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本文引用的文献

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Pharmacokinetic Modeling and Model-Based Hypothesis Generation for Dose Optimization of Clonidine in Neonates With Neonatal Opioid Withdrawal Syndrome.用于新生儿阿片类药物戒断综合征患儿可乐定剂量优化的药代动力学建模与基于模型的假设生成
Clin Pharmacol Ther. 2025 May;117(5):1254-1263. doi: 10.1002/cpt.3507. Epub 2024 Nov 22.
2
Clonidine as Monotherapy for Neonatal Opioid Withdrawal Syndrome: A Randomized Trial.可乐定单药治疗新生儿阿片类戒断综合征的随机试验。
Pediatrics. 2024 Nov 1;154(5). doi: 10.1542/peds.2023-065610.
3
Developmental Outcomes after Opioid Exposure in the Fetus and Neonate.胎儿和新生儿暴露于阿片类药物后的发育结果。
Neoreviews. 2024 Jun 1;25(6):e325-e337. doi: 10.1542/neo.25-6-e325.
4
Pharmacologic profile of ITI-333: a novel molecule for treatment of substance use disorders.ITI-333 的药理学特征:一种用于治疗物质使用障碍的新型分子。
Psychopharmacology (Berl). 2024 Jul;241(7):1477-1490. doi: 10.1007/s00213-024-06578-w. Epub 2024 May 6.
5
Advances in the Care of Infants With Prenatal Opioid Exposure and Neonatal Opioid Withdrawal Syndrome.产前阿片暴露和新生儿阿片戒断综合征婴儿护理的进展。
Pediatrics. 2024 Jan 1;153(2). doi: 10.1542/peds.2023-062871.
6
The Impact of P-Glycoprotein on Opioid Analgesics: What's the Real Meaning in Pain Management and Palliative Care?P-糖蛋白对阿片类镇痛药的影响:在疼痛管理和姑息治疗中的真正意义是什么?
Int J Mol Sci. 2022 Nov 16;23(22):14125. doi: 10.3390/ijms232214125.
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Optimizing a therapy for opiate use disorders: Characterizing ondansetron pharmacokinetics in blood and brain.优化阿片类药物使用障碍的治疗方法:在血液和大脑中表征昂丹司琼的药代动力学。
Clin Transl Sci. 2023 Feb;16(2):216-223. doi: 10.1111/cts.13440. Epub 2022 Nov 9.
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Ondansetron to reduce neonatal opioid withdrawal severity a randomized clinical trial.昂丹司琼减少新生儿阿片类药物戒断严重程度的随机临床试验。
J Perinatol. 2023 Mar;43(3):271-276. doi: 10.1038/s41372-022-01487-2. Epub 2022 Aug 27.
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Selective Targeting of Serotonin 5-HT1a and 5-HT3 Receptors Attenuates Acute and Long-Term Hypersensitivity Associated With Neonatal Procedural Pain.对5-羟色胺5-HT1a和5-HT3受体的选择性靶向作用可减轻与新生儿程序性疼痛相关的急性和长期超敏反应。
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5-羟色胺调节在阿片类药物戒断及新生儿阿片类药物戒断综合征中的作用:机制及潜在的5-羟色胺能靶点

The role of 5-HT modulation in opioid withdrawal and neonatal opioid withdrawal syndrome: mechanisms and potential serotonergic targets.

作者信息

Lam Kevin, Peltz Gary, Kraft Walter K

机构信息

Department of Pharmacology, Physiology, and Cancer Biology, Thomas Jefferson University, Philadelphia, PA, USA.

Department of Anesthesiology, Pain and Perioperative Medicine, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Expert Opin Investig Drugs. 2025 Jan-Feb;34(1-2):49-59. doi: 10.1080/13543784.2025.2462615. Epub 2025 Feb 8.

DOI:10.1080/13543784.2025.2462615
PMID:39900407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11899659/
Abstract

INTRODUCTION

Opioid use disorder and neonatal opioid withdrawal syndrome are persisting consequences of the opioid epidemic in the United States. Current pharmacologic approaches primarily utilize opioid replacement therapy, but non-opioid therapeutics could have advantages. Preclinical and clinical data suggest modulation of the serotonergic system as a novel therapeutic approach in relieving opioid withdrawal syndromes.

AREAS COVERED

Serotonin receptors that have been reported to mediate opioid withdrawal signs based on preclinical findings are identified and described. Extant clinical studies assessing the modulation of these receptors on opioid withdrawal outcomes are then summarized.

EXPERT OPINION

While medications that serve as agonists or antagonists to serotonin receptor subtypes have the potential for treatment of opioid withdrawal and neonatal opioid withdrawal syndrome, much of the evidence is tenuous. The supportive data are mainly derived from preclinical studies, and the measured clinical efficacy has been variable, but reductions in symptom severity are consistently noted. Serotonergic modulation offers a non-opioid pathway to relieving opioid withdrawal manifestations, which is especially useful for neonates as changes in neuroplasticity have been noted with postnatal opioid use. Potential benefits warrant additional studies to clarify the mechanisms for their effect and for measuring how effective these agents are in human disease.

摘要

引言

阿片类药物使用障碍和新生儿阿片类药物戒断综合征是美国阿片类药物流行持续存在的后果。目前的药物治疗方法主要采用阿片类药物替代疗法,但非阿片类治疗方法可能具有优势。临床前和临床数据表明,调节血清素能系统是缓解阿片类药物戒断综合征的一种新的治疗方法。

涵盖领域

根据临床前研究结果,确定并描述了据报道介导阿片类药物戒断症状的血清素受体。然后总结了评估这些受体调节对阿片类药物戒断结果影响的现有临床研究。

专家意见

虽然作为血清素受体亚型激动剂或拮抗剂的药物有可能用于治疗阿片类药物戒断和新生儿阿片类药物戒断综合征,但许多证据并不确凿。支持性数据主要来自临床前研究,所测得的临床疗效各不相同,但症状严重程度的减轻是一致的。血清素能调节为缓解阿片类药物戒断表现提供了一条非阿片类途径,这对新生儿尤其有用,因为已注意到产后使用阿片类药物会导致神经可塑性的变化。潜在的益处值得进一步研究,以阐明其作用机制,并衡量这些药物在人类疾病中的有效性。