Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, United States; Translational Neuroscience Program, Wayne State University School of Medicine, Detroit, MI, United States.
Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, United States.
Drug Alcohol Depend. 2021 Dec 1;229(Pt A):109101. doi: 10.1016/j.drugalcdep.2021.109101. Epub 2021 Sep 24.
Although fentanyl has gained widespread prominence, there remains a lack of knowledge on this opioid synthetic agonist, particularly related to sex effects. Therefore, we conducted behavioral tests in female and male rats to measure drug abuse-related responses to fentanyl hypothesizing sex-specific responses.
Using female and male rats, we measured the effects of acute or repeated administration of fentanyl (20 μg/kg) on locomotor activity (LMA) and behavioral sensitization in an open field test. We further measured contextual-reward and associated locomotor activity during training in a conditioned place preference (CPP) paradigm using a low (4 μg/kg) or high (16 μg/kg) dose of fentanyl. Vaginal lavage samples were collected from female rats in the CPP study, and the estrous phase was determined based on the cytological characterization.
Female, but not male, rats showed elevated LMA in response to acute fentanyl and behavioral sensitization to repeated administration of fentanyl. Fentanyl produced significant CPP in both sexes, but it was more potent in males. Finally, our secondary investigation of the estrous cycle on fentanyl-CPP suggests that non-estrus phases, likely reflecting high estradiol, may predict the degree of fentanyl preference in females.
Fentanyl was more potent and/or effective to produce LMA and LMA sensitization in females but more potent to produce CPP in males. Furthermore, the role of sex in fentanyl responses varied across endpoints, and sex differences in LMA were not predictive of sex differences in CPP.
尽管芬太尼已广泛受到关注,但人们对这种阿片类合成激动剂的了解仍然有限,特别是与性别相关的作用机制。因此,我们在雌性和雄性大鼠中进行了行为测试,以测量芬太尼滥用相关的反应,假设存在性别特异性的反应。
使用雌性和雄性大鼠,我们测量了单次或重复给予芬太尼(20μg/kg)对旷场试验中运动活动(LMA)和行为敏化的影响。我们进一步在条件性位置偏好(CPP)范式中使用低(4μg/kg)或高(16μg/kg)剂量的芬太尼测量训练期间的情境奖励和相关的运动活动。在 CPP 研究中从雌性大鼠收集阴道冲洗样本,并根据细胞学特征确定动情期。
雌性大鼠而非雄性大鼠对急性芬太尼表现出升高的 LMA,并且对重复给予芬太尼表现出行为敏化。芬太尼在两性中均产生了显著的 CPP,但在雄性中更为强烈。最后,我们对芬太尼-CPP 中发情周期的二次研究表明,非发情期,可能反映出高雌激素水平,可能预测雌性对芬太尼的偏好程度。
芬太尼在雌性中产生 LMA 和 LMA 敏化的效力更强/或更有效,但在雄性中产生 CPP 的效力更强。此外,性别在芬太尼反应中的作用因终点而异,LMA 中的性别差异不能预测 CPP 中的性别差异。