Department of Psychological Science, Northern Kentucky University, 1 Nunn Drive, Highland Heights, KY 41099, USA.
Department of Biological Sciences, Northern Kentucky University, 1 Nunn Drive, Highland Heights, KY 41099, USA.
Drug Alcohol Depend. 2023 Nov 1;252:110970. doi: 10.1016/j.drugalcdep.2023.110970. Epub 2023 Sep 22.
Individuals with attention-deficit/hyperactivity disorder (ADHD) are more likely to be diagnosed with a substance use disorder; however, the effects of long-term psychostimulant treatment on addiction are mixed. Preclinical studies are useful for further elucidating the relationship between ADHD and addiction-like behaviors, but these studies have focused on male subjects only. The goal of the current study was to determine if early-life administration of methylphenidate (MPH) augments methamphetamine (METH) conditioned place preference (CPP) and/or potentiates reinstatement of CPP in both male and female rats.
Male and female spontaneously hypertensive rats (SHRs) and Wistar-Kyoto rats (WKYs) received either MPH (1.5mg/kg; p.o.) or vehicle (1.0ml/kg) during adolescence (postnatal day [PND] ~29-57). Two weeks after cessation of MPH treatment, rats were tested for METH CPP (1.0mg/kg or 2.0mg/kg; s.c.). Rats were then given extinction sessions. Once rats met extinction criteria, they were tested for reinstatement of CPP following a priming injection of METH (0.25mg/kg; s.c.).
All groups developed METH CPP, except vehicle-treated SHR males and vehicle-treated WKY females conditioned with the higher dose of METH (2.0mg/kg). Female SHRs treated with MPH showed greater reinstatement of METH CPP compared to female SHRs treated with vehicle. Adolescent MPH treatment did not augment the locomotor-stimulant effects of METH in adulthood.
These results demonstrate the importance of considering biological sex when prescribing psychostimulant medications for ADHD as long-term MPH administration may increase the risk of continued drug use in females with ADHD following a period of abstinence.
患有注意力缺陷/多动障碍(ADHD)的个体更有可能被诊断出患有物质使用障碍;然而,长期使用精神兴奋剂治疗对成瘾的影响好坏参半。临床前研究对于进一步阐明 ADHD 与类似成瘾行为之间的关系很有用,但这些研究仅集中在雄性动物身上。本研究的目的是确定在生命早期给予哌醋甲酯(MPH)是否会增强 methamphetamine(METH)条件性位置偏好(CPP),并/或增强雄性和雌性大鼠 CPP 的复吸。
雄性和雌性自发性高血压大鼠(SHRs)和 Wistar-Kyoto 大鼠(WKYs)在青春期(出生后第 29-57 天)接受 MPH(1.5mg/kg;p.o.)或载体(1.0ml/kg)治疗。MPH 治疗停止两周后,大鼠接受 METH CPP 测试(1.0mg/kg 或 2.0mg/kg;s.c.)。然后,大鼠进行消退测试。一旦大鼠达到消退标准,它们就会接受 METH (0.25mg/kg;s.c.)引发的 CPP 复吸测试。
除了接受 METH(2.0mg/kg)高剂量处理的雄性 SHR 大鼠和接受载体处理的雌性 WKY 大鼠外,所有组均形成 METH CPP。与接受载体处理的 SHR 大鼠相比,接受 MPH 处理的雌性 SHR 大鼠表现出更大的 METH CPP 复吸。青春期 MPH 治疗不会增强成年后 METH 的运动兴奋剂效应。
这些结果表明,在为 ADHD 患者开具精神兴奋剂药物时,考虑到生物学性别非常重要,因为长期 MPH 治疗可能会增加 ADHD 女性在戒断期后继续使用药物的风险。