Xylazine potentiates the interoceptive effects of fentanyl in male and female rats.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Brooke N Bender, Joseph M Carew, Madigan L Bedard, Zoe A McElligott, Joyce Besheer
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引用次数: 0

Abstract

Rationale: Xylazine, a sedative typically used in veterinary medicine, has been increasingly detected as an adulterant in the unregulated opioid supply and present in opioid overdose deaths. Therefore, xylazine-adulterated fentanyl is a growing public health concern. People who use drugs have reported that xylazine changes and prolongs the effects of fentanyl.

Objectives: We used standard operant drug discrimination procedures to better understand how xylazine impacts the discriminative stimulus/interoceptive effects of fentanyl.

Methods: Male and female Long-Evans rats (n = 23) were trained to discriminate fentanyl (0.032 mg/kg intraperitoneal) such that one lever was reinforced with sucrose on days when fentanyl was administered, and the other lever was reinforced when vehicle was administered. Once rats met testing criteria, we tested a dose range of fentanyl to confirm discriminative stimulus control, then we tested if xylazine alone produced fentanyl-like effects and if the addition of xylazine to fentanyl impacted fentanyl interoceptive effects.

Results: Stimulus control was confirmed, as rats showed increased percent responses on the fentanyl-appropriate lever as well as decreased response rates for increasing doses of fentanyl. Xylazine alone did not substitute for the stimulus effects of fentanyl but produced similar response rate reductions as fentanyl alone. Xylazine co-administered with fentanyl potentiated the stimulus effects of lower doses of fentanyl in both males and females and potentiated response rate reductions.

Conclusions: These results indicate that xylazine enhances the interoceptive effects of fentanyl, which may inform clinical research about xylazine-adulterated fentanyl.

二甲嗪增强芬太尼对雌雄大鼠的内感受作用。
理由:甲嗪是一种通常用于兽药的镇静剂,越来越多地被发现是不受管制的阿片类药物供应中的掺假剂,并出现在阿片类药物过量死亡中。因此,掺杂氯嗪的芬太尼是一个日益严重的公共卫生问题。吸毒者报告说,二甲肼改变并延长了芬太尼的效果。目的:采用标准的可操作药物鉴别程序,更好地了解噻嗪如何影响芬太尼的鉴别刺激/内感受效应。方法:对雄性和雌性Long-Evans大鼠(n = 23)进行识别芬太尼(0.032 mg/kg腹腔注射)的训练,在芬太尼给药的当天用蔗糖加强另一水平,在给药的当天用对照物加强另一水平。一旦大鼠达到测试标准,我们测试了芬太尼的剂量范围,以确认区分刺激控制,然后我们测试了羟嗪是否单独产生类似芬太尼的作用,以及羟嗪加入芬太尼是否影响芬太尼的内感受作用。结果:刺激控制得到证实,大鼠在芬太尼适当水平上的反应百分比增加,而芬太尼剂量增加时反应率降低。单独使用噻嗪不能替代芬太尼的刺激作用,但与单独使用芬太尼产生相似的反应率降低。在男性和女性中,与芬太尼合用的噻嗪增强了低剂量芬太尼的刺激作用,并增强了反应率的降低。结论:这些结果表明,羟嗪可增强芬太尼的内感受作用,为临床研究掺杂羟嗪的芬太尼提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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