Canseco-Alba Ana, Rodríguez-Manzo Gabriela
Departamento de Farmacobiología, Centro de Investigación y de Estudios Avanzados (Cinvestav-Sede Sur), Ciudad de México, México.
Front Behav Neurosci. 2019 Aug 14;13:184. doi: 10.3389/fnbeh.2019.00184. eCollection 2019.
In male rats, copulation to satiety induces a long-lasting sexual inhibitory state, considered to rely on a decreased sexual motivation. Dopaminergic transmission at the mesolimbic system plays a central role in the regulation of male sexual motivation. Endocannabinoids (eCBs) modulate the activity of the mesolimbic system and both dopamine (DA) and cannabinoid receptor activation reverses the sexual inhibition that characterizes sexually satiated rats. The eCB anandamide reverses sexual satiety when systemically administered or infused into the ventral tegmental area (VTA), the region where the activity of mesolimbic dopaminergic neurons is regulated. Thus, it could be thought that sexual motivation is diminished during the long-lasting sexual inhibition of sexually satiated rats and that eCBs reverse that inhibition through the modulation of the dopaminergic system. To test this hypothesis, we assessed the motivational state of sexually satiated male rats and determined if 2-arachidonoylglycerol (2-AG), the most abundant eCB and a full cannabinoid receptor agonist, also reversed the sexual inhibitory state. To establish the possible interaction between 2-AG and anandamide with the dopaminergic system for the reversal of sexual satiety, we analyzed the effects of the co-administration of each eCB and DA receptor agonists or antagonists. Results showed that 24-h after copulation to satiety, when the sexual inhibition is well established, the males' sexual motivation is diminished as measured in the sexual incentive motivation test. 2-AG, similarly to anandamide, reverses sexual satiety through the activation of CB1 receptors and both eCBs interact with the dopaminergic system to reverse the sexual inhibitory state. 2-AG effects are mediated by the modulation of the D2-like DA receptor family, whereas anandamide's effects are clearly mediated by the modulation of the D1-like DA receptor family and the activation of D2-like DA receptors. Present results evidence that a reduced sexual motivation underlies the sexual inhibitory state of sexually satiated rats and support the notion that eCBs reverse sexual satiety by modulating dopaminergic transmission, presumably at the mesolimbic system. Anandamide and 2-AG have a different interaction with D1-like and D2-like DA receptor families. Altogether present data endorse the association of the eCB system with the regulation of the motivational tone at the mesolimbic system.
在雄性大鼠中,交配至满足会诱导一种持久的性抑制状态,这种状态被认为依赖于性动机的降低。中脑边缘系统的多巴胺能传递在雄性性动机的调节中起着核心作用。内源性大麻素(eCBs)调节中脑边缘系统的活动,多巴胺(DA)和大麻素受体的激活均可逆转性满足大鼠所特有的性抑制。当全身给药或注入腹侧被盖区(VTA,中脑边缘多巴胺能神经元活动受调节的区域)时,eCB花生四烯乙醇胺可逆转性满足。因此,可以认为在性满足的大鼠长期性抑制过程中性动机降低,且eCBs通过调节多巴胺能系统来逆转这种抑制。为了验证这一假设,我们评估了性满足的雄性大鼠的动机状态,并确定最丰富的eCB和完全大麻素受体激动剂2-花生四烯酸甘油(2-AG)是否也能逆转性抑制状态。为了确定2-AG和花生四烯乙醇胺与多巴胺能系统之间可能存在的相互作用以逆转性满足,我们分析了每种eCB与DA受体激动剂或拮抗剂联合给药的效果。结果显示,在交配至满足24小时后,当性抑制充分建立时,在性激励动机测试中测得雄性大鼠的性动机降低。与花生四烯乙醇胺类似,2-AG通过激活CB1受体来逆转性满足,且两种eCB均与多巴胺能系统相互作用以逆转性抑制状态。2-AG的作用是通过调节D2样DA受体家族介导的,而花生四烯乙醇胺的作用显然是通过调节D1样DA受体家族和激活D2样DA受体介导的。目前的结果表明,性动机降低是性满足大鼠性抑制状态的基础,并支持eCBs通过调节多巴胺能传递(可能是在中脑边缘系统)来逆转性满足的观点。花生四烯乙醇胺和2-AG与D1样和D2样DA受体家族有不同的相互作用。总之,目前的数据支持eCB系统与中脑边缘系统动机基调调节之间的关联。