Department of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario N6A5C1, Canada.
J Neurosci. 2011 Nov 9;31(45):16473-82. doi: 10.1523/JNEUROSCI.4013-11.2011.
Methamphetamine (Meth) users report having heightened sexual pleasure, numerous sexual partners, and engaging in unprotected sex due to loss of inhibitory control. This compulsive sexual behavior contributes to increased prevalence of sexually transmitted infections, but the neural basis for this is unknown. We previously established a paradigm for compulsive sexual behavior in male rats in which visceral illness induced by lithium chloride was paired with sexual behavior (Davis et al., 2010; Frohmader et al., 2010a). The current study examined the effects of repeated Meth administration on sexual performance, compulsive sexual behavior, and sex or Meth reward. First, results demonstrated that seven daily administrations of 2 mg/kg, but not 1 mg/kg, Meth increased latencies to initiate mating. This impairment was evident 30 min after last Meth administration, but dissipated after 1 or 7 d of subsequent drug abstinence. Repeated 1 mg/kg Meth exposure resulted in compulsive sex-seeking behavior 2 weeks following last Meth administration. This effect was dependent on Meth administration being concurrent with sexual experience and was not observed in sexually experienced animals that received Meth alone. Moreover, concurrent Meth and sexual experience enhanced conditioned place preference (CPP) for Meth, and for concurrent Meth and mating compared with Meth or mating alone. In contrast, CPP for mating alone was decreased. Together, these data indicate that the association between drug use and mating may be required for expression of compulsive sexual behavior and is correlated with increased reward seeking for concurrent Meth exposure and mating.
甲基苯丙胺(冰毒)使用者报告称,由于抑制控制的丧失,他们会有更高的性快感、更多的性伴侣,并进行无保护性行为。这种强迫性行为导致性传播感染的发病率增加,但这种行为的神经基础尚不清楚。我们之前建立了一个雄性大鼠强迫性性行为的范式,即在锂盐引起的内脏疾病与性行为配对(Davis 等人,2010 年;Frohmader 等人,2010a)。本研究考察了重复给予甲基苯丙胺对性行为表现、强迫性性行为以及性或甲基苯丙胺奖励的影响。首先,结果表明,每天给予 2 毫克/千克、而不是 1 毫克/千克的甲基苯丙胺 7 次,会延长开始交配的潜伏期。这种损伤在最后一次甲基苯丙胺给药后 30 分钟明显,但在随后的 1 或 7 天药物戒断后消失。重复给予 1 毫克/千克的甲基苯丙胺暴露会导致在最后一次甲基苯丙胺给药后 2 周出现强迫性性行为。这种影响取决于甲基苯丙胺的给药与性经验同时进行,并且在单独接受甲基苯丙胺的有性经验的动物中没有观察到。此外,同时给予甲基苯丙胺和性经验会增强对甲基苯丙胺的条件性位置偏好(CPP),以及对同时给予甲基苯丙胺和交配的 CPP,而单独给予交配的 CPP 则减少。总之,这些数据表明,药物使用和交配之间的关联可能是表达强迫性性行为所必需的,并且与增强对同时给予甲基苯丙胺暴露和交配的奖励寻求有关。