实验者给药Δ9-THC减少了大鼠模型中的尼古丁自我给药

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES Pharmacology Biochemistry and Behavior Pub Date : 2023-10-01 DOI:10.1016/j.pbb.2023.173632
Antony D. Abraham, Jenny L. Wiley, Julie A. Marusich
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引用次数: 0

摘要

背景在美国,尼古丁和大麻的共同使用一直在稳步上升。啮齿动物研究表明,德尔塔-9-四氢大麻酚(THC)可以增加尼古丁的成瘾性,但反复接触THC是否会改变尼古丁的自我给药尚未得到测试。我们假设四氢大麻酚会增加尼古丁的增强作用,并改变尼古丁的摄入。方法成年雄性和雌性Sprague-Dawley大鼠在训练前和训练期间每天用四氢大麻酚(0,3,30mg/kg)治疗14天。大鼠被允许自行服用尼古丁数周,然后通过多次测定含或不含四氢大麻酚预处理的尼古丁剂量-效应曲线来测试其对尼古丁剂量的敏感性。对一组单独的大鼠进行蔗糖固定比例反应训练,并评估四氢大麻酚对行为的影响。结果用药后四氢大麻酚在整个获取和维持过程中减少了雄性和雌性大鼠的尼古丁自我给药,并增加了获取过程中尼古丁摄入稳定率的潜伏期。治疗后四氢大麻酚使尼古丁剂量效应曲线向下移动,治疗前四氢大麻黄酮在较高的尼古丁剂量下抑制反应。与尼古丁不同,对蔗糖的反应不受治疗后四氢大麻酚的影响。用药前四氢大麻酚降低了对蔗糖的反应,尤其是对四氢大麻黄酮缺乏的大鼠。结论用药后重复的四氢大麻酚降低了尼古丁的摄取行为,但不改变蔗糖的反应。因此,疗程后的四氢大麻酚可能会改变对尼古丁的敏感性。在蔗糖和尼古丁研究中,用药前四氢大麻酚治疗均降低了杠杆按压,表明这种作用是非特异性的。这些研究表明,四氢大麻酚可以调节大鼠模型的尼古丁摄入模式。
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Experimenter administered Δ9-THC decreases nicotine self-administration in a rat model

Background

The co-use of nicotine and cannabis has been steadily rising in the United States. Rodent studies suggest that delta-9-tetrahydrocannabinol (THC) could increase addictive qualities of nicotine, but whether repeated THC exposure alters self-administration of nicotine has not been tested. We hypothesized that THC would increase the reinforcing effects of nicotine and alter nicotine intake.

Methods

Adult male and female Sprague-Dawley rats were treated with THC (0, 3, 30 mg/kg) daily for 14 days prior to and during training for intravenous self-administration of nicotine. Rats were allowed to self-administer nicotine for several weeks, then tested for sensitivity to nicotine dose through multiple determinations of a nicotine dose-effect curve with or without THC pretreatment. A separate set of rats were trained on fixed ratio responding for sucrose and assessed for THC effects on behavior.

Results

Post-session THC decreased nicotine self-administration in male and female rats throughout acquisition and maintenance and increased the latency to stable rates of nicotine intake during acquisition. Post-session THC shifted nicotine dose-effect curves downward, and pre-session THC suppressed responding at higher nicotine doses. Unlike nicotine, responding for sucrose was not affected by post-session THC. Pre-session THC decreased responding for sucrose, particularly for THC-naïve rats.

Conclusions

Repeated post-session THC decreased nicotine-taking behaviors but did not alter sucrose responding. Thus, post-session THC may alter sensitivity to nicotine. Pre-session THC treatment decreased lever pressing in both sucrose and nicotine studies, indicating this effect was nonspecific. These studies show that THC modulates patterns of nicotine intake in rat models.

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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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