Psychopharmacology Laboratory, Center for Neuroscience and Behavior, Department of Neuroscience, American University, 4400 Massachusetts Ave, NW, Washington, D.C 20016, USA.
Psychopharmacology Laboratory, Center for Neuroscience and Behavior, Department of Neuroscience, American University, 4400 Massachusetts Ave, NW, Washington, D.C 20016, USA.
Neurotoxicol Teratol. 2021 Jul-Aug;86:106977. doi: 10.1016/j.ntt.2021.106977. Epub 2021 Apr 5.
Methylone's rewarding effects have been well characterized; however, little is known about its aversive effects and how such effects may be impacted by sex. In this context, the present study investigated the aversive effects of methylone (vehicle, 5.6, 10 or 18 mg/kg, IP) in 35 male and 31 female Sprague-Dawley rats assessed by conditioned taste avoidance and changes in body temperature and activity/stereotypies. Methylone induced significant taste avoidance, changes in temperature and increased activity and stereotypies in both males and females. Similar to work with other synthetic cathinones, methylone has aversive effects as indexed by significant taste avoidance and changes in temperature and activity (two characteristics of methylone overdose in humans). The only endpoint for which there were significant sex differences was in general activity with males displaying a faster onset and females displaying a longer duration. Although sex was not a factor with taste avoidance and temperature, separate analyses for males and females revealed different patterns, e.g., males displayed a more rapid acquisition of taste avoidance and females displayed changes in temperature at lower doses. Males displayed a faster onset and females displayed a longer duration of activity (consistent with the analyses considering sex as a factor), while time- and dose-dependent stereotypies did not show consistent pattern differences. Although sex differences were relatively limited when sex was specifically assessed as a factor (or only evident when sex comparisons were made in the patterns of effects), sex as a biological variable in the study of drugs should be made to determine if differences exist and, if evident, the basis for these differences.
3-甲基己基酮的奖赏效应已得到充分的研究,但其厌恶效应及其可能受性别的影响却鲜为人知。在这种情况下,本研究通过条件性味觉回避和体温及活动/刻板行为的变化,来探究 35 只雄性和 31 只雌性 Sprague-Dawley 大鼠对 3-甲基己基酮(载体、5.6、10 或 18mg/kg,腹腔注射)的厌恶效应。3-甲基己基酮引起了显著的味觉回避、体温变化、活动增加和刻板行为,雄性和雌性大鼠均出现了这些现象。与其他合成卡西酮的研究类似,3-甲基己基酮具有厌恶效应,表现为显著的味觉回避、体温变化和活动增加(这是人类 3-甲基己基酮过量的两个特征)。唯一存在显著性别差异的终点是一般活动,雄性大鼠表现出更快的发作,而雌性大鼠表现出更长的持续时间。尽管在味觉回避和体温方面,性别不是一个因素,但对雄性和雌性大鼠进行单独分析,发现了不同的模式,例如,雄性大鼠更快地获得味觉回避,而雌性大鼠在较低剂量时出现体温变化。雄性大鼠表现出更快的发作,而雌性大鼠表现出更长的活动持续时间(与考虑性别为因素的分析一致),而时间和剂量依赖性刻板行为没有表现出一致的模式差异。尽管当性别被专门评估为一个因素时,性别差异相对有限(或者只有在比较不同性别的效应模式时才会发现差异),但在研究药物时,应将性别作为生物学变量来确定是否存在差异,如果存在,差异的基础是什么。