Flores-Ramirez Francisco J, Garcia-Carachure Israel, Sanchez David O, Gonzalez Celene, Castillo Samuel A, Arenivar Miguel A, Themann Anapaula, Lira Omar, Rodriguez Minerva, Preciado-Piña Joshua, Iñiguez Sergio D
1 Department of Psychology, The University of Texas at El Paso, El Paso, USA.
2 Department of Psychology, California State University, San Bernardino, USA.
J Psychopharmacol. 2018 Oct 18:269881118805488. doi: 10.1177/0269881118805488.
Preclinical evidence from male subjects indicates that exposure to psychotropic medications, during early development, results in long-lasting altered responses to reward-related stimuli. However, it is not known if exposure to the antidepressant fluoxetine, in female subjects specifically, changes sensitivity to natural and drug rewards, later in life.
The aim of this work was to investigate if exposure to fluoxetine mediates enduring changes in sensitivity to the rewarding properties of cocaine and sucrose, using female mice as a model system.
We exposed C57BL/6 female mice to fluoxetine (250 mg/L in their drinking water) for 15 consecutive days, either during adolescence (postnatal day 35-49) or adulthood (postnatal day 70-84). Twenty-one days later, mice were examined on their behavioral reactivity to cocaine (0, 2.5, 5, 7.5 mg/kg) using the conditioned place preference paradigm, or assessed on the two-bottle sucrose (1%) test.
We found that regardless of age of antidepressant exposure, female mice pre-exposed to fluoxetine displayed reliable conditioning to the cocaine-paired compartment. However, when compared to respective age-matched controls, antidepressant pre-exposure decreased the magnitude of conditioning at the 5 and 7.5 mg/kg cocaine doses. Furthermore, fluoxetine pre-exposure reduced sucrose preference without altering total liquid intake.
The data suggest that pre-exposure to fluoxetine, during adolescence or adulthood, results in a prolonged decrease in sensitivity to the rewarding properties of both natural and drug rewards in female C57BL/6 mice.
来自雄性受试者的临床前证据表明,在早期发育过程中接触精神药物会导致对奖励相关刺激的反应长期改变。然而,尚不清楚在雌性受试者中,特别是接触抗抑郁药氟西汀是否会改变其在生命后期对自然奖励和药物奖励的敏感性。
本研究的目的是使用雌性小鼠作为模型系统,研究接触氟西汀是否会介导对可卡因和蔗糖奖励特性的敏感性的持久变化。
我们将C57BL/6雌性小鼠连续15天暴露于氟西汀(饮用水中浓度为250mg/L),暴露时间分别为青春期(出生后第35 - 49天)或成年期(出生后第70 - 84天)。21天后,使用条件性位置偏爱范式检测小鼠对可卡因(0、2.5、5、7.5mg/kg)的行为反应性,或通过双瓶蔗糖(1%)试验进行评估。
我们发现,无论抗抑郁药暴露的年龄如何,预先接触氟西汀的雌性小鼠对与可卡因配对的隔室表现出可靠的条件反射。然而,与各自年龄匹配的对照组相比,预先接触抗抑郁药会降低在5mg/kg和7.5mg/kg可卡因剂量下的条件反射强度。此外,预先接触氟西汀会降低蔗糖偏好,但不会改变总液体摄入量。
数据表明,在青春期或成年期预先接触氟西汀会导致雌性C57BL/6小鼠对自然奖励和药物奖励的奖励特性的敏感性长期降低。