10.1016/j.actatropica.2013.06.010. Epub 2013 Jun 24.
9
Effect of high-fat meal intake on the pharmacokinetic profile of ivermectin in Japanese patients with scabies.
J Dermatol. 2016 Sep;43(9):1030-6. doi: 10.1111/1346-8138.13321. Epub 2016 Feb 26.
10
Preclinical development of moxidectin as a novel therapeutic for alcohol use disorder.
Neuropharmacology. 2017 Feb;113(Pt A):60-70. doi: 10.1016/j.neuropharm.2016.09.016. Epub 2016 Sep 15.

引用本文的文献

2
The P2X4 Receptor: Cellular and Molecular Characteristics of a Promising Neuroinflammatory Target.
Int J Mol Sci. 2022 May 20;23(10):5739. doi: 10.3390/ijms23105739.
4
To Inhibit or Enhance? Is There a Benefit to Positive Allosteric Modulation of P2X Receptors?
Front Pharmacol. 2020 May 12;11:627. doi: 10.3389/fphar.2020.00627. eCollection 2020.
5
Inclusion of Cannabis Users in Alcohol Research Samples: Screening In, Screening Out, and Implications.
Alcohol Alcohol. 2020 Jun 25;55(4):416-423. doi: 10.1093/alcalc/agaa023.
7
Neurochemical Evidence of Preclinical and Clinical Reports on Target-Based Therapy in Alcohol Used Disorder.
Neurochem Res. 2020 Feb;45(2):491-507. doi: 10.1007/s11064-019-02944-9. Epub 2020 Jan 2.
8
Convergence between the Penn Alcohol Craving Scale and diagnostic interview for the assessment of alcohol craving.
Addict Behav Rep. 2019 Jun 18;10:100198. doi: 10.1016/j.abrep.2019.100198. eCollection 2019 Dec.
9
Alcohol, tobacco, and marijuana consumption is associated with increased odds of same-day substance co- and tri-use.
Drug Alcohol Depend. 2019 Jul 1;200:40-49. doi: 10.1016/j.drugalcdep.2019.02.035. Epub 2019 May 7.
10
Overcoming the "Valley of Death" in Medications Development for Alcohol Use Disorder.
Alcohol Clin Exp Res. 2018 Sep;42(9):1612-1622. doi: 10.1111/acer.13829. Epub 2018 Jul 30.

本文引用的文献

1
Subjective Response to Alcohol as a Research Domain Criterion.
Alcohol Clin Exp Res. 2016 Jan;40(1):6-17. doi: 10.1111/acer.12927.
2
P2X4 receptors (P2X4Rs) represent a novel target for the development of drugs to prevent and/or treat alcohol use disorders.
Front Neurosci. 2014 Jun 24;8:176. doi: 10.3389/fnins.2014.00176. eCollection 2014.
3
Contribution of P2X4 receptors to ethanol intake in male C57BL/6 mice.
Neurochem Res. 2014 Jun;39(6):1127-39. doi: 10.1007/s11064-014-1271-9. Epub 2014 Mar 27.
4
Avermectins differentially affect ethanol intake and receptor function: implications for developing new therapeutics for alcohol use disorders.
Int J Neuropsychopharmacol. 2014 Jun;17(6):907-16. doi: 10.1017/S1461145713001703. Epub 2014 Jan 22.
5
Subjective response to alcohol among alcohol-dependent individuals: effects of the μ-opioid receptor (OPRM1) gene and alcoholism severity.
Alcohol Clin Exp Res. 2013 Jan;37 Suppl 1(Suppl 1):E116-24. doi: 10.1111/j.1530-0277.2012.01916.x. Epub 2012 Dec 14.
6
Pharmacological insights into the role of P2X4 receptors in behavioural regulation: lessons from ivermectin.
Int J Neuropsychopharmacol. 2013 Jun;16(5):1059-70. doi: 10.1017/S1461145712000909. Epub 2012 Sep 17.
7
Ivermectin reduces alcohol intake and preference in mice.
Neuropharmacology. 2012 Aug;63(2):190-201. doi: 10.1016/j.neuropharm.2012.03.014. Epub 2012 Mar 23.
8
Medications development to treat alcohol dependence: a vision for the next decade.
Addict Biol. 2012 May;17(3):513-27. doi: 10.1111/j.1369-1600.2012.00454.x. Epub 2012 Mar 28.
9
Medical treatment of alcohol dependence: a systematic review.
Int J Psychiatry Med. 2011;42(3):227-66. doi: 10.2190/PM.42.3.b.
10
Human laboratory paradigms in alcohol research.
Alcohol Clin Exp Res. 2012 Jun;36(6):972-83. doi: 10.1111/j.1530-0277.2011.01704.x. Epub 2012 Feb 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验